Conversion of 2-acetamido-2-deoxy-β-D-glucopyranose (N-acetylglucosamine) into 2-acetamido-2-deoxy-β-D-galactopyranose (N-acetylgalactosamine) using a biotransformation to generate a selectively deprotected substrate for SN2 inversion-Reference-Cited by-同舟云学术

Conversion of 2-acetamido-2-deoxy-β-D-glucopyranose (N-acetylglucosamine) into 2-acetamido-2-deoxy-β-D-galactopyranose (N-acetylgalactosamine) using a biotransformation to generate a selectively deprotected substrate for SN2 inversion

Published:1992 Issue:2 Volume: Page:235-237
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Chaplin David,Crout David H. G.,Bornemann Stephen,Hutchinson David W.,Khan Riaz

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1992/P1/P19920000235

Reference9 articles.

1. “Standardized intermediates” for oligosaccharide synthesis: convenient preparation of 2-amino-2-deoxy-d-glucose derivatives and their conversion into the d-galactose analogues

2. 958. The preparation and properties of acetochloroglucosamine and its use in the synthesis of 2-acetamido-2-deoxy-β-D-glucosides (N-acetyl-β-D-glucosaminides)

3. An Acyl Migration in Acetohalogenoglucosamines1

4. Preparative routes to methyl 2-acetamido-2,6-dideoxy-α-d-glucopyranoside

5. The Anomeric 1,3,4,6-Tetra-O-acetyl-2-deoxy-2-(2,4-dinitroanilino)-D-glucopyranoses

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