Total synthesis of Palmarumycin BGs, C1 and Guignardin E?

RSC Advances Pub Date: 2020-01-08 DOI: 10.1039/C9RA10316C

Abstract

The first total synthesis of Palmarumycin BG1–3, BG5–6, C1 and Guignardin E (1–7) were achieved by the same intermediate Palmarumycin C2 through a N-benzyl cinchoninium chloride-catalyzed epoxidation, an organoselenium-mediated reduction, and a cerium(III) chloride hydrate-promoted regioselective ring-opening and elimination of cyclic α,β-epoxy ketone as the key steps via 6–7 step routes using 1,8-dihydroxynaphthalene (DHN) and 5-methoxytetralone as the starting materials in overall yields of 1.0–17.4%, respectively. Their structures and absolute configurations were characterized and determined by 1H, 13C NMR, IR, HR-ESI-MS and X-ray diffraction data. These compounds displayed significant inhibition activities against HCT116, U87-MG, HepG2, BGC823 and PC9 cell lines.

Graphical abstract: Total synthesis of Palmarumycin BGs, C1 and Guignardin E
Recommended Literature