期刊
TETRAHEDRON LETTERS
卷 52, 期 3, 页码 377-380出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2010.11.045
关键词
Acid base organocatalyst; Domino reaction; Aza-MBH reaction; Tetrahydropyridines; Enantioselective reaction
资金
- Ministry of Education, Culture, Sports, Science and Technology, Japan
- Naito Foundation
- Grants-in-Aid for Scientific Research [22790010] Funding Source: KAKEN
A chiral acid-base organocatalyst was found to promote an aza-MBH domino process between alpha,beta-unsaturated carbonyl compounds and N-tosylimines to afford tetrahydropyridine derivatives with high enantioselectivity. (C) 2010 Elsevier Ltd. All rights reserved.
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