Literature DB >> 17127056

A convenient and efficient protocol for oxidative aromatization of Hantzsch 1,4-dihydropyridines using benzyltriphenylphosphonium peroxymonosulfate under almost neutral reaction conditions.

Hadi Adibi1, Abdol Reza Hajipour.   

Abstract

Oxidative aromatization of 4-alkyl or aryl and heterocyclic-substituted derivatives of Hantzsch 1,4-dihydropyridines to the corresponding pyridine derivatives has been studied using benzyltriphenylphosphonium peroxymonosulfate as an oxidant in the presence of BiCl(3) under nearly neutral reaction conditions at ambient temperature.

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Year:  2006        PMID: 17127056     DOI: 10.1016/j.bmcl.2006.11.033

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Accelerated Hantzsch electrospray synthesis with temporal control of reaction intermediates.

Authors:  Ryan M Bain; Christopher J Pulliam; R Graham Cooks
Journal:  Chem Sci       Date:  2014-09-09       Impact factor: 9.825

2.  Ammonium metavanadate (NH4VO3): a highly efficient and eco-friendly catalyst for one-pot synthesis of pyridines and 1,4-dihydropyridines.

Authors:  Jamal Rahimi; Maryam Niksefat; Marzieh Heidari; Mehdi Naderi; Hadis Abbasi; Mohammad Tajik Ijdani; Ali Maleki
Journal:  Sci Rep       Date:  2022-08-11       Impact factor: 4.996

  2 in total

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