## Abstract Two analogues of the antibiotic fusidic acid with photolabile groups, 4‐azidophenyl and 4‐benzoylphenyl, were successfully labelled with tritium via Pd/C catalysed tritiation of unsaturated precursors. Specific activities of 36 and 44 Ci/mmol were obtained. Copyright © 2007 John Wiley &
Synthesis of radiolabelled clenbuterol analogues
✍ Scribed by Graham G. Pegg; Martin N. Sillence; Madonna J. Sleeman; Derek B. Lindsay
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- French
- Weight
- 327 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
Oxidation of clenbuterol 1a with pyridinium chlorochromate yielded 4‐amino‐3,5‐dichloro‐α‐tert‐butylaminoacetophenone 5. Tritiated clenbuterol 1b was produced by reduction of 5 with sodium [^3^H]borohydride. Radioiodination of the clenbuterol precursor [2‐tert‐butylamino‐1‐(4‐aminophenyl)‐ethanol] 2 yielded [2‐tert.‐butylamino‐1‐(4‐amino‐3‐[^125^I] iodophenyl)‐ethanol] 3b.
📜 SIMILAR VOLUMES
The synthesis of D,-clenbuterol (I) and D,-clenbuterol ( ) is described. D,-clenbuterol (I) was prepared from 4-amino-a-bromo-3,5-dichloroacetophenone by reaction with D,-tert-butylamine followed by reduction of the keto group with NaBH,. D,-clenbuterol (11) was prepared from 4-amino-cl-tert-butylam
## Abstract The synthesis of nonadeutero‐clenbuterol, a useful tool for the quantitation of clenbuterol by gas chromatography‐mass spectrometry, is described.
## Abstract Tritiated clenbuterol was prepared starting from 4‐aminoacetophenone (I) which was selectively brominated to 4‐amino‐3,5‐dibromoacetopheno ne (II), then to 4‐amino‐α,3,5‐tribromoacetophenone (III) and reacted with tert.butylamine to 4‐amino‐3,5‐dibromo‐α‐tert.butylaminoacetoph‐none(IV).
## METHODS. A 7-amino acid analogue of bombesin (BBN) was synthesized through solid-phase techniques. The peptide was conjugated to trisuccin prior to cleavage 1 Department of Radiation Oncology, University from the resin. The conjugate was hydrogenated to remove the hydroxamateof Alabama at Birmi