Asymmetric synthesis of N-acetylneuraminic acid

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A highly diastereoselective synthesis of N-acetylneuraminic acid 1 has been completed by stereoselective functionalization of cis-olefin 6 and trans-olefin 10 via intramolecular phenylselenoamidation and osmylation, respectively.
Publisher
ROYAL SOC CHEMISTRY
Issue Date
2000
Language
English
Article Type
Article
Keywords

CMP-SIALATE SYNTHASE; STRUCTURAL VARIATIONS; SIALIC ACIDS; AQUEOUS-MEDIA; BEHAVIOR; ENANTIOMERS; DERIVATIVES

Citation

CHEMICAL COMMUNICATIONS, v.2, no.3, pp.227 - 228

ISSN
1359-7345
URI
http://hdl.handle.net/10203/75357
Appears in Collection
CH-Journal Papers(저널논문)
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