期刊
TETRAHEDRON LETTERS
卷 47, 期 48, 页码 8547-8551出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2006.09.135
关键词
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A highly enantio selective catalytic asymmetric synthesis of 2H-1-benzothiopyrans is presented. The organocatalytic asymmetric domino reactions between 2-mercaptobenzaldehyde and alpha,beta-unsaturated aldehydes proceed with excellent chemoand enantioselectivities to give the corresponding pharmaceutically valuable benzothiopyrans in high yields with 91-98% ee. (c) 2006 Elsevier Ltd. All rights reserved.
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