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- W4382987918 abstract "An efficient, concise, and green visible-light-mediated [3+2] cycloaddition reaction for the diastereoselective synthesis of naphtho[2,3-b]furan-4,9-diones starting from readily available 2-hydroxy-1,4-naphthoquinones and alkynes in the absence of any bases, metals, ligands, or other catalysts is described. The products could be obtained under blue LED (460 nm) irradiation at ambient temperature in 6 h with perfect regioselectivity and remarkable functional group tolerance. This approach provides an original, powerful, green, efficient, and facile way to expand the structural diversity of compounds with the structure motifs of naphtho[2,3-b]furan-4,9-diones and dihydronaphtho[2,3-b]furan-4,9-diones as promising scaffolds for novel drug discovery." @default.
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- W4382987918 date "2023-11-01" @default.
- W4382987918 modified "2023-09-23" @default.
- W4382987918 title "Visible-light-mediated synthesis, NMR analysis and X-ray crystal structure of naphtho[2,3-b]furan-4,9-diones" @default.
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- W4382987918 doi "https://doi.org/10.1016/j.molstruc.2023.136140" @default.
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