Abstract
A novel protocol to synthetic transformation of 4H-chromenes into dihydrofurans (3) and 2H-chromenes (11) promoted by hypervalent iodine has been accomplished in a one-pot reaction at ambient temperature. Dihydrofurans are exclusively formed under basic reaction conditions, whereas, 2H-chromenes are the products under acidic condition. Simple reaction conditions with a broad substrate scope inclusive of various heterocycles and high yields are the attractive features of this protocol.
Graphical Abstract
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Acknowledgements
We gratefully acknowledge the help received from Centre for NMR & Structural Chemistry and Analytical Chemistry & Mass Spectrometry, CSIR–IICT.