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Эта публикация цитируется в 9 научных статьях (всего в 9 статьях)
Synthesis of 1-iodo-1,2,3,4,4a,9a-hexahydrocarbazole, 2a,3,4,5,5a,10a-hexahydrooxazolocarbazolium iodide and 4-bromo-1,2,3,4,4a,11b-hexahydrodibenzoxazepine from N-benzoyl-2-(cyclohex-2-en-1-yl)aniline
R. R. Gataullin, R. R. Ishberdina, O. V. Shitikova, L. V. Spirikhin, T. V. Kazhanova, I. B. Abdrakhmanov
Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation
Аннотация:
The reaction of N-benzoyl-2-(cyclohex-2-en-1-yl)aniline 1 with molecular oxygen in the presence of NaHCO3 results in N-benzoyl-1-iodo-1,2,3,4,4a,9a-hexahydrocarbazole, which was isomerised to 1-phenyl-2a,3,4,5,5a,10a-hexahydro[1,3]oxazolo-[5,4,3-j,k]carbazol-10-ium iodide, whereas the reaction of amide 1 with molecular bromine results in dibromide, but the interaction with NBS leads to 4-bromo-6-phenyl-1,2,3,4,4a,11b-hexahydrodibenzo[d,f][1,3] oxazepine.
Образец цитирования:
R. R. Gataullin, R. R. Ishberdina, O. V. Shitikova, L. V. Spirikhin, T. V. Kazhanova, I. B. Abdrakhmanov, “Synthesis of 1-iodo-1,2,3,4,4a,9a-hexahydrocarbazole, 2a,3,4,5,5a,10a-hexahydrooxazolocarbazolium iodide and 4-bromo-1,2,3,4,4a,11b-hexahydrodibenzoxazepine from N-benzoyl-2-(cyclohex-2-en-1-yl)aniline”, Mendeleev Commun., 14:5 (2004), 219–221
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3885 https://www.mathnet.ru/rus/mendc/v14/i5/p219
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