Sciact
  • EN
  • RU

Diazabicycloalkanes with nitrogen atoms in the nodal positions. 7. Synthesis and configuration of 2,3-diphenyl-1,4-diazabicyclo[2.2.2]-octane Научная публикация

Журнал Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Вых. Данные Год: 1982, Том: 18, Номер: 1, Страницы: 80-84 Страниц : DOI: 10.1007/BF00513296
Авторы Shishkin G. V. , Naumenko I. I. , Anisimova I. L. , Yudina O. B. , Storozhenko V. G.
Организации
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, Novosibirsk, 630090, Russian Federation

Реферат: The reaction of ethylene oxide with the meso and d, l diasteromers of 1,2-diphenyl-ethylenediamine gave N,N'-bis(β-hydroxyethyl)-1,2-diphenylethylenediamines, which upon refluxing with SOCl2 form N,N'-bis (β-chloroethyl)-1,2-ethylenediamines. The latter upon heating in dimethylformamide (DMF) at 150 ° C undergo cyclization to give, respectivley, cis- and trans-2,3-diphenyl-1,4-diazabicyclo[2.2.2]octane. Evidence for the spatial orientation of the phenyl substituents in the diazabicyclooctanes obtained was obtained by means of an analysis of the multiplicity of the methylene protons in the PMR spectra. The vicinal spin-spin coupling constants for the benzyl protons of the isomeric 2,3-diphenyl-1,4-diazabicyclo[2.2.2]octanes in the 13C-H satellites were measured. The values obtained were compared with the literature data and with the dihedral angles calculated from mechanical models of the molecules. © 1982 Plenum Publishing Corporation.
Библиографическая ссылка: Shishkin G.V. , Naumenko I.I. , Anisimova I.L. , Yudina O.B. , Storozhenko V.G.
Diazabicycloalkanes with nitrogen atoms in the nodal positions. 7. Synthesis and configuration of 2,3-diphenyl-1,4-diazabicyclo[2.2.2]-octane
Chemistry of Heterocyclic Compounds. 1982. V.18. N1. P.80-84. DOI: 10.1007/BF00513296 Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 янв. 1982 г.
Идентификаторы БД:
Scopus: 2-s2.0-34250231099
РИНЦ: 30892970
OpenAlex: W2061356465
Цитирование в БД:
БД Цитирований
Scopus 1
РИНЦ 1
OpenAlex 1
Альметрики: