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

  • Okamoto K
  • Kondo T
  • Goto T
Bulletin of the Chemical Society of Japan (1987) 60(2) 631-636
DOI: 10.1246/bcsj.60.631
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Abstract

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.

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APA

Okamoto, K., Kondo, T., & Goto, T. (1987). Functionalization of 2-Deoxy-2,3-dehydro- N -acetylneuraminic Acid Methyl Ester. Bulletin of the Chemical Society of Japan, 60(2), 631–636. https://doi.org/10.1246/bcsj.60.631

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