An unprecedented catalytic reaction using gold(I) complexes

被引:33
作者
Ito, H
Yajima, T
Tateiwa, J
Hosomi, A [1 ]
机构
[1] Univ Tsukuba, Dept Chem, Tsukuba, Ibaraki 3058571, Japan
[2] Univ Tsukuba, Grad Sch Chem, Tsukuba, Ibaraki 3058571, Japan
关键词
gold; gold compounds; catalysis; tin; tin compounds;
D O I
10.1016/S0040-4039(99)01621-4
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
This paper describes an unprecedented catalytic reaction using Au(I) complexes. Au complexes efficiently catalyze dehydrogenative dimerization of trialkylstannanes. Catalytic activity of the Au(I) complex toward dehydrogenative dimerization of the trialkylstannane is extremely high (0.1 mol%, 48 h) comparable to that of Pd catalysts. The synthetic generality of this reaction was demonstrated for the reaction using tributyl-, trioctyl-, triphenylstannane. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:7807 / 7810
页数:4
相关论文
共 21 条
[1]  
DAVIES AG, 1997, ORGANOTIN CHEM, P203
[2]   EFFECTIVE TRANSFORMATION OF UNACTIVATED ALKYNES INTO KETONES OR ACETALS BY MEANS OF AU(III) CATALYST [J].
FUKUDA, Y ;
UTIMOTO, K .
JOURNAL OF ORGANIC CHEMISTRY, 1991, 56 (11) :3729-3731
[3]  
GROHMANN A, 1995, COMPREHENSIVE ORGA 2, V3, P1, DOI DOI 10.1016/B978-008046519-7.00021-6
[4]   Studies on organosilicon chemistry.: Part 145.: New method for introduction of a silyl group into α,β-enones using a disilane catalyzed by a copper(I) salt [J].
Ito, H ;
Ishizuka, T ;
Tateiwa, J ;
Sonoda, M ;
Hosomi, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (43) :11196-11197
[5]   Studies on organosilicon chemistry. 138. Generation of a reducing reagent from copper(I) salt and hydrosilane. New practical method for conjugate reduction [J].
Ito, H ;
Ishizuka, T ;
Arimoto, K ;
Miura, K ;
Hosomi, A .
TETRAHEDRON LETTERS, 1997, 38 (51) :8887-8890
[6]   Direct alkynyl group transfer from silicon to copper: New preparation method of alkynylcopper (I) reagents [J].
Ito, H ;
Arimoto, K ;
Sensui, H ;
Hosomi, A .
TETRAHEDRON LETTERS, 1997, 38 (22) :3977-3980
[7]   Highly stereoselective metathesis reaction between optically active hydrosilane and copper(I) salt in 1,3-dimethyl-2-imidazolidinone [J].
Ito, H ;
Ishizuka, T ;
Okumura, T ;
Yamanaka, H ;
Tateiwa, J ;
Sonoda, M ;
Hosomi, A .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1999, 574 (01) :102-106
[8]   New access to cross-coupling reaction between arylsilanes or heteroarylsilanes and aryl halides mediated by a copper(I) salt [J].
Ito, H ;
Sensui, H ;
Arimoto, K ;
Miura, K ;
Hosomi, A .
CHEMISTRY LETTERS, 1997, (07) :639-640
[9]   CATALYTIC ASYMMETRIC ALDOL REACTION - REACTION OF ALDEHYDES WITH ISOCYANOACETATE CATALYZED BY A CHIRAL FERROCENYLPHOSPHINE-GOLD(I) COMPLEX [J].
ITO, Y ;
SAWAMURA, M ;
HAYASHI, T .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (20) :6405-6406
[10]   REDUCTIVE ELIMINATION AND ISOMERIZATION OF ORGANOGOLD COMPLEXES - THEORETICAL STUDIES OF TRIALKYLGOLD SPECIES AS REACTIVE INTERMEDIATES [J].
KOMIYA, S ;
ALBRIGHT, TA ;
HOFFMANN, R ;
KOCHI, JK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1976, 98 (23) :7255-7265