Highly Efficient Copper(I) Iodide-Tolyl-BINAP-Catalyzed Asymmetric Conjugate Addition of Methylmagnesium Bromide to α,β-Unsaturated Esters

2008 ◽  
Vol 350 (5) ◽  
pp. 673-677 ◽  
Author(s):  
Shun-Yi Wang ◽  
Tze-Keong Lum ◽  
Shun-Jun Ji ◽  
Teck-Peng Loh
Keyword(s):  
Conjugate Addition ◽  
Unsaturated Esters ◽  
Highly Efficient

scholarly journals Conjugate Addition of Grignard Reagents to alpha,beta-Unsaturated Esters. XVI. Reactions with sec-Butyl Cinnamate.

1970 ◽  
Vol 24 ◽  
pp. 2641-2647 ◽  
Author(s):  
S. Rosendal Jensen ◽  
A.-M. Kristiansen ◽  
J. Munch-Petersen ◽  
Ragnar Ohlson ◽  
Akira Shimizu
Keyword(s):  
Conjugate Addition ◽  
Grignard Reagents ◽  
Unsaturated Esters ◽  
Alpha Beta

Enantioselective conjugate addition of hydroxylamines to α,β-unsaturated 2-acyl imidazoles catalyzed by a chiral-at-metal Rh(iii) complex

2017 ◽  
Vol 4 (4) ◽  
pp. 573-577 ◽  
Author(s):  
Tao Deng ◽  
Ganesh Kumar Thota ◽  
Yi Li ◽  
Qiang Kang
Keyword(s):  
Amino Acid ◽  
Michael Addition ◽  
Conjugate Addition ◽  
Amino Acid Derivatives ◽  
Highly Efficient

A highly efficient chiral-at-metal Rh(iii) complex catalyzed asymmetric aza-Michael addition was developed, affordingN-protected β-amino acid derivatives with excellent enantioselectivity.

Highly efficient procedure for the conjugate addition of amines to electron deficient alkenes

2010 ◽  
Vol 51 (2) ◽  
pp. 225-228 ◽  
Author(s):  
An-ping Liao ◽  
Ping Lan ◽  
Mei Li ◽  
Li-hong Lan
Keyword(s):  
Conjugate Addition ◽  
Efficient Procedure ◽  
Highly Efficient
Sign in / Sign up

Export Citation Format

Share Document