## Abstract {0‐methyl ^14^C} and {0‐methyl ^3^H} bergaptene were prepared by methylation of bergaptol with {^14^C} methyl iodide and {^3^H} methyl iodide in radioactive yields respectively 77 % and 59 %. {^14^C} methyl iodide and 11‐hydroxy ibogamine gave {0‐methyl C} tabernanthine with a 60 % radi
Synthese de [14 C] - sulfometuron methyle et de [14 C] - metsulfuron methyle
✍ Scribed by Jean Bastide; Robert Badon
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- French
- Weight
- 188 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
12-f 4 ~/ r v i ~~y f ~s u f f o m e t u r o n methyl
a n d / ~-f 4 ~) -triuhyy//metsuHuron methy4 two suflonyfurea herbicides has been prepared by muffisrep synthesis /2-f dCI 2-amino-$6 fimerhyf pyrimi&ne was obtahed by two steps from / f 4~~guanidne and 12-f 4~1.2-amino-4 methoxy-4 methyl f,.x-T triaahe was obtained from //"c/ cyanamide The two herbicides were prepared by mndensation ol'heterocycfe with meth,vl-2 huffonykwyanate) benzoate.
📜 SIMILAR VOLUMES
## Abstract 1‐O‐ and 5‐O‐Methyl‐^14^C‐myo‐inositols (methyf‐^14^C‐bornesitol and ‐sequoyitol) were synthesized by methylation of appropriately blocked myo‐inositol derivatives with methyl = ^14^C iodide and potassium hydroxide. The benzyl blocking groups of 1‐O‐methyl‐^14^C‐3,4,5, 6‐tetra‐O‐benzyl‐
The synthesis of ^14^C Norfenfluramine is described. The starting materials ^14^C‐Trifluoromethylbenzoic acid and ^14^C bistrifluoromethyl‐3‐benzophenone were prepared by carbonation of appropriate Grignard reagents. The labelled benzophenone was oxidized in high yield to give ^14^C‐trifluoromethylb
## Abstract A simple one‐step syntheses of 2‐([^14^C]‐methyl) furan and 4‐oxo‐[5‐^14^C]‐2‐pentenal have been described. Carbon‐14 labeled 2‐methylfuran was synthesized by treatment of 2‐furyl lithium with ^14^C‐methyl iodide, and ^14^C‐acetylacrolein was obtained by peracid oxidation of labeled 2‐m