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

Asymmetric Induction ◽

Insertion Reactions ◽

ChemInform Abstract: Double Asymmetric Induction in Intramolecular C-H Insertion Reactions of α-Diazo β-Keto Esters.

ChemInform ◽

10.1002/chin.199519046 ◽

2010 ◽

Vol 26 (19) ◽

pp. no-no

Author(s):

S. HASHIMOTO ◽

N. WATANABE ◽

K. KAWANO ◽

S. IKEGAMI

Keyword(s):

Asymmetric Induction ◽

Insertion Reactions ◽

Double Asymmetric Induction in Intramolecular C-H Insertion Reactions ofα-Diazoβ-Keto Esters

Synthetic Communications ◽

10.1080/00397919408010251 ◽

1994 ◽

Vol 24 (22) ◽

pp. 3277-3287 ◽

Cited By ~ 17

Author(s):

Shun-ichi Hashimoto ◽

Nobuhide Watanabe ◽

Katsuhiro Kawano ◽

Shiro Ikegami

Keyword(s):

Asymmetric Induction ◽

Insertion Reactions ◽

A Highly Chemo- and Stereoselective Synthesis of β-Keto Esters via a Polymer-Supported Lipase Catalyzed Transesterfication

The Journal of Organic Chemistry ◽

10.1021/jo001478o ◽

2001 ◽

Vol 66 (5) ◽

pp. 1906-1909 ◽

Cited By ~ 30

Author(s):

Armando Córdova ◽

Kim D. Janda

Keyword(s):

Keto Esters ◽

Polymer Supported

Stereoselective Synthesis of syn β-Hydroxy Cycloalkane Carboxylates: Transfer Hydrogenation of Cyclic β-Keto Esters via Dynamic Kinetic Resolution.

ChemInform ◽

10.1002/chin.200746026 ◽

2007 ◽

Vol 38 (46) ◽

Author(s):

Abel Ros ◽

Antonio Magriz ◽

Hansjoerg Dietrich ◽

Jose M. Lassaletta ◽

Rosario Fernandez

Keyword(s):

Kinetic Resolution ◽

Transfer Hydrogenation ◽

Dynamic Kinetic Resolution ◽

Asymmetric Induction in the [2,3] Wittig Rearrangement The Stereoselective Synthesis of Unsaturated Alcohols with Three Contiguous Stereogenic Centers

Chemische Berichte ◽

10.1002/cber.19891220130 ◽

1989 ◽

Vol 122 (1) ◽

pp. 193-198 ◽

Cited By ~ 19

Author(s):

Reinhard Brückner

Keyword(s):

Asymmetric Induction ◽

Wittig Rearrangement ◽

Unsaturated Alcohols ◽

Stereogenic Centers

Stereoselective Synthesis of Skipped Polyols by Substrate-Directed Asymmetric Induction

Organic Letters ◽

10.1021/ol0056325 ◽

2000 ◽

Vol 2 (9) ◽

pp. 1209-1212 ◽

Cited By ~ 11

Author(s):

Thomas Trieselmann ◽

Reinhard W. Hoffmann

Keyword(s):

Asymmetric Induction

ChemInform Abstract: Copper-Catalyzed Enantioselective Intramolecular C-H Insertion Reactions of α-Diazo-β-keto Esters and α-Diazo-β-keto Phosphonates.

ChemInform ◽

10.1002/chin.201336049 ◽

2013 ◽

Vol 44 (36) ◽

pp. no-no

Author(s):

Catherine N. Slattery ◽

Anita R. Maguire

Keyword(s):

Insertion Reactions ◽

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 ◽

ChemInform Abstract: STEREOSELECTIVE REDUCTION OF β-KETO ESTERS WITH ZINC BOROHYDRIDE. STEREOSELECTIVE SYNTHESIS OF ERYTHRO-3-HYDROXY-2-ALKYLPROPIONATES

Chemischer Informationsdienst ◽

10.1002/chin.198031103 ◽

1980 ◽

Vol 11 (31) ◽

Author(s):

T. NAKATA ◽

T. OISHI

Keyword(s):

Stereoselective Reduction ◽

A Facile and Mild Approach for Stereoselective Synthesis of α-Fluoro-α,β-unsaturated Esters from α-Fluoro-β-keto Esters via Deacylation

Synlett ◽

10.1055/s-0034-1378917 ◽

2014 ◽

Vol 26 (01) ◽

pp. 127-132 ◽

Cited By ~ 3

Author(s):

Wenbin Yi ◽

Jinlong Qian ◽

Meifang Lv ◽

Chun Cai

Keyword(s):

Unsaturated Esters ◽