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ChemInform Abstract: Analogues of Sialic Acids as Potential Sialidase Inhibitors. Synthesis of 2‐C‐Hydroxymethyl Derivatives of N‐Acetyl‐6‐amino‐2,6‐dideoxy‐neuraminic Acid.

Bruno Bernet, A. R. C. Bulusu Murty, Andrea Vasella

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Abstract

Abstract A variety of title compounds such as (VI) possessing an additional C‐2 hydroxymethyl substituent on the piperidine ring of the aza analogue (VII) of N‐acetylneuraminic acid (Neu5Ac)‐(VIII) are prepared starting from known azidoalkenes such as (I) in order to investigate the influence of the C‐2 substituent on the inhibition of sialidases.

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Abstract A variety of title compounds such as (VI) possessing an additional C‐2 hydroxymethyl substituent on the piperidine ring of the aza analogue (VII) of N‐acetylneuraminic acid (Neu5Ac)‐(VIII) are prepared starting from known azidoalkenes such as (I) in order to investigate the influence of the C‐2 substituent on the inhibition of sialidases.

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Available abstract

Abstract A variety of title compounds such as (VI) possessing an additional C‐2 hydroxymethyl substituent on the piperidine ring of the aza analogue (VII) of N‐acetylneuraminic acid (Neu5Ac)‐(VIII) are prepared starting from known azidoalkenes such as (I) in order to investigate the influence of the C‐2 substituent on the inhibition of sialidases.

Key concepts: Chemistry, Substituent, Sialidase, Hydroxymethyl, Neuraminic acid, Stereochemistry, Sialic acid, N-Acetylneuraminic acid

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ChemInform Abstract: Analogues of Sialic Acids as Potential Sialidase Inhibitors. Synthesis of 2‐C‐Hydroxymethyl Derivatives of N‐Acetyl‐6‐amino‐2,6‐dideoxy‐neuraminic Acid. — Research Paper | ScholarLens