Highly Efficient Synthesis of trans-β,γ-Unsaturated α-Keto Amides

被引:25
作者
Allais, Christophe [1 ]
Constantieux, Thierry [1 ]
Rodriguez, Jean [1 ]
机构
[1] Aix Marseille Univ, Inst Sci Mol Marseille, CNRS, UMR 6263,iSm2, F-13397 Marseille 20, France
来源
SYNTHESIS-STUTTGART | 2009年 / 15期
关键词
beta; gamma-unsaturated alpha-keto amide; alpha-keto acid; amine; peptidic coupling; Michael acceptor; DIELS-ALDER REACTIONS; AMINO-ACID DERIVATIVES; ONE-POT SYNTHESIS; MICHAEL ADDITION; RAPID SYNTHESIS; ENANTIOSELECTIVE SYNTHESIS; MULTICOMPONENT REACTIONS; DOUBLE-CARBONYLATION; PROTEASE INHIBITORS; AEROBIC OXIDATION;
D O I
10.1055/s-0029-1216869
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A highly efficient, metal-free, and selective access to trans-beta,gamma-unsaturated alpha-keto amides is described via peptidic coupling, involving easy to prepare trans-beta,gamma-unsaturated alpha-keto acids and commercially available amines.
引用
收藏
页码:2523 / 2530
页数:8
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