A convenient enantioselective synthesis of natural (1R,3S)-amidinomycin

被引:7
作者
Nagata, H [1 ]
Taniguchi, T [1 ]
Ogasawara, K [1 ]
机构
[1] TOHOKU UNIV,INST PHARMACEUT,SENDAI,MIYAGI 98077,JAPAN
关键词
D O I
10.1016/S0957-4166(97)00342-X
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Natural (1R,3S)-amidinomycin, an antiviral metabolite isolated from Streptomyces species, has been synthesized conveniently from (+)-norcamphor in an enantioselective manner. (C) 1997 Published by Elsevier Science Ltd.
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页码:2679 / 2681
页数:3
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