Functionalization of 2-Deoxy-2,3-dehydro-N-acetylneuraminic Acid Methyl Ester

DOI: 10.1246/bcsj.60.631

Source and publish data:

Bulletin of the Chemical Society of Japan p. 631 - 636 (1987)

Update date:2022-08-11

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Authors:

Okamoto, Kaoru

Kondo, Tadao

Goto, Toshio

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Article abstract of DOI:10.1246/bcsj.60.631

The acetyl protected 2-deoxy-2,3-dehydroneuraminic acid methyl ester was functionalized by modifying its 2,3-double bond to convert it into new glycosyl donors such as 2,3-dibromo-, 2,3-epoxy-, and 2-halo-3-hydroxyneuraminic acid derivatives.

Full text of DOI:10.1246/bcsj.60.631

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