A STEREOSPECIFIC β-GLYCOSYLATION OF 2β,3α-DIBROMO-N-ACETYLNEURAMINIC ACID

DOI: 10.1016/S0040-4020(01)87796-6

Source and publish data:

Tetrahedron p. 5909 - 5918 (1987)

Update date:2022-09-26

Topics: Stereospecific Experimental terms N-Acetylneuraminic Acid

Authors:

Okamoto, Kaoru

Kondo, Tadao

Goto, Toshio

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Article abstract of DOI:10.1016/S0040-4020(01)87796-6

Condensation of a new glycosyl donor, methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-2,3-dibromo-2,3,5-trideoxy-β-D-erythro-L-manno-2-nonulopyranosonate with various acceptors such as methyl 2,3,4-tri-O-benzyl-α-D-glucopyranoside, cholesterol, methyl 2,4,6-tri

Full text of DOI:10.1016/S0040-4020(01)87796-6

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Product name:5-acetamido-2-(5-chloesten-3β-yl)-3,5-dideoxy-D-glycero-β-D-galacto-nonulopyranosonic acid

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