Weak bonding strategies for achieving regio- and site-selective transformations

被引:48
|
作者
Jiao, Yang [1 ]
Chen, Xiao-Yang [1 ]
Stoddart, J. Fraser [1 ,2 ,3 ,4 ]
机构
[1] Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA
[2] Univ New South Wales, Sch Chem, Sydney, NSW 2052, Australia
[3] Zhejiang Univ, Stoddart Inst Mol Sci, Dept Chem, Hangzhou 310027, Peoples R China
[4] ZJU Hangzhou Global Sci & Technol Innovat Ctr, Hangzhou 311215, Peoples R China
来源
CHEM | 2022年 / 8卷 / 02期
关键词
C-H BORYLATION; COUPLED ELECTRON-TRANSFER; ATTRACTIVE NONCOVALENT INTERACTIONS; SUPRAMOLECULAR CATALYSIS; CRYSTAL-STRUCTURE; DIRECTING GROUPS; REMOTE; FUNCTIONALIZATION; ACTIVATION; HYDROFORMYLATION;
D O I
10.1016/j.chempr.2021.12.012
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The ability to identify and transform selectively similar constitutional fragments in molecules in a predetermined direction over all other possible directions remains a fundamental challenge in relation to the growth and reach of synthetic chemistry. A rapidly emerging approach toward this goal is to leverage weak bonding interactions, including both noncovalent and dynamic covalent bonds to control regio-and site selectivities. Drawing inspiration from the reactions catalyzed by enzymes, chemists have developed a wide variety of weak bonding strategies to facilitate regio-and site -selective transformations without the need to introduce additional handles onto molecular frameworks. Here, by classifying these weak bonding protocols into four categories, namely, bond-destabilizing, masking, pre-organizing, and templating strategies, we summarize the advances that have been made during the past two decades, highlighting their relative simplicity in promoting regio-and site -selective reactions that would otherwise be difficult to perform on molecules.
引用
收藏
页码:414 / 438
页数:25
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