Stereoselective Synthesis of Highly Substituted .gamma.-Lactones and Butenolides by Intramolecular Michael Addition of Enantiomerically Enriched .gamma.-[(Phenylthio)acyl]oxy .alpha.,.beta.-Unsaturated Esters

Carmen M. Rodriguez; Tomas Martin; Miguel A. Ramirez; Victor S. Martin

doi:10.1021/jo00095a022

Stereoselective Synthesis of Highly Substituted .gamma.-Lactones and Butenolides by Intramolecular Michael Addition of Enantiomerically Enriched .gamma.-[(Phenylthio)acyl]oxy .alpha.,.beta.-Unsaturated Esters

The Journal of Organic Chemistry ◽

10.1021/jo00095a022 ◽

1994 ◽

Vol 59 (16) ◽

pp. 4461-4472 ◽

Cited By ~ 21

Author(s):

Carmen M. Rodriguez ◽

Tomas Martin ◽

Miguel A. Ramirez ◽

Victor S. Martin

Keyword(s):

Michael Addition ◽

Stereoselective Synthesis ◽

Unsaturated Esters ◽

Alpha Beta

A stereoselective synthesis of (Z)- and (E)-trifluoromethylated .alpha.,.beta.-unsaturated esters via intramolecular Wittig reaction

The Journal of Organic Chemistry ◽

10.1021/jo00069a014 ◽

1993 ◽

Vol 58 (17) ◽

pp. 4564-4566 ◽

Cited By ~ 37

Author(s):

Yanchang Shen ◽

Shu Gao

Keyword(s):

Wittig Reaction ◽

Stereoselective Synthesis ◽

Unsaturated Esters ◽

Intramolecular Wittig Reaction ◽

Alpha Beta

Stereoselective synthesis of tetrasubstituted .alpha.,.beta.-unsaturated esters

The Journal of Organic Chemistry ◽

10.1021/jo00035a043 ◽

1992 ◽

Vol 57 (9) ◽

pp. 2753-2755 ◽

Cited By ~ 8

Author(s):

Jacob Mathew

Keyword(s):

Stereoselective Synthesis ◽

Unsaturated Esters ◽

Alpha Beta

Carbamate-mediated functionalization of unsaturated alcohols. 3. Intramolecular Michael addition of O-carbamates to .alpha.,.beta.-unsaturated esters. A new diastereoselective amination in an acyclic system

Journal of the American Chemical Society ◽

10.1021/ja00292a077 ◽

1985 ◽

Vol 107 (6) ◽

pp. 1797-1798 ◽

Cited By ~ 68

Author(s):

Masahiro Hirama ◽

Takeo Shigemoto ◽

Yutaka Yamazaki ◽

Sho Ito

Keyword(s):

Michael Addition ◽

Unsaturated Esters ◽

Unsaturated Alcohols ◽

Alpha Beta

threo-Selective Michael Addition ofN,N-Dibenzylglycinate and Alaninate Enolates to α,β-Unsaturated Esters. A Concise and Stereoselective Synthesis of (±)-CCG-II

Chemistry Letters ◽

10.1246/cl.1990.377 ◽

1990 ◽

Vol 19 (3) ◽

pp. 377-380 ◽

Cited By ~ 8

Author(s):

Masahiko Yamaguchi ◽

Kazuhiko Torisu ◽

Toru Minami

Keyword(s):

Michael Addition ◽

Stereoselective Synthesis ◽

Unsaturated Esters

Highly diastereoselective Michael addition of lithiated camphor imines of glycine esters to .alpha.,.beta.-unsaturated esters. Synthesis of optically pure 5-oxo-2,4-pyrrolidinedicarboxylates of unnatural stereochemistry

The Journal of Organic Chemistry ◽

10.1021/jo00008a052 ◽

1991 ◽

Vol 56 (8) ◽

pp. 2875-2883 ◽

Cited By ~ 46

Author(s):

Shuji Kanemasa ◽

Akira Tatsukawa ◽

Eiji Wada

Keyword(s):

Michael Addition ◽

Unsaturated Esters ◽

Alpha Beta ◽

Optically Pure

Michael addition of silylated telluronium allylide to α,β-unsaturated esters: facile and stereoselective synthesis of trimethylsilylvinylcyclopropane derivatives

Journal of the Chemical Society Chemical Communications ◽

10.1039/c39930000007 ◽

1993 ◽

pp. 7-9 ◽

Cited By ~ 12

Author(s):

Yao-Zeng Huang ◽

Yong Tang ◽

Zhang-Lin Zhou ◽

Ji-Ling Huang

Keyword(s):

Michael Addition ◽

Stereoselective Synthesis ◽

Unsaturated Esters

ChemInform Abstract: Michael Addition of Silylated Telluronium Allylide to α,β- Unsaturated Esters: Facile and Stereoselective Synthesis of Trimethylsilylvinylcyclopropane Derivatives.

ChemInform ◽

10.1002/chin.199317081 ◽

2010 ◽

Vol 24 (17) ◽

pp. no-no

Author(s):

Y.-Z. HUANG ◽

Y. TANG ◽

Z.-L. ZHOU ◽

J.-L. HUANG

Keyword(s):

Michael Addition ◽

Stereoselective Synthesis ◽

Unsaturated Esters

ChemInform Abstract: A Facile and Mild Approach for Stereoselective Synthesis of α-Fluoro-.alpha±beta.-unsaturated Esters from α-Fluoro-β-keto Esters via Deacylation.

ChemInform ◽

10.1002/chin.201523084 ◽

2015 ◽

Vol 46 (23) ◽

pp. no-no

Author(s):

Jinlong Qian ◽

Wenbin Yi ◽

Meifang Lv ◽

Chun Cai

Keyword(s):

Stereoselective Synthesis ◽

Unsaturated Esters ◽

Keto Esters ◽

Alpha Beta

ChemInform Abstract: A Diastereo- and Enantioselective Michael Addition of Chiral Amide Enolates to α,β-Unsaturated Esters: A Stereoselective Synthesis of (+)-Dehydroiridodiol and (-)-Isodehydroiridodiol.

Chemischer Informationsdienst ◽

10.1002/chin.198631111 ◽

1986 ◽

Vol 17 (31) ◽

Author(s):

M. YAMAGUCHI ◽

K. HASEBE ◽

S. TANAKA ◽

T. MINAMI

Keyword(s):

Michael Addition ◽

Stereoselective Synthesis ◽

Unsaturated Esters

Stereoselective synthesis of trisubstituted .alpha.,.beta.-unsaturated esters and amides via reactions of tantalum-alkyne complexes derived from acetylenic esters and amides with carbonyl compounds

The Journal of Organic Chemistry ◽

10.1021/jo00021a005 ◽

1991 ◽

Vol 56 (21) ◽

pp. 5980-5982 ◽

Cited By ~ 20

Author(s):

Kazuhiko Takai ◽

Makoto Tezuka ◽

Kiitiro Utimoto

Keyword(s):

Carbonyl Compounds ◽

Stereoselective Synthesis ◽

Acetylenic Esters ◽

Unsaturated Esters ◽

Alpha Beta ◽

Alkyne Complexes