Issue 14, 2001

First intramolecular trapping and structural proof of the key intermediate in the formation of indolizine photochromicsElectronic supplementary information (ESI) available: Figs. S1 and S2. See http://www.rsc.org/suppdata/cc/b1/b101044l/

Abstract

The reaction of substituted spirocyclopropenes 1 with 1-(3,5-dinitrophenyl)-3,4-dihydroisoquinoline 2 in dry ether solution afforded not only the expected THI 4 by 1,5-electrocyclization but also novel fluorenespiroazanorcaradienes 5 which is the first intramolecularly trapped product of the key intermediate in the formation of indolizine photochromics.

Supplementary files

Article information

Article type
Communication
Submitted
30 Jan 2001
Accepted
22 May 2001
First published
20 Jun 2001

Chem. Commun., 2001, 1246-1247

First intramolecular trapping and structural proof of the key intermediate in the formation of indolizine photochromics

Y. Tan, S. A. Ahmed, H. Dürr, V. Huch and A. Abdel-Wahab, Chem. Commun., 2001, 1246 DOI: 10.1039/B101044L

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