Synthesis of hyaluronic acid-related di-, tri-, and tetra-saccharides having an N-acetylglucosamine residue at the reducing end

DOI: 10.1016/S0008-6215(00)90971-6

Source and publish data:

Carbohydrate Research p. 61 - 85 (1994)

Update date:2022-08-03

Topics: Characterization Deprotection Purification Protection of Functional Groups Glycosylation Structural Elaboration

Authors:

Slaghek Slaghek

Nakahara

Ogawa Ogawa

Kamerling

Vliegenthart

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Article abstract of DOI:10.1016/S0008-6215(00)90971-6

The synthesis is reported of 4-methoxyphenyl O-(β-D-glucopyranosyluronic acid)-(1 → 3)-2-acetamido-2-deoxy β-D-glucopyranoside (1), 4-methoxyphenyl O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1 → 4)-O-(β-D-glucopyranosyluronic acid)-(1 → 3)-2-acetamido-2-

Full text of DOI:10.1016/S0008-6215(00)90971-6

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Product name:4-methoxyphenyl O-(6-levulinoyl-2,3,4-tri-O-p-toluoyl-β-D-glucopyranosyl)-(1->3)-O-(2-deoxy-4,6-O-isopropylidene-2-phthalimido-β-D-glucopyranosyl)-(1->4)-O-(6-O-levulinoyl-2,3-di-O-p-toluoyl-β-D-glucopyranosyl)-(1->3)-4,6-di-O-acetyl-2-deoxy-2-pht...

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