Chinese Journal of Organic Chemistry >
Progress in the Asymmetric Metal-Catalyzed 1,2-Addition Reactions of Arylboronic Acids with Ketones
Received date: 2013-05-27
Revised date: 2013-06-24
Online published: 2013-07-03
Supported by
Project supported by the Science Foundation of Gannan Medical University (No. YB201014).
A number of biologically active compounds and drugs contain the structural unit of chiral aryl-substituted tertiary alcohol. The catalytic asymmetric arylation of ketones is a powerful tool for the efficient construction of such compounds. Arylboron reagents have attracted considerable attention due to their availability, relative insensitivity to air and moisture, high functional group tolerance and generally low toxicity. Recent progress of the catalytic asymmetric arylation of highly activated ketones such as isatins, trifluoromethyl ketones, α-ketoesters, 1, 2-diketones and unactivated ketones is reviewed.
Key words： metal-catalyzed; arylboronic acid; ketone; asymmetric; 1,2-addition; progress
Luo Renshi , Liao Jianhua , Zhang Jian . Progress in the Asymmetric Metal-Catalyzed 1,2-Addition Reactions of Arylboronic Acids with Ketones[J]. Chinese Journal of Organic Chemistry, 2013 , 33(11) : 2298 -2309 . DOI: 10.6023/cjoc201305044
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