Asymmetric Kumada-Corriu cross-coupling reaction with Pd2(dba)3 and an N-Ar axially chiral mimetic-type ligand catalyst

被引:38
作者
Hideo, H
Fukuda, Y
Kondo, K
Okuno, H
Murakami, Y
Aoyama, T
机构
[1] Nagoya City Univ, Grad Sch Pharmaceut Sci, Mizuho Ku, Nagoya, Aichi 4678603, Japan
[2] Toho Univ, Fac Pharmaceut Sci, Funabashi, Chiba 2748510, Japan
关键词
Kumada-Corriu cross-coupling reaction; N-ar axially chiral; mimetic-type ligand; enantioselectivity;
D O I
10.1016/j.tet.2004.09.010
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A catalyst comprised of Pd-2(dba)(3).CHCl3 and an N-Ar axially chiral mimetic-type ligand, (S)-N-[2-(diphenyl-phosphanyl)naphthalene-1-yl]-2-(piperidinylmethyl)piperidine, provides good enantioselectivities for the asymmetric Kumada-Corriu cross-coupling reaction of 1-phenylethylmagnesium chloride and E-beta-bromostyrene derivatives with which it is more difficult to achieve high enantioselectivity. Furthermore, in the case of styrene derivatives bearing both vinyl and aryl bromide groups, the chemoselective asymmetric cross-coupling reaction of the vinyl bromide group is observed. This N-Ar axially chiral mimetic-type ligand allows easy synthesis of a wide variety of analogues, and starting from the initial ligand, the enantioselectivity of coupling products is improved by modifying the structure in the ligand. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:10701 / 10709
页数:9
相关论文
共 65 条
[1]   ASYMMETRIC REDUCTION OF PROCHIRAL KETONES WITH CHIRAL HYDRIDE REAGENTS PREPARED FROM LITHIUM ALUMINUM-HYDRIDE AND (S)-2-(N-SUBSTITUTED AMINOMETHYL)PYRROLIDINES [J].
ASAMI, M ;
OHNO, H ;
KOBAYASHI, S ;
MUKAIYAMA, T .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1978, 51 (06) :1869-1873
[2]   REACTIVE INTERMEDIATES IN ASYMMETRIC CROSS-COUPLING CATALYZED BY PALLADIUM P-N CHELATES [J].
BAKER, KV ;
BROWN, JM ;
COOLEY, NA ;
HUGHES, GD ;
TAYLOR, RJ .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1989, 370 (1-3) :397-406
[3]   ASYMMETRIC INDUCTION IN THE ELECTROCYCLISATIONS OF 1,3 DIPOLAR INTERMEDIATES - THE 1.7 CYCLIZATION OF DIENE-CONJUGATED DIAZO-COMPOUNDS TO GIVE 1H-2,3-BENZODIAZEPINES [J].
BLAKE, AJ ;
HARDING, M ;
SHARP, JT .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1994, (21) :3149-3161
[4]   Steric hindrance versus asymmetric induction: new PN-ligands for carbon-carbon coupling reactions [J].
Bourghida, M ;
Widhalm, M .
TETRAHEDRON-ASYMMETRY, 1998, 9 (06) :1073-1083
[5]   trans-2,5-dialkylpyrrolidinyl-containing phosphinamines.: Synthetic and mechanistic studies in Pd-catalysed asymmetric allylic alkylation [J].
Cahill, JP ;
Cunneen, D ;
Guiry, PJ .
TETRAHEDRON-ASYMMETRY, 1999, 10 (21) :4157-4173
[6]   The first asymmetric Suzuki cross-coupling reaction [J].
Cammidge, AN ;
Crépy, KVL .
CHEMICAL COMMUNICATIONS, 2000, (18) :1723-1724
[7]   Asymmetric Suzuki cross-coupling reaction: chirality reversal depending on the palladium-chiral phosphine ratio [J].
Castanet, AS ;
Colobert, F ;
Broutin, PE ;
Obringer, M .
TETRAHEDRON-ASYMMETRY, 2002, 13 (06) :659-665
[8]   The asymmetric synthesis of cyclopentane derivatives by palladium-catalyzed coupling of prochiral alkylboron compounds [J].
Cho, SY ;
Shibasaki, M .
TETRAHEDRON-ASYMMETRY, 1998, 9 (21) :3751-3754
[9]   Nickel(0)-catalysed asymmetric cross-coupling reactions of allylic compounds with Grignard reagents using optically active oxazolinylferrocenylphosphines as ligands [J].
Chung, KG ;
Miyake, Y ;
Uemura, S .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 2000, (16) :2725-2729
[10]   Nickel(0)-catalyzed asymmetric cross-coupling reactions of allylic compounds with arylboronic acids [J].
Chung, KG ;
Miyake, Y ;
Uemura, S .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 2000, (01) :15-18