740817-20-3

Upstream product

• 740817-18-9 1-O-acetyl-2,3,4-tri-O-benzyl-1-C-(2-thiazolyl)-α-L-fucopyranose 
• 740817-09-8 2,6-anhydro-3,4,5-tri-O-benzyl-7-deoxy-1-C-phenyl-aldehydo-L-glycero-D-manno-heptose 
• 740816-90-4 2,3,4-tri-O-benzyl-1-C-(2-thiazolyl)-L-fucopyranose 
• 740816-91-5 2-(2,3,4-tri-O-benzyl-β-L-fucopyranosyl)thiazole 
• 740817-19-0 2,6-anhydro-3,4,5-tri-O-benzyl-7-deoxy-aldehydo-L-glycero-D-manno-heptose 
• 100-39-0 benzyl bromide 
• 740817-10-1 (1R)-2,6-anhydro-3,4,5-tri-O-benzyl-7-deoxy-1-C-phenyl-1-C-(2-thiazolyl)-L-glycero-D-manno-heptitol 
• 162118-38-9 (3S,4R,5R,6S)-3,4,5-tris(benzyloxy)-6-methyltetrahydro-2H-pyran-2-ol 

Downstream Products

• 740817-12-3 methyl 3,7-anhydro-2,4,5,6-tetra-O-benzyl-8-deoxy-2-C-phenyl-L-threo-D-gulo-octonate 
• 740817-11-2 3,7-anhydro-2,4,5,6-tetra-O-benzyl-8-deoxy-2-C-phenyl-aldehydo-L-threo-D-gulo-octose 

Relevant academic research and scientific papers

Stereoselective synthesis of α- and β-L-C-fucosyl aldehydes and their utility in the assembly of C-fucosides of biological relevance

An efficient synthesis of O-benzylated derivatives of the title sugar aldehydes via thiazole addition to tri-O-benzyl-L-fuconolactone followed by highly stereoselective deoxygenation of the resulting thiazolylketose and thiazole to formyl transformation i