Issue 16, 1998
From the journal:

Chemical Communications

A new synthesis of benzoporphyrins using 4,7-dihydro-4,7-ethano-2H-isoindole as a synthon of isoindole

Satoshi Ito,   Takashi Murashima,   Noboru Ono  and  Hidemitsu Uno  

Abstract

Heating 4,7-dihydro-4,7-ethano-2H-isoindole at 200 °C induces the retro-Diels–Alder reaction to give isoindole in essentially quantitative yield, which can be applied to a new synthesis of tetrabenzoporphyrins and monobenzoporphyrins.

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Article information

DOI
https://doi.org/10.1039/A803656J
Article type
Paper

Chem. Commun., 1998, 1661-1662

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A new synthesis of benzoporphyrins using 4,7-dihydro-4,7-ethano-2H-isoindole as a synthon of isoindole

S. Ito, T. Murashima, N. Ono and H. Uno, Chem. Commun., 1998, 1661 DOI: 10.1039/A803656J

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