ICCAS OpenIR
Regio- and stereo-selective reaction of chiral alkoxy- and aminomethyl-substituted alpha-silylallyl carbanions with aldehydes
Liu, L; Wang, D
1998-09-01
Source PublicationJOURNAL OF CHEMICAL RESEARCH-S
ISSN0308-2342
Issue9Pages:612-613
AbstractThe reactions of chiral alkoxy- and aminomethyl-substituted alpha-silylallyl carbanions with aldehydes gave 1-silyl homoallylic alcohols with high gamma-regioselection and E-stereoselection, as well as a diastereomeric excess of 8-69%, depending on the chiral substituents on silicon, the aldehydes and the base used.
Indexed BySCI ; CCR
Language英语
WOS IDWOS:000077722900065
PublisherROYAL SOC CHEMISTRY
Citation statistics
Cited Times:3[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/74408
Collection中国科学院化学研究所
Corresponding AuthorWang, D
AffiliationChinese Acad Sci, Inst Chem, Beijing 100080, Peoples R China
Recommended Citation
GB/T 7714
Liu, L,Wang, D. Regio- and stereo-selective reaction of chiral alkoxy- and aminomethyl-substituted alpha-silylallyl carbanions with aldehydes[J]. JOURNAL OF CHEMICAL RESEARCH-S,1998(9):612-613.
APA Liu, L,&Wang, D.(1998).Regio- and stereo-selective reaction of chiral alkoxy- and aminomethyl-substituted alpha-silylallyl carbanions with aldehydes.JOURNAL OF CHEMICAL RESEARCH-S(9),612-613.
MLA Liu, L,et al."Regio- and stereo-selective reaction of chiral alkoxy- and aminomethyl-substituted alpha-silylallyl carbanions with aldehydes".JOURNAL OF CHEMICAL RESEARCH-S .9(1998):612-613.
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