Reaction of guanidine with peri-substituted (R-ethynyl)-9,10-anthraquinones bearing electron-donating substituents

D. S. Baranov, S. F. Vasilevsky

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

2-Amino-3-aroyl-7H-dibenzo[de,h]quinolin-7-ones were synthesized by the reaction of guanidine with peri-(R-ethynyl)-9,10-anthraquinones in boiling n-butanol.

Original languageEnglish
Pages (from-to)1031-1034
Number of pages4
JournalRussian Chemical Bulletin
Volume59
Issue number5
DOIs
Publication statusPublished - 1 May 2010
Externally publishedYes

Fingerprint

Bearings (structural)
1-Butanol
Guanidine
Boiling liquids
Electrons
9,10-anthraquinone

Keywords

  • 7H-dibenzo[de,h]- quinolin-7-ones
  • alkynes
  • cross-coupling
  • guanidine
  • heterocyclization

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Reaction of guanidine with peri-substituted (R-ethynyl)-9,10-anthraquinones bearing electron-donating substituents. / Baranov, D. S.; Vasilevsky, S. F.

In: Russian Chemical Bulletin, Vol. 59, No. 5, 01.05.2010, p. 1031-1034.

Research output: Contribution to journalArticle

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AB - 2-Amino-3-aroyl-7H-dibenzo[de,h]quinolin-7-ones were synthesized by the reaction of guanidine with peri-(R-ethynyl)-9,10-anthraquinones in boiling n-butanol.

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KW - heterocyclization

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