A general procedure to enantiopure conduritols:: Sulfur-mediated synthesis of (+)-conduritol B and (-)-conduritol F derivatives and of (-)-conduritol E and F

被引：35

作者：

Cerè, V ^{[1
]}

Mantovani, G ^{[1
]}

Peri, F ^{[1
]}

Pollicino, S ^{[1
]}

Ricci, A ^{[1
]}

机构：

[1] Univ Bologna, Dept Organ Chem, I-40136 Bologna, Italy

来源：

TETRAHEDRON | 2000年 / 56卷 / 09期

关键词：

biologically active compounds; cyclitols; enantiomeric purity; thiosugars;

D O I：

10.1016/S0040-4020(00)00011-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

We have demonstrated the generality of a simple procedure, synthesizing enatiomerically pare (+)-conduritol B and (-)-conduritol F derivatives, starting, starting from D-mannitol and D-sorbitol, respectively. This method, slightly modified, can also be applied to the synthesis of unprotected conduritols: (-)-conduritol E and (-)-conduritol F were obtained. (C) 2000 Elsevier Science Ltd. All rights reserved.

引用

页码：1225 / 1231

页数：7

共 24 条

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