Skip to main content
Journal ArticleOPEN ACCESS

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
N/ACitations
Citations of this article
13Readers
Mendeley users who have this article in their library.
Get full text

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.

Cite

CITATION STYLE

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free