Literature DB >> 25684444

Lewis acid activation of pyridines for nucleophilic aromatic substitution and conjugate addition.

Sarah Abou-Shehada1, Matthew C Teasdale, Steven D Bull, Charles E Wade, Jonathan M J Williams.   

Abstract

A clean, mild and sustainable method for the functionalization of pyridines and their analogues is reported. A zinc-based Lewis acid is used to activate pyridine and its analogues towards nucleophilic aromatic substitution, conjugate addition, and cyclization reactions by binding to the nitrogen on the pyridine ring and activating the pyridine ring core towards further functionalization.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  SNAr; amination; conjugate addition; lewis acid; pyridine

Mesh:

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Year:  2015        PMID: 25684444     DOI: 10.1002/cssc.201403154

Source DB:  PubMed          Journal:  ChemSusChem        ISSN: 1864-5631            Impact factor:   8.928


  1 in total

1.  Vinylazaarenes as dienophiles in Lewis acid-promoted Diels-Alder reactions.

Authors:  Anna E Davis; Jared M Lowe; Michael K Hilinski
Journal:  Chem Sci       Date:  2021-11-24       Impact factor: 9.825

  1 in total

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