Issue 16, 2024

Deconstructive annulation mediated one-pot synthesis of xanthene derivatives

Abstract

Direct conversion of naphthoxazines to diverse xanthene derivatives was achieved under one-pot operation through deconstructive annulation methodology. Sequential oxidative C(sp3)–O/C(sp3)–N cleavage followed by intramolecular/intermolecular annulation reaction was carried out under aerobic reaction conditions. Mechanistic analyses performed on the substrate revealed that the C(sp3)–O bond cleavage supersedes the C(sp3)–N bond scission. The in situ generated Betti base intermediate through the C(sp3)–O cleavage was successfully isolated. Based on a molecular docking investigation, the intermolecular annulated products demonstrated good α-glucosidase inhibitory properties.

Graphical abstract: Deconstructive annulation mediated one-pot synthesis of xanthene derivatives

Supplementary files

Article information

Article type
Paper
Submitted
18 Jan 2024
Accepted
28 Mar 2024
First published
04 Apr 2024

Org. Biomol. Chem., 2024,22, 3279-3286

Deconstructive annulation mediated one-pot synthesis of xanthene derivatives

B. Manikandan, S. Thamotharan, O. Blacque and S. Selva Ganesan, Org. Biomol. Chem., 2024, 22, 3279 DOI: 10.1039/D4OB00093E

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