Synthesis of deramciclane labeled with tritium in various positions
[(1R)‐endo]‐(+)‐3‐bromocamphor was dehalogenated with tritium gas to [3‐3H]camphor and via [3‐3H]phenylborneol converted to [3‐3H]deramciclane isolated as the fumarate salt (specific activity 51.8 GBq/mmol). This three step synthesis from [3‐3H]camphor gave an overall yield of 22%. Benzyloxy‐acetic...
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Veröffentlicht in: | Journal of labelled compounds & radiopharmaceuticals 2005-08, Vol.48 (9), p.693-700 |
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Sprache: | eng |
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