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Easy Access to cis-3-(Benzoxazol-2-yl)cyclopentanecarboxylic Acids from Camphorquinone and o-Aminophenols via an Unexpected Opening of Camphor Ring
Authors:Joanna Nowicka-Scheibe
Institution:1. West Pomeranian University of Technology , Szczecin, Institute of Chemistry and Environmental Protection , Szczecin , Poland joannans@zut.edu.pl
Abstract:An unexpected formation of cis-1,2,2-trimethyl-3-(benzoxazol-2-yl)cyclopenta-necarboxylic acids was observed as the result of an oxidative C-C bond cleavage of the camphor ring in the intermediate imine during the condensation reactions between camphoroquinone and o-aminophenols conducted under open air conditions.

Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications® to view the free supplemental file.
Keywords:Air oxidation  benzoxazole  caphoroquinone  condensation  o-aminophenols  ring opening
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