AN EFFICIENT DIPOLAR-CYCLOADDITION ROUTE TO THE PTEROSIN FAMILY OF SESQUITERPENES

被引:36
作者
CURTIS, EA [1 ]
SANDANAYAKA, VP [1 ]
PADWA, A [1 ]
机构
[1] EMORY UNIV,DEPT CHEM,ATLANTA,GA 30322
关键词
D O I
10.1016/0040-4039(95)00209-U
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A short synthesis of several members of the pterosin family of sesquiterpenes is described in which the key step involves a dipolar-cycloaddition using a carbonyl ylide.
引用
收藏
页码:1989 / 1992
页数:4
相关论文
共 26 条
[21]   REACTIONS OF PHOSPHORUS COMPOUNDS .24. PREPARATION AND REACTIONS OF PHOSPHONIUM BETAINES [J].
SCHWEIZER, EE ;
KOPAY, CM .
JOURNAL OF ORGANIC CHEMISTRY, 1971, 36 (11) :1489-+
[22]   AQUILIDE-A, A NEW MUTAGENIC COMPOUND ISOLATED FROM BRACKEN FERN (PTERIDIUM-AQUILINUM (L) KUHN) [J].
VANDERHOEVEN, JCM ;
LAGERWEIJ, WJ ;
POSTHUMUS, MA ;
VANVELDHUIZEN, A ;
HOLTERMAN, HAJ .
CARCINOGENESIS, 1983, 4 (12) :1587-1590
[23]   TOTAL SYNTHESIS OF ILLUDININE, ILLUDALIC ACID, AND ILLUDACETALIC ACID [J].
WOODWARD, RB ;
HOYE, TR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1977, 99 (24) :8007-8014
[24]  
YOSHIHIRA K, 1971, CHEM PHARM BULL, V19, P1491
[25]  
YOSHISHIRA K, 1978, PHYTOCHEMISTRY, V17, P275
[26]  
YOSHISHIRA K, 1978, CHEM PHARM BULL, V26, P2365