Applications of Azoalkenes in the Synthesis of Fused Ring Pyridazine Derivatives

Santosh L. Gaonkar, K. M. Lokanatha Rai

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Cyclic ketohydrazones containing α-methylene group are oxidized by chloramine-T followed by treatment with triethylamine leads to the formation of azoalkenes via azochloride, which are trapped by olefinic compounds to produce fused ring pyridazine derivatives in good yield.

Original languageEnglish
Pages (from-to)1346-1348
Number of pages3
JournalJournal of Heterocyclic Chemistry
Volume52
Issue number5
DOIs
Publication statusPublished - 01-09-2015

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Derivatives
triethylamine
chloramine-T
pyridazine

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

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abstract = "Cyclic ketohydrazones containing α-methylene group are oxidized by chloramine-T followed by treatment with triethylamine leads to the formation of azoalkenes via azochloride, which are trapped by olefinic compounds to produce fused ring pyridazine derivatives in good yield.",
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Applications of Azoalkenes in the Synthesis of Fused Ring Pyridazine Derivatives. / Gaonkar, Santosh L.; Lokanatha Rai, K. M.

In: Journal of Heterocyclic Chemistry, Vol. 52, No. 5, 01.09.2015, p. 1346-1348.

Research output: Contribution to journalArticle

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AB - Cyclic ketohydrazones containing α-methylene group are oxidized by chloramine-T followed by treatment with triethylamine leads to the formation of azoalkenes via azochloride, which are trapped by olefinic compounds to produce fused ring pyridazine derivatives in good yield.

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