Abstract
Re-examination of the thermal and photochemical decomposition of 2-azidophenazine reveals new pathways. Thus, besides reduction to the amine, the triplet nitrene yields the azo derivative and phenazino[1',2':5,6]pyridazino[4,3-a]phenazine while the singlet nitrene rearranges to the dehydroazepine and adds a further molecule of azide to yield an open-chain imine. The factors leading to the predominance of «dimeric» products from this type of heterocyclic azides are discussed
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: 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.
