Highly stereoselective glycosidation of ribose solubilized in apolar organic media via host-guest complexation

DOI: 10.1016/S0040-4039(00)97022-9

Source and publish data:

Tetrahedron Letters p. 6193 - 6196 (1990)

Update date:2022-08-11

Topics:

Authors:

Tanaka, Yasutaka

Khare, Chinmai

Yonezawa, Masaki

Aoyama, Yasuhiro

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Article abstract of DOI:10.1016/S0040-4039(00)97022-9

Ribose complexed with resorcinol-dodecanal cyclotetramer via hydrogen bonding in CCl₄ undergoes highly stereoselective glycosidation with methanol to give methyl β-ribofuranoside under mild and neutral conditions.

Full text of DOI:10.1016/S0040-4039(00)97022-9

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