Preparation of 2-substituted naphth[2,3-d]oxazole-4,9-diones via a radicalchain process

Citation
P. Rathelot et al., Preparation of 2-substituted naphth[2,3-d]oxazole-4,9-diones via a radicalchain process, HETEROCYCLE, 53(5), 2000, pp. 1075
Citations number
26
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
HETEROCYCLES
ISSN journal
03855414 → ACNP
Volume
53
Issue
5
Year of publication
2000
Database
ISI
SICI code
0385-5414(20000501)53:5<1075:PO2NVA>2.0.ZU;2-Z
Abstract
A novel series of ethylenic naphth[2,3-d]oxazole-4,9-diones was synthesized via an S(RN)1 mechanism from the 2-chloromethylnaphth[2,3-d]oxazole-4,9-di one. This mechanism was confirmed by the inhibitory effects of the use of d ark, bubbling oxygen, cupric chloride, p-dinitrobenzene and TEMPO.