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
Synthesis of deuterated dihydrochalcones
β Scribed by Daniel J. Comeskey; Janine M. Cooney; Daryl D. Rowan
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- French
- Weight
- 128 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
The dihydrochalcones phloretin and phloridzin are major phenolic constituents of apple fruit. Phloretin-d 4 , deuterated at both the a and b positions, was prepared by hydrogenolysis of naringenin and by deuterium exchange from unlabelled phloretin using Pd/C and sodium formate with methanol-d 1 as the source of deuterium. Deuterated derivatives of the glycosides, phloridzin and naringin dihydrochalcone, were similarly prepared.
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