Chemistry Letters
Online ISSN : 1348-0715
Print ISSN : 0366-7022
ISSN-L : 0366-7022
Remarkable Differences in Photo and Thermal (Acid-catalyzed) Reactivities between ortho- and para-Acylcyclohexadienones as Essential Factors Determining the Overall Efficiency of the Photo-Fries Rearrangement
Tadashi MoriMakoto TakamotoHideaki SaitoTakahiro FuroTakehiko WadaYoshihisa Inoue
Author information

2004 Volume 33 Issue 3 Pages 256-257


Successful isolation of “ortho” and “para”-acylcyclohexadienones allowed us to comparatively study their ground- and excited-state behavior under a variety of conditions. In neutral solutions, the two isomeric cyclohexdienones showed completely different reactivities for photochemical and thermal reactions, while in acidic methanol both quantitatively afforded the corresponding transesterification product and naphthol. These studies help us understand the detailed photo-Fries rearrangement mechanism, which involves several crucial photochemical and thermal steps.

Information related to the author

This article cannot obtain the latest cited-by information.

© 2004 The Chemical Society of Japan
Previous article Next article