Harnessing non-covalent interactions to exert control over regioselectivity and site-selectivity in catalytic reactions

被引:291
作者
Davis, Holly J. [1 ]
Phipps, Robert J. [1 ]
机构
[1] Univ Cambridge, Dept Chem, Lensfield Rd, Cambridge CB2 1EW, England
基金
英国工程与自然科学研究理事会;
关键词
TRANSITION-METAL CATALYSIS; C-H BORYLATION; ASYMMETRIC CATALYSIS; SUPRAMOLECULAR CONTROL; HYDROGEN-BOND; ARTIFICIAL CYTOCHROME-P-450; MOLECULAR RECOGNITION; CARBOXYLIC-ACIDS; ENZYME MIMICS; DIELS-ALDER;
D O I
10.1039/c6sc04157d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Asymmetric catalysis has been revolutionised by the realisation that attractive non-covalent interactions such as hydrogen bonds and ion pairs can act as powerful controllers of enantioselectivity when incorporated into appropriate small molecule chiral scaffolds. Given these tremendous advances it is surprising that there are still a relatively limited number of examples of non-covalent interactions being harnessed for control of regioselectivity or site-selectivity in catalysis, two other fundamental selectivity aspects facing the synthetic chemist. This perspective examines the progress that has been made in this area thus far using non-covalent interactions in conjunction with transition metal catalysis as well as in the context of purely organic catalysts. We hope this will highlight the great potential in this approach for designing selective catalytic reactions.
引用
收藏
页码:864 / 877
页数:14
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