ASYMMETRIC-SYNTHESIS OF THE MACROLIDE (-)-ASPICILIN

被引：40

作者：

SOLLADIE, G

FERNANDEZ, I

MAESTRO, C

机构：

[1] Ecole Européenne des Hautes Etudes des Industries Chimiques (URA du CNRS 466)

来源：

TETRAHEDRON-ASYMMETRY | 1991年 / 2卷 / 08期

关键词：

D O I：

10.1016/S0957-4166(00)80464-4

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The asymmetric synthesis of 4(S), 5(R), 6(S), 17(R)-(-)-Aspicilin is described. The chiral parts of the molecule were obtained by asymmetric synthesis monitored by a chiral sulfoxide group.

引用

页码：801 / 819

页数：19

共 19 条

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[13]

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[16] REDUCTION OF BETA-HYDROXYSULFOXIDES - APPLICATION TO THE SYNTHESIS OF OPTICALLY-ACTIVE EPOXIDES [J].

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[17]

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[18] STEREOCONTROLLED TOTAL SYNTHESIS OF THE MACROCYCLIC LACTONE (-)-ASPICILIN [J].

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TETRAHEDRON LETTERS, 1987, 28 (21) :2409-2412

[19]

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