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
收藏
页码：1221 / 1230
页数：10
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