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 |
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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 |
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