Author:
Plé Nelly,Turck Alain,Queguiner Guy
Abstract
Covalent addition of various nucleophiles to pyrido-as-triazines was studied and the σ-adduct structures were determined by NMR. A remarkable reactivity toward carbon nucleophiles has been highlighted for pyrido-as-triazines bearing a pyridinic nitrogen in the β position: only in the pteridine series has a similar reactivity been encountered. Complete regioselectivity of the nucleophilic attack on the pyridine nucleus peri to the triazine was observed.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
4 articles.
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