Regioselective deprotection of p-methoxybenzyl ethers of furanose derivatives

DOI: 10.1016/S0040-4039(99)00396-2

Source and publish data:

Tetrahedron Letters p. 2883 - 2886 (1999)

Update date:2022-09-26

Topics:

Authors:

Bouzide, Abderrahim

Sauve, Gilles

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Article abstract of DOI:10.1016/S0040-4039(99)00396-2

Reaction of per-p-methoxybenzylated hexofuranoses and pentofuranoses with either a catalytic amount of tin chloride dihydrate (SnCl₂·2H₂O) or 0.5-10% solution of trifluoroaoetic acid in dichloromethane afforded regioselectively the corresponding monosaccharide derivatives having a single free hydroxyl group at C(5) in good yields.

Full text of DOI:10.1016/S0040-4039(99)00396-2

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