Novel and highly efficient bifunctional calixarene thiourea derivatives as organocatalysts for enantioselective Michael reaction of nitroolefins with diketones

被引:11
|
作者
Genc, Hayriye Nevin [1 ]
Sirit, Abdulkadir [1 ]
机构
[1] Necmettin Erbakan Univ, Dept Chem, TR-42090 Konya, Turkey
关键词
Calixarenes; Asymmetric Michael addition reactions; Thiourea; Organocatalysis; Enantioselectivity; AMINO-ACID-DERIVATIVES; BOND-DONOR CATALYSTS; 1,3-DICARBONYL COMPOUNDS; CONJUGATE ADDITION; RECOGNITION; STRECKER; LIGANDS; HYDROGENATION; ACETYLACETONE; NITROALKENES;
D O I
10.1007/s10847-017-0761-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
New bifunctional calixarene thiourea organocatalysts were synthesized and applied in catalytic asymmetric Michael addition of acetylacetone to various nitroolefins at room temperature. The corresponding adducts were obtained in good to excellent yields with excellent enantioselectivities (up to 92% ee). The present research demonstrates the advantages of incorporating two stereocontrolling structures into a single catalyst. Notably, it offers a simple and convenient doubly stereocontrolled approach for the catalytic asymmetric synthesis of a chiral organic molecule.
引用
收藏
页码:39 / 49
页数:11
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