ICCAS OpenIR
Highly stereoselective alpha-O-glucosylation of heterocyclic ketene aminals
Chen, XM; Li, ZJ; Huang, ZT
2000-09-22
Source PublicationCARBOHYDRATE RESEARCH
ISSN0008-6215
Volume328Issue:3Pages:253-261
AbstractA new series of a-glucosides of heterocyclic ketene aminals have been synthesized. The double bonds of the glucosides resulted in Z or E configuration by using CaH2 or a Lewis acid as catalyst, respectively. A special complex of mercuric cyanide with glucopyranosides was the result when Hg(CN), was used to catalyze the reaction. (C) 2000 Elsevier Science Ltd. All rights reserved.
KeywordSynthesis Glucosylation Heterocyclic Ketene Aminal
Indexed ByIC ; CCR ; SCI
Language英语
WOS IDWOS:000089551400002
PublisherELSEVIER SCI LTD
Citation statistics
Cited Times:5[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/75634
Collection中国科学院化学研究所
Corresponding AuthorHuang, ZT
AffiliationChinese Acad Sci, Inst Chem, Ctr Mol Sci, Beijing 100080, Peoples R China
Recommended Citation
GB/T 7714
Chen, XM,Li, ZJ,Huang, ZT. Highly stereoselective alpha-O-glucosylation of heterocyclic ketene aminals[J]. CARBOHYDRATE RESEARCH,2000,328(3):253-261.
APA Chen, XM,Li, ZJ,&Huang, ZT.(2000).Highly stereoselective alpha-O-glucosylation of heterocyclic ketene aminals.CARBOHYDRATE RESEARCH,328(3),253-261.
MLA Chen, XM,et al."Highly stereoselective alpha-O-glucosylation of heterocyclic ketene aminals".CARBOHYDRATE RESEARCH 328.3(2000):253-261.
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