Easy Access to cis-3-(Benzoxazol-2-yl)cyclopentanecarboxylic Acids from Camphorquinone and o-Aminophenols via an Unexpected Opening of Camphor Ring

Autor: J. Nowicka-Scheibe
Rok vydání: 2013
Předmět:
Zdroj: Synthetic Communications. 43:2198-2207
ISSN: 1532-2432
0039-7911
DOI: 10.1080/00397911.2012.696302
Popis: 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.
Databáze: OpenAIRE
Nepřihlášeným uživatelům se plný text nezobrazuje