期刊
TETRAHEDRON-ASYMMETRY
卷 21, 期 19, 页码 2372-2375出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2010.08.012
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资金
- CSIR, New Delhi
- DST, New Delhi [SR/S1/OC-65/2009]
A new hydroxyphthalimide-coupled triazole-pyrrolidine derivative has been synthesized and demonstrated as an efficient and stereoselective organocatalyst for the asymmetric Michael addition reaction of ketones to nitro olefins at room temperature. Good yields and high selectivities were achieved when benzoic acid was used in combination with organocatalyst 1, employing water as the reaction medium. (C) 2010 Elsevier Ltd. All rights reserved.
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