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The Allyl Ester as Carboxy-Protecting Group in the Stereoselective Construction of Neuraminic-Acid Glycosides

✍ Scribed by Horst Kunz; Herbert Waldmann; Uwe Klinkhammer

Publisher
John Wiley and Sons
Year
1988
Tongue
German
Weight
415 KB
Volume
71
Category
Article
ISSN
0018-019X

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✦ Synopsis

j For glycosylations of N-acetylneuraminic acid based on the use of 2-chloro and 2-hromo derivatives, see e.g. ~41.

*) The analogous methyl ester has been described in [lo].

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