Catalytic activation of the leaving group in the SN2 reaction

被引:31
|
作者
Yamamoto, Hirofumi [1 ]
Pandey, Ghanshyam [1 ]
Asai, Yumiko [1 ]
Nakano, Mayo [1 ]
Kinoshita, Atsushi [1 ]
Namba, Kosuke [1 ]
Imagawa, Hiroshi [1 ]
Nishizawa, Mugio [1 ]
机构
[1] Tokushima Bunri Univ, Fac Pharmaceut Sci, Tokushima 7708514, Japan
关键词
D O I
10.1021/ol701737x
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A novel catalytic activation of the leaving group in the S(N)2 reaction is achieved as an extension of our mercuric triflate-catalyzed reactions. Derivatives of anilinoethyl 4-pentynoate reacted smoothly with catalytic amounts of Hg(OTf)(2) to give indoline derivatives in excellent yield with efficient catalytic turnovers under very mild conditions. The reaction of optically pure secondary alcohol derivatives resulted in inversion of stereochemistry, which is a definitive feature of the SN2 reaction. The procedure is applicable for benzoazepine synthesis.
引用
收藏
页码:4029 / 4032
页数:4
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