Direct Asymmetric Alkylation of Ketones: Still Unconquered

被引:80
作者
Cano, Rafael [1 ,2 ]
Zakarian, Armen [3 ]
McGlacken, Gerard P. [1 ,2 ]
机构
[1] Univ Coll Cork, Dept Chem, Cork, Ireland
[2] Univ Coll Cork, Analyt & Biol Chem Res Facil, Cork, Ireland
[3] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
基金
美国国家卫生研究院;
关键词
asymmetric; ketones; organocatalysis; transition-metal catalysis; alpha-alkylation; ENANTIOSELECTIVE ALLYLIC ALKYLATION; IRIDIUM-CATALYZED ALLYLATION; CHIRAL LITHIUM AMIDES; ALPHA-ALKYLATION; CYCLIC-KETONES; PRIMARY AMINE; QUATERNARY STEREOCENTERS; PHOTOCHEMICAL ACTIVITY; CROSS-COUPLINGS; DUAL CATALYSIS;
D O I
10.1002/anie.201703079
中图分类号
O6 [化学];
学科分类号
0703 ;
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.
引用
收藏
页码:9278 / 9290
页数:13
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