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Synthesis and properties of 2,2,4-trisubstituted 2,3-dihydro-1H-1,5-benzodiazepines

✍ Scribed by V. D. Orlov; S. M. Desenko; N. N. Kolos

Book ID
112348685
Publisher
Springer US
Year
1984
Tongue
English
Weight
519 KB
Volume
20
Category
Article
ISSN
0009-3122

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πŸ“œ SIMILAR VOLUMES

Chemical properties of 2,2,4-trisubstitu
Chemical properties of 2,2,4-trisubstituted 2,3-dihydro-1H-1,5-benzodiazepines
✍ V. D. Orlov; S. M. Desenko; N. S. Pivnenko πŸ“‚ Article πŸ“… 1987 πŸ› Springer US 🌐 English βš– 328 KB

Acetylation and nitrosation of 2,4-diaryl-2-methyl-2,3-dihydro-iH-l,5-benzodiazepines take place at the azomethyne nitrogen. Reduction is stereoselective.

Synthesis of 4-styryl-2,3-dihydro-1H-1,5
Synthesis of 4-styryl-2,3-dihydro-1H-1,5-benzodiazepin-2-ones
✍ Z. F. Solomko; A. A. Gaponov; V. I. Avramenko; M. P. Khmel' πŸ“‚ Article πŸ“… 1987 πŸ› Springer US 🌐 English βš– 265 KB

UDC 547.892.07:543. 422.25'51 4-Styryl-2,3-dihydro-iH-l,5-benzodiazepin-2-ones were synthesized and their structure was established by means of PMR spectra and mass spectroscopy. There is no unequivocal information on the structure of the reaction products of 4methyl-2,3-dihydro-iH-l,5-benzodiazepi