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

DOI: 10.3762/bjoc.8.164

Keywords: anhydride opening , catalytic asymmetric Biginelli reaction , organocatalysis , sulfoximines , thioureas

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Abstract:

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.

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