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Action de Divers Dienophiles Sur Quelques 2-(3-Indolyl)-1,4-Naphtoqui-Nones-N-Substituees. Synthese D'une Nouvelle Serie de Naphto-[2,3-c]-Carbazole-5,13-Quinones

✍ Scribed by Claude Lion; Michel Hocquaux; Patricia Amouzegh; Michel Philippe; Jean-Christophe Henrion; Emmanuelle Caron; Sylvette Briand


Publisher
Wiley (John Wiley & Sons)
Year
2010
Weight
289 KB
Volume
104
Category
Article
ISSN
0037-9646

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✦ Synopsis


Addition of an N-substituted indole without any substitution in the 2 and 3 positions to 1 ,Gnaphtoquinone leads to the expected, 2-(3-indolyl)-l,4-naphtoquinone. The latter reacts with some dienophiles via a Diels -Alder reaction and gives new N-substituted naphto-[2,3-C]-carbazoIe-5-13-quinones.