4.7 Article

Atom-Economic Synthesis of Optically Active Warfarin Anticoagulant over a Chiral MOF Organocatalyst

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 355, Issue 13, Pages 2538-2543

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201300554

Keywords

asymmetric synthesis; catalyst design; heterogeneous catalysis; Michael addition; warfarin

Funding

  1. Program for Changjiang Scholars and Innovative Research Team in Chinese Universities [IRT0980]
  2. National Natural Science Foundation of China [21036006, 21272214]
  3. Zhejiang Leading Team of Science and Technology Innovation [2009R50020]

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A novel chiral metal-organic framework (MOF) organocatalyst has been developed, based on readily available MIL-101 and the chiral primary diamine (1R,2R)-1,2-diphenylethylenediamine, by the post-synthetic modification. Over the developed chiral heterogeneous catalyst the asymmetric synthesis of (S)-warfarin with high enantioselectivity can be fulfilled on a gram-scale (2.8g) with excellent yield (92%) at low cost, making the synthesis method an ideal alternative to existing methods.

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