C-Deuteration and cyclization of 2-hydroxypropiophenones

V. Szabó, J. Borbély, J. Borda

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

For planning of the conditions of Claisen condensation the relationship between CH-acidity and reactivity of 2-hydroxypropiophenones was investigated. It was found that there is a linear correlation between the acidity of the α-methylene group of these compounds and the rate of base-catalyzed Claisen condensation in the synthesis of chromones.

Original languageEnglish
Pages (from-to)127-131
Number of pages5
JournalReaction Kinetics and Catalysis Letters
Volume17
Issue number1-2
DOIs
Publication statusPublished - Aug 1981

Fingerprint

Hydroxypropiophenone
Cyclization
Acidity
acidity
Condensation
condensation
Chromones
methylene
planning
reactivity
methylidyne
Planning
synthesis

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Catalysis

Cite this

C-Deuteration and cyclization of 2-hydroxypropiophenones. / Szabó, V.; Borbély, J.; Borda, J.

In: Reaction Kinetics and Catalysis Letters, Vol. 17, No. 1-2, 08.1981, p. 127-131.

Research output: Contribution to journalArticle

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