Issue 19, 1977

Chemical behaviour of αβ-acetylenic α′-hydroxy quaternary ammonium salts in basic media

Abstract

According to the nature of their substituents hydroxy-ammonium salts, R1C[triple bond, length half m-dash]CCH(NMe3+I)CR2R3-OH, when treated with a weak base in aqueous solution, are either cleaved into a carbonyl compound and a quaternary prop-2-ynylic ammonium compound, or cyclize to form an oxiran or a furan.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1977, 679-679

Chemical behaviour of αβ-acetylenic α′-hydroxy quaternary ammonium salts in basic media

R. Epsztein and N. Le Goff, J. Chem. Soc., Chem. Commun., 1977, 679 DOI: 10.1039/C39770000679

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