Papers

Peer-reviewed
2013

Synthesis, structure and properties of ethyl naphth[2,3-f]isoindole-1-carboxylate

RSC ADVANCES
  • Aya Seike
  • ,
  • Kaoru Yamagami
  • ,
  • Yoshimasa Kakitani
  • ,
  • Miki Kuwajima
  • ,
  • Hiroki Uoyama
  • ,
  • Shin-ichi Nagaoka
  • ,
  • Takahiro Nakae
  • ,
  • Shigeki Mori
  • ,
  • Tetsuo Okujima
  • ,
  • Hidemitsu Uno

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
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

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