期刊
TETRAHEDRON-ASYMMETRY
卷 22, 期 11, 页码 1205-1211出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2011.06.028
关键词
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资金
- Welch Foundation [AX-1593]
- NIH [SC1GM082718]
The organocatalytic enantioselective tandem aldol-cyclization reactions of a-isothiocyanato imides and activated carbonyl compounds, such as isatins, an alpha-ketolactone and a 1,2-dione, have been studied with cinchona alkaloid-derived thiourea-catalysts. This methodology provided an easy way to access enantiomerically enriched spirobicyclic thiocarbamates with high yields and good to excellent stereoselectivity, which have been demonstrated to be useful precursors for the synthesis of biologically active molecules. (C) 2011 Elsevier Ltd. All rights reserved.
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