Synthesis of fully and partially benzylated glycosyl azides via thioalkyl glycosides as precursors for the preparation of N-glycopeptides

DOI: 10.1016/S0040-4039(98)01540-8

Source and publish data:

Tetrahedron Letters p. 7189 - 7192 (1998)

Update date:2022-08-05

Topics:

Authors:

Kerekgyarto, Janos

Agoston, Karoly

Batta, Gyula

Kamerling, Johannis P.

Vliegenthart, Johannes F. G.

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Article abstract of DOI:10.1016/S0040-4039(98)01540-8

Fully O-benzylated mono-, di- and trisaccharide glycosyl azides representing the reducing terminal of the core structure of N-glycans were synthesized. Totally and partially benzylated thioalkyl glucosamine glycosides were converted into the corresponding

Full text of DOI:10.1016/S0040-4039(98)01540-8

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Product name:Acetic acid (2S,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-[(2R,3S,4R,5R,6S)-4-benzyloxy-2-benzyloxymethyl-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-6-ethylsulfanyl-tetrahydro-pyran-3-yloxy]-6-benzyloxymethyl-tetrahydro-pyran-3-yl ester

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