67965-12-2

Usage

Chemical class

Hexopyranose derivatives

Structure

Highly functionalized sugar molecule with multiple acetyl, benzyl, and trityl groups attached

Applications

Widely used in organic and medicinal chemistry as a building block for the synthesis of various drugs and natural products

Molecular architecture

Valuable tool for the creation of novel molecular architectures and pharmaceutical compounds

Reactivity

High reactivity and versatile reactivity

Field of importance

Important reagent in the field of carbohydrate chemistry and drug discovery

Upstream product

• 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 
• 64-19-7 acetic acid 
• 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 

Downstream Products

• 67965-13-3 1,2-di-O-acetyl-3,4-di-O-benzyl-β-D-glucopyranose 
• 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 
• 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