Literature DB >> 21755915

An unexpected directing effect in the asymmetric transfer hydrogenation of α,α-disubstituted ketones.

Rina Soni1, John-Michael Collinson, Guy C Clarkson, Martin Wills.   

Abstract

α,α-Disubstituted ketones containing an aromatic ring or alkene are reduced in high enantiomeric excess using an asymmetric transfer hydrogenation catalyst. The sense of reduction indicates that the unsaturated region of the ketone adopts a position adjacent to the Ru-bound η(6)-arene ring in the reduction transition state.
© 2011 American Chemical Society

Entities:  

Year:  2011        PMID: 21755915     DOI: 10.1021/ol201643v

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


  3 in total

1.  Biomimetic kinetic resolution: highly enantio- and diastereoselective transfer hydrogenation of aglain ketones to access flavagline natural products.

Authors:  Steven D Stone; Neil J Lajkiewicz; Luke Whitesell; Ahmed Hilmy; John A Porco
Journal:  J Am Chem Soc       Date:  2014-12-29       Impact factor: 15.419

2.  Direct formation of tethered Ru(II) catalysts using arene exchange.

Authors:  Rina Soni; Katherine E Jolley; Guy J Clarkson; Martin Wills
Journal:  Org Lett       Date:  2013-09-26       Impact factor: 6.005

3.  Design, synthesis and anti-fibrosis activity study of N₁-substituted phenylhydroquinolinone derivatives.

Authors:  Ling Wu; Bin Liu; Qianbin Li; Jun Chen; Lijian Tao; Gaoyun Hu
Journal:  Molecules       Date:  2012-02-02       Impact factor: 4.411

  3 in total

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