## Abstract Reaction of adriamycinone with excess ^14^CH~3~Mgl and periodate cleavage of the resulting glycol (5) affords daunomycinone‐14‐^14^C (6). Bromination and hydrolysis of 6 gives adriamycinone‐14‐^14^C (8). Coupling of 6 and the 14‐0‐p‐anisyldiphenyl‐methyl derivative (9) with 1‐chloro‐3‐N
Synthesis of [14C]-fenfluramine and [14C]-S780
✍ Scribed by D. R. Hawkins; I. Midgley
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- French
- Weight
- 261 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
The syntheses of 1‐m‐trifluoromethylphenyl‐2‐N‐ethylaminopropane (I; Ponderax®) and 1‐m‐trifluoromethylphenyl‐2‐N‐β‐benzoyloxyethylaminopropane (II; S780) labelled with carbon‐14 at the benzylic position have been accomplished in seven stages starting from Ba^14^CO~3~. The overall radiochemical yield was 9% and both products were obtained with a radiochemical purity in excess of 98%.
📜 SIMILAR VOLUMES
The synthesis of lanosterol [la] and desmosterol [Ira] Iabeled with 14C in the 25 position by a Wittig reaction between triphenyl-214C isopropylidene-phosphorane [IVb] and the corresponding aldehydes are described. The specijic activities obtained are, respectively, 0.539 mClmM and 0.752 mClmM and t
14-14C-Adriamycin HC1 has been prepared from unlabeled adriamycin. The 14C-Diazald served as the source of the label. This synthesis does not require protection of the phenolic hydroxyl groups.
The s y n t h e s i s o f " C -c h l o r o e t h e n e and. 1 4 C -t r i c h l o r o e t h e n e i s d e s c r i b e d , t h e f o r m e r i n 4 s t a t e of h i g h chemicaZ p ur i t y s u i t a b l e f o r p o l y m e r i s a t i o n s t u d i e s . RESUME La s y n t h P s e d e 1 4 C -c h l o r
## Abstract [5‐^14^C]‐Dodecane and [8‐^14^C]‐Hexadecane were synthesized starting with [1‐^14^C]‐octanoic acid. The carboxylic acid was reduced to 1‐octanol, which was esterified to n‐octyl p‐toluenesulfonate. Following a Corey‐House procedure, the sulfonate was either reacted with Li[Cu(butyl)~2~]
## Abstract Org 37462 (1) is the active ingredient in Orgalutran^®^, an innovative product that reduces the time of treatment in __in vitro__ fertilization from four to less than two weeks. Org 37462 is a synthetic decapeptide containing several amino acids that are unnatural in stereochemistry and