Synthesis of Analogues of the Antitumor (1→6)-Branched (1→3)-Glucohexaose  被引量:2

Synthesis of Analogues of the Antitumor (1→6)-Branched (1→3)-Glucohexaose

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作  者:曾佑林 张建军 孔繁祚 

机构地区:[1]Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China

出  处:《Chinese Journal of Chemistry》2004年第5期460-466,共7页中国化学(英文版)

基  金:Project supported by Chinese Academy of Sciences (No. KZCX3-J-08) and the National Science Foundation of China (Nos. 30070185 and 39970964).

摘  要:b-D-Glcp-(13)-[b-D-Glcp-(16)-]a-D-Manp-(13)-b-D-Glcp-(13)-[b-D-Glcp-(16)-]D-Glcp (18) and b-D-Glcp-(13)-[b-D-Glcp-(16)-]a-D-Manp-(13)-b-D-Glcp-(13)-[b-D-Glcp-(16)-]b-D-Glcp-D-(13)-Glcp-1OMe (29) were synthesized as the analogues of the immunomodulator b-D-Glcp-(13)-[b-D-Glcp- (16)-]a-D-Glcp-(13)-b-D-Glcp-(13)-[b-D-Glcp-(16)-]D-Glcp through coupling of trisaccharide donors 9 with trisaccharide acceptor 16 and tetrasaccharide acceptor 27 followed by deprotection, respectively.b-D-Glcp-(13)-[b-D-Glcp-(16)-]a-D-Manp-(13)-b-D-Glcp-(13)-[b-D-Glcp-(16)-]D-Glcp (18) and b-D-Glcp-(13)-[b-D-Glcp-(16)-]a-D-Manp-(13)-b-D-Glcp-(13)-[b-D-Glcp-(16)-]b-D-Glcp-D-(13)-Glcp-1OMe (29) were synthesized as the analogues of the immunomodulator b-D-Glcp-(13)-[b-D-Glcp- (16)-]a-D-Glcp-(13)-b-D-Glcp-(13)-[b-D-Glcp-(16)-]D-Glcp through coupling of trisaccharide donors 9 with trisaccharide acceptor 16 and tetrasaccharide acceptor 27 followed by deprotection, respectively.

关 键 词:OLIGOSACCHARIDE trichloroacetimidate regio- and stereoselective synthesis 

分 类 号:O621[理学—有机化学]

 

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