Experimental and Theoretical Studies in Hydrogen-Bonding Organocatalysis

被引:59
|
作者
Zabka, Matej [1 ]
Sebesta, Radovan [1 ]
机构
[1] Comenius Univ, Fac Nat Sci, Dept Organ Chem, SK-84215 Bratislava, Slovakia
关键词
organocatalysis; hydrogen bonding; thiourea; squaramide; experimental and computational studies; reaction mechanisms; ENANTIOSELECTIVE CONSTRUCTION; 1,3-DICARBONYL COMPOUNDS; EQUILIBRIUM ACIDITIES; ASYMMETRIC CATALYSIS; MICHAEL ADDITION; MECHANISM; ACTIVATION; INSIGHTS; DERIVATIVES; SQUARAMIDES;
D O I
10.3390/molecules200915500
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chiral thioureas and squaramides are among the most prominent hydrogen-bond bifunctional organocatalysts now extensively used for various transformations, including aldol, Michael, Mannich and Diels-Alder reactions. More importantly, the experimental and computational study of the mode of activation has begun to attract considerable attention. Various experimental, spectroscopic and calculation methods are now frequently used, often as an integrated approach, to establish the reaction mechanism, the mode of activation or explain the stereochemical outcome of the reaction. This article comprises several case studies, sorted according to the method used in their study. The aim of this review is to give the investigators an overview of the methods currently utilized for mechanistic investigations in hydrogen-bonding organocatalysis.
引用
收藏
页码:15500 / 15524
页数:25
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