887480-16-2

Upstream product

• 142789-96-6 1,2-O-anhydro-3-O-benzyl-4,6-O-benzylidene-5a-carba-β-D-mannopyranose 
• 887480-12-8 2-O-acetyl-3-O-benzyl-4,6-O-benzylidene-5a-carba-α-D-mannopyranosyl-(1->4)-1,5-anhydro-3,6-di-O-benzyl-2-deoxy-D-arabino-hex-1-enitol 
• 887480-08-2 3-O-benzyl-4,6-O-benzylidene-5a-carba-α-D-mannopyranosyl-(1->4)-1,5-anhydro-3,6-di-O-benzyl-2-deoxy-D-arabino-hex-1-enitol 

Downstream Products

• 887480-20-8 3-O-benzyl-4,6-O-benzylidene-5a-carba-β-D-arabino-hex-2-ulopyranosyl-(1->4)-1,5-anhydro-3,6-di-O-benzyl-2-deoxy-D-arabino-hex-1-enitol 
• 887480-08-2 3-O-benzyl-4,6-O-benzylidene-5a-carba-α-D-mannopyranosyl-(1->4)-1,5-anhydro-3,6-di-O-benzyl-2-deoxy-D-arabino-hex-1-enitol 
• 887480-24-2 3-O-benzyl-4,6-O-benzylidene-5a-carba-α-D-glucopyranosyl-(1->4)-1,5-anhydro-3,6-di-O-benzyl-2-deoxy-D-arabino-hex-1-enitol 

Relevant academic research and scientific papers

Preparation of building blocks for carba-oligosaccharides: Some protected 5a′-carba-D-hexopyranosyl-1,5-anhydro-2-deoxy-D-arabino-hex-1-enitols, and 5a,5a′-dicarba congeners thereof

Four configurational types of two protected O-linked (5a-carba-D- hexopyranosyl)-D-glucal and carba-D-glucal derivatives were prepared in order to provide versatile synthetic intermediates readily convertible into carba-oligosaccharides of biological inte