𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A novel method for the preparation of adenosine 3′5′ cyclic phosphate labelled with 14C or 3H

✍ Scribed by V. N. Pandey; C. K. K. Nair; D. S. Pradhan

Publisher
John Wiley and Sons
Year
1983
Tongue
French
Weight
240 KB
Volume
20
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Convenient methods for the preparation o
Convenient methods for the preparation of [5-14C]-4-ipomeanol and [3H(G)]-4-ipomeanol of high specific radioactivity
✍ Michael R. Boyd; John S. Dutcher 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 French ⚖ 226 KB 👁 1 views

## Abstract Procedures are described for the preparation of radiolabeled 4‐ipomeanol [1‐(3‐furyl)‐4‐hydroxypentanone], a highly selective pulmonary alkylating agent, of sufficiently high specific radioactivity for biochemical and autoradiographic studies. The ^14^C‐labeled material is prepared from

A method for the preparation of 14C-labe
A method for the preparation of 14C-labeled carboxylic acids. Synthesis of 6,11-dihydro[b,e]thiepin-11-one-3-yl acetic 14C-acid
✍ Howard Parnes 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 French ⚖ 198 KB

## Abstract An example of a potentially general method for the preparation of ^14^C‐carboxylic acids based on the carbonation of an α‐lithiated carboxylate is described. This procedure requires only the unlabeled analog of the desired ^14^C‐acid as the precursor. The possibility of carrying out the

A novel method for the preparation of hi
A novel method for the preparation of highly tritiated methyl iodide, and its use for the syntheses of methyl-3H-labelled diazepam and the methiodides of (+)- and (−)-bicuculline
✍ R. Schwob; J. Wuersch 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 French ⚖ 227 KB

## Abstract The syntheses of methyl‐^3^H‐labelled diazepam (4) and the methiodides of (+)‐ and (−)‐bicuculline (5) labelled with tritium in their methyl groups are described. Also reported here is a novel method for the preparation of triti‐ated methyl iodide (3) serving as the radioactive precurso

Synthesis of isotopically labelled [3-14
Synthesis of isotopically labelled [3-14C]- and [3,3-2H2]-5-fluoro-1,3-dihydro-1-hydroxy-2,1-benzoxaborole (AN2690), a new antifungal agent for the potential treatment of onychomycosis
✍ Stephen J. Baker; Yong-Kang Zhang; Tsutomu Akama; Conrad Wheeler; Jacob J. Platt 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 French ⚖ 113 KB

## Abstract 5‐Fluoro‐1,3‐dihydro‐1‐hydroxy‐2,1‐benzoxaborole (AN2690) is a new antifungal agent for the potential treatment of onychomycosis. During the preclinical development phase, it was necessary to synthesize the radioisotope [3‐^14^C]‐5‐fluoro‐1,3‐dihydro‐1‐hydroxy‐2,1‐benzoxaborole and the

A novel method for the synthesis of carb
A novel method for the synthesis of carbon-14-labeled N-[3-(1-methyl-4-piperidinyl)-1H-pyrrolo[3,2-b]pyridin-5-yl]propanamide and its use in quantitative whole-body autoradiography studies
✍ William J. Wheeler; Sylvia H. Chay; Jennifer L. Herman; Douglas D. O'Bannon 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 French ⚖ 183 KB 👁 1 views

## Abstract Sumitriptan (1), a non‐selective 5‐HT~1B/1D~ agonist is an effective therapeutic agent for the acute treatment of migraine, but it is contraindicated for use in patients with known heart disease. The first Selective Serotonin One F Receptor Agonist (SSOFRA), 5‐(4′‐fluorobenz‐amido)‐3‐(_