Picolinyl group as an efficient alcohol protecting group: Cleavage with Zn(OAc)2·2H2O under a neutral condition

Article abstract of DOI:10.1016/j.tetlet.2005.05.125

As an efficient alcohol protecting group, picolinates (Pic), prepared from the corresponding alcohols using commercial picolinoyl chloride, are readily cleaved by Zn(OAc)₂ or Cu(OAc)₂, even in the presence of other common alcohol protecting groups. Moreover, the picolinyl group at C-2 position in carbohydrates can be selectively cleaved to give methyl 4,6-O-benzylidene-3-O-picolinyl-α-d-glucopyranoside and 3-O-picolinyl methyl-4,6-O-benzylidene-α-d-galactopyranoside in good yields.