Synthesis of 14C-ochratoxin A
✍ Scribed by D. Rousseau; G. Slegers; C. Van Peteghem; A. Claeys
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- French
- Weight
- 344 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
14C-0chratoxin A s obtained by coupling t h e N-hydroxysuccinimide d e r i v a t i v e of t h e l a c t o n e a c i d h y d r o l y s a t e o f n a t u r a l o c h r a t o x i n A w t h 14C-L-8-phenylalanine methylester. 14C-Ochratoxin A inethylester i s converted i n t o 14Gochratox i n A by a l k a l i n e h y d r o l y s i s . P u r i f i c a t i o n o f t h e intermedia t e s and t h e 1 4 C -o c h r a t o x i n A i s achieved by HPLC. For an amount o f 0.05 pmole L-6-phenylalanine methylester t h e y i e l d o f ochratoxin A i s 0.02 pmole o r 40 % and t h e s p e c i f i c a c t iv i t y 130 Ci/mole. S t e r e o s p e c i f i c i t y i s 100 % and radiochemic a l p u r i t y is 96 96.
The y i e l d o f 1%-ochratoxin A increases w i t h increasing amounts o f 14C-L-pphenylalanine methylester and reaches 80% under t h e best conditions.
📜 SIMILAR VOLUMES
Ochratoxin A is a mycotoxin produced by Asperqillus and Penici1l.w moulds. The toxin is an amide formed between phenylalanine and the isocoumarin acid ochratoxin a . Ochratoxin A with high specific radioactivity can be obtained, by sub titution of the natural phenylalanine for I4C or %-labelled phe
## 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
## Abstract An efficient one‐vessel synthesis of camphene‐8–^14^C was developed. Methyl‐^14^C iodide was reacted with triphenylphosphine; treatment of the resulting phosphonium salt with methyllithium produced methylene[‐^14^C]‐triphenylphosphorane, which was condensed with camphenilone to provide
## Abstract A convenient synthesis with analytical monitoring of ^14^C‐cotinine is reported. ^14^C‐Nicotine was converted into ^14^C‐dibromocotinine hydrobromide perbromide. Debromination, achieved by using Zn dust/acetic acid, resulted in high yields (71%) of ^14^C‐cotinine.