Abstract
This review summarizes the main strategies aimed at the total synthesis of vincamine and congeners. Then, our contribution in this field is presented: we describe (+)-vincamine semi-synthesis using tabersonine as starting material. Characterization and quantification of the main impurities are discussed, and HPLC conditions, structural elucidation and NMR data of four of them are reported.
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Bonandi, E., Foschi, F., Marucci, C. et al. Vincamine by synthesis and semi-synthesis. Phytochem Rev 20, 343–365 (2021). https://doi.org/10.1007/s11101-020-09702-8
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DOI: https://doi.org/10.1007/s11101-020-09702-8