Reduction of alpha-halo carbonyl compounds with NaBH4-SbBr3

被引：13

作者：

Sayama, S

Inamura, Y

机构：

[1] Department of Chemistry, Fukushima Medical College, Hikarigaoka

来源：

CHEMISTRY LETTERS | 1996年 / 08期

关键词：

D O I：

10.1246/cl.1996.633

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The reagent NaBH4-SbBr3 was found to be chemoselective for the reductive debromination of aromatic alpha-bromo carbonyl compounds and 2,3-dibromo-1,4-butanediones.

引用

页码：633 / 634

页数：2

共 4 条

[1] DEHALOGENATION OF ALPHA-HALO CARBONYL-COMPOUNDS BY A NEW EFFICIENT REAGENT, TRIPHENYLPHOSPHONIUM IODIDE
KAMIYA, N
TANMATU, H
ISHII, Y
[J]. CHEMISTRY LETTERS, 1992, (02) : 293 - 296
[2] LAROCK RC, 1989, COMPREHENSIVE ORGANI, P21
[3] Studies on unsaturated 1,4-diketones. III. The mode of addition of halogen to dibenzoylethylene
Lutz, RE
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1927, 49 : 1106 - 1111
[4] CONJUGATE REDUCTION OF 2-BUTENE-1,4-DIONES WITH LIALH4-SBCL3
SAYAMA, S
INAMURA, Y
[J]. BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1991, 64 (01) : 306 - 308

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