A novel double 'inverse electron-demand' Diels-Alder reaction of azolyldienamines and tetrazines

A Kotschy, Z Novak, Z Vincze, D M Smith, G Hajos

Research output: Contribution to journalArticlepeer-review

17 Citations (Scopus)

Abstract

Appropriately substituted azolyldienamines were found to undergo double 'inverse electron-demand' Diels-Alder reactions with tetrazine derivatives, yielding azolylpyridazines and dihydropyridazines as products. (C) 1999 Elsevier Science Ltd. All rights reserved.

Original languageEnglish
Pages (from-to)6313-6316
Number of pages4
JournalTetrahedron Letters
Volume40
Publication statusPublished - 20 Aug 1999

Keywords

  • Diels-Alder reactions
  • dienamines
  • pyridazines
  • tetrazines
  • DIENAMINES

Fingerprint

Dive into the research topics of 'A novel double 'inverse electron-demand' Diels-Alder reaction of azolyldienamines and tetrazines'. Together they form a unique fingerprint.

Cite this