4.7 Article

Amano lipase DF-catalyzed efficient synthesis of 2,2 '-arylmethylene dicyclohexane-1,3-dione derivatives in anhydrous media

Journal

CHINESE CHEMICAL LETTERS
Volume 25, Issue 8, Pages 1190-1192

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cclet.2014.04.007

Keywords

Amano lipase DF; Knoevenagel condensation; Michael addition; Catalytic promiscuity

Funding

  1. Outstanding Young Scholar Grant of Zhejiang University [R4110092]
  2. National Natural Science Foundation of China [21176215/21176102]
  3. Program for Zhejiang leading team of ST Innovation [2011R50007]

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A simple and efficient method was developed for the synthesis of 2,2'-arylmethylene dicyclohexane-1,3-dione derivatives via the Knoevenagel Michael cascade reactions of aromatic aldehydes and 1,3-cyclic diketones catalyzed by Amano lipase DF, which expands the application field of enzyme catalytic promiscuity. This protocol provides several advantages over the traditional chemical synthesis, such as simple work-up procedure, high yields (up to 94%) and environmental friendliness. (C) 2014 Li-Dan Ye. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.

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