Abstract
Ozonolysis is a widely used and practical synthetic technique for the deconstructive oxidation of olefins using ozone. While there are numerous ozonolysis reactions that give a myriad of products and functionalities, almost all of them involve scission at the olefin double bond. Using ozone as a constructive reagent rather than a deconstructive one would open new domains of chemical reactivity and amplify molecular complexity in synthetic methodology. Here we report the use of primary ozonides as preparative synthetic intermediates for a safe and green olefin syn-dihydroxylation reaction. Furthermore, we have demonstrated this method using a continuous flow reactor that virtually eliminates peroxide accumulation and extended these applications towards the synthesis of pharmaceutically relevant small molecules such as guaifenesin, the active ingredient in Mucinex, and a precursor to ponesimod, a drug to treat multiple sclerosis.
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Acknowledgements
A.A.T. and D.K.A. are grateful for the generous financial support from Texas A&M University and the Welch Foundation (grant no. A-2081-20210327). A.A.T. and D.K.A. thank M. Garcia for his preliminary experiments performed before the research described here.
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A.A.T. conceived the work. A.A.T. and D.K.A. designed the experiments. D.K.A. conducted the synthetic experiments including NMR experiments, synthesis of starting materials, titrations, purifications and flow experiments. A.A.T. and D.K.A. wrote the manuscript.
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Supplementary Figs. 1–80, Tables 1–17 and Experimental procedures and spectra.
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Arriaga, D.K., Thomas, A.A. Capturing primary ozonides for a syn-dihydroxylation of olefins. Nat. Chem. 15, 1262–1266 (2023). https://doi.org/10.1038/s41557-023-01247-5
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DOI: https://doi.org/10.1038/s41557-023-01247-5