中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Stereoselective synthesis of D-alpha-glucopyranosides, di- and tri-saccharides via 6-O-acetyl-glucopyranosyl bromides

文献类型:期刊论文

作者Fei, CP; Ma, Y; Chan, TH
刊名CHINESE JOURNAL OF CHEMISTRY
出版日期1995-09-01
卷号13期号:5页码:454-459
关键词Stereoselection Alpha-d-pyranosyl Bromide Glycosidation C-13 Nmr
ISSN号1001-604X
英文摘要Acetyl bromide cleaved 2,3,4-tri-O-benzyl-1,6-anhydro-beta-glucopuranose (1a) or 2,3,4-tri-O-benzyl-1,6-anhydro-beta-D-galactopyrane (1a') to give the corresponding alpha-D-pyranosyl bromides (2). Reaction of 2 with ROH/diisopropylethylamine gave the corresponding alpha-glucopyranosides, di- and tri-saccharides with good yield. It was available to use C-13 NMR to monitor the glycosidation reaction.
语种英语
WOS记录号WOS:A1995TU13900011
出版者SCIENCE CHINA PRESS
源URL[http://ir.iccas.ac.cn/handle/121111/43617]  
专题中国科学院化学研究所
作者单位1.CHINESE ACAD SCI,INST CHEM,BEIJING 100080,PEOPLES R CHINA
2.MCGILL UNIV,DEPT CHEM,MONTREAL,PQ,CANADA
推荐引用方式
GB/T 7714
Fei, CP,Ma, Y,Chan, TH. Stereoselective synthesis of D-alpha-glucopyranosides, di- and tri-saccharides via 6-O-acetyl-glucopyranosyl bromides[J]. CHINESE JOURNAL OF CHEMISTRY,1995,13(5):454-459.
APA Fei, CP,Ma, Y,&Chan, TH.(1995).Stereoselective synthesis of D-alpha-glucopyranosides, di- and tri-saccharides via 6-O-acetyl-glucopyranosyl bromides.CHINESE JOURNAL OF CHEMISTRY,13(5),454-459.
MLA Fei, CP,et al."Stereoselective synthesis of D-alpha-glucopyranosides, di- and tri-saccharides via 6-O-acetyl-glucopyranosyl bromides".CHINESE JOURNAL OF CHEMISTRY 13.5(1995):454-459.

入库方式: OAI收割

来源:化学研究所

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