Institut de Chimie Moléculaire et des Matériaux d'Orsay

Laboratoire de Catalyse Moléculaire - LCM

HENRI B. KAGAN


Professeur Emerite
Equipe de Catalyse Moléculaire-ICMMO - Bât 420
Université Paris-Sud 11
15, rue Georges Clemenceau
91405 Orsay Cedex
FRANCE

Tél : 01.69.15.78.95
Fax : 01.69.15.46.80
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publications

Annual Index : 1956-1960, 61-65, 66-70, 71-75, 76-80, 81-85,86-90,91, 92, 93, 94, 95, 96, 97, 98, 99, 2000-2011

1956 - 1960

(1) Sur la dismutation de certains dérivés dihydro-naphtaléniques et dihydro-phénanthréniques.
J. Jacques, H. B. Kagan, Bull. Soc. Chim. Fr, 1956, 128.

(2) Préparation et propriétés de quelques dioxolanes dérivés des acides biliaires.
H. B. Kagan, J. Jacques, Bull. Soc. Chim. Fr. , 1957, 699.

(3) Nouveaux dérivés d'acides biliaires: acides D6 choléniques et acides 6,7-dihydroxy-cholaniques.
H. B. Kagan, C. R. Acad. Sciences, Paris, 1957, 244, 1373.

(4) Acide 3a-hydroxy D6 cholénique et acide 3 a , 6 a, 7a-trihydroxy-cholanique.
H. B. Kagan, J. Jacques, C. R. Acad. Sciences, Paris, 1957, 245, 2417.

(5) Note sur les quelques essais concernant la préparation de stéroïdes possédant un noyau B "ouvert".
H. B. Kagan, J. Jacques, Bull. Soc. Chim. Fr., 1958, 1600.

(6)Sur la bromuration des cétals cycliques.
A. Marquet, H. B. Kagan, M. Dvolaitzky, L. Mamlok, C. Weidman, J. Jacques.
C. R. Acad. Sciences, Fr., 1959, 248, 984.

(7)Un nouveau type de stéroïdes modifiés: "Les stéroïdes inversés". Synthèse d'une "cortisone inversée".
H. B. Kagan, C. R. Acad. Sciences, Paris, 1960, 250, 1738.

(8)Stéroïdes inversés - I. Introduction générale.
H. B. Kagan, Bull. Soc. Chim. Fr., 1960, 535.

(9) Stéroïdes inversés - II. Dérivés du (5a) androstane substitué en 3 par un groupe éthynyle, vinyle ou éthyle.
A. Marquet, H. B. Kagan, M. Dvolaitzky, J. Lematre, J. Jacques,
Bull. Soc. Chim.Fr., 1960, 539.

(10) Acides biliaires comportant des hydroxyles en positions 6 et 7.
H. B. Kagan, J. Jacques, Bull. Soc. Chim. Fr, 1960, 871.

(11) Stéroïdes inversés - III. Dérivés du (5a) androstane possédant en 3 une chaine dihydroxyacétonique.
H. B. Kagan, A. Marquet, J. Jacques, Bull. Soc. Chim.Fr., 1960, 1079.

(12) Stéroïdes inversés - IV. Première approximation d'une cortisone inversée.
H. B. Kagan, J. Jacques, Bull. Soc. Chim. Fr., 1960, 1551.


Annual Index
1961 - 1965

(13) Stéroïdes inversés - V. Progestérone et désoxycorticostérone inversés. Dérivés de l'androstane possédant en 3 une chaine acétyle ou acétoxycétyle.
M. Dvolaitzky, H. B. Kagan, J. Jacques, Bull. Soc. Chim. Fr., 1961, 598.

(14) Halogénation par les perhalogénures d'ammonium quaternaires dans le tétrahydrofuranne. -1. Choix d'un réactif, bromuration des cétals cycliques.
A. Marquet, M. Dvolaitzky, H. B. Kagan, L. Mamlok, C. Ouannes, J. Jacques, Bull. Soc. Chim.Fr., 1961, 1822.

(15) Action du réactif de Réformatsky sur les nitriles - Structures des soi-disants "acidylimines b-esters obtenus".
A. Horeau, J. Jacques, H. B. Kagan, Y. Heng Suen, C. R. Acad. Sciences, Paris, 1962, 255, 717.

(16) Influence du noyau A et effet du solvant sur la vitesse de saponification d'esters d'hydroxy-17 b stéroïdes.
Tran-Luu-Kim-Phuong, H. B. Kagan, C. R. Acad. Sciences, Paris, 1963, 256, 4036.

(17) Synthèse d'acides seco-doisynolique et seco homo deshydro-doisynolique.
J. C. Dubois, A. Horeau, H. B. Kagan, C. R. Acad. Sciences, Paris, 1963, 256, 5596.

(18) Stéréochimie en série b -lactame: stéréochimie de la réaction de Réformatsky sur les bases de Schiff.
H. B. Kagan, J. J. Basselier, J. L. Luche, Tetrahedron Lett., 1964, 5, 941.

(19) Détermination des configurations par la méthode du dédoublement partiel - IV. Alcools stéroïdes.
A. Horeau, H. B. Kagan, Tetrahedron, 1964, 20, 2431.

(20) Iminomagnésiens - I. Action sur les chlorures d'acide.
Y-Heng Suen, A. Horeau, H. B. Kagan, Bull. Soc. Chim. Fr., 1965, 1454.

(21) Iminomagnésiens - II. Action sur les esters.
H. B. Kagan, A. Horeau, Y-Heng Suen, Bull. Soc. Chim., 1965, 1457.

(22) Iminomagnésiens - III. Propriétés d'acylimines et acylénamines.
Y-Heng Suen, H. B. Kagan, Bull. Soc. Chim. Fr., 1965, 1460.

(23) Méthodes d'études de substances actives sur le métabolisme du cholestérol- II. Application à quelques dérivés de l'androstane.
L. Chevillard, C. Bournique, H. B. Kagan, R. Portet, Thérapie, 1965, XX, 371.

(24) Psilostachyin, a new type of sesquiterpene lactone.
H. E. Miller, H. B. Kagan, W. Renold, T. J. Mabry, Tetrahedron Lett., 1965, 6, 3397.


Annual Index
1966 - 1970

(25) The structure of Ambrosiol, a new sesquiterpene lactone from Ambrosia Psilostachya.
T. J. Mabry, H. E. Miller, W. Renold, H. B. Kagan, J. Org. Chem., 1966, 31, 681.

(26) The structure of Psilostachyin, a new sesquiterpene Dilactone from A. Psilostachya.
T. J. Mabry, H. E. Miller, H. B. Kagan, W. Renold, Tetrahedron, 1966, 22, 1139.

(27) Psilostachyin B, a new sesquiterpene Dilactone from A. Psilostachya.
T. J. Mabry, H. B. Kagan, H. E. Miller, Tetrahedron, 1966, 22, 1948.

(28) The structure of Psilostachyin C, a new sesquiterpene Dilactone from A. Psilostachya.
H. B. Kagan, H. E. Miller, W. Renold, M. V. Laksmikantham, L. R. Tether, W. Herz, T. J. Mabry, J. Org. Chem., 1966, 31, 1629.

(29) Réaction de Réformatsky sur les nitriles - I. Préparation de cétoesters non substitués, mono ou disubstitués en a.
H. B. Kagan, Y-Heng Suen, Bull. Soc. Chim. Fr., 1966, 1819.

(30) Réaction de Réformatsky sur les nitriles - II. Structure des produits secondaires obtenus à partir des esters a -bromoisobutyriques.
A. Horeau, J. Jacques, H. B. Kagan, Y-Heng Suen, Bull. Soc. Chim. Fr., 1966, 1823.

(31) Addition 1,4 du réactif de Réformatsky sur les cétones éthyléniques.
J. C. Dubois, J. P. Guetté, H. B. Kagan, Bull. Soc. Chim. Fr., 1966, 3008.

(32) Determination of absolute configuration of hydroxylated sesquiterpene lactones by Horeau's method of asymmetric esterification.
W. Herz, H. B. Kagan, J. Org. Chem., 1967, 32, 216.

(33) Structure et activité oestrogène - XXV. Synthèse d'acides seco-11,23 doisynoliques.
J. C. Dubois, A. Horeau, H. B. Kagan, Bull. Soc. Chim. Fr., 1967, 1827.

(34) Stéréochimie dans la série des b-lactames - II. Influence de la stéréoisomérie sur la fragmentation en spectrométrie de masse. Etude d'isomères cis-trans de [beta]-lactames substituées.
H. E. Audier, M. Fetizon, H. B. Kagan, J. L. Luche, Bull. Soc. Chim. Fr., 1967, 2297.

(35) Stereochemistry in the b -lactam series - III.
J. L. Luche, H. B. Kagan, R. Parthasarathy, G. Tsoucaris, C. de Rango, C. Zelwer; Tetrahedron, 1968, 24, 1275.

(36) Stéréochimie en série b -lactame - IV. Cycloaddition d'aldocétènes sur la benzalaniline.
J. L. Luche, H. B. Kagan, Bull. Soc. Chim. Fr., 1968, 2450.

(37) Cycloaddition des cétènes sur les imines - II. Mise en évidence d'un intermédiaire de réaction au cours de l'addition diphénylcétène-benzalaniline.
H. B. Kagan, J. L. Luche, Tetrahedron Lett., 1968, 9, 3093.

(38) The dehydration of Coronopilin.
J. Kagan, H. B. Kagan, J. Org. Chem., 1968, 33, 2807.

(39) Synthèses asymétriques par double induction.
A. Horeau, H. B. Kagan, J. P. Vigneron, Bull. Soc. Chim. Fr., 1968, 3795.

(40) Synthèse asymétrique de l'acide aspartique optiquement pur.
J. P. Vigneron, H. B. Kagan, A. Horeau, Tetrahedron Lett., 1968, 9, 5681.

(41) The structure of Tamaulipin A, a new germacranolide from Ambrosia Confertiflora Dc. (Compositae).
N. H. Fisher, T. J. Mabry, H. B. Kagan, Tetrahedron, 1968, 24, 4091.

(42) Stéréochimie en série b -lactame - V. Effet isotopique du deutérium et mécanisme des réactions de Réformatsky ou des cétènes sur les bases de Schiff.
J. L. Luche, H. B. Kagan, Bull. Soc. Chim. Fr., 1969, 1680.

(43) Stéréochimie en série b -lactame - VI. Réaction de Réformatsky sur les bases de Schiff.
J. L. Luche, H. B. Kagan, Bull. Soc. Chim., 1969, 3500.

(44) Réduction de l'acétophénone par des amine-boranes optiquement actifs.
J. C. Fiaud, H. B. Kagan, Bull. Soc. Chim.. Fr., 1969, 2742.

(45) Synthèse totale de stéroïdes - II. Synthèse dans la série de l'oestrone.
A. Horeau, L. Ménager, H. B. Kagan, C. R. Acad. Sciences, Paris, 1968, 269, 602.

(46) Détermination du pouvoir rotatoire maximum de la méthyl-2 cyclohexanone par corrélation directe avec la méthyl-3 cyclohexanone.
J. Barry, A. Horeau, H. B. Kagan, Bull. Soc. Chim. Fr., 1969, 989.

(47) Préparation du t-butyl-2 méthylène cyclohexane, des cis et trans méthyl-1 t-butyl-2 cyclohexanols et de leurs produits de deshydratation.
Y-Heng Suen, H. B. Kagan, Bull. Soc. Chim. Fr., 1969, 2270.

(48) Application de la méthode du dédoublement partiel en série stéroïde - II. Mise en évidence d'un effet à longue distance sur les hydroxy-3b D5 stéroïdes.
G. Balavoine, A. Horeau, H. B. Kagan, Bull. Soc. Chim. Fr., 1969, 1910.

(49) Une nouvelle synthèse d'a-amino acides. Synthèse asymétrique de l'alanine.

J. C. Fiaud, H. B. Kagan, Tetrahedron Lett., 1969, 10, 1813.

(50) Narcissistic reactions.
L. Salem, J. Durup, G. Bergeron, X. Chapuisat, H. B. Kagan, J. Am. Chem. Soc., 1969, 92, 4472.

(51) Conformational analysis by X-ray crystallography. Prelog's rule and conformation of (-) menthyl p-bromophenylglyoxylate.
R. Parthasarathy, A. Horeau, H. B. Kagan, J. P. Vigneron, Tetrahedron,1969, 26, 4705.

(52) Cycloaddition des cétènes sur les bases de Schiff - III. Détermination par RMN de la configuration de triphényl-1,3,4 alcoyls-3 azétidinones-2.
J. Decazes, J. L. Luche, H. B. Kagan, Tetrahedron Lett, 1969, 10, 3361.

(53) Cycloaddition des cétènes sur les bases de Schiff - IV. Stéréochimie de l'addition des aldocétènes sur la benzalaniline.
J. Decazes, J. L. Luche, H. B. Kagan, Tetrahedron Lett., 1969, 10, 3665.

(54) Spectroscopie RMN dans la série des glucides en présence de chélates de terres rares.
P. Girard, H. B. Kagan, S. David, Bull. Soc. Chim.Fr., 1970, 4515.

(55) Stabilité relative de cyclohexènes isomères par la position de la double liaison. Equilibre entre cyclohexènes 1,3 et 1,5 substitués.
Y-Heng Suen, H. B. Kagan, Bull. Soc. Chim.Fr., 1970, 3552.


Annual Index
1971 - 1975

(56) The asymmetric synthesis of hydratropic acid and amino-acids by homogeneous catalytic hydrogenation.
T. P. Dang., H. B. Kagan, Chem. Comm., 1971, 481.

(57) Photochemistry with circularly polarized light. The synthesis of optically active hexahelicene.
A. Moradpour, J. F. Nicoud, G. Balavoine, G. Tsoucaris, H. B. Kagan,
J. Am. Chem. Soc., 1971, 93, 2353.

(58) Intérêt des structures hélicoîdales en synthèse asymétrique par la lumière polarisée circulairement.
G. Tsoucaris, G. Balavoine, A. Moradpour, J. F. Nicoud, H. B. Kagan,
C. R. Acad. Sciences,Paris, 1971, 272, Série B, 1271.

(59) Photochemistry with circularly polarized light - II. Asymmetric synthesis of octa and nona helicene.
H. B. Kagan, A. Moradpour, J. F. Nicoud, O. Balavoine, R. H. Martin, J. P. Cosyn,
Tetrahedon Lett., 1971, 12, 2479.

(60) Alcaloïdes stéroïdiques - Attribution en RMN des protons d'un système AB par complexation avec Eu(dpm)3.
G. Lukacs, X. Lusinchi, P. Girard, H. B. Kagan, Bull. Soc. Chim. Fr., 1971, 3200.

(61) Synthèse asymétrique d'acides aminés. Etude de l'addition d'organométalliques sur les imines glyoxyliques.
J. C. Fiaud, H. B. Kagan, Tetrahedron Lett., 1971, 12, 1019.

(62) Une nouvelle synthèse asymétrique de l'alanine par insertion d'un carbène sur une liaison NH.
J. F. Nicoud, H. B. Kagan, Tetrahedron Lett., 1971, 12, 2065.

(63) Influence de stéroïdes substitués en 3 par une chaine carbonée, sur la synthèse des enzymes induites par Pseudomonas testosteroni. Y. M. Briand, G. Balavoine, H. B. Kagan, J. P. Vigneron, Eur. J. Biochem., 1971, 19, 219.

(64) Spectroscopie RMN de quelques dérivés de sucres en présence de chélates de terres rares.
P. Girard, H. B. Kagan, S. David, Tetrahedron, 1971, 27, 5911.

(65) Stéréochimie de l'acylation du (-)-menthol par le phényléthylcétène.
G. Balavoine, H. B. Kagan, C. R. Acad. Sciences, Paris, 1971, 272, Série C, 1511.

(66) Quelques compléments concernant l'addition de réactifs de Réformatsky sur les imines.
J. L. Luche, H. B. Kagan, Bull. Soc. Chim. Fr., 1971, 2260.

(67) Synthèse de méthyl-tétralones-1 et de méthyl-tétralines optiquement actives. Etude de leurs conformations par dichroïsme circulaire.
J. Barry, H. B. Kagan, G. Snatzke, Tetrahedron, 1971, 27, 4747.

(68) Synthèses totales de stéroïdes - III. Synthèse dans la série de l'oestrone.
A. Horeau, L. Ménager, H. B. Kagan, Bull. Soc. Chim. Fr., 1971, 3571.

(69) Conformational analysis by X-ray crystallography - III. Geometry and the conformation of trans-4-t-butylcyclohexanol parabromobenzoate.
R. Parthasarathy, J. Ohrt, H. B. Kagan, J. C. Fiaud, Tetrahedron, 1972, 28, 1529.

(70) Chromatographie en phase vapeur d'hélicènes et de diaryl-1,2 éthylènes.
J. F. Nicoud, A. Moradpour, G. Balavoine, H. B. Kagan, R. H. Martin, M. Deblecker, J. of Chromat., 1972, 66, 43.

(71) Asymmetric catalytic reduction with transition metal complexes. -I. A catalytic system of rhodium(I) with (-)-2,3-O-isopropylidene-2,3-dihydroxy-1,4-(diphenylphosphino)butane, a new chiral diphosphine., H. B. Kagan, T. P. Dang,
J. Am. Chem. Soc., 1972, 94, 6429.

(72) Synthèse asymétrique stéréospécifique: préparation quantitative de l'acide aspartique optiquement pur.
J. P. Vigneron, A. Horeau, H. B. Kagan, Bull. Soc. Chim. Fr., 1972, 3836.

(73) Cycloaddition of ketenes with Schiff bases -V. Structure and stereochemistry of adducts formed in liquid SO2.
J. M. Decazes, J. L. Luche, H. B. Kagan, R. Parthasarathy, J. Ohrt, Tetrahedron Lett., 1972, 13, 3838.

(74) Préparation d'une diphosphine chirale liée à une résine polystyrène insoluble et exemple d'utilisation en catalyse asymétrique.
J. C. Poulin, W. Dumont, T. P. Dang, H. B. Kagan, C. R. Acad. Sciences, Paris, 1973, C, 277, 41.

(75) Le brome en insertion dans le graphite, un composé de bromation en chimie organique.
A. Page-Lecuyer, J. L Luche, H. B. Kagan, C. Colin, C. Mazière,
Bull. Soc. Chim. Fr., 1973, 1690.

(76) Photoactivation optique du méthyl p-tolyl sulfoxyde racémique par emploi d'un sensibilisateur chiral.
G. Balavoine, S. Jugé, H. B. Kagan, Tetrahedron Lett., 1973, 14, 4159.

(77) Asymmetric catalytic reduction with transition metal complexes - II. Asymmetric catalysis by a supported chiral rhodium complex.
W. Dumont, J. C. Poulin, T. P. Dang, H. B. Kagan, J. Am. Chem. Soc., 1973, 95, 8295.

(78) Synthèse asymétrique d'amines par hydrosilylation d'imines catalysées par un complexe chiral du rhodium.
N. Langlois, T. P. Dang, H. B. Kagan, Tetrahedron Lett., 1973, 14, 4865.

(79) a-Chloration de bromures d'alkyles par le pentachlorure d'antimoine.
J. L. Luche, J. Bertin, H. B. Kagan, Tetrahedron Lett., 1974, 15, 759.

(80) Réactifs en insertion dans le graphite. Réactivité du système graphite pentachlorure d'antimoine.
J. Bertin, J. L. Luche, H. B. Kagan, R. Setton, Tetrahedron Lett., 1974, 15, 763.

(81) Preparation of chiral compounds of high optical purity by irradiation with circularly polarized light, a model reaction for the prebiotic generation of optical activity.
G. Balavoine, A. Moradpour, H. B. Kagan, J. Am. Chem. Soc., 1974, 86, 5152.

(82) Can circularly polarized light be used to obtain chiral compounds of high optical purity ?.
H. B. Kagan, G. Balavoine, A. Moradpour, J. Mol. Ev. 1974, 4, 41.

(83) Graphite electrolytic lamellar reagents in organic chemistry. Esterification in the presence of graphite bisulfate.
J. Bertin, H. B. Kagan, J. L. Luche, R. Setton, J. Am. Chem. Soc., 1974, 96, 2113.

(84) Hydrogénation catalytique homogène à l'aide de complexes rhodium-diphosphines.
J. C. Poulin, T. P. Dang, H. B. Kagan, J. Organometal. Chem., 1975, 84, 87.

(85) Réduction asymétrique catalysée par des complexes de métaux de transition - III. Diphosphines chirales dérivées de l'isopropylidène dihydroxy-2,3 bis (diphényl phosphino)-1,4 butane (DIOP).
H. B. Kagan, N. Langlois, T. P. Dang, J. Organomet. Chem., 1975, 90, 353.

(86) Détermination de la configuration absolue des énantiomères de sulfoxydes racémiques par dédoublement cinétique.
S. Jugé, H. B. Kagan, Tetrahedron Lett., 1975, 16, 2733.

(87) Lanthanide reagents in organic chemistry. A convenient catalytic oxidation of benzoins to benzils using lanthanum nitrates.
P. Girard, H. B. Kagan, Tetrahedron Lett., 1975, 16, 4513.

(88) Photochemistry with circularly polarized light - III. Synthesis of helicenes using bis (arylvinyl) arenes as precursors.
A. Moradpour, H. B. Kagan, M. Baes, G. Marrens, R. H. Martin, Tetrahedron, 1975, 31, 2139.

(89) Asymmetric catalysis by chiral rhodium complexes in hydrogenation and hydrosilylation reactions.
H. B. Kagan, Pure App. Chem., 1975, 43, 3.

 

Annual Index
1976 - 1980

(90) Catalyse asymétrique avec des complexes chiraux de rhodium DIOP - V. Effets des substituants lors de la réduction d'acides N-acylamino-cinnamiques.
G. Gelbard, H. B. Kagan, R. Stern, Tetrahedron, 1976, 32, 233.

(91) Graphite insertion compounds as chemical reagents in organic chemistry.
H. B. Kagan, Pure Appl Chem, 1976, 46, 177.

(92) Catalyse asymétrique et structure du complexe IrCOD((+)-DIOP)Cl.
S. Brunie, J. Mazan, N. Langlois, H. B. Kagan, J. Organometal. Chem., 1976, 114, 225.

(93) Catalyse asymétrique par le complexe cationique [Rh(COD)(+)-DIOP]+ClO4-.
D. Sinou, H. B. Kagan, J. Organometal. Chem., 1976, 114, 325.

(94) A new preparation of some divalent lanthanides iodides and their usefulness in organic synthesis.
J. L. Namy, P. Girard, H. B. Kagan, Nouv. J. Chim., 1977, I, 5.

(95) Nouveaux exemples d'utilisation du bisulfate de graphite et du nitrate de graphite en synthèse organique.
J. P. Alazard, H. B. Kagan, R. Setton, Bull. Soc. Chim. Fr., 1977, 499.

(96) A new case of asymmetric synthesis using circularly polarized light
F. Nicoud, H. B. Kagan, Israel J. Chem., 1977, 15, 78.

(97) Photochemistry with circularly polarized light of a ketone of a reportedly unusually high optical activity.
J. F. Nicoud, C. Eskenazi, H. B. Kagan, J. Org. Chem., 1977, 42, 4270.

(98) Determination of stereochemistry by chemical correlation methods.
J. C. Fiaud, H. B. Kagan, in Stereochemistry, Fundamentals and Methods, 1977, Vol.3, 1, H. B. Kagan Ed., Georg Thieme Verlag (Stuttgart, 1977).

(99) Synthesis of new ligands for transition metal complexes: menthyl and neomenthyl-cyclopentadienes.
E. Cesarotti, H. B. Kagan, R. Goddard, C. Krueger, J. Organometal. Chem., 1978, 162, 297.

(100) A graphite supported chiral catalyst.
H. B. Kagan, T. Yamagishi, J. C. Motte, R. Setton, Israel J. Chem., 1978, 17, 274.

(101) Asymmetric catalysis with chiral complexes of Rhodium-O-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)-butane - V. On the mechanism of reduction of (E,Z)-a-acylaminocinnamic acids with homogeneous rhodium catalysts.
C. Detellier, G. Gelbard, H. B. Kagan, J. Am. Chem. Soc., 1978, 100, 7556.

(102) Hydrogen production by visible light irradiation of aqueous solutions of Ru(bipy)32+.
A. Moradpour, E. Amouyal, P. Keller, H. B. Kagan, Nouv. J. Chim., 1978, 2, 547.

(103) Spin trapping experiments on an hydrosilylation catalytic system, mechanistic implications.
J. F. Peyronel, H. B. Kagan, Nouv. J. Chim., 1978, 2, 211.

(104) Asymmetric catalytic allylation of b-diketones or b-ketoesters with allylic ethers using a palladium-diop catalyst: a mechanistic study.
J. C. Fiaud, A. Hibon de Gournay, M. Larchevêque, H. B. Kagan, J. Organometal. Chem., 1978, 154, 175.

(105) Asymmetric hydrosilylation.
H. B. Kagan, J. F. Peyronel, T. Yamagishi, in Inorganic Compounds with Unusual Properties II, R. B. King Ed., Advances in Chem. Series, 1979, 173, 50, (Am. Chem. Soc.).

(106) Asymmetric induction in cholesteric media revisited.
C. Eskenazi, J. F. Nicoud, H. B. Kagan, J. Org. Chem., 1979, 44, 995.

(107) Synthesis of new chiral phosphines for asymmetric catalysis.
H. B. Kagan, J. C. Fiaud, C. Hoornaert, D. Meyer, J. C. Poulin, Bull. Soc. Chim. Belg., 1979, 88, 923.

(108) Complexes with chiral alkylcyclopentadienyl ligands for homogeneous catalytic hydrogenation of 2-phenyl-1-butene.
E. Cesarotti, R. Ugo, H. B. Kagan, Angew. Chem. Intern Ed. Engl., 1979, 18, 770.

(109) Asymmetric epoxidation of simple olefins with an optically active molybdenum (VI) peroxo complex.
H. B. Kagan, H. Mimoun, C. Mark, V. Schurig, Angew. Chem. Intern. Ed. Engl., 1979, 18, 485.

(110) Synthesis of phellanphos, an efficient chiral 1,2-diphosphine for asymmetric catalysis.
M. Lauer, O. Samuel, H. B. Kagan, J. Organometal. Chem., 1979, 177, 309.

(111) Storage of light energy by chemical systems: comment on long-term efficiency of iterative cyclic reactions.
O. Samuel, A. Moradpour, H. B. Kagan, Solar Energy, 1979, 23, 543.

(112) Synthèse asymétrique de dipeptides par réduction d'un bisdéhydro-peptide.
J. C. Poulin, D. Meyer, H. B. Kagan C. R. Acad. Sciences,Paris, 1980, C, 291, 69.

(113) Etablissement de la courbe de Karplus 3J(P-P) caractéristique des sulfures de diphosphines.
R. Couffignal, H. B. Kagan, F. Mathey, O. Samuel, C. Santini, C. R. Acad. Sciences, Paris, 1980, C, 291, 29.

(114) Asymmetric hydrosilylation of ketones catalysed by chiral rhodium complexes.
J. F. Peyronel, J. C. Fiaud, H. B. Kagan, J. Chem. Res., (S), 1980, (M), 1980, 4057-4080.

(114) The use of (-) diop and the cluster Rh6CO16 as a catalyst precursor in asymmetric hydrogenation.
G. Balavoine, T. P. Dang, C. Eskenazi, H. B. Kagan, J. Mol. Cat., 1980, 7, 531.

(115) Chiral ligands in asymmetric catalysis by transition metal complexes.
H. B. Kagan, in Ann. N. Y. Acad. Sciences, 1980, 333, 1.

(116) Hydrogen production by visible-light using viologen-dye mediated redox cycles.
P. Keller, A. Moradpour, E. Amouyal, H. B. Kagan, Nouv. J. Chim., 1980, 4, 377.

(117) Divalent lanthanide derivatives in organic synthesis - I. Mild preparation of SmI2 and YbI2 and their use as reducing or coupling agents.
P. Girard, J. L. Namy, H. B. Kagan, J. Am. Chem. Soc., 1980, 102, 2693.

(118) Selective fluorination by C19XeF6.
S. S. Yemul, H. B. Kagan, R. Setton, Tetrahedron Lett., 1980, 21, 287.

(119) Stereoselective synthesis of dipeptides by asymmetric reduction of dehydropeptides catalyzed by chiral rhodium complexes.
D. Meyer, J. C. Poulin, H. B. Kagan, H. Levine-Pinto, J. L. Morgat, P. Fromageot, J. Org. Chem., 1980, 45, 4680.

(120) Structure cristalline du complexe [FeCp((-)DIOP)I], analyse conformationnelle du cycle de chélation de la (-)-DIOP.
G. Balavoine, S. Brunie, H. B. Kagan, J. Organometal. Chem., 1980, 187.

(121) Visible-light photoreduction of water. Hydrogen formation yields as a function of the structure of the viologen-dye relays.
P. Keller, A. Moradpour, E. Amouyal, H. B. Kagan, J. Mol. Cat, 1980, 7, 539.


Annual Index
1981 - 1985

(122) Phellanphos and nopaphos, new diphosphines for asymmetric catalysis.
O. Samuel, R. Couffignal, M. Lauer, S. Y. Zhang, H. B. Kagan, Nouv. J. Chim., 1981, 5, 15.

(123) Divalent lanthanide derivatives in organic synthesis - II. Mechanism of SmI2 reactions in presence of ketones and organic halides.
H. B. Kagan, J. L. Namy, P. Girard, Tetrahedron, 1981, 37, suppl. ndeg.1, 175.

(124) Smooth synthesis and characterization of divalent samarium and ytterbium derivatives.
J. L. Namy, P. Girard, H. B. Kagan, P. E. Caro, Nouv. J. Chim., 1981, 8, 479.

(125) An easy coupling of acid chlorides into a-diketones promoted by diiodosamarium.
P. Girard, R. Couffignal, H. B. Kagan, Tetrahedron Lett., 1981, 22, 3959.

(126) Cyclodiop, an example of a new class of chiral diphosphines.
S. Y. Zhang, S. Yemul, H. B. Kagan, R. Stern, D. Commereuc, Y. Chauvin, Tetrahedron Lett., 1981, 22, 3955.

(127) Synthesis of enantiomers of 1,2-heptanediol.
J. Barry, H. B. Kagan, Synthesis, 1981, 453.

(128) Samarium diiodide as coupling agent between aldehydes and organic halides for the synthesis of homoallylic and homobenzylic alcohols.
J. Souppe, J. L. Namy, H. B. Kagan, Tetrahedron Lett., 1982, 23, 3497.

(129) Asymmetric tritiation of N-acetyl dehydrophenylalanyl-(S)-phenylalanine methyl ester catalyzed with a rhodium-(+)-DIOP complex.
H. Levine-Pinto, J. L. Morgat, P. Fromageot, D. Meyer, J. C. Poulin, H. B. Kagan, Tetrahedron, 1982, 38, 119.

(130) Asymmetric hydrogenation with chiral rhodium complexes: synthetic aspects and stereochemical problems.
H. B. Kagan, Chimia, 1982, 36, 247.

(131) A direct preparation of N-acetyl-(S)-phenylalanyl-(S)-phenylalanine methyl ester by a double asymmetric hydrogenation.
J. C. Poulin, H. B. Kagan, J. C. S. Chem. Commun., 1982, 1261.

(132) The easy preparation of many benzylic bromides using molecular bromine as halogenating agent in presence of catalytic amounts of lanthanum triacetate.
M. Ouertani, P. Girard, H. B. Kagan, Bull. Soc. Chim. Fr., 1982, II, 327.

(133) Selective nitration of phenols catalyzed by lanthanum (III) nitrate.
M. Ouertani, P. Girard, H. B. Kagan, Tetrahedron Lett., 1982, 23, 4315.

(134) Efficient formation of pinacols from aldehydes or ketones mediated by samarium diiodide.
J. L. Namy, J. Souppe, H. B. Kagan, Tetrahedron Lett., 1983, 24, 765.

(135) Some organic reactions promoted by samarium diiodide.
J. Souppe, L. Danon, J. L. Namy, H. B. Kagan, J. Organometal. Chem., 1983, 250, 227.

(136) An efficient asymmetric oxidation of sulfides to sulfoxides.
P. Pitchen, H. B. Kagan, Tetrahedron Lett., 1984, 25, 1049.

(137) Reactions of acyl anions generated froml acid chlorides and diiodosamarium.
J. Souppe, J. L.Namy, H. B. Kagan, Tetrahedron Lett., 1984, 25, 2869.

(138) A convenient family of chiral shift reagents for measurement of enantiomeric excesses of sulfoxides.
M. Deshmukh, E. Dunach, S. Jugé, H. B. Kagan, Tetrahedron Lett., 1984, 25, 3467.

(139) An efficient asymmetric oxidation of sulfides into sulfoxides.
P. Pitchen, E. Dunach, M. N. Deshmukh, H. B. Kagan, J. Am. Chem. Soc., 1984, 106, 8188.

(140) Stereochemistry and structure of phellanphos and nopaphos, two chiral diphosphines for asymmetric hydrogenation : X-ray crystal structure of their sulfides.
O. Samuel, S. Y. Zhang, H. B. Kagan, Phosphorus and Sulfur, 1984, 21, 145.

(141) New preparations of lanthanide alkoxides and their catalytic activity in Meerwein-Ponndorf-Verley-Oppenauer reactions.
J. L Namy, J. Souppe, J. Collin, H. B. Kagan, J. Org. Chem., 1984, 49, 2045.

(142) Partial resolution through chiral synthesis using a racemic mixture.
S. El Baba, J. C. Poulin, H. B. Kagan, Tetrahedron, 1984, 40, 4275.

(143) Asymmetric oxidation of functionnalized sulfides into sulfoxides.
E. Dunach, H. B. Kagan, Nouv. J. Chim., 1985, 9, 1.

(144) Asymmetric oxidation of sulfides to sulfoxides.
H. B. Kagan, E. Dunach, M. N. Deshmukh, P. Pitchen, Chem. Scripta, 1985, 25, 101.

(145) A short route to chiral sulfoxides using titanium-mediated asymmetric oxidation.
H. B. Kagan, E. Dunach, C. Nemecek, O. Samuel, S. Zhao, Pure Appl Chem. , 1985, 57, 1911.

(146) A simple chiral shift reagent for measurement of enantiomeric excesses of phosphines oxides.
E. Dunach, H. B. Kagan, Tetrahedron Lett., 1985, 26, 2649.

(147) Differentiation of diastereomeric dipeptides by mass spectrometry.
J. C. Tabet, D. Fraisse, H. B. Kagan, J. C. Poulin, D. Meyer, Spectroscop. Int. J., 1985, 4, 81.

(149) Selective catalyzed-rearrangement of terminal epoxides to methyl ketones.
J. Prandi, J. L. Namy, G. Menoret, H. B. Kagan, J. Organometal. Chem., 1985, 285, 449.

(150) Ether formation from allyl alcohols catalyzed by samarium trichloride.
M. Ouertani, J. Collin, H. B. Kagan, Tetrahedron, 1985, 41, 3689.


Annual Index
1986 - 1990

(151) Epoxidation of isolated double bonds with 30% hydrogen peroxide catalyzed by pertungstate salts.
J. Prandi, H. B. Kagan, H. Mimoun, Tetrahedron Lett., 1986, 27, 2617.

(152) Asymmetric oxidation of some sulfur derivatives.
C. Nemecek, E. Dunach, H. B. Kagan, Nouv.J.Chim., 1986, 10, 761.

(153) Synthesis of chiral sulfoxides by asymmetric oxidation.
H. B. Kagan, Phosphorus and Sulfur, 1986, 27, 127.

(154).Formation of a crystalline molecular complex between a chiral sulfoxide and a chiral amide.
P. Charpin, E. Dunach, H. B. Kagan, F. R. Theobald,Tetrahedron Lett., 1986, 27, 2989.

(155) Nonlinear effects in asymmetric synthesis. Examples in asymmetric oxidation and aldolization reactions.
C. Puchot, O.Samuel, E. Dunach, S. Zhao, C. Agami, H. B. Kagan, J. Am. Chem. Soc.,1986, 108, 2353.

(156) Synthesis of a protected monodehydro Leu-Eukephalin and its hydrogenation catalyzed by chiral rhodium complexes.
J. M. Nuzillard, J. C. Poulin, H. B. Kagan, Tetrahedron Lett., 1986, 27, 2993.

(157) Asymmetric homogeneous reduction of dehydropeptides.
S. El Baba, J. M. Nuzillard, J. C. Poulin, H. B. Kagan,Tetrahedron, 1986, 42, 3851.

(158) Samarium diiodide, an efficient catalyst precursor in some Oppenauer oxidations.
J. Collin, J. L. Namy, H. B. Kagan, Nouv. J. Chim., 1986, 10, 229.

(159) Oxydation asymétrique de sulfures en sulfoxides.
S. Zhao, O. Samuel, H. B. Kagan, C.R.Acad.Sciences,Paris, 1987, 304, II. 273.

(160) The evaluation of dicyclopentadienylsamarium as a reagent in organic synthesis.
J. Collin, J. L. Namy, J. Zhang, H. B. Kagan,Organometal. Chem., 1987, 328, 81.

(161) Benzylsamarium complexes and their reactivity.
J. Collin, J. L. Namy, H. B. Kagan, Inorg. Chim. Acta, 1987, 140, 29.

(162) Lanthanides as Lewis-acid catalysts in aldol addition, cyanohydrin-forming and oxirane ring opening reactions.
A. E. Vougioukas, H. B. Kagan, Tetrahedron Lett., 1987, 28, 5513.

(163) Asymmetric oxidation of sulfides mediated by chiral titanium complexes: mechanistic and synthetic aspects.
S. H. Zhao, O. Samuel, H. B. Kagan, Tetrahedron, 1987, 43, 5135.

(164) Oxirane ring opening reactions with thiols catalyzed by lanthanide complexes.
A. E. Vougioukas, H. B. Kagan,Tetrahedron Lett. 1987, 28, 6065.

(165) Synthesis of 1,2-glycol monoethers utilizing decarbonylation of a-alkoxyacids chlorides mediated by samarium diiodide.
M. Sasaki, J. Collin, H. B. Kagan, Tetrahedron Lett., 1988, 29, 4847.

(166) Asymmetric additions of a-sulfoxide carbanions on imines.
B. Ronan, S. Marchalin, O. Samuel, H. B. Kagan,Tetrahedron Lett., 1988, 29, 6101.

(167) Double cyclisation of allylloxybenzoic acid chlorides mediated by samarium diiodide giving cyclopropanols.
M. Sasaki, J. Collin, H. B. Kagan, Tetrahedron Lett., 1988, 29, 6105.

(168) Carbonylations mediated by dicyclopentadienyl samarium.
J. Collin, H. B. Kagan, Tetrahedron Lett., 1988, 29, 6097.

(169) Asymmetric catalysis in organic synthesis with industrial perspectives.
H. B. Kagan, Bull. Soc. Chim. Fr. II, 1988, 846.

(170) Tritium and deuterium selective stereospecific labelling of peptide inhibitors of bacterial collagenases.
C. Roumestand, A. Yotakis, V. Dive, J. L. Morgat, P. Fromageot, F. Toma, A. Hammadi, J. C. Poulin, H. B. Kagan dans "Proceedings II Peptide Forum", J. Libbrey Eurotext, London 1988, 22

(171) Asymmetric oxidation of some 1,3-dithianes in presence of chiral titanium complexes
O. Samuel, B. Ronan, H.B. Kagan, J. Organomet. Chem., 1989, 370, 43.

(172) Enantioselective epoxidation of unfunctionalized simple olefins by non-racemic molybdenum (VI) (oxo-diperoxo) complexes.
V. Schurig, K. Hintzer, U. Leyrer, C. Mark, P. Pitchen, H.B. Kagan.
J. Organomet. Chem., 1989, 370, 81.

(173) Enantioselective oxidation of a sulfide : (S)-(-)-methyl p-tolylsulfoxide.
S. H. Zhao, O. Samuel, H. B. Kagan, Organic Syntheses, 1989, Vol. 68, 49.

(174) An efficient route to chiral t-butyl sulfoxides,
F. Rebiere, H. B. Kagan, Tetrahedron Lett., 1989, 30, 3659.

(175) Asymmetric Diels-Alder reaction catalyzed by chiral bases,
O. Riant, H. B. Kagan, Tetrahedron Lett., 1989, 30, 7403.

(176) A convenient method for the preparation of monolithioferrocene,
F. Rebiere, O. Samuel, H. B. Kagan, Tetrahedron Lett., 1990, 31, 3121.

(177) Asymmetric Diels-Alder reaction catalysed by some chiral Lewis acids
F. Rebiere, O. Riant , H. B. Kagan, Tetrahedron:Asymmetry, 1990, 1, 199.

(178) Synthesis of new optically active sulfoxides with chelating properties,
K. U. Baldenius, H. B. Kagan, Tetrahedron: Asymmetry, 1990,1 ,597.

(179) Reductive couplings of acid chlorides mediated by SmI2,
J. Collin, F. Dallemer, J. L. Namy, H. B. Kagan, Tetrahedron Lett., 1990, 30, 7407.


Annual Index
1991

(180) Structure d'un sulfite cyclique clé dans une méthode générale de synthèse de sulfoxydes chiraux,
L. Ricard, F. Rebiere, H. B. Kagan, C. R. Acad. Sci. Paris, 1991, 312, Ser.II, 225.

(181) Synthesis of a-ketols mediated by divalent samarium compounds,
J. Collin, J. L. Namy, F. Dallemer, H. B. Kagan, J. Org. Chem., 1991, 56, 3118.

(182) Synthesis and reactivity of allyl samarium complexes,
J. Collin, C. Bied, H. B. Kagan, Tetrahedron Lett., 1991, 32, 629.

(183) Highly diastereoselective Diels-Alder reactions with (R) ethoxy p-tolyl vinyl sulfonium tetrafluoroborate,
B. Ronan, H. B. Kagan, Tetrahedron : Asymmetry, 1991, 2, 75.

(184) Reaction of P-Cl compounds in presence of SmI2,
M. Sasaki, J. Collin, H. B. Kagan, Tetrahedron Lett, 1991, 32, 2493.

(185) A new preparation of lanthanide alkoxides, and some applications in catalysis,
A. Lebrun, J. L. Namy, H. B. Kagan, Tetrahedron Lett, 1991, 32, 2355.

(186) New approaches for asymmetric synthesis of sulfoxides,
H. B. Kagan, F. Rebiere, O. Samuel, Phosphorus, Sulfur, Silicon, 1991, 58, 89.

(187) A general route to enantiomerically pure sulfoxides from a chiral sulfite,
F. Rebière, O. Samuel, L. Ricard, H. B. Kagan, J. Org. Chem., 1991, 56, 5991.

(189) Solid angle as a steric parameter of acyclic saturated groups,
R. Chauvin, H. B. Kagan, Chirality, 1991, 3, 242.

(190) Visualisation simultanée d'un cristal liquide, le 8CB, et de son support graphitique par
microscopie à balayage par effet tunnel (STM),
J. C. Poulin, H. B. Kagan, C. R. Acad.Sci. Paris, 1991, Série II, 313, 242.

(191) 2-Hydroxyalkyl diphenylphosphines: biocatalytic resolution and use as ligands for transition-metal catalysts,
H. B. Kagan, M. Tahar, J. C. Fiaud, Tetrahedron Lett., 1991, 32, 5959.


Annual Index
1992

(192) Divalent lanthanide derivatives in organic synthesis: new developments in SmI2 mediated Barbier type reactions,
M. Sasaki, J. Collin, H. B. Kagan, New J. Chem., 1992, 16, 89.

(193) Highly enantioselective synthesis of a Corey Prostaglandin intermediate
B. Ronan, H. B. Kagan , Tetrahedron: Asymmetry, 1992, 3, 115.

(194) Synthesis and reactivity of benzylic and allylic samarium compounds,
C. Bied, J. Collin, H. B. Kagan, Tetrahedron, 1992, 48, 3877.

(195) Reaction of protected amino acid chlorides mediated by SmI2,
J. Collin, J. L. Namy, G. Jones, H. B. Kagan, Tetrahedron Lett, 1992, 33, 2973.

(196) Organosamariums from reaction of alkyl halides on samarium (II) derivatives,
J. L. Namy, J. Collin, C. Bied, H. B. Kagan, Synlett, 1992, 733.

(197) Synthesis of 6-endo-hydroxy norphos, a potential ligand for construction of chiral bimetallic catalysts,
J. Ward, A. Börner, H. B. Kagan, Tetrahedron : Asymmetry, 1992, 3, 849.

(198) Diastereoselective hydrogenation of monodehydroenkephalins controlled by chiral rhodium complexes,
A. Hammadi, J. M. Nuzillard, J. C. Poulin, H. B. Kagan, Tetrahedron:Asymmetry, 1992, 3, 1247.


Annual Index
1993

(199) Asymmetric synthesis and highly diastereoselective ortholithiation of some ferrocenyl sulfoxides. Application to synthesis of ferrocenyl derivatives with planar chirality
F. Rebière, O. Riant, L. Ricard, H. B. Kagan, Angew. Chem. Int. Ed. Eng., 1993, 32, 568-570.

(200) A general asymmetric synthesis of ferrocenes with planar chirality
O. Riant, O. Samuel, H. B. Kagan, J. Am. Chem. Soc., 1993, 115, 5835-5836.

(201) New chiral building blocks and their application to the construction of chiral
aminoalcohols: enantiomerically pure cis-and trans-3 mesyloxy-4-hydroxy tetrahydrofuranes,
A. Börner, J. Holz, H. B. Kagan, Tetrahedron Lett., 1993, 34,5273-5276

(202) Concise synthesis of enantiomerically pure cis-and trans-3-(Diphenylphosphino)-4-
hydroxytetrahydrofurans
A. Börner, J. Holz, J. Ward, H. B. Kagan, J. Org. Chem., 1993, 58, 6814-6817.

(203) A boron analog of DIOP: synthesis and properties,
A. Börner, J. Ward, K. Kortus, H. B. Kagan, Tetrahedron: Asymmetry, 1993, 4, 2219-2228.

(204) Samarium dibromide, an efficient reagent for the pinacol coupling reactions,
A. Lebrun, J.L. Namy, H. B. Kagan, Tetrahedron Lett., 1993, 34, 2311-2314.


Annual Index
1994

(205) Rabbit gastric lipase in biocatalytic resolution of 2-hydroxyalkyldiphenylphosphines,
H. B. Kagan, M. Tahar, J. C. Fiaud, Bioorganic and Medicinal Chem., 1994, 2, 15-21.

(206) Asymmetric base-catalyzed cycloaddition between anthrone and some dienophiles,
O. Riant, H. B. Kagan, L. Ricard, Tetrahedron, 1994, 50, 4543-4554.

(207) Samarium diiodide in tetrahydropyran: preparation and some reactions in organic chemistry
J. L. Namy, M. Colomb, H. B. Kagan, Tetrahedron Lett., 1994, 35, 1723-1726.

(208) Enantiomeric enrichment of sulfoxides by preparative flash chromatography on an achiral phase,
P. Diter, S. Taudien, O. Samuel, H. B. Kagan, J. Org. Chem., 1994, 59, 370-373.

(209) Highly enantioselective oxidation of ferrocenyl sulfides,
P. Diter, O. Samuel, S. Taudien, H. B. Kagan, Tetrahedron:Asymmetry,, 1994, 5S, 549-552.

(210) Synthesis and catalytic properties of an acyclic analogue of hydroxy norphos
A. Börner, J. Ward, W. Ruth, J. Holz, A. Kless, D. Heller, H. B. Kagan, Tetrahedron, 1994, 50, 10419-10430.

(211) Tandem asymmetric syntheses from achiral precursors. Asymmetric homogeneous reduction of bisdehydrodipeptides,
S. El Baba, K. Sartor, J. C. Poulin, H. Kagan, Bull Soc. Chim. Fr., 1994, 131, 525-533.

(212) Nonlinear effects in asymmetric catalysis,
D. Guillaneux, S. H. Zhao, O. Samuel, D. Rainford, H. B. Kagan,
J. Am. Chem. Soc., 1994, 116, 9430-9439.

(213) Kinetic resolution by asymmetric oxidation of racemic 3-azetidinyl p. tolyl sulfide with t-butyl-hydroperoxide in presence of a chiral titanium complex
C. Nemecek, H. B. Kagan, Polish J. Chem., 1994, 68, 2467-2475.


Annual Index
1995

(214) Scanning tunneling microscopy observation of giant palladium-561 clusters,
J-C. Poulin, H. B. Kagan, M. N. Vargaftik, I. P. Stolarov, I.I. Moiseev,
J. Mol. Catal., 1995, 95, 109-113.

(215) Synthesis of chiral lithium dialkoxyaminoborohydrides,
L. Dubois, J. C. Fiaud, H. B. Kagan, Tetrahedron, 1995, 51, 3803-3812.

(216) Synthesis of chiral carbocations linked to a ferrocene unit,
S. Taudien, O. Riant, H. B. Kagan, Tetrahedron Lett., 1995, 36, 3513-3516.

(217) High yield synthesis of monosubstituted ferrocenes,
D. Guillaneux, H. B. Kagan, J. Org. Chem., 1995, 60, 2502-2505.

(218) Dibromosamarium : new preparation and evaluation as a reducing agent,
A. Lebrun, E. Rantze, J.-L. Namy, H. B. Kagan, New J. Chem. , 1995, 19, 699-705.

(219) Enantioselective reduction of acetophenone with oxazaborolidines derived from chiral diethanolamines,
L. Dubois, J.-C. Fiaud, H. B. Kagan, Tetrahedron : Asymmetry, 1995, 6, 1097-1104.

(220) Nonlinear effects in the reduction of acetophenone by diisopino-camphenylchloroborane : influence of the reagent preparation,
C. Girard, H. B. Kagan, Tetrahedron : Asymmetry, 1995, 6, 1881-1884.

(221) Is there a preferred expression for the composition of a mixture of enantiomers ?
H. B. Kagan, Recl. Trav. Chim. Pays-Bas, 1995, 114, 203-205.

(222) A new chiral multidentate ligand for asymmetric catalysis,
A. Kless, R. Kadyrov, A. Börner, J. Holz, H. B. Kagan, Tetrahedron Lett., 1995, 36, 4601-4602.

(223) Highly enantioselective oxidation of sulfides mediated by a chiral titanium complex,
J. M. Brunel, P. Diter, M. Duetsch, H. B. Kagan, J. Org. Chem., 1995, 60, 8086-8088.

(224) Nonlinear effects involving two competing pseudo enantiomeric catalysts: example in asymmetric dihydroxylation of olefins,
S. Zhang, C. Girard, H. B. Kagan, Tetrahedron : Asymmetry, 1995, 6, 2637-2640.

(225) Synthesis of tertiary phosphine oxides mediated by SmCp2 or SmI2,
F. Dallemer, J. Collin, H. B. Kagan, Applied Organometallic Chemistry, 1995, 9, 431-435.

(226) Towards new ferrocenyl ligands for asymmetric catalysis,
H. B. Kagan, P. Diter, A. Gref, D. Guillaneux, A. Masson-Szymzak, F. Rebière, O. Riant,
O. Samuel, S. Taudien, Pure Appl. Chem., 1995, 68, 29-36.


Annual Index
1996

(227) Nonlinear effects in asymmetric catalysis : some recent aspects,
H. B. Kagan, C. Girard, D. Guillaneux, D. Rainford, O. Samuel, S. H. Zhao, S. Y. Zhang,
Acta Chem. Scand., 1996, 50, 345-352.

(228) Asymmetric synthesis of chiral tetradentate ligand based on a bis [diphenylphosphinoferrocenyl]
moiety. Electrochemical behavior of free ligand and its RuII and CuI complexes,
A. Masson-Szymczak, O. Riant, A. Gref, H. B. Kagan, J. Organometal. Chem., 1996, 511, 193-197.

(229)Catalytic asymmetric oxidation of sulfides with high enantioselectivities,
J. M. Brunel, H. B. Kagan, Synlett, 1996, 404-406.

(230) Development of asymmetric catalysis by chiral metal complexes: the example of asymmetric hydrogenation,
H. B. Kagan, C. R. Acad. Sci. Paris, 1996, t. 322, Série IIb, 131-143.

(231) Transformation of a racemic mixture by a chiral reagent or catalyst to give regioisomeric products,
H. B. Kagan, Croatica Chem. Acta, 1996, 69, 669-680 (special issue for the 90th anniversary of V. Prelog).

(232) Improved reactivity of diodosamarium by catalysis with transition metal salts,
F. Machroui, B. Hamann, J. L. Namy, H. B. Kagan, Synlett, 1996, 633-634.

(233) Preparation and reactions of samarium diiodide in nitriles,
B. Hamann, J. L. Namy, H. B. Kagan, Tetrahedron, 1996, 52, 14225-14234.

(234) Catalytic enantioselective oxidation of sulfides with a chiral titanium complex,
J. M. Brunel, H. B. Kagan, Bull. Soc. Chim. Fr., 1996, 133, 1109-1115.


Annual Index
1997

(235) Stereoselective synthesis of some chiral a-ferrocenyl carbenium ions,
A. Brunner, S. Taudien, O. Riant, H. B. Kagan,Chirality, 1997, 9, 478-485.

(236) Nucleophilic acylation of esters by acid chlorides mediated by samarium diiodide: formation and use of samarium enediolates,
F. Machroui, J. L. Namy, H. B. Kagan, Tetrahedron Lett., 1997, 38; 7183-7186.

(237) Generation and reactivity of compounds using diiodosamarium in tetrahydropyran,
B. Hamman-Gaudinet, J. L. Namy, H. B. Kagan, Tetrahedron Lett., 1997, 38, 6585-6588.

(238) Asymmetric catalytic reduction of ketones with hypervalent trialkoxysilanes,
R. Schiffers, H. B. Kagan, Synlett, 1997, 1175-1178.

(239) An efficient asymmetric synthesis of 2-substituted ferrocenecarboxaldehyde
O. Riant, O. Samuel, T. Flessner, S. Taudien, H. B. Kagan, J. Org. Chem., 1997, 62, 6733-6745.

(240) Nonlinear effects in the reduction of acetophenone by diisopino-campheyl chloroborane :
influence of stoichiometry of the reagent.
C. Girard, H.B. Kagan, Tetrahedron:Asymmetry, 1997, 8, 3851.


Annual Index
1998

(241) One-pot multi-substrate screening in asymmetric catalysis.
X. Gao, H. B. Kagan, Chirality, 1998, 10, 120-124.

(242) Asymmetric PTC C-alkylation mediated by TADDOL-novel route to enantiomerically enriched, a-alkyl-a-aminoacids
Y. N. Belokon, K. A. Kotchekov, T. D. Churkina, N. S. Ikonnikov, A. E. Chesnokov, O. V. Larionov, V. S. Parmar, R. Kumar, H. B. Kagan, Tetrahedron : Asymmetry, 1998, 9, 851-857.

(243) A straightforward asymmetric synthesis of enantiopure 1,2-disubstituted ferrocenes,
O. Riant, G. Argouarch, D. Guillaneux, O. Samuel, H. B. Kagan, J. Org.Chem., 1998, 63, 3511-3514.

(244) Nonlinear effects as "indicators" in the tuning of asymmetric catalysts
T. Luukas, J. M. Brunel, H. B. Kagan, Tetrahedron : Asymmetry, 1998, 9, 1941-1946.

(245) Dioxygen oxidation of alcohols and aldehydes over a cerium dioxide-ruthenium system,
F. Vocanson, Y. P. Guo, J. L. Namy, H. B. Kagan, Synthetic Commun., 1998, 28, 2577-2582.

(246) Organosamariums : preparation using diiodosamarium and reactivity in tetrahydropyran,
B. Hamman-Gaudinet, J.L. Namy, H.B. Kagan, J. Organometal. Chem., 1998, 567, 39-47.

(247) Chiral hydroxythiols as catalysts for enantioselective borane ketone reduction,
J.C. Fiaud, F. Mazé, H.B. Kagan, Tetrahedron : Asymmetry, 1998, 9, 3647-3655.


Annual Index
1999

(248) Enantiomerically pure (R)- and (S)-2-methylphenylalanine via asymmetric PTCC-alkylation catalyzed by NOBIN.
Y. N. Belokon, K. A. Kochetkov, T. D. Churkina, N. S. Ikonnikov, S. Vyskocil, H. B. Kagan, Tetrahedron: Asymmetry, 1999, 10, 1723-1728.

(249) Asymmetric alkylation catalyzed by chiral alkali metal alkoxides of TADDOL. Synthesis of a-methyl amino acids, Y. N. Belokon, K. A. Kotchekov, T. D. Churkina, N. S. Ikonnikov, A. A. Chesnokov, O. V. Larionov, H. B. Kagan, Russian Chemical Bulletin, 1999, 48, 917-923.

(250) Kinetic resolution when the chiral auxiliary is not enantiomerically pure: normal or abnormal behavior,
T. O. Luukas, C. Girard, D. R. Fenwick, H. B. Kagan, J. Am. Chem. Soc., 1999, 121, 9299-9306.


Annual Index
2000 - 2011

(251) Diferrocenylphosphine: easy synthesis and its use to prepare chiral phosphines,
D. Guillaneux, L. Martiny, H. B. Kagan, Coll. Czech. Chem. Commun., 2000, 65, 717-728.

(252) Asymmetric PTC C-alkylation catalyzed by chiral derivatives of tartaric acid and aminophenols. Synthesis of (R)- and (S)-a-methyl aminoacids,
Y. N. Belokon, A. Konstantin, A. Kochetkov, Tatiana D. Churkina, N. S. Ikonnikov, A. A. Chesnokov, O. V. Larionov, V. S. Parmar, J. Org. Chem., 2000, 65, 7041-7048.

(253) A synthesis of some ferrocene-based 1,3-bis(phosphanes) with planar chirality as the sole source of chirality,
G. Argouarch, O. Samuel, H. B. Kagan, Eur. J. Org. Chem., 2000, 2885-2891.

(254) A new class of ferrocene-based 1,2-bis(phosphanes) possessing only planar chirality,
G. Argouarch, O. Samuel, O. Riant, J.-C. Daran, H. B. Kagan, Eur. J. Org. Chem., 2000, 2893-2899.

(255) The asymmetric addition of trimethylsilylcyanide to aldehydes catalysed by anionic chiral nucleophiles 1
Holmes, I. P.; Kagan, H. B. Tetrahedron Lett., 2000, 41, 7453-7456.

(256) The asymmetric addition of trimethylsilylcyanide to aldehydes catalysed by anionic chiral
nucleophiles 2
Holmes, I. P.; Kagan, H. B. Tetrahedron Lett., 2000, 41 , 7457-7460.

(257) Various aspects of the reaction of a chiral catalyst or reagent with a racemic or enantio-pure substrate,
H. B. Kagan, Tetrahedron, 2001, 57, 2449-2459.

(258) Asymmetric catalysis. Part 137: nickel catalysed enantioselective a-ketol rearrangement of 1-benzoylcycloalkanols,
H. Brunner, H. B. Kagan, G. Kreutzer, Tetrahedron:Asymmetry, 2001, 12, 497-499.

(259) Highly efficient catalytic synthesis of a-amino acids under phase-transfer conditions with novel catalyst/substrate pair,
Y. N. Belokon, K. A. Kochetkov, T. D. Churkina, N. S. Ikonnikov, O. V. Larionov, S. Vyskosil, M. North, H. B. Kagan, Angew. Chem. Int. Ed., 2001, 40, 1948-1951.

(260) A practical kinetic resolution of 4-acetyl[2.2]paracyclophane,
P. Dorizon, C. Martin, J.-C. Daran, J.-C. Fiaud, H. B. Kagan, Tetrahedron: Asymmetry, 2001, 12, 2625-2630.

(261) A one-pot esterification of chiral O-trimethylsilyl-cyanohydrins with retention of stereochemistry,
S. Norsikian, I. Holmes, F. Lagasse, H. B. Kagan, Tetrahedron Lett., 2002, 43, 5715-5717.

(262) Presence or absence of nonlinear effect according to the asymmetric catalyst preparation in the alkylation of benzaldehyde,
T. O. Luukas, D. R. Fenwick, H. B. Kagan, C. R. Chimie, 2002, 5, 487-491.

(263) Is it possible to estimate the enantioselectivity of a chiral catalyst from its racemic mixture ?
F. Lagasse, M. Tsukamoto, C. J. Welch, H. B. Kagan, J. Am. Chem. Soc., 2003, 125, 7490-7491

(264) Asymmetric catalysis. Part 153 : metal-catalyzed enantioselective a-ketol rearrangement,
H. Brunner, H. B. Kagan, G. Kreutzer, Tetrahedron :Asymmetry, 2003, 14, 2177-2187.

(265) Synthesis of a-aminoacids via asymmetric phase transfer-catalyzed alkylation of a chiral Nickel(II) complexes of glycine-derived Schiff bases,
Y. N. Belokon, N. B. Bespalova, T. D. Churkina, I. Cisarova, M. G. Ezernitskaya, S. R. Harutyunyan, R. Hrdina, H. B. Kagan, P. Kocovsky, K. A. Kochetkov, O. V. Larionov, K. A. Lyssenko, M. North, M. Polasek, A. S. Peregudov, V. V ; Prisyazhnyuk, S. Vyskocil, J. Am. Chem. Soc. 2003, 125, 12860-12871. 

(266) In situ formation of a heterobimetallic chiral [(Salen)Ti(IV)][(Salen)V(V)] catalyst for the asymmetric addition of TMSCN to benzaldehyde,
Y. N. Belokon, M. North, V. I. Maleev, N. V. Voskoboev, M. A. Moskalenko, A.S.Peregudov, A. V. Dimitriev, N. S. Ikonnikov, H. B. Kagan
Angew. Chem. Int. Ed., 2004, 43, 4085-4089.

(267) Study of molecular rotational isomerism using deuterium NMR in chiral oriented solvents,
P. Lesot, O. Lafon, H. B. Kagan, C. Fan Chem. Commun, 2005, 389-391.

(268) Chemo-, regio- and stereoselective 1,3-dipolar cycloaddition of C-aryl-N-phenylnitrones over 3,5-bis(arylidene)-1-methylpiperidin-4-ones : synthesis of highly susbtituted  novel spiro-isoxazolidines,
R.R. Kumar, S.Perumal, H. B. Kagan, R. Guillot, Tetrahedron, 2006, 62, 12380-12391.

(269) Asymmetric amplification by kinetic resolution using a racemic reagent : example in amine acetylation,
T. Satyanarayana, H. B. Kagan, Chem. Eur. J., 2006, 12, 5785-5789.

(270) Asymmetric amplification in catalysis by trans-1,2-diaminocyclohexane bistriflamide,
T. Satyanaryana, B. Ferber, H. B. Kagan Org. Lett., 2007, 9, 251-253.

(271)   Amplification of enantiomeric excess of a compound in kinetic resolution by a racemic
  reagent, T. Satyanarayana. ,  H. B. Kagan, Tetrahedron, 2007, 63, 6415-6422.

(272)  Analysis of intramolecular dynamic processes in enantiomeric diaryl atropoisomers and  related derivatives by 2H NMR spectroscopy in polypeptide liquid crystals.  O. Lafon, P. Lesot, C. Fan, H. B. Kagan Chem. Eur. J., 2007, 13, 3772-3786.

(273)   1,3-dipolar cycloaddition of nitrile oxides to (R)-1-(1-phenylethyl)-3[(E)- arylmethylidene]tetrahydro-4(1H)-pyridinones: synthesis of enantiomerically pure spiro heterocycles, R. S. Kumar, S. Perumal, H. B. Kagan, R. Guillot, Tetrahedron :Asymmetry, 2007, 18, 170-180.

(274)    Equilibrium of homochiral dimerization of a mixture of enantiomers, its relevance to nonlinear effects in asymmetric catalysis, M. Tsukamoto, K. Gopalaiah, H. B. Kagan,  J. Chem. Phys. B, 2008112, 15361-15368.

(275) Two aspects of the desymmetrization of selected prochiral aromatic or vinylic dihalides, enantioselective halogen lithium exchange and prochiral recognition in chiral liquid crystals, C.A. Fan, B. Ferber, H.B. Kagan, O. Lafon, P. Lesot, Tetrahedron :Asymmetry, 2008, 19, 2666-2677.

(276) Asymmetric meso-epoxide ring-openng with trimethylsilylcyanide promoted by binuclear complexes of titanium. Dichotomy of C-C versus C-N bond formation. Y. N. Belokon, D. Chusov, A. S. Pereegudov, L. V. Yashkina, G. I. Timofeeva, V. I. Maleev, M. North, H. B. Kagan Adv. Synth. Catal. 2009, 351, 3157-3167.

(277) Routes toward enantiopure 2-substituted indolines : an overview. A. Saithalavi, H. B. Kagan Tetrahedron Asymmetry 2009, 20, 2193-2199.

(278) Nonlinear effects in asymmetric catalysis T. Satyanarayana, S. Abraham, H. B. Kagan  Angew. Chem. Int. Ed. 2009, 48, 456-494.

(279) Regioselective reactions on a chiral substrate controlled by the configuration of a chiral catalyst. R. R. Kumar, H. B. Kagan Adv. Synth. Catal 2010, 352, 231-242.

(280) Enantioselective synthesis of 2-methyl indoline by palladium catalysed asymmetric C(sp3)-H activation. A. Saithalavi, A. Cordi , H. B. Kagan Chem. Commun 2011, 11483-11485.

(281) A mild one-pot method for conversion of various steroidal secondary alcohols into the corresponding olefins. R. R. Kumar, S. D. Haveli, H. B. Kagan Synlett 2011, 1709-1712.

(282) Use of nonfunctionalized enamides and enecarbamates in asymmetric synthesis. G. Kovuru, H. B. Kagan Chem. Rev. 2011, 111, 4599-4657.