Direct Asymmetric Michael Additions of Ketones to Nitroolefins and Chalcones Catalyzed by a Chiral C2-Symmetric Pyrrolidine-based Tetraamine
C2-Symmetric pyrrolidine-based tetraamine, available from commercially starting materials, showed good cata- lytic activity for asymmetric Michael additions of ketones to nitroalkenes especially to chalcones. The reactions proceeded to give the corresponding products in good yields and in a highly s...
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Published in | Chinese journal of chemistry Vol. 30; no. 11; pp. 2707 - 2713 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
01.11.2012
WILEY‐VCH Verlag Wiley Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | C2-Symmetric pyrrolidine-based tetraamine, available from commercially starting materials, showed good cata- lytic activity for asymmetric Michael additions of ketones to nitroalkenes especially to chalcones. The reactions proceeded to give the corresponding products in good yields and in a highly selective manner. |
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Bibliography: | 31-1547/O6 C2-Symmetric pyrrolidine-based tetraamine, available from commercially starting materials, showed good cata- lytic activity for asymmetric Michael additions of ketones to nitroalkenes especially to chalcones. The reactions proceeded to give the corresponding products in good yields and in a highly selective manner. asymmetric catalysis, Michael addition, tetraamine, chalcones, enantioselectivity Ma, Shijun Wu, Lulu Liu, Ming Wang, Yongmei Department of Chemistry, The Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China ark:/67375/WNG-4X62D6WB-W istex:9E249E850270F2F01D3CBC6AC0D186A397F80B8E the Nankai University State Key Laboratory of Elemento-Organic Chemistry National Basic Research Program of China (973 Program) - No. 2010CB833300 ArticleID:CJOC201200214 the Ph.D. Programs Foundation of Ministry of Education of China - No. 20090031110019 ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 14 |
ISSN: | 1001-604X 1614-7065 |
DOI: | 10.1002/cjoc.201200214 |