A highly enantioselective Michael reaction between α, β-unsaturated ketones and malonic acid half-thioesters. (20th May 2015)
- Record Type:
- Journal Article
- Title:
- A highly enantioselective Michael reaction between α, β-unsaturated ketones and malonic acid half-thioesters. (20th May 2015)
- Main Title:
- A highly enantioselective Michael reaction between α, β-unsaturated ketones and malonic acid half-thioesters
- Authors:
- Ren, Qiao
Gao, Tao
Li, Wenjun
Wan, Li
Hu, Yimin
Peng, Yanhong
Sun, Shaofa
Hu, Liqiang
Wu, Minghu
Guo, Haibing
Wang, Jian - Abstract:
- Abstract : An organocatalytic Michael reaction of enones and malonic acid half thioesters catalyzed by a chiral amine has been developed. Abstract : We disclose herein an efficient enantioselective organocatalytic Michael reaction between α, β-unsaturated ketones and malonic acid half thioesters (MAHTs). The reactions are catalyzed by a primary amine to generate Michael addition products in good to excellent yields (62–87%) with high to excellent enantioselectivities (80–98%).
- Is Part Of:
- New journal of chemistry. Volume 39:Number 7(2015:Jul.)
- Journal:
- New journal of chemistry
- Issue:
- Volume 39:Number 7(2015:Jul.)
- Issue Display:
- Volume 39, Issue 7 (2015)
- Year:
- 2015
- Volume:
- 39
- Issue:
- 7
- Issue Sort Value:
- 2015-0039-0007-0000
- Page Start:
- 5100
- Page End:
- 5103
- Publication Date:
- 2015-05-20
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/c5nj00719d ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 6652.xml