Applications of Azoalkenes in the Synthesis of Fused Ring Pyridazine Derivatives

Santosh L. Gaonkar; K. M. Lokanatha Rai

doi:10.1002/jhet.2172

Applications of Azoalkenes in the Synthesis of Fused Ring Pyridazine Derivatives

Santosh L. Gaonkar^*, K. M. Lokanatha Rai

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

8 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 language	English
Pages (from-to)	1346-1348
Number of pages	3
Journal	Journal of Heterocyclic Chemistry
Volume	52
Issue number	5
DOIs	https://doi.org/10.1002/jhet.2172
Publication status	Published - 01-09-2015

All Science Journal Classification (ASJC) codes

Organic Chemistry

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10.1002/jhet.2172

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title = "Applications of Azoalkenes in the Synthesis of Fused Ring Pyridazine Derivatives",

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.",

author = "Gaonkar, \{Santosh L.\} and \{Lokanatha Rai\}, \{K. M.\}",

note = "Publisher Copyright: {\textcopyright} 2014 HeteroCorporation.",

year = "2015",

month = sep,

day = "1",

doi = "10.1002/jhet.2172",

language = "English",

volume = "52",

pages = "1346--1348",

journal = "Journal of Heterocyclic Chemistry",

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T1 - Applications of Azoalkenes in the Synthesis of Fused Ring Pyridazine Derivatives

AU - Gaonkar, Santosh L.

AU - Lokanatha Rai, K. M.

PY - 2015/9/1

Y1 - 2015/9/1

N2 - 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.

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.

UR - https://www.scopus.com/pages/publications/84942510865

UR - https://www.scopus.com/inward/citedby.url?scp=84942510865&partnerID=8YFLogxK

U2 - 10.1002/jhet.2172

DO - 10.1002/jhet.2172

M3 - Article

AN - SCOPUS:84942510865

SN - 0022-152X

VL - 52

SP - 1346

EP - 1348

JO - Journal of Heterocyclic Chemistry

JF - Journal of Heterocyclic Chemistry

IS - 5

ER -

Applications of Azoalkenes in the Synthesis of Fused Ring Pyridazine Derivatives

Abstract

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