烷基化
立体中心
试剂
化学
组合化学
有机催化
转化(遗传学)
催化作用
简单
对映选择合成
有机化学
物理
生物化学
量子力学
基因
作者
Rafael Cano,Armen Zakarian,Gerard P. McGlacken
标识
DOI:10.1002/anie.201703079
摘要
The alkylation of ketones is taught at basic undergraduate level. In many cases this transformation leads to the formation of a new stereogenic center. However, the apparent simplicity of the transformation is belied by a number of problems. So much so, that a general method for the direct asymmetric alkylation of ketones remains an unmet target. Despite the advancement of organocatalysis and transition-metal catalysis, neither field has provided an adequate solution. Indeed, even use of an efficient and general stoichiometric chiral reagent has yet to be reported. Herein we describe the state-of-the-art in terms of direct alkylation reactions of some carbonyl groups. We outline the limited progress that has been made with ketones, and potential routes towards ultimately achieving a widely applicable methodology for the asymmetric alkylation of ketones.
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