Literature DB >> 21186828

Synthesis and reactivity of highly nucleophilic pyridines.

Nicolas De Rycke1, Guillaume Berionni, François Couty, Herbert Mayr, Regis Goumont, Olivier R P David.   

Abstract

3,4,5-Triamino-substituted pyridines are avid for electrophiles but are still willing to give them back. In these compounds three amino groups conjoin their forces into the heterocyclic nitrogen, making it a powerful Lewis base. A short and efficient synthesis is described, and the origin of its unique activity in nucleophilic organocatalysis is rationalized by kinetics and thermodynamic quantifications.

Entities:  

Year:  2010        PMID: 21186828     DOI: 10.1021/ol1029589

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  Cation affinity numbers of Lewis bases.

Authors:  Christoph Lindner; Raman Tandon; Boris Maryasin; Evgeny Larionov; Hendrik Zipse
Journal:  Beilstein J Org Chem       Date:  2012-08-31       Impact factor: 2.883

  1 in total

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