Sequential reactions promoted by manganese:: Completely stereoselective synthesis of (E)-α,β-unsaturated amides, ketones, aldehydes, and carboxylic acids

被引:33
作者
Concellon, Jose M. [1 ]
Rodriguez-Solla, Humberto [1 ]
Diaz, Pamela [1 ]
机构
[1] Univ Oviedo, Dept Quim Organ & Inorgan, E-33071 Oviedo, Spain
关键词
D O I
10.1021/jo701417z
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A complete E-selective synthesis of a,alpha,beta-unsaturated amides through a sequential reaction of a range of dichloroamides with a variety of aldehydes promoted by Rieke manganese (Mn*) is reported. A mechanism based on a sequential aldol-type reaction and a completely stereoselective beta-elimination is proposed to explain these results. The unsaturated amides obtained are readily and efficiently transformed into alpha,beta-unsaturated ketones, aldehydes, or carboxylic acids without loss of the diastereoisomeric purity of the C-C double bond.
引用
收藏
页码:7974 / 7979
页数:6
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