3-Phenyl-3H-naphtho[1,2-e][1,2,3]oxadiazine

Autor: Alia D. Aouant, George Varvounis
Jazyk: angličtina
Rok vydání: 2022
Předmět:
Zdroj: Molbank, Vol 2022, Iss 3, p M1432 (2022)
Druh dokumentu: article
ISSN: 1422-8599
DOI: 10.3390/M1432
Popis: In this study, we considered the reaction of (E)-1-[(2-phenylhydrazono)methyl]naphthalen-2-ol with iodobenzene diacetate in dichloromethane-produced novel 3-phenyl-3H-naphtho[1,2-e][1,2,3]oxadiazine in 11% yield. By analogy to previously published work, we suggested that the reaction proceeds via the intermediacy of an o-naphthoquinone azomethide that undergoes conjugated 6π-electrocylization to produce the product. 1D, 2D NMR, HRMS, IR, and UV-VIS spectra provided information that supported the structure of the product.
Databáze: Directory of Open Access Journals
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