ICCAS OpenIR
Asymmetric allylation of aldehydes and alkylation using "carbon-centered" chiral organosilicon compounds
Wang, D
1999-09-01
Source PublicationCHINESE JOURNAL OF CHEMISTRY
ISSN1001-604X
Volume17Issue:5Pages:429-437
AbstractThe effects of the chiral substituents attached to silicon on the stereoselectivity of the reactions of C-centered chiral silicon compounds was examined. The investigation was focused on the asymmetric C-C bond formation reaction of chiral allylsilanes and a-silylallyl anions with aldehydes. The functionalities of the substituents on silicon can be manipulated to improve the stereoselectivities of the reactions remote from silicon atom.
KeywordCarbon-centered Chiral Organosilicon Compoung Asymmetric C-c Bond Formation Reaction Allylsilane Alpha-silylallyl Anion
Indexed BySCI
Language英语
WOS IDWOS:000083814600001
PublisherSCIENCE PRESS
Citation statistics
Cited Times:2[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/74924
Collection中国科学院化学研究所
Corresponding AuthorWang, D
AffiliationAcad Sinica, Inst Chem, Beijing 100080, Peoples R China
Recommended Citation
GB/T 7714
Wang, D. Asymmetric allylation of aldehydes and alkylation using "carbon-centered" chiral organosilicon compounds[J]. CHINESE JOURNAL OF CHEMISTRY,1999,17(5):429-437.
APA Wang, D.(1999).Asymmetric allylation of aldehydes and alkylation using "carbon-centered" chiral organosilicon compounds.CHINESE JOURNAL OF CHEMISTRY,17(5),429-437.
MLA Wang, D."Asymmetric allylation of aldehydes and alkylation using "carbon-centered" chiral organosilicon compounds".CHINESE JOURNAL OF CHEMISTRY 17.5(1999):429-437.
Files in This Item:
There are no files associated with this item.
Related Services
Recommend this item
Bookmark
Usage statistics
Export to Endnote
Google Scholar
Similar articles in Google Scholar
[Wang, D]'s Articles
Baidu academic
Similar articles in Baidu academic
[Wang, D]'s Articles
Bing Scholar
Similar articles in Bing Scholar
[Wang, D]'s Articles
Terms of Use
No data!
Social Bookmark/Share
All comments (0)
No comment.
 

Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.