Alkali-catalysed alkoxy exchange, alcohol elimination, and hydrolysis of acetals having a dissociable α-proton

S. Antus, Ferenc Boross, Mihály Nógrádi

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

Some acetals with strong anionic activation in the α-position are prone to alkali-catalysed acetal exchange and/or alcohol elimination or, in the presence of water, to hydrolysis.

Original languageEnglish
Pages (from-to)333-334
Number of pages2
JournalJournal of the Chemical Society, Chemical Communications
Issue number10
DOIs
Publication statusPublished - 1977

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Acetals
Alkalies
Protons
Hydrolysis
Alcohols
Chemical activation
Prone Position
Water
alkoxyl radical

ASJC Scopus subject areas

  • Molecular Medicine

Cite this

Alkali-catalysed alkoxy exchange, alcohol elimination, and hydrolysis of acetals having a dissociable α-proton. / Antus, S.; Boross, Ferenc; Nógrádi, Mihály.

In: Journal of the Chemical Society, Chemical Communications, No. 10, 1977, p. 333-334.

Research output: Contribution to journalArticle

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