๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Selenium heterocycles VIII: Synthesis and antibacterial activity of selenosemicarbazide and 1,3,4-selenadiazolylcarbamic acid esters

โœ Scribed by A. Shafiee; I. Lalezari; S. Yazdany; A. Pournorouz

Publisher
John Wiley and Sons
Year
1973
Tongue
English
Weight
151 KB
Volume
62
Category
Article
ISSN
0022-3549

No coin nor oath required. For personal study only.

โœฆ Synopsis

The antibacterial activity of selenosemicarbazide and its acyl derivatives was compared with the activity of their sulfur and oxygen analogs. A series of 1,3,4-selenadiazolylcarbamic acid esters was also prepared and tested. Some of these compounds showed significant antibacterial activity.

Keyphrases 0 Selenosemicarbazide and acyl derivatives-synthesis,antibacterial activity compared with sulfur and oxygen analogs 0 1,3,4-Selenadiazolylcarbamic acid esters-synthesis, antibacterial activity 0 Antibacterial activity-synthesis of selenosemicarbazide derivatives and I ,3,4-selenadiazolylcarbamjc acid esters

๐Ÿ“œ SIMILAR VOLUMES

Selenium heterocycles X: Synthesis and a
Selenium heterocycles X: Synthesis and antibacterial activity of pyridyl-1,2,3-thiadiazoles and pyridyl-1,2,3-selenadiazoles
โœ I. Lalezari; A. Shafiee; S. Yazdany ๐Ÿ“‚ Article ๐Ÿ“… 1974 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 180 KB

acidic carboxylic group of aspirin may be achieved by making derivatives similar to Compound I. One possible advantage of a compound such as I is that the mucous membranes of the stomach are in contact with a neutral molecule. As I dissolves, however, it will rapidly hydrolyze, generating aspirin in