Asymmetric Supramolecular Organocatalysis: A Complementary Upgrade to Organocatalysis

被引:24
|
作者
Anebouselvy, Kengadarane [1 ]
Shruthi, Kodambahalli S. [1 ]
Ramachary, Dhevalapally B. [1 ]
机构
[1] Univ Hyderabad, Sch Chem, Catalysis Lab, Hyderabad 500046, Andhra Prades, India
关键词
Organocatalysis; C-C bond formation; Weak interactions; Asymmetric catalysis; Supramolecular chemistry; Pre-transition states; DIELS-ALDER REACTIONS; MODULARLY DESIGNED ORGANOCATALYSTS; DIRECT ALDOL REACTION; ALPHA; BETA-UNSATURATED KETONES; ENANTIOSELECTIVE SYNTHESIS; ORGANIC-SYNTHESIS; ENZYME CATALYSIS; AMINO-ACID; ENAMINE ACTIVATION; MICHAEL REACTIONS;
D O I
10.1002/ejoc.201700611
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The recent past has witnessed tremendous growth in the field of asymmetric synthesis through "asymmetric supramolecular organocatalysis (ASO)". ASO emerges from many interactions between substrates and catalysts: namely substratecatalyst, catalyst-catalyst and substrate-substrate interactions. As a result, ASO has come to be the fourth pillar of asymmetric catalysis. This review summarizes recent advances in the high-yielding asymmetric synthesis of chiral compounds from functionally rich substrates with the aid of combinations of two or more organocatalysts working synergistically through relatively stable pre-transition states. ASO not only assists in product formation from highly functionalized substrates with high rate/selectivity, but also sheds some light on understanding of the fundamental aspects of the pre-transition state structures.
引用
收藏
页码:5460 / 5483
页数:24
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