期刊
TETRAHEDRON LETTERS
卷 61, 期 13, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2020.151657
关键词
Organocatalyst; Proline; Fluorous; Activation; Aldol reaction
资金
- JSPS KAKENHI [JP19K07006]
- Professor Y. Uozumi's JST-ACCEL program [JPMJAC1401]
A recyclable fluorous proline catalyst with high stereoselectivity that functions as a catalyst for asymmetric aldol reactions is described. Its high stereoselectivity and facile recovery are achieved by employing a multi-fluorous tag attachment strategy. Although a gradual decrease was observed with respect to the catalytic activity, the catalyst can be separated from the reaction mixture by adsorption onto FluoroFlash (R) and can be reused in that form for a maximum of five times while maintaining a high stereoselectivity.2019 Elsevier Ltd. All rights reserved. (C) 2020 Elsevier Ltd. All rights reserved.
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