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Chiral pyrrolidine-azole conjugates: Simple and efficient asymmetric organocatalysts for Michael addition to nitrostyrenes
Zhang Long2,3; Xu Hui1; Mi XueLing2,3; Luo SanZhong1; Cheng Jin-Pei1,2,3
2010-06-01
Source PublicationCHINESE SCIENCE BULLETIN
ISSN1001-6538
Volume55Issue:17Pages:1735-1741
AbstractSimple pyrrolidine-azole conjugates have been synthesized and found to be efficient catalysts for asymmetric Michael addition to nitrostyrenes. The identified optimal catalysts, pyrrolidine-azoles 2, 8 and 13, could catalyze the asymmetric Michael addition of a range of Michael donors and nitrostyrenes in high yields (up to 99%) and excellent stereoselectivities (up to 99: 1 dr and 97% ee).
KeywordPyrrolidine Azole Organocatalysis Michael Addition Nitrostyrene
DOI10.1007/s11434-010-3120-9
Indexed BySCI
Language英语
WOS IDWOS:000278900800007
PublisherSCIENCE PRESS
Citation statistics
Cited Times:3[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/70130
Collection中国科学院化学研究所
Corresponding AuthorLuo SanZhong
Affiliation1.Chinese Acad Sci, BNLMS, CAS Key Lab Mol Recognit & Funct, Inst Chem, Beijing 100190, Peoples R China
2.Nankai Univ, Dept Chem, Tianjin 300071, Peoples R China
3.Nankai Univ, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China
Recommended Citation
GB/T 7714
Zhang Long,Xu Hui,Mi XueLing,et al. Chiral pyrrolidine-azole conjugates: Simple and efficient asymmetric organocatalysts for Michael addition to nitrostyrenes[J]. CHINESE SCIENCE BULLETIN,2010,55(17):1735-1741.
APA Zhang Long,Xu Hui,Mi XueLing,Luo SanZhong,&Cheng Jin-Pei.(2010).Chiral pyrrolidine-azole conjugates: Simple and efficient asymmetric organocatalysts for Michael addition to nitrostyrenes.CHINESE SCIENCE BULLETIN,55(17),1735-1741.
MLA Zhang Long,et al."Chiral pyrrolidine-azole conjugates: Simple and efficient asymmetric organocatalysts for Michael addition to nitrostyrenes".CHINESE SCIENCE BULLETIN 55.17(2010):1735-1741.
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