STEREOSELECTION IN IODOLACTONISATIONS OF 3-SILYLOXY-5-ALKENOIC ACIDS

被引：10

作者：

BEDFORD, SB

FENTON, G

KNIGHT, DW

SHAW, D

机构：

[1] DEPT CHEM,UNIV PK,NOTTINGHAM NG7 2RD,ENGLAND

[2] 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)79027-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Iodolactonisations of (Z)- or (E) 3 silyloxy-5-alkenoic acids [1 and 7] both lead to trans-disubstituted valerolactones [6 and 8]. which differ only in the stereochemistry of the iodine substituent.

引用

页码：6505 / 6506

页数：2

共 7 条

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