Literature DB >> 18817401

Highly efficient route for enantioselective preparation of chlorohydrins via dynamic kinetic resolution.

Annika Träff1, Krisztián Bogár, Madeleine Warner, Jan-E Bäckvall.   

Abstract

Dynamic kinetic resolution (DKR) of various aromatic chlorohydrins with the use of Pseudomonas cepacia lipase (PS-C "Amano" II) and ruthenium catalyst 1 afforded chlorohydrin acetates in high yields and high enantiomeric excesses. These optically pure chlorohydrin acetates are useful synthetic intermediates and can be transformed to a range of important chiral compounds.

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Year:  2008        PMID: 18817401     DOI: 10.1021/ol801749z

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Chiral epoxides via borane reduction of 2-haloketones catalyzed by spiroborate ester: application to the synthesis of optically pure 1,2-hydroxy ethers and 1,2-azido alcohols.

Authors:  Kun Huang; Haiyang Wang; Viatcheslav Stepanenko; Melvin De Jesús; Carilyn Torruellas; Wildeliz Correa; Margarita Ortiz-Marciales
Journal:  J Org Chem       Date:  2011-02-04       Impact factor: 4.354

Review 2.  Chemoenzymatic dynamic kinetic resolution: a powerful tool for the preparation of enantiomerically pure alcohols and amines.

Authors:  Oscar Verho; Jan-E Bäckvall
Journal:  J Am Chem Soc       Date:  2015-03-19       Impact factor: 15.419

3.  Preparation of (S)-1-Halo-2-octanols Using Ionic Liquids and Biocatalysts.

Authors:  Mireia Oromí-Farrús; Jordi Eras; Núria Sala; Mercè Torres; Ramon Canela
Journal:  Molecules       Date:  2009-10-23       Impact factor: 4.411

  3 in total

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