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.

Vincamine by synthesis and semi-synthesis / E. Bonandi, F. Foschi, C. Marucci, G. Paladino, M. Luzzani, D. Passarella. - In: PHYTOCHEMISTRY REVIEWS. - ISSN 1568-7767. - (2020). [Epub ahead of print] [10.1007/s11101-020-09702-8]

Vincamine by synthesis and semi-synthesis

E. Bonandi
Primo
;
C. Marucci;G. Paladino;D. Passarella
Ultimo
2020

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.
Indole alkaloids; Semi-synthesis; Tabersonine; Vincamine;
Settore CHIM/06 - Chimica Organica
2020
5-lug-2020
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/754221
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