✦ LIBER ✦

Synthesis of [14-14C] dexclamol hydrochloride and [14-14C] butaclamol hydrochloride

✍ Scribed by E. S. Ferdinandi; P. Raman; V. Ross

Book ID: 111700786
Publisher: John Wiley and Sons
Year: 1978
Tongue: French
Weight: 426 KB
Volume: 14
Category: Article
ISSN: 0022-2135
DOI: 10.1002/jlcr.2580140514

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of 14C-radiolabeled ractopamin

Synthesis of 14C-radiolabeled ractopamine hydrochloride

✍ Norman H. Terando 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 French ⚖ 311 KB 👁 1 views

## Abstract Ractopamine HCl was uniformly labeled with carbon‐14 in one of two phenyl rings as a requirement for animal metabolism studies. The six‐step synthesis was completed in a 14% yield. Product instability on silica gel complicated purification, but development of a chromatographic method af

A synthesis of [14C]alfuzosine hydrochlo

A synthesis of [14C]alfuzosine hydrochloride

✍ J. Allen 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 French ⚖ 158 KB

## Labelled w i t h catbon-14 wan nynthe-4hed in h i g h ouch& yield dmm p o t a n h i m [ 14C]cyunaCe doh p h m a c o k i n d c and me,tabvLbm h t u d i a . Alfuzosine hydrochloride, ~-[3-[(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino]propyl] tetrahydro-2-furancarboxamide hydrochloride, herei

Synthesis of 14C labelled drotaverinum h

Synthesis of 14C labelled drotaverinum hydrochloride

✍ E. Koltai; D. Bánfi; J. Engler; J. Volford; Z. Mészáros 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 French ⚖ 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

Synthesis of 14C-labelled etintidine hydrochloride

✍ Stephen M. Stefanick; Charles F. Kasulanis; Seymour D. Levine; Arthur C. Fabian 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 French ⚖ 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 14C-bucromarone succinate a

Synthesis of 14C-bucromarone succinate and hydrochloride

✍ Colette Nicolas; Michel Verny; Jean-Claude Maurizis; Marc Payard; Michel Faurie 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 French ⚖ 287 KB

[2] [3] [4]N dibutylamino propoxy) 3,S-dirnethyl benzoyl] chromone, was synthesized from (U-14C) oxalic acid. The labelling takes place at the first step of the synthesis, and allowed the obtention o f -14C-Bucromarone succinate, with a specific activity o f 7.45 mCi/mmol, i.e. 275.6 MBq/mmol ; -

Synthesis of 4′-iodo-4′-[14-14C]-deoxydo

Synthesis of 4′-iodo-4′-[14-14C]-deoxydoxorubicin hydrochloride (FCE 21954)

✍ Erminia Fontana; Antonino Suarato; Michele Caruso; Gian Piero Vicario 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 French ⚖ 242 KB

The synthesis of 4' -iodo-4 l -[ 14-l4C1 -deoxydoxorubicin hydrochloride (PCE 21954) in five steps is described. 4 -Epi-N-trif luoroacetyl-[ 14-14C] -daunorubicin has been employed as starting material. substitution of C-4l-OH with iodine and subsequent hydroxylation of the side chain, via the 14-br