Document Type
Conference Proceeding
Keywords
carbohydrates, glycosylation, ICS-28, oligosaccharides, synthesis
Abstract
This article describes the development of alkylated S-benzimidazolyl (SBiz) imidates as versatile building blocks for chemical glycosylation. The SBiz imidates have been originally developed as a new platform for active-latent glycosylations and its utility was further extended to other common strategies for oligosaccharide synthesis. This article expands upon the utility of these compounds. We developed a general protocol for the synthesis of a series of N-alkylated SBiz glycosides from N-protected SBiz aglycones by Lewis acid-mediated coupling with glucose pentaacetate. The N-alkylated SBiz moiety was found to be stable under strong basic conditions which allowed us to obtain both armed and disarmed N-alkylated SBiz donors. These donors showed good reactivity at a variety of activation conditions, and generally provided high yields in glycosylations.
Publication Date
9-1-2017
Publication Title
Pure and Applied Chemistry
ISSN
00334545
E-ISSN
13653075
Volume
89
Issue
9
First Page
1321
Last Page
1331
Rights
other-closed
DOI
10.1515/pac-2017-0112
Funding Number
GM111835
Funding Sponsor
National Institute of General Medical Sciences
Recommended Citation
Hasty, Scott J.; Rath, Nigam P.; and Demchenko, Alexei V., "Extending the S-benzimidazolyl (SBiz) platform: N-alkylated SBiz glycosyl donors with the universal activation profile" (2017). Chemistry & Biochemistry Faculty Works. 107.
DOI: https://doi.org/10.1515/pac-2017-0112
Available at:
https://irl.umsl.edu/chemistry-faculty/107