IODOETHERIFICATION OF HOMOALLYLIC ALCOHOLS - A STEREOSELECTIVE APPROACH TO TETRAHYDROFURANS

被引：44

作者：

BEDFORD, SB ^{[1
]}

BELL, KE ^{[1
]}

FENTON, G ^{[1
]}

HAYES, CJ ^{[1
]}

KNIGHT, DW ^{[1
]}

SHAW, D ^{[1
]}

机构：

[1] RHONE POULENC RORER,CENT RES,DAGENHAM RM10 7XS,ESSEX,ENGLAND

来源：

TETRAHEDRON LETTERS | 1992年 / 33卷 / 43期

关键词：

D O I：

10.1016/S0040-4039(00)79029-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Iodoetherification of homoallylic alcohols proceeds efficiently and with high levels of stereoselection by a 5-endo-trig process when anhydrous acetonitrile is used as the solvent.

引用

页码：6511 / 6514

页数：4

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