Ionic hydrogenation of acylferrocenes using zinc borohydride: An efficient, mild method for the preparation of alkylferrocenes

被引:10
作者
Bhattacharyya, S
机构
[1] Department of Chemistry, Vijoygarh College
[2] Department of Chemistry, University of Mississippi, University
关键词
D O I
10.1021/om950751n
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
An effective mild procedure for the reductive deoxygenation of alpha-ferrocenyl aldehydes, ketones, and alcohols into the corresponding alkylferrocenes is described using a combination of zinc borohydride and zinc chloride. This is the first example of such reactivity of zinc borohydride. The present method allows the synthesis of alkylferrocenes bearing terminally functionalized pendant chains.
引用
收藏
页码:1065 / 1066
页数:2
相关论文
共 48 条
[1]   NEW POLYAZA AND POLYAMMONIUM FERROCENE MACROCYCLIC LIGANDS THAT COMPLEX AND ELECTROCHEMICALLY RECOGNIZE TRANSITION-METAL CATIONS AND PHOSPHATE ANIONS IN WATER [J].
BEER, PD ;
CHEN, Z ;
DREW, MGB ;
KINGSTON, J ;
OGDEN, M ;
SPENCER, P .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1993, (13) :1046-1048
[2]   TITANIUM(IV) ISOPROPOXIDE AND SODIUM-BOROHYDRIDE - A REAGENT OF CHOICE FOR REDUCTIVE AMINATION [J].
BHATTACHARYYA, S .
TETRAHEDRON LETTERS, 1994, 35 (15) :2401-2404
[3]  
BHATTACHARYYA S, 1994, SYNLETT, P1029
[4]   REDUCTIVE ALKYLATIONS OF DIMETHYLAMINE USING TITANIUM(IV) ISOPROPOXIDE AND SODIUM-BOROHYDRIDE - AN EFFICIENT, SAFE, AND CONVENIENT METHOD FOR THE SYNTHESIS OF N,N-DIMETHYLATED TERTIARY-AMINES [J].
BHATTACHARYYA, S .
JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (15) :4928-4929
[5]   USE OF ZINC BOROHYDRIDE IN REDUCTIVE AMINATION - AN EFFICIENT AND MILD METHOD FOR N-METHYLATION OF AMINES [J].
BHATTACHARYYA, S ;
CHATTERJEE, A ;
DUTTACHOWDHURY, SK .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1994, (01) :1-2
[6]  
BHATTACHARYYA S, IN PRESS SYNLETT
[7]   RING MIGRATION IN ALKYLATED FERROCENES [J].
BUBLITZ, DE .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1964, 42 (11) :2381-&
[8]  
BUBLITZ DE, 1969, ORG REACTIONS, V17, P24
[9]  
BUBLITZ DE, 1969, ORG REACTIONS, V17, P28
[10]  
Cais M, 1966, ORGANOMET CHEM REV, V1, P435