Literature DB >> 10814336

Concerted catalytic reactions for conversion of ketones or enol acetates to chiral acetates

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Abstract

[reaction: see text] Enol acetates or ketones asymmetrically transformed to chiral acetates in high yields with high optical purities through multistep reactions catalyzed by a lipase and a ruthenium complex. 2,6-Dimethylheptan-4-ol was chosen as a suitable hydrogen donor, and 4-chlorophenyl acetate was used as an acyl donor for the conversion of ketones.

Entities:  

Year:  2000        PMID: 10814336     DOI: 10.1021/ol9914043

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


  2 in total

1.  Chemoenzymatic Dynamic Kinetic Asymmetric Transformations of β-Hydroxyketones.

Authors:  Simon Hilker; Daniels Posevins; C Rikard Unelius; Jan-E Bäckvall
Journal:  Chemistry       Date:  2021-10-05       Impact factor: 5.020

2.  One-pot synthesis of enantiopure syn-1,3-diacetates from racemic syn/anti mixtures of 1,3-diols by dynamic kinetic asymmetric transformation.

Authors:  Michaela Edin; Johannes Steinreiber; Jan-E Bäckvall
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-06       Impact factor: 11.205

  2 in total

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