The benzyloxycarbonyl protective group: A good alternative to the benzyl protective group in the glycopyranoside and glycofuranoside series

DOI: 10.1016/S0040-4039(97)10021-1

Source and publish data:

Tetrahedron Letters p. 7519 - 7522 (1997)

Update date:2022-08-05

Topics:

Authors:

Morere, Alain

Mouffouk, Fouzi

Chavis, Claude

Montero, Jean-Louis

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Article abstract of DOI:10.1016/S0040-4039(97)10021-1

A procedure for the O-benzyloxycarbonylation of secondary alcohols in the glucose, galactose, mannose, ribose and deoxyribose series is described. Starting from the (4-methoxy)tritylated derivatives on the primary hydroxyl group, the fully protected compounds were obtained for the first time in high yields.

Full text of DOI:10.1016/S0040-4039(97)10021-1

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