Issue 11, 1998

Some Rearrangements of Gibberellins Catalysed by Tetracyanoethylene

Abstract

Tetracyanoethylene in methanol has been shown to catalyse the rearrangement of ring A of gibberellic acid to the3β-methyl ether of gibberellenic acid and to the 19-2α-isolactone whilst the 13-hydroxygibberellin 16,17-epoxides are converted to 8:13-isogibberellins.

Article information

Article type
Paper

J. Chem. Res. (S), 1998, 676-676

Some Rearrangements of Gibberellins Catalysed by Tetracyanoethylene

J. R. Hanson and C. Uyanik, J. Chem. Res. (S), 1998, 676 DOI: 10.1039/A804144J

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