Issue 7, 1983

Regioselective synthesis of 4,10-dihydro-3-hydroxy-3-methyl-1H,3H-pyrano[4,3-b][1]benzopyran-10-one, the basic skeleton in fulvic acid

Abstract

The first synthesis of 4,10-dihydro-3-hydroxy-3-methyl-1H,3H-pyrano[4,3-b][1]benzopyran-10-one, the basic skeleton in fulvic acid, was achieved by sequential cyclization, which involved hydrogenation of the boron complex of the dione (5) obtained by regioselective cyclization of the acetal (4) with HCl in tetrahydrofuran.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 335-336

Regioselective synthesis of 4,10-dihydro-3-hydroxy-3-methyl-1H,3H-pyrano[4,3-b][1]benzopyran-10-one, the basic skeleton in fulvic acid

M. Yamauchi, S. Katayama, Y. Nakashita and T. Watanabe, J. Chem. Soc., Chem. Commun., 1983, 335 DOI: 10.1039/C39830000335

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