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Photocycloaddition Reactions of 5,5‐Dimethyl‐3‐(3‐methylbut‐3‐en‐1‐ynyl)cyclohex‐2‐en‐1‐one
Authors:Inga Inhülsen  Jürgen Kopf  Paul Margaretha
Affiliation:1. Chemistry Department, University of Hamburg, Martin‐Luther‐King Platz 6, D‐20146 Hamburg, (phone: +4940428384316;2. fax: +4940428385592)
Abstract:The title cyclohexenone 1d undergoes photodimerization selectively at the exocyclic C?C bond to give a 1 : 1 mixture of 1,2‐dialkynyl‐1,2‐dimethylcyclobutanes 6 and 7 . On irradiation in the presence of 2,3‐dimethylbuta‐1,3‐diene, 1d affords bicyclo[8.4.0]tetradeca‐1,2,3,7‐tetraen‐11‐one 9 . This – formal – (6+4)‐cycloadduct undergoes quantitative isomerization to 3‐cycloheptadienyl‐2,5,5‐trimethylcyclohex‐2‐enone 11 on treatment with basic silica gel.
Keywords:Cyclodeca‐1,2.3,7‐tetraenes  Cyclohexenone photodimerization  Photocycloaddition reactions  X‐Ray crystallography  Hexa‐1,5‐dien‐2‐ynes, 1‐acyl‐
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