Issue 8, 1994

An imrpoved practical method for synthesis of aryl C-glycosides from unprotected methyl glycosides and 1-hydroxy sugars

Abstract

Aryl C-glycosidations of the unprotected methyl glycosides 9–12 and the unprotected 1-hydroxy sugars 14 and 15 with 2-naphthol 6 using TMSOTf proceed much more effectively than those of the acylated methyl glycosides 4 and 5; the unprotected methyl glycoside 10 is also smoothly coupled with other phenol and naphthol derivatives 25–27 to give the corresponding unprotected o-hydroxyaryl β-C-glycosides in high yields (TMSOTf = trimethylsilyloxytrifluoromethanesulfonate).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 997-998

An imrpoved practical method for synthesis of aryl C-glycosides from unprotected methyl glycosides and 1-hydroxy sugars

K. Toshima, G. Matsuo and M. Nakata, J. Chem. Soc., Chem. Commun., 1994, 997 DOI: 10.1039/C39940000997

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