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Synthesis of the epimeric 2‐bromocholesterols and their conversion into (2α‐ 3 H)cholesterol and [2ß‐ 3 H]cholesterol
Author(s) -
Römer J.,
Wagner H.,
Ponsold K.
Publication year - 1984
Publication title -
journal of labelled compounds and radiopharmaceuticals
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.432
H-Index - 47
eISSN - 1099-1344
pISSN - 0362-4803
DOI - 10.1002/jlcr.2580210810
Subject(s) - chemistry , labelling , cholesterol , catalysis , specific activity , stereochemistry , radiochemistry , medicinal chemistry , organic chemistry , enzyme , biochemistry
The synthesis of the epimeric 2‐bromocholesterols is described. Their reductive catalyzed debromination with T 2 affords [2α‐ 3 H]‐ and [2ß‐ 3 H]cholesterol respectively. The [2‐ 3 H] cholesterols can be synthesised with a radiochemical purity >98% and specific activities of about 600–700 GBq/mmol. The labelling reactions proceed under retention.

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