𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Marquage par 14C et 3H du 4,4-dimethyl-1-(methylendioxy-3,4 phenyl)-1-pentene-3- ol ou stiripentol

✍ Scribed by J. C. Madelmont; J. M. Dupuy; M. Rapp; P. Labarre; J. C. Maurizis; F. Lepage; A. Veyre


Publisher
John Wiley and Sons
Year
1992
Tongue
French
Weight
264 KB
Volume
31
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

4,4‐dimethyl‐1‐(3‐4‐methylenedioxyphenyl)‐1‐pentene‐3‐ol or stiripentol was labelled by ^14^C and ^3^H.

^14^C labelling was performed on the carbone 1 of the pentene group via a four steps procedure after the carbonatation. The radiochemical yield calculated from the precursor (Ba^14^CO~3~) is 28%.

^3^H labelling was performed on the position 3 of the pentene chain by reduction of the corresponding cetone via NaBT~4~. The radiochemical yield calculated from the precursor (NaBT~4~) is 40%.


📜 SIMILAR VOLUMES


Synthese radioactive de sels d'ammonium
✍ C. Nicolas; J. C. Madelmont; J. C. Maurizis; H. Garrigue; J. M. Meyniel; P. Deme 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 French ⚖ 357 KB 👁 1 views

The ^14^C labelling of three compounds : HI‐6, TMB‐4 and pyrimidoxime is described from ^14^C‐formic acid, sodium salt. The compounds were prepared by lithiation and formylation with N‐methyl (^14^C)‐formanilide followed by introduction of the hydroxylamine moieties and alkylation of the pyridine. R

14C-labeling of a novel fungicide. I. Sy
✍ Iwao Nakatsuka; Hiroshi Kanamaru; Takeshi Kamada; Kazuo Kawahara; Akira Yoshitak 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 French ⚖ 384 KB

A novel fungicide, (-) (E)-1-( 2,4-di chlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-1-penten-3-ol (S-3308 L) and i t s three o p t i c a l l y active stereoisaners were labeled w i t h carbon-14 a t the t r i a z o l e r i n g f o r use i n the metabolic and environmental f a t e studies. 1 ,2,

Synthese de l'hydroxy-9 ellipticine (14C
✍ Nguyen Van-Bac; Michel Herbert; Louis Pichat; Maurice-Marie Janot; Nguyen Dat-Xu 📂 Article 📅 1975 🏛 John Wiley and Sons 🌐 French ⚖ 286 KB

## Abstract 9‐Hydroxy‐ellipticine (^14^C‐1), specific activity: 2,13 mCi/mM, has been synthesized for molecular biology and cancer research, from N‐methyl‐formanilide (^14^C‐formyl). The radioactive overall yield was 13,5% based on sodium formate ^14^C.

Synthese radioactive de sels d'ammonium
✍ J. C. Madelmont; C. Nicolas; J. C. Maurizis; J. M. Dupuy; H. Garrigue; J. M. Mey 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 French ⚖ 306 KB 👁 1 views

The two compounds were labelled by ^14^C on the hydroxyimino methyl group substituted on the 2 positions of the pyridinium ring. The convenient pyridinium lithiated intermediates were formylated with N‐methyl ^14^C‐formanilide. The hydroxyimino methyl groups were synthezised by reaction of the ^14^