Synthesis of 1-Azabenzanthracene

Epimerization with the Use of 1,3-Dihydrobenzo(C)Thiophene -S,S Dioxide As a Source of Ortho-Quinodimethane

Murthy Akula, Louis A. Levy

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

The cycloaddition of o-quinodimethane, from l,3-dihydrobenzo(c)-S,S dioxide, to 5,6-dihydroquinoline yields a mixture of adducts isomeric at the newly created ring junction. The cycloadducts can be dehydrogenated to the fully aromatic 1-azabenzanthracene.

Original languageEnglish (US)
Pages (from-to)2765-2771
Number of pages7
JournalSynthetic Communications
Volume19
Issue number15
DOIs
StatePublished - Jan 1 1989

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Thiophenes
Cycloaddition

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

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Synthesis of 1-Azabenzanthracene : Epimerization with the Use of 1,3-Dihydrobenzo(C)Thiophene -S,S Dioxide As a Source of Ortho-Quinodimethane. / Akula, Murthy; Levy, Louis A.

In: Synthetic Communications, Vol. 19, No. 15, 01.01.1989, p. 2765-2771.

Research output: Contribution to journalArticle

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