Catalytic asymmetric aldol reaction of trimethoxysilyl enol ethers using 2,2′-bis(di-p-tolylphosphino)-1,1′-binaphthyl•AgF complex

被引:35
作者
Yanagisawa, A [1 ]
Nakatsuka, Y [1 ]
Asakawa, K [1 ]
Wadamoto, M [1 ]
Kageyama, H [1 ]
Yamamoto, H [1 ]
机构
[1] Nagoya Univ, Grad Sch Engn, Japan Sci & Technol Corp, CREST,Chikusa Ku, Nagoya, Aichi 4648603, Japan
关键词
D O I
10.1246/bcsj.74.1477
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Catalytic asymmetric Mukaiyama-type aldol reaction using trimethoxysilyl enol ethers was achieved using 2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl (p-Tol-BINAP). AgF complex as a catalyst. The chiral silver(I) catalyst was easily generated by mixing p-Tol-BINAP and silver(I) fluoride in MeOH at room temperature, High syn- and enantioselectivities were obtained from both the E- and Z-silyl enol ethers. Use of a 1: 1 mixture of MeOH and acetone as a solvent in the reaction of cyclohexanone-derived trimethoxysilyl enol ethers resulted in higher enantioselectivity.
引用
收藏
页码:1477 / 1484
页数:8
相关论文
共 67 条
[1]   NEW METHODS AND REAGENTS IN ORGANIC-SYNTHESIS .85. ENANTIOSELECTIVE SYNTHESIS OF BETA-HYDROXY-ALPHA-METHYL CARBONYL-COMPOUNDS BY ALDOL REACTION [J].
ANDO, A ;
SHIOIRI, T .
TETRAHEDRON, 1989, 45 (16) :4969-4988
[2]  
ANDO A, 1991, CHEM PHARM BULL, V39, P1967
[3]   Advances in asymmetric enolate methodology [J].
Arya, P ;
Qin, HP .
TETRAHEDRON, 2000, 56 (07) :917-947
[4]   CATALYTIC ENANTIOSELECTIVE C-C COUPLING - ALLYL TRANSFER AND MUKAIYAMA ALDOL REACTION [J].
BACH, T .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1994, 33 (04) :417-419
[5]   New computational and experimental evidence for the mechanism of the Sakurai reaction [J].
Bottoni, A ;
Costa, AL ;
Di Tommaso, D ;
Rossi, I ;
Tagliavini, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (50) :12131-12135
[6]  
BRAUN M, 1995, HOUBENWEYL METHODS E, V21, P1730
[7]  
Cai DW, 1999, ORG SYNTH, V76, P6
[8]   Synthesis and evaluation of a new chiral ligand:: 2-diphenylarsino-2′-diphenylphosphino-1,1′ (BINAPAs) [J].
Cho, SY ;
Shibasaki, M .
TETRAHEDRON LETTERS, 1998, 39 (13) :1773-1776
[9]   Chemistry of trichlorosilyl enolates .1. New reagents for catalytic, asymmetric aldol additions [J].
Denmark, SE ;
Winter, SBD ;
Su, XP ;
Wong, KT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (31) :7404-7405
[10]   The chemistry of trichlorosilyl enolates .2. Highly-selective asymmetric aldol additions of ketone enolates [J].
Denmark, SE ;
Wong, KT ;
Stavenger, RA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (09) :2333-2334