Abstract
1- and 4-Azaphenanthrene N-oxides undergo solvent-dependent photoisomerization, yielding naphtho-1,3-oxazepines in aprotic solvents and benzoquinolin-1 (2H)-ones in water. No ring enlargement but only isomerization to the corresponding lactam is observed to take place in the case of 9-azaphenanthrene N-oxide. Measurements of the quantum yield of two photoprocesses (lactam formation and ring enlargement) confirm the difference between the photochemical behaviour of 9-azaphenanthrene N-oxide and that of the other two N-oxides examined
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of the Chemical Society, Perkin Transactions 2
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.