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A highly efficient and enantioselective synthesis of EEHP and EMHP: intermediates of PPAR agonists

Publication Type : Journal Article

Publisher : Elsevier

Source : Tetrahedron Letters, 2016

Url : https://www.sciencedirect.com/science/article/pii/S0040403916307626?casa_token=3QPCrkL5-Z8AAAAA:ALeDaDN5wLIIBHCjJz9uwlzz4HLQcr79VuUFx2834oCoxE8VaodqtpSrNPiZ77nZNlNihpRmJj8

Campus : Amritapuri

School : School of Biotechnology

Verified : No

Year : 2016

Abstract : Glycolate alkylation reactions of (S)-4-isopropyl-1-[(R)-1-phenylethyl]imidazolidin-2-one auxiliary has been optimised with high yields and diastereoselectivity on substituted benzyl and allyl bromides. The standardised reaction condition was employed for the stereoselective synthesis of EEHP and EMHP intermediates of PPAR agonists.

Cite this Research Publication : Mukesh Gangar, Harikrishnan M., Sandeep Goyal, Maulik N. Mungalpara and Vipin A. Nair, "A highly efficient and enantioselective synthesis of EEHP and EMHP: intermediates of PPAR agonists", Tetrahedron Letters 2016, 57, 3462-3467

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