CIS-FUSED AND TRANS-FUSED DI-TETRAHYDROPYRANS BY REARRANGEMENT STEROIDAL SPIROACETALS

被引：4

作者：

DORTA, RL

FREIRE, R

MARTIN, A

SUAREZ, E

PRANGE, T

机构：

[1] CSIC,INST PROD NAT & AGROBIOL,E-38206 LA LAGUNA,SPAIN

[2] UNIV PARIS 11,LURE,F-91405 ORSAY,FRANCE

来源：

TETRAHEDRON LETTERS | 1995年 / 36卷 / 40期

关键词：

D O I：

10.1016/0040-4039(95)01472-T

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A new method for the synthesis of steroidal cis- and trans-fused di-tetrahydropyrans (1,6-dioxadecalins) by reduction with DIBAH of derivatives of 1,6-dioxaspiro[4.5]decan-10-yl methanesulfonate is described.

引用

页码：7309 / 7312

页数：4

共 19 条

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[6] STRUCTURE OF MAITOTOXIN
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[7] PARTIAL STRUCTURES OF MAITOTOXIN, THE MOST POTENT MARINE TOXIN FROM DINOFLAGELLATE GAMBIERDISCUS-TOXICUS
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[8] TOTAL SYNTHESIS OF BREVETOXIN-B .2. COMPLETION
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[9] TOTAL SYNTHESIS OF BREVETOXIN-B .1. CDEFG FRAMEWORK
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[10] HIGHLY REGIOSELECTIVE AND STEREOSELECTIVE REDUCTIONS OF SPIROKETALS
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[J]. TETRAHEDRON LETTERS, 1993, 34 (33) : 5303 - 5306

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