Abstract
A simple and highly efficient one-pot protocol for the synthesis of novel polysubstituted 1,2-dihydronaphtho[2,1-b] furans has been developed by three-component coupling reaction of 2-aminopyridines, naphthols, and glyoxal in the presence of guanidinium chloride as a polyfunctional organocatalyst under solvent-free conditions. The protocol avoids the use of expensive catalysts, toxic solvents, and chromatographic separation and provides a wide range of novel dihydronaphthofurans in good to excellent yields.
GRAPHICAL ABSTRACT
SUPPORTING INFORMATION
Full experimental detail, IR, CHN analysis, and 1H and 13C NMR spectra for this article can be accessed on the publisher’s website.