BROMINATION OF AROMATIC RING OF TETRAHYDRO-1,5-BENZODIAZEPIN-2-ONES

Авторы

  • B. Puodziunaite Editorial Office "Chemistry of Heterocyclic Compounds"
  • R. Janciene Institute of Biochemistry, Vilnius
  • Z. Stumbreviciute Institute of Biochemistry, Vilnius
  • L. Kosychova Institute of Biochemistry, Vilnius

DOI:

https://doi.org/10.1007/240

Ключевые слова:

tetrahydro-1, 5-benzodiazepin-2-ones, bromination

Аннотация

Novel mono- or dibromo-substituted tetrahydro-1,5-benzodiazepinones were obtained by direct bromination of the corresponding 2,3,4,5-tetrahydro-(1H)-1,5-benzodiazepin-2-ones and 5‑N‑alkyl (or formyl) derivatives with bromine. Substituent effects and the orientation of the entering groups in the bromination reaction are discussed.

Also published in Chemistry of Heterocyclic Compounds, 2000, 36 (6), pp 698-704

http://link.springer.com/article/10.1007/BF02297679

Загрузки

Опубликован

2013-02-04

Выпуск

Раздел

Оригинальные статьи