2013
Synthesis, structure and properties of ethyl naphth[2,3-f]isoindole-1-carboxylate
RSC ADVANCES
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- Volume
- 3
- Number
- 9
- First page
- 3006
- Last page
- 3016
- Language
- English
- Publishing type
- Research paper (scientific journal)
- DOI
- 10.1039/c2ra22870j
- Publisher
- ROYAL SOC CHEMISTRY
Ethyl 12-oxo-4,11-dihydro-4,11-ethanonaphth[2,3-f]isoindole-1-carboxylate (2) was prepared from 7-tert-butoxynorbornadiene and quantitatively converted to ethyl naphth[2,3-f]isoindole-1-carboxylate (3) by the thermal or photochemical cheletropic reaction. Ethyl naphth[2,3-f] isoindole-1-carboxylate (3) existed in a 2H-form both in solution and as a solid, and gradually dimerized to give a dianthradiazafulvalene derivative under aerobic conditions.
- Link information
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- DOI
- https://doi.org/10.1039/c2ra22870j
- Web of Science
- https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000314475700019&DestApp=WOS_CPL
- URL
- http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84874427782&origin=inward
- ID information
-
- DOI : 10.1039/c2ra22870j
- ISSN : 2046-2069
- SCOPUS ID : 84874427782
- Web of Science ID : WOS:000314475700019