Diastereoselective routes to side-chain truncated analogues of N-acetylneuraminic acid†

1 January 1998

journal article
research article
Published by Royal Society of Chemistry (RSC) in Chemical Communications

No. 6,p. 645-646
https://doi.org/10.1039/a708594j

Abstract

Vitamin C 3 has been converted, in a completely stereocontrolled manner, into the side-chain truncated analogues 4 and 5 of N-acetylneuraminic acid 1.

Keywords

DIASTEREOSELECTIVE ROUTES
COMPLETELY STEREOCONTROLLED
STEREOCONTROLLED MANNER
CONVERTED
VITAMIN
CHAIN TRUNCATED
SIDE CHAIN

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