THE ISOXAZOLINE-5-SPIROCYCLOPROPANE ROUTE TO (+/-)-PUMILIOTOXIN-C

被引：33

作者：

BRANDI, A ^{[1
]}

CORDERO, FM ^{[1
]}

GOTI, A ^{[1
]}

GUARNA, A ^{[1
]}

机构：

[1] UNIV FLORENCE,CNR,CTR COMPOSTI ETEROCICLICI,I-50121 FLORENCE,ITALY

来源：

TETRAHEDRON LETTERS | 1992年 / 33卷 / 44期

关键词：

D O I：

10.1016/S0040-4039(00)61023-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A new total synthesis of (+/-)-Pumiliotoxin C has been achieved by the key thermal rearrangement of an appropriate 5-spirocyclopropane isoxazoline.

引用

页码：6697 / 6700

页数：4

共 14 条

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[5] REARRANGEMENT OF ISOXAZOLINE-5-SPIRO DERIVATIVES .5. DIASTEREOFACIAL SELECTIVITY IN THE CYCLOADDITION OF SUBSTITUTED 5-MEMBERED CYCLIC NITRONES AND METHYLENECYCLOPROPANES - STEREOSELECTIVE SYNTHESIS OF 3,5-SUBSTITUTED INDOLIZIDINONES
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