## 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,
Syntheses du Bergaptene [0 — methyl 14C et 3H] et de la Tabernanthine [0-methyl 14C]
✍ Scribed by N. V. Bac; M. Audinot; L. Pichat; M. Herbert; N. Dat Xuong
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- French
- Weight
- 199 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
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 % radioactive yield.
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