The electrochemical reduction of the amide group of echinosporine on mercury leads to the corresponding alcohol or aldehyde according to the operative conditions, with no hydrolysis of the lactone function. © 1987.
CITATION STYLE
Deprez, D., Margraff, R., Bizot, J., & Pulicani, J. P. (1987). Reduction electrochimique de la fonction amide d’un compose antitumoral, l’echinosporine. Tetrahedron Letters, 28(40), 4679–4680. https://doi.org/10.1016/S0040-4039(00)96595-X
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