Synthese De La Beta-naphtoflavone 14C-4 OU 14C-5 A Partir De L'Acide Phenylpropiolique (CARBOXYLE14C) Ou Du β-Naphtol 14C-8
✍ Scribed by Nguyen-Hoang Nam; Do-Cao Thang; P. Queval; L. Pichat
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- French
- Weight
- 235 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Carbonation with ^14^CO~2~ of penylethynyl‐lithium has given rise to (carboxyl‐^14^C) phenylpropiolic acid with 75 % yield based on ^14^CO^2^. The latter condensed with 2‐naphthol by treating with polyphosphoric acid afforded (4‐^14^C) β‐naphthoflavone, purified by silicagel low pressure liquid chromatography; 22 % overall yield based on ^14^CO~2~, SA = 13 mCi/mM. Similar run of 2‐(8‐^14^C) naphthol with phenylpropiolic acid gave (5‐ ^14^C) β‐naphthoflavone; 28 % yield based on radioactive 2‐naphthol, SA = 7.2 mCi/mM.
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S y n t h e s i s o f a c e t o x y 4 -t r i f l y t r o m e t h y l b e n z o i c a c i d [ r i n g U-i ' C] o r " [ r i n g U -C] T r i f u s a l " ( R i n g U-14C) A n i l i n e 1 was c o n v e r t e i n t o ( r i n g U -1 4 C ) i d o b e n z e n e 2 t h r o u g h t h e ( r i n g U -f 4 C ) p h e
The ^14^C labelling of three compounds : HI‐6, TMB‐4 and pyrimidoxime is described from ^14^C‐formic acid, sodium salt. The compounds were prepared by lithiation and formylation with N‐methyl (^14^C)‐formanilide followed by introduction of the hydroxylamine moieties and alkylation of the pyridine. R
## Abstract 9‐Hydroxy‐ellipticine (^14^C‐1), specific activity: 2,13 mCi/mM, has been synthesized for molecular biology and cancer research, from N‐methyl‐formanilide (^14^C‐formyl). The radioactive overall yield was 13,5% based on sodium formate ^14^C.
The two compounds were labelled by ^14^C on the hydroxyimino methyl group substituted on the 2 positions of the pyridinium ring. The convenient pyridinium lithiated intermediates were formylated with N‐methyl ^14^C‐formanilide. The hydroxyimino methyl groups were synthezised by reaction of the ^14^