(Thio)urea organocatalysis - What can be learnt from anion recognition?

被引:799
作者
Zhang, Zhiguo [1 ]
Schreiner, Peter R. [1 ]
机构
[1] Univ Giessen, Inst Organ Chem, D-35392 Giessen, Germany
关键词
ENANTIOSELECTIVE CONJUGATE ADDITION; ION-PAIR BINDING; MOLECULAR RECOGNITION; HENRY REACTION; CARBOXYLATE COMPLEXATION; ASYMMETRIC CATALYSIS; NITROALDOL REACTION; ORGANIC FRAMEWORKS; MICHAEL REACTION; THIOUREA GROUPS;
D O I
10.1039/b801793j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The present critical review outlines the close relationship and mutual interplay between molecular recognition, active site considerations in enzyme catalysis involving anions, and organocatalysis utilizing explicit hydrogen bonding. These interconnections are generally not made although, as we demonstrate, they are quite apparent as exemplified with pertinent examples in the field of (thio) urea organocatalysis. Indeed, the concepts of anion binding or binding with negatively (partially) charged heteroatoms is key for designing new organocatalytic transformations. Utilizing anions through recognition with hydrogen-bonding organocatalysts is still in its infancy but bears great potential. In turn, the discovery and mechanistic elucidation of such reactions is likely to improve the understanding of enzyme active sites (108 references).
引用
收藏
页码:1187 / 1198
页数:12
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