Carbohydrates (also known as saccharides or glycans) occupy a central role among biomolecules due to their participation in a number of signaling and recognition processes in biology. Moreover, carbohydrates are essential structural components of numerous vaccines, anti-diabetic and anti-viral drugs, and anti-tumor drug candidates. Despite significant advances in chemical glycosylation methods, general technologies which offer a precise control of anomeric configuration of the glycosidic bond are in demand. In this proposal we aim to develop methods and strategies for efficient and practical synthesis of bioactive oligosaccharides.
In Aim 1, we will expand the toolset of nucleophilic glycosyl donors.
In Aim 2, we will develop and apply oxidative glycosylation method for the preparation of oligosaccharides with defined anomeric configuration. This novel method will establish a robust protocol for which the configuration of the anomeric bond is pre-defined in the configuration of nucleophilic glycosyl donor and is independent from the structure of the carbohydrate chain, protective groups, and alcohol acceptors. This method, in combination with C-glycosylation, will address the critical challenges of oligosaccharides synthesis and can be incorporated into automated and high-throughput synthesis. Given the generality and a predictable nature of the glycosylation step, this new technology can be used by researchers with minimal training in organic synthesis, and the discoveries of this study can have important impact on the development of new diagnostic tools and therapies.

Public Health Relevance

Carbohydrates are important structural elements found in numerous bioactive natural products of medical relevance, commercially available drugs, and diagnostic agents. This proposal seeks to develop chemical methods and strategies to enable the synthesis of a diverse set of oligosaccharides of biomedical relevance with high efficiency and selectivity.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01GM125284-02
Application #
9548712
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Marino, Pamela
Project Start
2017-09-01
Project End
2021-06-30
Budget Start
2018-07-01
Budget End
2019-06-30
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Colorado at Boulder
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
007431505
City
Boulder
State
CO
Country
United States
Zip Code
80303
Yang, Tianyi; Zhu, Feng; Walczak, Maciej A (2018) Stereoselective oxidative glycosylation of anomeric nucleophiles with alcohols and carboxylic acids. Nat Commun 9:3650
Zhu, Feng; Rodriguez, Jacob; Yang, Tianyi et al. (2017) Glycosyl Cross-Coupling of Anomeric Nucleophiles: Scope, Mechanism, and Applications in the Synthesis of Aryl C-Glycosides. J Am Chem Soc 139:17908-17922