Synthesis of new stable pseudobases

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Pyrido[1,2-b][1,2,4]triazinium salts easily form covalent hydrates in the presence of traces of water and readily react with various nucleophilic anions (e.g. hydoxide, alkoxide, or cyanide ions) to yield stable crystalline addition products (i.e. pseudobases). All these transformations were found to be regioselective and afforded 2-substituted products as revealed by NMR experiments.

Original languageEnglish
Pages (from-to)155-161
Number of pages7
JournalArkivoc
Volume2003
Issue number14
Publication statusPublished - Dec 1 2003

Keywords

  • Covalent hydrate
  • Fused 1,2,4-triazinium salt
  • Pseudobase
  • Regioselective addition

ASJC Scopus subject areas

  • Organic Chemistry

Fingerprint Dive into the research topics of 'Synthesis of new stable pseudobases'. Together they form a unique fingerprint.

  • Cite this