## Abstract A reaction sequence employing a fungus mediated oxidation of arteether, an experimental antimalarial drug, was used to introduce a hydroxyl group on Cβ14. The hydroxyl group was replaced by a deuterium by preparing the tosylate and reductively cleaving it with sodium borodeuteride in DM
β¦ LIBER β¦
Synthesis of 11-[3H]-arteether, an experimental antimalarial drug
β Scribed by Yu-Ming Pu; Herman Ziffer
- Book ID
- 102369288
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- French
- Weight
- 262 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
The triphenylphosphine hydrobromideβcatalyzed addition of a proton from ethanol to anhydrodihydroartemisinin (5) has been employed for the synthesis of 2 and 4 Use of 1.5 equivalents of EtO^2^H or EtO^3^H yielded 11β[~3~H]βΞ²βarteether as the major product.
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