STRUCTURAL ELUCIDATION OF THE CYCLIC PRODUCTS FORMED BY THE REACTION OF 2,3-O-ISOPROPYLIDENE DERIVATIVES OF ALDEHYDO-ALDOSE WITH ALLYLSILANES, VINYL ETHERS, OR VINYL SULFIDES IN THE PRESENCE OF BORON-TRIFLUORIDE ETHERATE

被引：29

作者：

SUGIMURA, H

机构：

[1] The Noguchi Institute, Itabashi-ku, Tokyo, 173, 1-8-1, Kaga

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 41期

关键词：

D O I：

10.1016/S0040-4039(00)97991-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The structural elucidation of the cyclic products derived from 2,3-O-isopropylidene derivatives of aldehydo-aldose and allylsilanes, vinyl ethers, or vinyl sulfides indicated that tetrahydrofuran derivatives were formed by cyclization accompanied with migration of the isopropylidene group. © 1990.

引用

页码：5909 / 5912

页数：4

共 14 条

[1]

COLVIN E, 1980, SILICON ORGANIC SYNT, P97

[2] LATENT ACETONYLATION OF ALPHA,BETA-ENONES WITH ALLYLTRIMETHYLSILANE OR 2-METHYL-2-PROPENYLTRIMETHYLSILANE - SYNTHESIS OF 1,5-DIKETONES AND ANNELATION TO FUSED CYCLOHEXENONES [J].