Asymmetric induction in the epoxidation of alkenes by optically active peroxy-acids

Journal of the Chemical Society D Chemical Communications ◽

10.1039/c29690000135 ◽

1969 ◽

pp. 135 ◽

Author(s):

F. Montanari ◽

I. Moretti ◽

G. Torre

Keyword(s):

Optically Active ◽

Asymmetric Induction ◽

Peroxy Acids ◽

Epoxidation Of Alkenes

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Asymmetric induction and configurational correlations in oxidations at sulphur. Part V. Oxidations of optically active esters of o-(methylthio)benzoic acid by achiral peroxy-acids

Journal of the Chemical Society C Organic ◽

10.1039/j39690000731 ◽

1969 ◽

pp. 731 ◽

Author(s):

G. Barbieri ◽

V. Davoli ◽

I. Moretti ◽

F. Montanari ◽

G. Torre

Keyword(s):

Benzoic Acid ◽

Optically Active ◽

Asymmetric Induction ◽

Active Esters ◽

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Asymmetric induction and configurational correlations in oxidations at sulphur. Part III. Oxidations of aryl alkyl sulphides to sulphoxides by optically active peroxy-acids

Journal of the Chemical Society C Organic ◽

10.1039/j39680001317 ◽

1968 ◽

pp. 1317 ◽

Author(s):

U. Folli ◽

D. Iarossi ◽

F. Montanari ◽

G. Torre

Keyword(s):

Optically Active ◽

Asymmetric Induction ◽

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ChemInform Abstract: INFLUENCE OF STRUCTURAL VARIATIONS IN THE SUBSTRATE ON THE ASYMMETRIC EPOXIDATION OF ALKENES BY OPTICALLY ACTIVE PEROXY-ACIDS

Chemischer Informationsdienst ◽

10.1002/chin.197428183 ◽

1974 ◽

Vol 5 (28) ◽

pp. no-no

Author(s):

FERNANDO MONTANARI ◽

IRENE MORETTI ◽

GIOVANNI TORRE

Keyword(s):

Optically Active ◽

Asymmetric Epoxidation ◽

Structural Variations ◽

Peroxy Acids ◽

Epoxidation Of Alkenes

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Asymmetric induction and configurational correlations in oxidations at sulphur. Part IV. Oxidation of aryl alkyl sulphoxides to sulphones by optically active peroxy-acids

Journal of the Chemical Society C Organic ◽

10.1039/j39680001372 ◽

1968 ◽

pp. 1372 ◽

Author(s):

U. Folli ◽

D. Iarossi ◽

F. Montanari

Keyword(s):

Optically Active ◽

Asymmetric Induction ◽

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Asymmetric induction copolymerization of optically active N-(l-menthyl carboxylatomethyl)citraconimide with styrene

Journal of Polymer Science Part A Polymer Chemistry ◽

10.1002/pola.1986.080240608 ◽

1986 ◽

Vol 24 (6) ◽

pp. 1185-1196 ◽

Author(s):

Tsutomu Oishi ◽

Nobushige Okamoto ◽

Minoru Fujimoto

Keyword(s):

Optically Active ◽

Asymmetric Induction

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ChemInform Abstract: CATALYTIC ASYMMETRIC INDUCTION IN OXIDATION REACTIONS. THE SYNTHESIS OF OPTICALLY ACTIVE EPOXIDES

Chemischer Informationsdienst ◽

10.1002/chin.197635153 ◽

1976 ◽

Vol 7 (35) ◽

pp. no-no

Author(s):

R. HELDER ◽

J. C. HUMMELEN ◽

R. W. P. M. LAANE ◽

J. S. WIERING ◽

H. WYNBERG

Keyword(s):

Optically Active ◽

Asymmetric Induction ◽

Oxidation Reactions ◽

Catalytic Asymmetric

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1,5-Asymmetric induction in addition reaction of aldehydes with chiral allyltitaniums having an amino group at the stereogenic center. Synthesis of optically active 2,6-cis-disubstituted piperidines

Tetrahedron Letters ◽

10.1016/s0040-4039(98)01455-5 ◽

1998 ◽

Vol 39 (38) ◽

pp. 6927-6930 ◽

Author(s):

Teng Xin ◽

Sentaro Okamoto ◽

Fumie Sato

Keyword(s):

Addition Reaction ◽

Optically Active ◽

Asymmetric Induction ◽

Amino Group ◽

Stereogenic Center

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ChemInform Abstract: The Preparation of Optically Active δ2-Isoxazolines. A Model for Asymmetric Induction in the Non Lewis Acid Catalyzed Reactions of Oppolzer′s Chiral Sultam.

10.1002/chin.198852160 ◽

1988 ◽

Vol 19 (52) ◽

Author(s):

D. P. CURRAN ◽

B. H. KIM ◽

J. DAUGHERTY ◽

T. A. HEFFNER

Keyword(s):

Optically Active ◽

Asymmetric Induction ◽

Acid Catalyzed ◽

Catalyzed Reactions

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Preparations of Chiral Menthyl α-Sulfinylacrylates. The Optically Active Dienophiles with Double Asymmetric-Induction Capability

Journal of the Chinese Chemical Society ◽

10.1002/jccs.199100063 ◽

1991 ◽

Vol 38 (4) ◽

pp. 375-378 ◽

Author(s):

Teng-Kuci Yang ◽

Tsung-Fan Teng ◽

Dong-Sheng Lec

Keyword(s):

Optically Active ◽

Asymmetric Induction

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A synthetic strategy for tricholomic acid and acivicin

Canadian Journal of Chemistry ◽

10.1139/v87-031 ◽

1987 ◽

Vol 65 (1) ◽

pp. 195-199 ◽

Author(s):

Stephen Hanessian ◽

Benoit Vanasse

Keyword(s):

Aldol Condensation ◽

Optically Active ◽

Asymmetric Induction ◽

Bond Forming ◽

Synthetic Strategy

A synthetic strategy towards tricholomic acid and acivicin has been established using the aldol condensation of N-pyruvilideneglycinatoaquocopper(II) and an optically active aldehyde derived from S-malic acid as the key bond-forming reaction. Although a viable strategy was developed, no asymmetric induction was observed.

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