## Abstract The title product was labelled with ^14^C at the ketone group, from 3‐methoxybromobenzene in six steps. Complete synthetic techniques of the labelled drug are presented.
Preparation of 14C labeled β-aminoisobutyric acid (3 Amino-2 methyl-propionic acid, 314C)
✍ Scribed by J. H. Lukas; G. B. Gerber
- Publisher
- John Wiley and Sons
- Year
- 1965
- Tongue
- French
- Weight
- 81 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Preparation of 14C labeled p-aminoisobutyric acid (3 Amino-2 methyl-propionic acid, 314C) *
In the course of studies on the catabolism of thymidine the need emerged to study in greater detail its metabolite (l), p aminoisobutyric acid (BAIBA). This substance, labeled with 14C in the 3-C position, was synthesized by the following procedure, which represents a modification of the synthesis of inactive BAIBA (2) :
📜 SIMILAR VOLUMES
A synthesis of 3-cyano-4-methyl-5 ( 14 C)-methyl-2-(5-14C)pyrrolyloxamic acid is described. The compound, having specific activity of 66.7 pCi/mmole, was obtained in 19.68% overall yield from uniformly labelled 14C-l-alanine. 14 14 Key Words: 3-Cyano-4-methyl-5( C)-methyl-2-(5-C)pyrrolyloxamic acid,
## D-Shikimic acids I-I4C, 6-14C and 7-(carboxyl) 14C have been biosyntheticaily prepared with specific activities of about 25 mCi/ mmole and with overall yields of 45% based on pyruvate 3,2 or I-1% as the respective starting materials. A crude cellfree homogenate of E. coli 83-24 was used to cat
## Abstract A relatively simple route to 2‐substituted adamantane derivatives labelled with ^14^C at the 2‐position in the adamantane skeleton was developed. The approach used (Figure I) involved ring expansion of adamantanone by labelled diazomethane, conversion of the resulting 4‐homoadamantanone