2,3,4-Tri-O-benzyl-D-glucopyranose NEW

Description of 2,3,4-Tri-O-benzyl-D-glucopyranose from Wuhan Fortuna Chemical Co.,Ltd

What is 2,3,4-Tri-O-benzyl-D-glucopyranose?

2,3,4-Tri-O-benzyl-D-glucopyranose** is a derivative of D-glucopyranose (a glucose molecule in its cyclic form) where three hydroxyl (-OH) groups on the sugar ring have been substituted with benzyl groups (-CH?C?H?). This chemical modification is often used in synthetic organic chemistry for protecting hydroxyl groups during multi-step reactions, particularly in carbohydrate and nucleoside chemistry.

Application of 2,3,4-Tri-O-benzyl-D-glucopyranose

2,3,4-Tri-O-benzyl-D-glucopyranose has several important applications in organic synthesis, particularly in the field of carbohydrate chemistry. Its main purpose is to serve as an intermediate or building block in complex synthetic reactions, where protecting specific functional groups is essential. Here are its key applications:

1. Protecting Group in Organic Synthesis - Selective Protection:The benzyl groups attached to the hydroxyl groups on the 2nd, 3rd, and 4th carbon atoms of the glucose molecule serve as protecting groups. Protecting groups prevent unwanted side reactions during multi-step synthesis, allowing for selective modification of other parts of the molecule. -Deprotection: After the desired reactions are completed, the benzyl groups can be removed under specific conditions, such as hydrogenation or treatment with strong acids, to regenerate the free hydroxyl groups. This makes it easier to manipulate the sugar while keeping the protected parts intact.

2. Carbohydrate Synthesis - Building Complex Sugars: 2,3,4-Tri-O-benzyl-D-glucopyranose is used as a starting material or intermediate in the synthesis of complex carbohydrates, such as oligosaccharides, disaccharides, and polysaccharides. In such syntheses, selectively protecting certain hydroxyl groups allows for the precise attachment of other sugar units or functional groups. -Glycoside Synthesis: It can be used in the preparation of glycosides, where the sugar molecule is linked to another molecule (like an alcohol or a protein) via a glycosidic bond. The selective protection of the hydroxyl groups ensures control over which hydroxyl group participates in forming the glycosidic bond.

3. Glycosylation Reactions -Selective Glycosylation: In reactions where sugars are attached to other molecules (proteins, lipids, or other sugars), the protected hydroxyl groups ensure selective glycosylation, allowing for the controlled formation of glycosidic bonds at specific positions on the sugar molecule. This is crucial for constructing biologically active molecules like glycoproteins, glycolipids, and other glycoconjugates. - Formation of Functional Biomolecules: The molecule can be involved in synthesizing complex bioactive molecules that play roles in biological processes such as cell signaling, immune responses, and energy storage.

4. Synthesis of Nucleosides and Nucleotides - In nucleoside chemistry, sugars like D-glucopyranose are essential components. Protecting the hydroxyl groups selectively using benzyl groups allows for the synthesis of nucleosides (sugar + base) or nucleotides (sugar + base + phosphate). This is important in the creation of synthetic DNA/RNA analogs, antiviral drugs, or other biomolecular applications.

5. Pharmaceutical and Drug Design - Drug Development: In some cases, 2,3,4-Tri-O-benzyl-D-glucopyranose derivatives may be used in the design and synthesis of glycosylated drugs or drug delivery systems. Carbohydrate-based drugs or prodrugs often require precise control over the structure, and protected intermediates like this are crucial for their synthesis.

6. Synthesis of Natural Products -Natural Product Chemistry:** Many natural products, including antibiotics, glycopeptides, and secondary metabolites, contain sugar moieties in their structure. 2,3,4-Tri-O-benzyl-D-glucopyranose is useful in synthesizing these natural products, enabling the controlled modification of sugar-containing structures.

Summary of Applications:

- Protecting group for selective reactions in organic and carbohydrate synthesis. - Intermediate in the synthesis of complex carbohydrates (oligosaccharides, disaccharides, polysaccharides).

- Glycosylation reactions to form glycosidic bonds in biologically active molecules.

- Nucleoside synthesis, which is important in nucleic acid chemistry.

- Drug design and development, especially in glycosylated compounds or drug delivery systems.

- Natural product synthesis  involving sugar moieties.

Overall, 2,3,4-Tri-O-benzyl-D-glucopyranose is a valuable tool in synthetic chemistry, enabling the controlled and selective modification of glucose and its derivatives for use in complex molecular structures.

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