Highly enantioselective synthesis of 2H-1-benzothiopyrans by a catalytic domino reaction

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Abstract

A highly enantioselective catalytic asymmetric synthesis of 2H-1-benzothiopyrans is presented. The organocatalytic asymmetric domino reactions between 2-mercaptobenzaldehyde and α,β-unsaturated aldehydes proceed with excellent chemo- and enantioselectivities to give the corresponding pharmaceutically valuable benzothiopyrans in high yields with 91-98% ee. © 2006 Elsevier Ltd. All rights reserved.

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Rios, R., Sundén, H., Ibrahem, I., Zhao, G. L., Eriksson, L., & Córdova, A. (2006). Highly enantioselective synthesis of 2H-1-benzothiopyrans by a catalytic domino reaction. Tetrahedron Letters, 47(48), 8547–8551. https://doi.org/10.1016/j.tetlet.2006.09.135

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