An expedient synthesis of 3-amino-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-one
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (9) , 939-942
- https://doi.org/10.1016/s0040-4039(00)95879-9
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Biochemical and pharmacological characterization of an extremely potent and selective nonpeptide cholecystokinin antagonist.Proceedings of the National Academy of Sciences, 1986
- Design of potent, orally effective, nonpeptidal antagonists of the peptide hormone cholecystokinin.Proceedings of the National Academy of Sciences, 1986
- A potent nonpeptide cholecystokinin antagonist selective for peripheral tissues isolated from Aspergillus alliaceusScience, 1985
- Identification of two related pentapeptides from the brain with potent opiate agonist activityNature, 1975
- Amidoalkylation of mercaptans with glyoxylic acid derivativesTetrahedron, 1975
- A general method for preparing 2-acetamidoacetanilides having a second functional group in the 2 position and affording an access to 3-acetamido-1,3-dihydro-2H-1,4-benzodiazepin-2-onesThe Journal of Organic Chemistry, 1968
- A novel elimination-addition reaction of a diacylated hydroxylamineTetrahedron Letters, 1965