Highly stereoselective glycosylation of N-acetylneuraminic acid aided by a phenylthio substituent as a stereocontrolling auxilliary
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Glycosidsynthese von N-acetylneuraminsäure mit sekundären Hydroxylgruppen
2. Synthesis of α-Neu5Acp-(2→3)-d-Gal and α-Neu5Acp-(2→3)-β-d-Galp-(1→4)-d-Glc
3. A stereospecific β-glycosylation of 2β,3α-dibromo-n-acetylneuraminic acid
4. An effective synthesis of α-glycosides of N-acetylneuraminic acid derivatives by use of 2-deoxy-2β-halo-3β-hydroxy-4,7,8,9-tetra-O-acetyl- N-acetylneuraminic acid methyl ester
5. An efficient approach to streoselective glycosylation of N-acetylneuraminic acid: Used of phenylselenyl group as a stereocontrolling auxillary
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