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
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