CONJUGATE HYDROBORATION-REDUCTION AND ORGANOLITHIUM ADDITIONS TO ACYLKETENE ACETALS - SYNTHESIS OF MONOPROTECTED BETA-DICARBONYLS

被引：9

作者：

EID, CN ^{[1
]}

KONOPELSKI, JP ^{[1
]}

机构：

[1] UNIV CALIF SANTA CRUZ,DEPT CHEM,SANTA CRUZ,CA 95064

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 03期

关键词：

D O I：

10.1016/S0040-4039(00)94539-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Hydride and organolithium additions to acylketene acetals are presented. Results indicate conjugate addition to be the dominant reaction pathway, resulting in the formation of monoprotected β-diketones and β-ketoaldehydes. © 1990.

引用

页码：305 / 306

页数：2

共 9 条

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