| Literature DB >> 25244630 |
Quentin Michaudel1, Guillaume Journot, Alicia Regueiro-Ren, Animesh Goswami, Zhiwei Guo, Thomas P Tully, Lufeng Zou, Raghunath O Ramabhadran, Kendall N Houk, Phil S Baran.
Abstract
Physicochemical properties constitute a key factor for the success of a drug candidate. Whereas many strategies to improve the physicochemical properties of small heterocycle-type leads exist, complex hydrocarbon skeletons are more challenging to derivatize because of the absence of functional groups. A variety of C-H oxidation methods have been explored on the betulin skeleton to improve the solubility of this very bioactive, yet poorly water-soluble, natural product. Capitalizing on the innate reactivity of the molecule, as well as the few molecular handles present on the core, allowed oxidations at different positions across the pentacyclic structure. Enzymatic oxidations afforded several orthogonal oxidations to chemical methods. Solubility measurements showed an enhancement for many of the synthesized compounds.Entities:
Keywords: CH activation; medicinal chemistry; oxidation; radical reactions; terpenoids
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Year: 2014 PMID: 25244630 PMCID: PMC4226272 DOI: 10.1002/anie.201407016
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336