Diels‐alder cycloadditions of diene‐substituted N‐ethoxycarbonyl‐2‐methyl‐1,2‐dihydropyridines with N‐phenylmaleimide

Grant R. Krow, Kevin C. Cannon, James T. Carey, Yoon B. Lee, Steven W. Szczepanski, Harri G. Ramjit

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

The ten possible substitution patterns for N‐Ethoxycarbonyl‐2‐methyl‐1,2‐dihydropyridines 5 in which one or two olefinic sites are alkyl substituted were synthesized and reacted with N‐phenylmaleimide 2 to provide cycloadducts 6. N‐Ethoxycarbonyl‐5,6‐cyclohexyl‐2‐methyl‐1,2‐dihydropyridine 51 provided the novel spirocycle 61.

Original languageEnglish (US)
Pages (from-to)131-135
Number of pages5
JournalJournal of Heterocyclic Chemistry
Volume22
Issue number1
DOIs
StatePublished - Jan 1 1985

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Cycloaddition
Substitution reactions

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Krow, Grant R. ; Cannon, Kevin C. ; Carey, James T. ; Lee, Yoon B. ; Szczepanski, Steven W. ; Ramjit, Harri G. / Diels‐alder cycloadditions of diene‐substituted N‐ethoxycarbonyl‐2‐methyl‐1,2‐dihydropyridines with N‐phenylmaleimide. In: Journal of Heterocyclic Chemistry. 1985 ; Vol. 22, No. 1. pp. 131-135.
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Diels‐alder cycloadditions of diene‐substituted N‐ethoxycarbonyl‐2‐methyl‐1,2‐dihydropyridines with N‐phenylmaleimide. / Krow, Grant R.; Cannon, Kevin C.; Carey, James T.; Lee, Yoon B.; Szczepanski, Steven W.; Ramjit, Harri G.

In: Journal of Heterocyclic Chemistry, Vol. 22, No. 1, 01.01.1985, p. 131-135.

Research output: Contribution to journalArticle

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