Enantioselective cyclopropanation of enals by oxidative N-heterocyclic carbene catalysis
Enantioselective cyclopropanation of enals by oxidative N-heterocyclic carbene catalysis
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DOI:
10.1039/c2cc31501g
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发表时间:
2012-01-01
影响因子:
4.9
通讯作者:
Studer, Armido
中科院分区:
文献类型:
--
作者:
Biswas, Anup;De Sarkar, Suman;Studer, Armido
Carbene catalysed redox activation of alpha,beta-unsaturated aldehydes is applied for generation of alpha,beta-unsaturated acyl azoliums which undergo cyclopropanation upon reaction with a sulfur ylide and an alcohol to give the corresponding cyclopropanecarboxylic acid esters. With chiral carbenes good to excellent diastereo and enantioselectivities are obtained.