67965-13-3

Usage

Chemical structure

A hexopyranose sugar with two acetyl groups and two benzyl groups attached to its hydroxyl (OH) functional groups.

Building block

Commonly used in the synthesis of complex carbohydrates and natural products.

Selective modification

Acetyl and benzyl groups can be selectively removed or modified for different chemical reactions and derivatization.

Structural diversity

Allows for the creation of a wide range of structurally diverse molecules.

Potential biological activities

Investigated for antimicrobial and anticancer properties.

Research interest

An interesting target for further research in medicinal chemistry.

Upstream product

• 67965-11-1 (3aR,5R,6R,7S,7aR)-6,7-Bis-benzyloxy-2-ethoxy-2-methyl-5-trityloxymethyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran 
• 53604-68-5 1,2-O-(1-ethoxyethylidene)-α-D-glucopyranose 
• 67965-10-0 1,2-O-(1-ethoxyethylidene)-6-O-(triphenylmethyl)-α-D-glucopyranose 
• 3254-17-9 3,4,6-tri-O-acetyl-1,2-O-(1-ethoxyethylidene)-α-D-glucopyranose 
• 67965-12-2 1,2-di-O-acetyl-3,4-di-O-benzyl-6-O-(triphenylmethyl)-β-D-glucopyranose 

Downstream Products

• 99605-02-4 1,2-di-O-acetyl-3,4-di-O-benzyl-β-D-glucodialdehydo-1,5-pyranose 
• 67965-18-8 3,4-di-O-Benzyl-1,6-anhydro-β-L-gulopyranose 
• 67999-94-4 2,3,4-tri-O-acetyl-1,6-anhydro-β-L-gulopyranose 
• 99605-10-4 2-O-allyl-1,6-anhydro-3,4-di-O-benzyl-β-L-gulopyranose 
• 99605-09-1 2-O-acetyl-1,6-anhydro-3,4-di-O-benzyl-β-L-gulopyranose 
• 67965-16-6 (β,β-dimethylhydrazino)-3,4-di-O-benzyl-L-gulopyranoside 

Relevant academic research and scientific papers

Synthesis of the Carbohydrate Moiety of Bleomycin. 1,3,4,6-Tetra-O-substituted L-Gulose Derivatives

To facilitate the synthesis of the carbohydrate moiety of bleomycin and its subsequent attachment to the remainder of the bleomycin molecule in a regio- and stereocelective fashion, a number of suita