๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Synthesis of 3H- and 14C-labelled 0-(3-morpholinoethoxy)-diphenylether hydrochloride

โœ Scribed by Tohru Horie; Takeshi Fujita


Publisher
John Wiley and Sons
Year
1972
Tongue
French
Weight
206 KB
Volume
8
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Synthesis of 2H- and 3H-labelled iptakal
โœ Cheng Zhang; Rifang Yang; Lanfu Chen; Bohua Zhong; Liuhong Yun; Hai Wang ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 110 KB

## Abstract Iptakalim hydrochloride (__N__โ€(1โ€methylethyl)โ€1,1,2โ€trimethylโ€propylamine hydrochloride) is a promising antihypertensive drug discovered and developed by Beijing Institute of Pharmacology and Toxicology. Deuteriumโ€ and tritiumโ€labelled compounds were designed and synthesized for pharma

Synthesis of 3H and 14C labelled SCH 484
โœ D. Hesk; C. Bowlen; S. Hendershot; D. Koharski; P. McNamara; D. Rettig; S. Saluj ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 404 KB ๐Ÿ‘ 1 views

3H-Sch 47949, racemic 3H-Sch 48461, was prepared at a specific activity of 40 mCi/mmole by Pt catalysed exchange with tritiated water. 3H-Sch 48461 was prepared at a specific activity of 64.6 Ci/mmole by a Pd/C catalysed reduction of an olefinic intermediate. 14C-Sch 48461 was prepared in 8 steps fr

Synthesis of 14C labelled drotaverinum h
โœ E. Koltai; D. Bรกnfi; J. Engler; J. Volford; Z. Mรฉszรกros ๐Ÿ“‚ Article ๐Ÿ“… 1979 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 182 KB

Drotaverinum hydrochloride was labelled with 14C isotope in position 1 of the isoquinoline ring. A rapid synthesis with high radiochemical yield was elaborated. ~ \* Kl'CN was prepared by BBnfi's method5 4C -Drotaverinwn Hydrochloride

Synthesis of 14C-labelled etintidine hyd
โœ Stephen M. Stefanick; Charles F. Kasulanis; Seymour D. Levine; Arthur C. Fabian ๐Ÿ“‚ Article ๐Ÿ“… 1985 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 279 KB

Two 14C preparations o f t h e Hz-antagonist e t i n t i d i n e hydrochloride a r e reported. I n one, t h e l a b e l I s introduced by r e a c t i n g [1-I4C] propargylamine w i t h t h e a p p r o p r i a t e i s o t h i ourea, f o l l o w e d by h y d r o c h l o r i d e formation. This a f f

Synthesis of 3H-, 13C3-, and 14C-labeled
โœ C. Flader Lavey; D. Hesk; D. Koharski; V. Truong; P. McNamara ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 152 KB

## Abstract The preparation of [^3^H]Sch 727965 from unlabeled compound and tritiated water was base catalyzed. Diethyl [^13^C~3~]malonate was used to prepare [^13^C~3~]Sch 727965 in five steps in 21.8% overall yield. In a similar manner, [^14^C]Sch 727965 was prepared in five steps from diethyl [2