On the synthesis and reactivity of 1-benzyl-2-arylquinoline-4-thiones

Edmund J. Niedzinski, Matthew R. Lashley, Michael H. Nantz

Research output: Contribution to journalArticle

5 Scopus citations

Abstract

A panel of 1-benzyl-2-aryl-4-quinolones was synthesized in three steps and converted to the corresponding 4-thione derivatives using Lawesson's reagent. The representative vinylogous thioamide (5a) was alkylated to afford a novel series of quinolinium salts.

Original languageEnglish (US)
Pages (from-to)623-627
Number of pages5
JournalHeterocycles
Volume55
Issue number4
StatePublished - Apr 1 2001

ASJC Scopus subject areas

  • Organic Chemistry

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    Niedzinski, E. J., Lashley, M. R., & Nantz, M. H. (2001). On the synthesis and reactivity of 1-benzyl-2-arylquinoline-4-thiones. Heterocycles, 55(4), 623-627.