DIASTEREOSELECTIVE [2,3] WITTIG REARRANGEMENT OF CARBOHYDRATE-DERIVED TERTIARY ALLYLIC ETHERS .2. SYNTHESIS OF AN ADVANCED RAPAMYCIN INTERMEDIATE FROM D-GLUCOSE

被引：0

作者：

NY, S ^{[1
]}

KALLMERTEN, J ^{[1
]}

机构：

[1] SYRACUSE UNIV,DEPT CHEM,SYRACUSE,NY 13244

来源：

TETRAHEDRON LETTERS | 1993年 / 34卷 / 05期

关键词：

D O I：

暂无

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The advanced rapamycin intermediate 26 has been prepared by an iterative sigmatropic sequence incorporating the diastereoselective [2,3] Wittig rearrangement of a D-glucofuranose-derived tertiary allylic ether.

引用

页码：753 / 756

页数：4

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