CHIRAL SYNTHONS FROM CARVONE .7. CHIRAL SYNTHONS FROM MONOTERPENES - STEREOSELECTIVE SYNTHESES OF (-)5S,6S,9R-6-ISOPROPYL-9-METHYL-2-OXASPIRO[4.4]NONAN-3-ONE AND (-)3AR,6R,7AR-3A-METHYL-6-ISOPROPENYLHEXAHYDROBENZOFURAN-2-ONE

被引：10

作者：

SRIKRISHNA, A

SHARMA, GVR

NAGARAJU, S

机构：

[1] Department of Organic Chemistry, Indian Institute of Science, Bangalore

来源：

SYNTHETIC COMMUNICATIONS | 1992年 / 22卷 / 09期

关键词：

D O I：

10.1080/00397919208019303

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Highly stereoselective syntheses of two C-12 chiral synthons 3 and 9, mentioned in the title, starting from the monoterpenes R-limonene and R-carvone, using radical cyclisation as key reaction, are described.

引用

页码：1221 / 1230

页数：10

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