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Preparation and photolysis of 2-diazo-6-oximino- and 2,6-bisdiazo-4-tert. Butylcyclohexanone
dc.creator | Tasovac, R. | |
dc.creator | Stefanović, Milutin | |
dc.creator | Stojiljković, A. | |
dc.date.accessioned | 2021-05-26T13:07:23Z | |
dc.date.available | 2021-05-26T13:07:23Z | |
dc.date.issued | 1967 | |
dc.identifier.issn | 0040-4039 | |
dc.identifier.issn | 1873-3581 | |
dc.identifier.uri | https://cer.ihtm.bg.ac.rs/handle/123456789/4666 | |
dc.description.abstract | Reaction mechanism of diazoketone photolysie is assumed to involve the formation ofd-keto-carbene intermediates, final products being dependent on the molecular structure and reaction medium. Numerous example8 of Wolff-rearrangement (1) 1,2-hydrogen shift (2) and intermolecular reactions (3) are available. | sr |
dc.language.iso | en | sr |
dc.publisher | Elsevier | sr |
dc.rights | restrictedAccess | sr |
dc.source | Tetrahedron Letters | sr |
dc.subject | photolysis of 2-diazo-6-oximino- and 2,6-bisdiazo-4-tert | sr |
dc.subject | Butylcyclohexanone | sr |
dc.subject | photolysie | sr |
dc.subject | molecular structure | sr |
dc.subject | hydrogen | sr |
dc.subject | intermolecular reaction | sr |
dc.title | Preparation and photolysis of 2-diazo-6-oximino- and 2,6-bisdiazo-4-tert. Butylcyclohexanone | sr |
dc.type | article | sr |
dc.rights.license | ARR | sr |
dcterms.abstract | Стојиљковић, A.; Тасовац, Р.; Стефановић, Милутин; | |
dc.citation.volume | 8 | |
dc.citation.issue | 28 | |
dc.citation.spage | 2729 | |
dc.citation.epage | 2732 | |
dc.identifier.doi | 10.1016/S0040-4039(01)89983-4 | |
dc.identifier.scopus | 2-s2.0-0005760829 | |
dc.type.version | publishedVersion | sr |