## Abstract 5′‐[^14^C~1~]Panadiplon was prepared in 3 steps starting from [^14^C~1~]cyclopropane carboxylic acid and 3‐(5′‐cyano‐1,2,4‐oxadiazol‐3‐yl)‐5‐(1‐methylethyl)‐imidazo‐[1,5a]‐quinoxalin‐4(5H)‐one. 3a, 4‐[^13^C~2~]Panadiplon was prepared in two steps from ^13^C~2~‐oxalic acid and N‐1‐(1‐met
Polychlorinated biphenyls V. + synthesis of14C-labelled 2,2′, 4,4′, 5,5′-hexachlorobiphenyl, a major component in PCB-mixtures
✍ Scribed by Goran Sundstrom
- Book ID
- 112589805
- Publisher
- Springer
- Year
- 1974
- Tongue
- English
- Weight
- 272 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0007-4861
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract ^14^C‐Labelled (S)‐(+)‐6‐(2‐chlorophenyl)‐3‐cyclopropanecarbonyl‐8,11‐dimethyl‐2,3,4,5‐ tetrahydro‐8H‐pyrido[4′,3′:4,5]thieno[3,2‐f][1,2,4]triazolo[4,3‐a][1,4] diazepine (^14^C‐E6123), a platelet activating factor receptor antagonist for studying the pharmacokinetic profile of E6123, wa
## Abstract 2‐Propyl‐8‐oxo‐1‐[(2′‐(1H‐tetrazole‐5‐yl) biphenyl‐4‐yl)methyl]‐4, 5, 6, 7‐tetrahydrocyclohept imidazole (KT3‐671), which has been found to be a potent and selective angiotesin II receptor antagonist, was synthesized in ^14^C‐labelled form by using potassium[^14^C]‐cyanide. [^14^C](KT3‐
Syn thes is of 14C -labe 1 led 4 -chloro -3 -s u l f amoyl -N -(3aa, 4a, 5 , 6 7a,7aa-hexahydro-4,7-methano-isoindolin-Z-yl)-benzamide.
## Abstract A group of radioactive 1,4‐benzodiazepine derivatives have been synthesized from glycine‐1‐^14^C. The subject compounds are labeled with carbon‐14 in the 2‐position of the 1,4‐benzodiazepine ring system.