𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Rapid synthesis of 14C forskolin by a route suitable for 11C labeling

✍ Scribed by T. Sasaki; I Ogihara-Umeda; H. Nishigori; S. Ikegami; M. Senda; K. Kitani; K. Ogawa; T. Nozaki


Publisher
John Wiley and Sons
Year
1991
Tongue
French
Weight
400 KB
Volume
29
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Radiolabeled forskolin was synthesized by acetylation of deacetylforskolin with ^14^C‐labeled acetic acid in the presence of dicyclohexylcarbodiimide. Separation of labeled forskolin of greater than 97% radiochemical purity was achieved by HPLC with a reversed‐phase column. The synthesis and purification of labeled forskolin were achieved in less than 30 min and the radiochemical yield of labeled forskolin after HPLC purification was about 30%, These methods are therefore applicable for production of ^11^C‐forskolin which may be useful for PET second messenger imaging.


📜 SIMILAR VOLUMES


Synthesis of [2-14C]thymidine: A potenti
✍ T. Vander Borght; Dr. S. Pauwels; L. Lambotte; C. De Saeger; C. Beckers 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 French ⚖ 201 KB

## Abstract We report a three‐step synthesis of thymidine, starting from trace amounts of urea, that allows rapid introduction of radioactivity in C2‐position of the pyrimidine ring. Thymine was produced within 5 min with a 60% yield by cyclocondensation of urea and diethyl β‐methylmalate in fuming

Synthesis of a 11C-labelled taxane deriv
✍ P. Mäding; J. Zessin; U. Pleiß; F. Füchtner; F. Wüst 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 French ⚖ 173 KB

## Abstract The ^11^C‐labelling of the taxane derivative BAY 59‐8862 (**1**), a potent anticancer drug, was carried out as a module‐assisted automated multi‐step synthesis procedure. The radiotracer **[^11^C]1** was synthesized by reacting [1‐^11^C]acetyl chloride (**6**) with the lithium salt of t

A method for synthesis of 14C-labelled s
✍ Andrzej Majcherczyk; Annette Braun-Lüllemann; Aloys Hüttermann 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 French ⚖ 388 KB

## Abstract Side‐chain and ring ^14^C‐labelled styrene were synthesised from labelled benzene and acetaldehyde via bromobenzene, Grignard‐reagent and 1‐phenylethanol. Uniformly ^14^C‐labelled styrene can be also prepared using this method. By‐products were identified and the purity of products was

Synthesis of 14C-labelled antitumor agen
✍ Ying-Tsung Lin; Robert J. Dummel; Morris A. Leaffer; Masato Tanabe 📂 Article 📅 1976 🏛 John Wiley and Sons 🌐 French ⚖ 156 KB 👁 1 views

## Abstract p‐Toluic acid‐ring‐^14^C was synthesized by the Friedel‐Crafts p‐carbamylation of toluene‐ring‐^14^C with N,N‐disubstituted carbamyl chloride and subsequent hydrolysis. The radiochemical yield was 61%. An attempt was made to apply this method for the synthesis of benzoic acid‐ring‐^14^C