Literature DB >> 16153067

Solid-phase synthesis of 3,4-dihydro-1H-pyrimidine-2-ones using sodium benzenesulfinate as a traceless linker.

Weiwei Li1, Yulin Lam.   

Abstract

The facile preparation of 3,4-dihydropyrimidine-2-one derivatives with traceless solid-phase sulfone linker strategy is described. Key steps involved in the solid-phase synthetic procedure include (i) sulfinate acidification, (ii) condensation of urea or thiourea with aldehydes and sulfinic acid, and (iii) traceless product release via a one-pot cyclization-dehydration process. A library of 18 compounds was synthesized.

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Year:  2005        PMID: 16153067     DOI: 10.1021/cc0500295

Source DB:  PubMed          Journal:  J Comb Chem        ISSN: 1520-4766


  3 in total

1.  An easy access to 2-Amino-5,6-dihydro-3H-pyrimidin-4-one building blocks: the reaction under conventional and microwave conditions.

Authors:  Konstantin S Ostras; Nikolay Yu Gorobets; Sergey M Desenko; Vladimir I Musatov
Journal:  Mol Divers       Date:  2006-09-12       Impact factor: 2.943

2.  Scalable organocatalytic asymmetric Strecker reactions catalysed by a chiral cyanide generator.

Authors:  Hailong Yan; Joong Suk Oh; Ji-Woong Lee; Choong Eui Song
Journal:  Nat Commun       Date:  2012       Impact factor: 14.919

3.  Decarboxylative allylation using sulfones as surrogates of alkanes.

Authors:  Jimmie D Weaver; Jon A Tunge
Journal:  Org Lett       Date:  2008-09-12       Impact factor: 6.005

  3 in total

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