## Abstract Synthesis of ^14^C‐labelled Lawsone or 2‐hydroxy‐1,4‐naphthoquinone was achieved by auto‐oxidation of [phenyl‐^14^C(U)]α‐tetralone; the latter was prepared from [^14^C(U)] benzene in a reaction sequence more convenient than reported earlier. Copyright © 2002 John Wiley & Sons, Ltd.
Synthesis of 4-hydroxy[phenyl-U-14C]coumarin
✍ Scribed by Allan K. Nadian
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- French
- Weight
- 229 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Radiolabeled 4‐hydroxycoumarin was synthesized on a microscale by condensing [U‐^14^C]phenol and malonic acid in the presence of anhydrous zinc chloride and phosphorus oxychloride. The yield was 14% on a 0.5 mmol scale at a specific activity of 107 μCi/mmol.
📜 SIMILAR VOLUMES
## 0-Ethyl-S-phenyl-ethylphosphonodithioate ( 1 ) a broad spectrum soil insecticide (2) was unqormly labeled in the benzene ring with Carbon-14 to expand the residue and metabolism information (3' gained from previous labelings of this compound ( 4 ) .
## Abstract Disodium [__benzene__‐U‐^14^C]‐(4‐chlorophenylthio)methylenediphosphonate, [__benzene__‐^14^C]‐Tiludronate, 2, has been prepared in six steps from [__benzene__‐U‐^14^C]‐acetanilide in an overall radiochemical yield of 41%. A key step in this transformation was the efficient conversion o
## Abstract N‐Phenyl‐2‐naphthylamine has been synthesized (1) with ^14^C in positions 1, 4, 5 and 8, (2) with ^13^C in position 8 (small amounts of [1‐^13^C] naphthalene and 2‐[8‐^13^C]naphthylamine are formed as by‐products), and (3) with the N‐phenyl nucleus uniformly labelled with ^14^C.
In support of a program to develop a treatment for advanced, refractory cutaneous T-cell lymphoma, two differentially [ 14 C]-labeled forms of vorinostat, a histone deacetylase inhibitor, were synthesized for use in metabolism studies.