A Novel Synthesis of Highly Branched-Alkyl Aryl Ketones Using the Conjugate Addition of the Gilman Lithio Cuprate toβ-Methylthio-α,β-unsaturated Ketones: Abnormal Reactivity of the Intermediary Enolates toward Molecular Oxygen

1999 ◽  
Vol 28 (2) ◽  
pp. 107-108 ◽  
Author(s):  
Takayuki Arai ◽  
Motohiro Akazome ◽  
Katsuyuki Ogura
1981 ◽  
Vol 34 (1) ◽  
pp. 181 ◽  
Author(s):  
DJ Hannah ◽  
RAJ Smith ◽  
I Teoh ◽  
RT Weavers

The reaction of a series of organocuprate systems containing alkyl, aryl, alkynyl, silylalkyl or phenylthio groups with (1) is reported. Some of these organocuprates showed electron transfer properties and were relatively unreactive toward conjugate addition, hence have potential synthetic application as organocuprates involving an external electrophile.


1980 ◽  
Vol 45 (15) ◽  
pp. 3053-3061 ◽  
Author(s):  
Jeffrey Schwartz ◽  
Denise B. Carr ◽  
Robert T. Hansen ◽  
Fabian M. Dayrit

2017 ◽  
Vol 15 (19) ◽  
pp. 4191-4198 ◽  
Author(s):  
Haojiang Wang ◽  
Yifeng Wang ◽  
Cheng Zhang ◽  
Yidong Jiang ◽  
Mingming Chu ◽  
...  

A highly enantioselective conjugate addition of 2-substituted benzofuran-3(2H)-ones to α,β-unsaturated ketones promoted by chiral copper complexes has been developed.


Sign in / Sign up

Export Citation Format

Share Document