ChemInform Abstract: CHROMIUM COMPLEXED CARBINOLS AS HIGHLY EFFECTIVE AUXILIARIES FOR USE IN ASYMMETRIC INDUCTION: REDUCTION OF α-KETO ESTERS

A. SOLLADIE-CAVALLO; J. SUFFERT

doi:10.1002/chin.198523293

ChemInform Abstract: CHROMIUM COMPLEXED CARBINOLS AS HIGHLY EFFECTIVE AUXILIARIES FOR USE IN ASYMMETRIC INDUCTION: REDUCTION OF α-KETO ESTERS

Chemischer Informationsdienst ◽

10.1002/chin.198523293 ◽

1985 ◽

Vol 16 (23) ◽

Author(s):

A. SOLLADIE-CAVALLO ◽

J. SUFFERT

Keyword(s):

Asymmetric Induction ◽

Keto Esters ◽

Highly Effective

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Highly Effective Chiral Ortho-Substituted BINAPO Ligands (o-BINAPO): Applications in Ru-Catalyzed Asymmetric Hydrogenations of β-Aryl-Substituted β-(Acylamino)acrylates and β-Keto Esters

Journal of the American Chemical Society ◽

10.1021/ja020121u ◽

2002 ◽

Vol 124 (18) ◽

pp. 4952-4953 ◽

Cited By ~ 150

Author(s):

Yong-Gui Zhou ◽

Wenjun Tang ◽

Wen-Bo Wang ◽

Wenge Li ◽

Xumu Zhang

Keyword(s):

Keto Esters ◽

Highly Effective ◽

Asymmetric Hydrogenations

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ChemInform Abstract: A New Approach to Remote Asymmetric Induction in the Stereoselective Reduction of γ-Keto Esters by Use of a Chiral Podand as Chiral Auxiliary.

ChemInform ◽

10.1002/chin.199205105 ◽

2010 ◽

Vol 23 (5) ◽

pp. no-no

Author(s):

Y. TAMAI ◽

S. KOIKE ◽

A. OGURA ◽

S. MIYANO

Keyword(s):

Chiral Auxiliary ◽

Asymmetric Induction ◽

New Approach ◽

Stereoselective Reduction ◽

Keto Esters

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ChemInform Abstract: Pseudo-Macrocyclic Chelation Control in Remote Asymmetric Induction. Highly Efficient 1,7-Asymmetric Inductive Hydride Reduction and Grignard Reaction of γ-Keto Esters of 1,1′-Binaphthalen-2-ols Bearing an Appropriate Oligoether Group

ChemInform ◽

10.1002/chin.199944041 ◽

2010 ◽

Vol 30 (44) ◽

pp. no-no

Author(s):

Yasufumi Tamai ◽

Tetsutaro Hattori ◽

Masamitsu Date ◽

Shinji Koike ◽

Yoshinori Kamikubo ◽

...

Keyword(s):

Asymmetric Induction ◽

Grignard Reaction ◽

Keto Esters ◽

Highly Efficient ◽

Hydride Reduction

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ChemInform Abstract: ASYMMETRIC SYNTHESIS OF β-SUBSTITUTED Δ-KETO ESTERS VIA MICHAEL ADDITIONS OF (S)-AMP/(R)-AMP HYDRAZONES (AMP = 1-AMINO-2-METHOXYMETHYLPYRROLIDINE) TO α,β-UNSATURATED ESTERS. VIRTUALLY COMPLETE 1,6-ASYMMETRIC INDUCTION

Chemischer Informationsdienst ◽

10.1002/chin.198409179 ◽

1984 ◽

Vol 15 (9) ◽

Author(s):

D. ENDERS ◽

K. PAPADOPOULOS

Keyword(s):

Asymmetric Synthesis ◽

Asymmetric Induction ◽

Unsaturated Esters ◽

Keto Esters ◽

Michael Additions

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Efficient 1,8- to 1,12-asymmetric induction in Grignard reactions of ω-keto esters by using BINOL or its 2′-oligoether derivatives as the chiral auxiliary

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/a901978b ◽

1999 ◽

pp. 1141-1142 ◽

Cited By ~ 10

Author(s):

Yasufumi Tamai ◽

Tetsutaro Hattori ◽

Masamitsu Date ◽

Hideki Takayama ◽

Yoshinori Kamikubo ◽

...

Keyword(s):

Chiral Auxiliary ◽

Asymmetric Induction ◽

Keto Esters ◽

Grignard Reactions

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ChemInform Abstract: CHELATION-CONTROLLED NUCLEOPHILIC ADDITIONS. 2. A HIGHLY EFFECTIVE SYSTEM FOR R ASYMMETRIC INDUCTION IN THE REACTION OF ORGANOMETALLICS WITH β-ALKOXY ALDEHYDES

Chemischer Informationsdienst ◽

10.1002/chin.198023111 ◽

1980 ◽

Vol 11 (23) ◽

Author(s):

W. C. STILL ◽

J. A. SCHNEIDER

Keyword(s):

Asymmetric Induction ◽

Nucleophilic Additions ◽

Highly Effective ◽

Effective System

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Stereoselective synthesis of disubstituted 3(2H)-furanones via catalytic intramolecular C-H insertion reactions of α-diazo-β-keto esters including asymmetric induction

Tetrahedron Letters ◽

10.1016/0040-4039(94)85379-7 ◽

1994 ◽

Vol 35 (39) ◽

pp. 7269-7272 ◽

Cited By ~ 24

Author(s):

Tao Ye ◽

M.Anthony McKervey ◽

Bridget D. Brandes ◽

Michael P. Doyle

Keyword(s):

Stereoselective Synthesis ◽

Asymmetric Induction ◽

Insertion Reactions ◽

Keto Esters

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A new approach to remote asymmetric induction in the diastereoselective reduction of γ-keto esters by use of a chiral podand as chiral auxiliary

Journal of the Chemical Society Chemical Communications ◽

10.1039/c39910000799 ◽

1991 ◽

pp. 799-800 ◽

Cited By ~ 13

Author(s):

Yasufumi Tamai ◽

Shinji Koike ◽

Atsuhiko Ogura ◽

Sotaro Miyano

Keyword(s):

Chiral Auxiliary ◽

Asymmetric Induction ◽

New Approach ◽

Keto Esters ◽

Diastereoselective Reduction

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ChemInform Abstract: Asymmetric Reactions Catalyzed by Chiral Metal Complexes. Part 24. Highly Effective Catalytic Asymmetric Hydrogenation of α-Keto Esters and an α-Keto Acetal with New Neutral Chiral Pyrrolidinebisphosphine- Rhodium Complexes.

ChemInform ◽

10.1002/chin.198750115 ◽

1987 ◽

Vol 18 (50) ◽

Author(s):

H. TAKAHASHI ◽

T. MORIMOTO ◽

K. ACHIWA

Keyword(s):

Metal Complexes ◽

Asymmetric Hydrogenation ◽

Asymmetric Reactions ◽

Rhodium Complexes ◽

Keto Esters ◽

Highly Effective ◽

Catalytic Asymmetric ◽

Catalytic Asymmetric Hydrogenation

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ChemInform Abstract: ASYMMETRIC INDUCTION. REDUCTION, NUCLEOPHILIC ADDITION TO, AND ENE REACTIONS OF CHIRAL α-KETO ESTERS

Chemischer Informationsdienst ◽

10.1002/chin.198349087 ◽

1983 ◽

Vol 14 (49) ◽

Author(s):

J. K. WHITESELL ◽

D. DEYO ◽

A. BHATTACHARYA

Keyword(s):

Nucleophilic Addition ◽

Asymmetric Induction ◽

Ene Reactions ◽

Keto Esters

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