期刊
TETRAHEDRON LETTERS
卷 48, 期 48, 页码 8456-8459出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2007.09.168
关键词
organocatalysis; Michael addition; salt catalysis; nitroalkenes; water
An enantioselective Michael addition of malonate to nitroalkenes is efficiently catalyzed by low loading demethylquinine salts in water; the yield range from 49% to 93% and the ee up to 90%. (c) 2007 Elsevier Ltd. All rights reserved.
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