((2R,3R,4S,5R,6S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)oxy)-5-(benzyloxy)-6-(ethylthio)-4-(naphthalen-2-ylmethoxy)tetrahydro-2H-pyran-2-yl)methyl 4-oxopentanoate

((2R,3R,4S,5R,6S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)oxy)-5-(benzyloxy)-6-(ethylthio)-4-(naphthalen-2-ylmethoxy)tetrahydro-2H-pyran-2-yl)methyl 4-oxopentanoate

Product Details

• CAS Number: 2411961-92-5
• Catalog Number: A23-1045
• Molecular Formula: C36H40O9S
• Molecular Weight: 648.76 g/mol
• Purity: ≥ 98%

Description

((2R,3R,4S,5R,6S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)oxy)-5-(benzyloxy)-6-(ethylthio)-4-(naphthalen-2-ylmethoxy)tetrahydro-2H-pyran-2-yl)methyl 4-oxopentanoate is a highly functionalized and stereochemically defined thioglycoside derivative used in advanced carbohydrate synthesis. The presence of the fluorenylmethoxycarbonyl group enables selective protection and deprotection strategies, providing precise control during multi-step synthetic processes.

The combination of benzyloxy and naphthylmethyl protecting groups allows fine-tuning of reactivity and regioselectivity, while the ethylthio functionality offers stability and controlled activation for glycosylation reactions. The appended 4-oxopentanoate moiety introduces additional functional versatility, making this compound suitable for constructing complex glycoconjugates and biologically relevant molecules.

This compound is widely used in glycosylation reactions, oligosaccharide synthesis, and medicinal chemistry research.

Applications

• Intermediate in stereoselective carbohydrate synthesis
• Precursor for glycosylation reactions
• Building block for complex oligosaccharides and glycoconjugates
• Used in pharmaceutical and chemical research