Synthesis of heptasaccharide and nonasaccharide analogues of the lentinan repeating unit
文献类型:期刊论文
作者 | Yang, GB; Kong, FZ |
刊名 | CARBOHYDRATE RESEARCH
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出版日期 | 2005 |
卷号 | 340期号:1页码:39-48 |
关键词 | Trichloroacetimidate Beta-(1 -> 6)-branched Beta-(1 -> 3)-glucan Synthesis |
DOI | 10.1016/j.carres.2004.11.005 |
英文摘要 | The allyl glycoside beta-D-Glcp-(1 --> 3)-beta-D-Glcp-(1 --> 3)-[beta-D-Glcp-(1 --> 6)]-beta-D-Glcp-(1 --> 3)-beta-D-Glcp-(1 --> 3)-[beta-D-Glcp(1 --> 6)]-alpha-D-Glcp (18) and the acetonyl glycoside of beta-D-Glcp-(1 --> 3)-[beta-D-Glcp-(1 --> 6)]-beta-D-Glcp-(1 --> 3)-beta-D-Glcp-(1 --> 3)-[beta-D-Glcp-(1 --> 6)]-beta-D-Glcp-(1 --> 3)-beta-D-Glcp-(1 --> 3)-[beta-D-Glcp-(1 --> 6)]-alpha-D-Glcp (28) were synthesized as analogues of the lentinan heptaose repeating unit. 4,6-O-Benzylidenated monosaccharide donor 3 and 4,6-0-benzylidenated tetrasaccharide acceptor 14 were used to ensure the P-linkage in the synthesis of 18, while 4,6-0-benzylidenated disaccharide acceptor 20, and 4,6-0-benzylidenated disaccharide donors 21 and 24 were used to ensure the beta-linkage in the synthesis of 28. (C) 2004 Elsevier Ltd. All rights reserved. |
学科主题 | Biochemistry & Molecular Biology ; Chemistry |
WOS研究方向 | Biochemistry & Molecular Biology ; Chemistry |
WOS记录号 | WOS:000226538800005 |
源URL | [http://ir.rcees.ac.cn/handle/311016/23382] ![]() |
专题 | 生态环境研究中心_中国科学院环境生物技术重点实验室 |
推荐引用方式 GB/T 7714 | Yang, GB,Kong, FZ. Synthesis of heptasaccharide and nonasaccharide analogues of the lentinan repeating unit[J]. CARBOHYDRATE RESEARCH,2005,340(1):39-48. |
APA | Yang, GB,&Kong, FZ.(2005).Synthesis of heptasaccharide and nonasaccharide analogues of the lentinan repeating unit.CARBOHYDRATE RESEARCH,340(1),39-48. |
MLA | Yang, GB,et al."Synthesis of heptasaccharide and nonasaccharide analogues of the lentinan repeating unit".CARBOHYDRATE RESEARCH 340.1(2005):39-48. |
入库方式: OAI收割
来源:生态环境研究中心
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