dc.contributor.author | Tuyun, AMAÇ FATİH | |
dc.date.accessioned | 2021-03-06T08:17:42Z | |
dc.date.available | 2021-03-06T08:17:42Z | |
dc.date.issued | 2014 | |
dc.identifier.citation | Tuyun A. F. , "Synthetic exploitation of halogenated alkenes containing EWG: benzotriazole-mediated synthesis of benzoazetines and thermal transformations", RSC ADVANCES, cilt.4, ss.19640-19645, 2014 | |
dc.identifier.issn | 2046-2069 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_e02abf07-2c94-498a-b5fd-09a5c9f0b9c5 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/147658 | |
dc.identifier.uri | https://doi.org/10.1039/c4ra01425a | |
dc.description.abstract | The series of stable benzoazetine derivatives (5a-d) based on nitrovinyl moieties have been synthesized via transamination of bisbenzotriazolyl derivatives (2a-c). Four new heptatomic aromatic cycloheterocumulenes (azacyclohepta-1,2,4,6-tetraene) occurring at the stage of the film-forming process by TVE have been obtained by rearrangement of benzoazetines. The highly strained products were characterized by IR spectroscopy. | |
dc.language.iso | eng | |
dc.subject | Temel Bilimler | |
dc.subject | Biyokimya | |
dc.subject | Temel Bilimler (SCI) | |
dc.subject | KİMYA, MULTİDİSİPLİNER | |
dc.subject | Alkoloidler | |
dc.subject | Kimya | |
dc.title | Synthetic exploitation of halogenated alkenes containing EWG: benzotriazole-mediated synthesis of benzoazetines and thermal transformations | |
dc.type | Makale | |
dc.relation.journal | RSC ADVANCES | |
dc.contributor.department | Beykent Üniversitesi , Mühendislik-Mimarlık Fakültesi , Kimya Mühendisliği | |
dc.identifier.volume | 4 | |
dc.identifier.issue | 38 | |
dc.identifier.startpage | 19640 | |
dc.identifier.endpage | 19645 | |
dc.contributor.firstauthorID | 718527 | |