Literature DB >> 17389979

A reductase-mimicking thiourea organocatalyst incorporating a covalently bound NADH analogue: efficient 1,2-diketone reduction with in situ prosthetic group generation and recycling.

Barbara Procuranti1, Stephen J Connon.   

Abstract

A new class of bifunctional organocatalyst promotes the chemoselective reduction of diketone electrophiles at catalytic loadings in the presence of an inorganic co-reductant.

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Year:  2007        PMID： 17389979     DOI： 10.1039/b618792g

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  3 in total

1.  Primary Amine-Catalyzed Biginelli Reaction for the Enantioselective Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones.

Authors:  Derong Ding; Cong-Gui Zhao
Journal:  European J Org Chem       Date:  2010-07-01

2.  Enantioselective, organocatalytic reduction of ketones using bifunctional thiourea-amine catalysts.

Authors:  De Run Li; Anyu He; J R Falck
Journal:  Org Lett       Date:  2010-04-16       Impact factor: 6.005

3.  A Novel Bis-Thiourea Organocatalyst for the Asymmetric Aza-Henry Reaction.

Authors:  Constantinos Rampalakos; William D Wulff
Journal:  Adv Synth Catal       Date:  2008-08-04       Impact factor: 5.837
  3 in total

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