Synthesis of chiral sulfoximine-based thioureas and their application in asymmetric organocatalysis

被引:80
作者
Frings, Marcus [1 ]
Thome, Isabelle [1 ]
Bolm, Carsten [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Organ Chem, D-52074 Aachen, Germany
来源
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY | 2012年 / 8卷
关键词
anhydride opening; catalytic asymmetric Biginelli reaction; organocatalysis; sulfoximines; thioureas; C-1-SYMMETRIC AMINOSULFOXIMINES; ANHYDRIDES; CATALYST; DESYMMETRIZATION; SULFINAMIDES; DERIVATIVES; INHIBITORS; LIGANDS; ANALOGS; DESIGN;
D O I
10.3762/bjoc.8.164
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
For the first time, chiral sulfoximine derivatives have been applied as asymmetric organocatalysts. In combination with a thiourea-type backbone the sulfonimidoyl moiety leads to organocatalysts showing good reactivity in the catalytic desymmetrization of a cyclic meso-anhydride and moderate enantioselectivity in the catalytic asymmetric Biginelli reaction. Straightforward synthetic routes provide the newly designed thiourea-sulfoximine catalysts in high overall yields without affecting the stereohomogeneity of the sulfur-containing core fragment.
引用
收藏
页码:1443 / 1451
页数:9
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