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The catalytic versatility of low toxicity dialkyltriazolium salts: in situ modification facilitates diametrically opposed catalysis modes in one pot.
Myles, Lauren; Gathergood, Nicholas; Connon, Stephen J.
Affiliation
  • Myles L; School of Chemistry, Centre for Synthesis and Chemical Biology, Trinity Biomedical Sciences Institute, University of Dublin, Trinity College, Dublin 2, Ireland.
Chem Commun (Camb) ; 49(46): 5316-8, 2013 Jun 11.
Article in En | MEDLINE | ID: mdl-23646348
ABSTRACT
The ability of triazolium salts to serve as a precatalyst for both an acid and a powerful base/nucleophile (controlled by additives) has been exploited in a process characterised by a unique in situ catalyst modification strategy.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Salts / Triazoles / Acids Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2013 Document type: Article Affiliation country: Ireland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Salts / Triazoles / Acids Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2013 Document type: Article Affiliation country: Ireland