Issue 8, 1982

The mechanism of photoinduced fragmentation of alkyl pyruvates

Abstract

The finding that t-butyl pyruvate is photostable and has a much longer triplet lifetime than methyl, ethyl, isopropyl, 2-deuterioisopropyl, and benzyl pyruvates, together with triplet quenching studies, shows that alkyl pyruvates fragment from the triplet state via a Type II and not a Type I process.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1982, 993-997

The mechanism of photoinduced fragmentation of alkyl pyruvates

R. S. Davidson and D. Goodwin, J. Chem. Soc., Perkin Trans. 2, 1982, 993 DOI: 10.1039/P29820000993

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