Abstract
Cyclopentenyl carbinols are oxidatively cleaved and cyclized into a class of terpenylic acid analogues in the presence of oxone and sodium periodate in good yields.
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Acknowledgements
This research was supported by the FRIEND (Fine Particle Research Initiative in East Asia Considering National Differences) Project through the National Research Foundation of Korea (NRF) funded by the Ministry of Science and ICT (NRF-2020M3G1A1114560).
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Dao, P.D.Q., Park, JH., Lim, HJ. et al. Synthesis of terpenylic acid and its analogues by oxidative cleavage and lactonization of cyclopentenyl carbinols. Chem. Pap. 76, 1885–1889 (2022). https://doi.org/10.1007/s11696-021-01964-6
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DOI: https://doi.org/10.1007/s11696-021-01964-6