Версия от 13:22, 21 февраля 2024; EducationBot(обсуждение | вклад)(Новая страница: «{{Английская Википедия/Панель перехода}} {{distinguish|Cope rearrangement}} {{Reactionbox | Name = Cope reaction | Type = Elimination reaction | NamedAfter = Arthur C. Cope | Section3 = {{Reactionbox Identifiers | OrganicChemistryNamed = cope-elimination | RSC_ontology_id = 0000539 }} }} The '''Cope reaction''' or '''Cope elimination''', developed by Arthur C. Cope, is an elimination reaction of the Amine...»)
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The reverse or retro-Cope elimination has been reported, in which an N,N-disubstituted hydroxylamine reacts with an alkene to form a tertiary N-oxide.[9][10] The reaction is a form of hydroamination and can be extended to the use of unsubstituted hydroxylamine, in which case oximes are produced.[11]
↑Amine Oxides. VIII. Medium-sized Cyclic Olefins from Amine Oxides and Quaternary Ammonium Hydroxides Arthur C. Cope, Engelbert Ciganek, Charles F. Howell, Edward E. Schweizer J. Am. Chem. Soc., 1960, 82 (17), pp 4663–4669 Шаблон:Doi
↑Amine Oxides. VII. The Thermal Decomposition of the N-Oxides of N-Methylazacycloalkanes Arthur C. Cope, Norman A. LeBel; J. Am. Chem. Soc.; 1960; 82(17); 4656-4662. Шаблон:Doi
