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Synthesis of the antiinflammatory prodrug RS‐42169‐ 14 C

Synthesis of the antiinflammatory prodrug RS‐42169‐ 14 C A facile synthesis of the antiinflammatory agent RS‐42169‐14C, based on a carbonation/cycloaddition sequence is described. The product was obtained in 36% yield from Ba14CO3 at a specific activity of 52 mCi/mmole. The design of the six step sequence was such that pure intermediates were isolated by extractive workup, and only a single chromatographic purification was required. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Journal of Labelled Compounds and Radiopharmaceuticals Wiley

Synthesis of the antiinflammatory prodrug RS‐42169‐ 14 C

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References (8)

Publisher
Wiley
Copyright
Copyright © 1995 John Wiley & Sons, Ltd.
ISSN
0362-4803
eISSN
1099-1344
DOI
10.1002/jlcr.2580360106
Publisher site
See Article on Publisher Site

Abstract

A facile synthesis of the antiinflammatory agent RS‐42169‐14C, based on a carbonation/cycloaddition sequence is described. The product was obtained in 36% yield from Ba14CO3 at a specific activity of 52 mCi/mmole. The design of the six step sequence was such that pure intermediates were isolated by extractive workup, and only a single chromatographic purification was required.

Journal

Journal of Labelled Compounds and RadiopharmaceuticalsWiley

Published: Jan 1, 1995

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