Glycosylation via Transition‐Metal Catalysis: Challenges and Opportunities
Гликозилирование с использованием катализа переходными металлами: проблемы и возможности
2016-07-21
SCID: 54.1/ypw4bk6e
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O-, N-, C-, and S-glycosidescomplex oligosaccharidesglycoconjugatesstereoselective glycosylationtransition-metal catalysis
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Abstract (AI)
Development of efficient, mild, and easily operable stereoselective glycosylations is of critical importance to access sufficient amounts of pure and structurally well‐defined carbohydrates for studies of their biological functions. Such studies will facilitate our understanding of the role of complex oligosaccharides and glycoconjugates in biological processes as well as the development of carbohydrate‐based effective therapeutic agents. This review highlights recent advances in the transition metal catalyzed stereoselective glycosylations for the synthesis of a variety of structurally complex and biologically significant O‐, N‐, C‐, and S‐glycosides.
Key Findings
1
Efficient, mild, and operationally simple stereoselective glycosylations are essential for producing pure, structurally defined carbohydrates.
2
Improved glycosylation methods can support studies of oligosaccharide and glycoconjugate biological functions and carbohydrate-based therapeutic development.
3
The review highlights recent advances in transition-metal-catalyzed stereoselective glycosylation methods.
4
Transition-metal catalysis enables synthesis of structurally complex and biologically significant O-, N-, C-, and S-glycosides.
Research Object
Transition-metal-catalyzed stereoselective glycosylation reactions for synthesizing structurally complex O-, N-, C-, and S-glycosides
Research Subject
Recent advances, challenges, and opportunities in the efficiency, mildness, operational simplicity, and stereoselectivity of transition-metal-catalyzed glycosylations
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2016-07-21
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