Literature DB >> 15678186

Combined epimerisation and acylation: Meerwein-Ponndorf-Verley-Oppenauer catalysts in action.

Dirk Klomp1, Kristina Djanashvili, Nina Cianfanelli Svennum, Nuttanun Chantapariyavat, Chung-Sing Wong, Filipe Vilela, Thomas Maschmeyer, Joop A Peters, Ulf Hanefeld.   

Abstract

A practical racemisation-epimerisation method for chiral secondary alcohols has been developed. Meerwein-Ponndorf-Verley-Oppenauer catalysts such as neodymium(III) isopropoxide are able to racemise these alcohols with retention of other stereocentres in the molecule. This is particularly useful for the recycling of the undesired products of kinetic resolutions of alcohols. By combination of such a racemisation with an acylation using isopropenyl or ethoxyvinyl esters as acyl donors, a fast straightforward recycling of starting materials may be achieved. The combined epimerisation and acylation process is demonstrated for the steroid estradiol methyl ether.

Entities:  

Year:  2004        PMID: 15678186     DOI: 10.1039/b413944e

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

Review 1.  Investigation of the Stereoselective Synthesis of the Indane Dimer PH46A, a New Potential Anti-inflammatory Agent.

Authors:  Graham R Cumming; Tao Zhang; Gaia Scalabrino; Neil Frankish; Helen Sheridan
Journal:  Org Process Res Dev       Date:  2017-11-27       Impact factor: 3.317

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.