Literature DB >> 15789566

A simple approach to the synthesis of highly functionalized pyrrole derivatives.

Issa Yavari1, Mohammad Anary-Abbasinejad, Farough Nasiri, Hoorieh Djahaniani, Abdolali Alizadeh, Hamid R Bijanzadeh.   

Abstract

The reaction of dibenzoylacetylene and enaminocarbonyl compounds leads to 3-alkylidene-2,3-dihydro-1H-pyrrol-2-ol derivatives in nearly quantitative yields. The reaction of this heterocyclic system with alcohols in the presence of a catalytic amount of HCl produces highly functionalized pyrroles in good yields.

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Year:  2005        PMID： 15789566     DOI： 10.1007/s11030-005-2175-z

Source DB:  PubMed          Journal:  Mol Divers        ISSN： 1381-1991            Impact factor:   2.943


  1 in total

1.  Cascade Reactions in Quantitative Solid-State Syntheses.

Authors: 
Journal:  Angew Chem Int Ed Engl       Date:  1999-10-04       Impact factor: 15.336
  1 in total
  2 in total

1.  Regioselective four-component synthesis of new tetrazolo[1,5-a]quinoline-based 2-amino-1,4-dihydropyridine and pyridin-2(1H)-one derivatives using nano-ZnO catalysis.

Authors:  Tooran Aghaalizadeh; Farough Nasiri
Journal:  Mol Divers       Date:  2018-06-27       Impact factor: 2.943

2.  A simple approach to the synthesis of highly functionalized 3-alkylidene-2,3-dihydro-1H-pyrrole-2-ol derivatives and related pyrroles.

Authors:  Farough Nasiri; Kourosh Pourdavaie
Journal:  Mol Divers       Date:  2007-04-04       Impact factor: 3.364
  2 in total

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