Literature DB >> 22053905

Catalytic, asymmetric, interrupted Feist-Bénary reactions of α-tosyloxyacetophenones.

Michael A Calter1, Alexander Korotkov.   

Abstract

A new variant of the Interrupted Feist-Bénary (IFB) reaction uses α-tosyloxyacetophenones as electrophiles and proceeds in good yields and excellent enantioselectivities.

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Year:  2011        PMID： 22053905      PMCID： PMC3226731          DOI： 10.1021/ol2026697

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


  5 in total

1.  Scope and diastereoselectivity of the "interrupted" Feist-Bénary reaction.

Authors:  Michael A Calter; Cheng Zhu
Journal:  Org Lett       Date:  2002-01-24       Impact factor: 6.005

2.  Rapid synthesis of the 7-deoxy zaragozic acid core.

Authors:  Michael A Calter; Cheng Zhu; Rene J Lachicotte
Journal:  Org Lett       Date:  2002-01-24       Impact factor: 6.005

3.  Heteroaromatic thioether-boronic acid cross-coupling under neutral reaction conditions.

Authors:  Lanny S Liebeskind; Jiri Srogl
Journal:  Org Lett       Date:  2002-03-21       Impact factor: 6.005

4.  Catalytic, asymmetric, "interrupted" Feist-Bénary reactions.

Authors:  Michael A Calter; Ryan M Phillips; Christine Flaschenriem
Journal:  J Am Chem Soc       Date:  2005-10-26       Impact factor: 15.419

5.  Catalytic, asymmetric Michael reactions of cyclic diketones with beta,gamma-unsaturated alpha-ketoesters.

Authors:  Michael A Calter; Jun Wang
Journal:  Org Lett       Date:  2009-05-21       Impact factor: 6.005
  5 in total
  1 in total

Review 1.  Dimeric Cinchona alkaloids.

Authors:  Przemysław J Boratyński
Journal:  Mol Divers       Date:  2015-01-15       Impact factor: 2.943
  1 in total

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