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Bioinspired Divergent Synthesis of Aspersteroids A and B

Ke Cen, Jiajing Bao, Xudong Wang, Hailong Tian, Yun Wang, Jinghan Gui

2024Journal of the American Chemical Society10 citationsDOIOpen Access PDF

Abstract

Aspersteroids A and B are novel ergostane-type 18,22-cyclosterols with immunosuppressive and antimicrobial activities. Herein, we report the first synthesis of these two natural products, which was accomplished in 15 and 14 steps, respectively, from commercially available ergosterol by means of a bioinspired divergent approach. Key features of this synthesis include an unprecedented radical relay cyclization that was initiated by iron(II)-mediated decomposition of an alkyl hydroperoxide to construct the E ring cyclopentane motif; a titanium(III)-mediated diastereoselective radical reduction of an epoxide to install the challenging C22 stereocenter; and highly regioselective, divergent late-stage oxidations to access the highly oxidized core framework.

Topics & Concepts

ChemistryStereocenterCyclopentaneRegioselectivityDivergent synthesisStereochemistryCombinatorial chemistryErgosterolEpoxideOrganic chemistryEnantioselective synthesisCatalysisBiochemistryMarine Sponges and Natural ProductsMicrobial Natural Products and BiosynthesisOxidative Organic Chemistry Reactions
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