𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of [phenyl-U-14C] tefluthrin

✍ Scribed by Raymond A Burrell

Book ID
103920327
Publisher
Elsevier Science
Year
1988
Weight
57 KB
Volume
39
Category
Article
ISSN
0883-2889

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of 4-hydroxy[phenyl-U-14C]coum
Synthesis of 4-hydroxy[phenyl-U-14C]coumarin
✍ Allan K. Nadian 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 French ⚖ 229 KB

## 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.

An improved synthesis of [phenyl-14C(U)]
An improved synthesis of [phenyl-14C(U)] Lawsone
✍ Christopher Wright; Giliyar V. Ullas 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 French ⚖ 71 KB

## 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 O-ethyl-S-phenyl-14C(U)-eth
Synthesis of O-ethyl-S-phenyl-14C(U)-ethylphosphonodithioate
✍ Jules Kalbfeld; Harold M. Pitt; Donald A. Hermann 📂 Article 📅 1969 🏛 John Wiley and Sons 🌐 French ⚖ 193 KB

## 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 ) .

Synthesis of [phenyl-U-14C]aryl and [8-1
Synthesis of [phenyl-U-14C]aryl and [8-14C]carboxy labeled tracers of vorinostat
✍ Eric D. Soli; Matthew P. Braun 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 French ⚖ 105 KB

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.

Synthese von [3-14C]- und [Phenyl-U-14C]
Synthese von [3-14C]- und [Phenyl-U-14C] Olaquindox
✍ W. Maul; D. Scherling; F. Seng 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 French ⚖ 360 KB

## Abstract Olaquindox is a new feed additive.[^14^C]Olaquindox, labelled in different positions, was needed for tracer‐studies of pharmacokinetics, biotransformation and residues in several species of animals. 2‐ [N‐(2‐hydroxethyl)‐carbamoyl] −3‐methyl‐[3‐^14^C] quinoxaline‐1,4‐dioxide ([3‐^14^C]