1,3-Dicarbonyl compounds in stereoselective domino and multicomponent reactions

被引:161
作者
Bonne, Damien [1 ]
Coquerel, Yoann [1 ]
Constantieux, Thierry [1 ]
Rodriguez, Jean [1 ]
机构
[1] Aix Marseille Univ, Inst Sci Mol Marseille, iSm2, CNRS,UMR 6263,Fac Sci & Tech,Ctr St Jerome, F-13397 Marseille 20, France
关键词
ONE-POT SYNTHESIS; HIGHLY ENANTIOSELECTIVE SYNTHESIS; ACETAMIDO CARBONYL-COMPOUNDS; CALCIUM-CHANNEL BLOCKERS; 3-COMPONENT REACTION; ASYMMETRIC-SYNTHESIS; EFFICIENT ACCESS; MICHAEL-ALDOL; MARDI CASCADE; DIELS-ALDER;
D O I
10.1016/j.tetasy.2010.04.045
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Modern organic synthesis focuses on the discovery and the development of stereoselective multiple bond-forming transformations allowing the creation of several covalent bonds in a single operation. Hence, the number of steps required to obtain a target molecule is reduced, which nicely addresses the efficiency and economy criteria of 'green chemistry'. In this context, 1,3-dicarbonyl compounds are exceptional synthetic platforms due to the presence of four contiguous reaction sites. This functional group density allows cascades of elemental steps from simple substrates leading to the selective formation of elaborated molecular architectures displaying a large functional diversity. (C) 2010 Published by Elsevier Ltd.
引用
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页码:1085 / 1109
页数:25
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