740817-13-4

Upstream product

• 79265-30-8 2-(trimethylsilyl)thiazole 
• 740817-19-0 2,6-anhydro-3,4,5-tri-O-benzyl-7-deoxy-aldehydo-L-glycero-D-manno-heptose 
• 869500-97-0 3-Methyl-2-thiazol-2-yl-2-((2S,3S,4R,5R,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yl)-2,3-dihydro-benzothiazole 
• 869500-65-2 2-(2,3,4-tri-O-benzyl-β-L-fucopyranosyl)benzothiazole 
• 869500-63-0 (2S,3S,4R,5R,6S)-2-Benzothiazol-2-yl-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-ol 
• 869500-64-1 1-O-acetyl-2,3,4-tri-O-benzyl-1-C-(2-benzothiazolyl)-α-L-fucopyranose 
• 162118-38-9 (3S,4R,5R,6S)-3,4,5-tris(benzyloxy)-6-methyltetrahydro-2H-pyran-2-ol 
• 144668-21-3 (3S,4R,5R,6S)-3,4,5-tris(benzyloxy)-6-methyltetrahydro-2H-pyran-2-one 
• 740816-91-5 2-(2,3,4-tri-O-benzyl-β-L-fucopyranosyl)thiazole 
• 740816-90-4 2,3,4-tri-O-benzyl-1-C-(2-thiazolyl)-L-fucopyranose 
• 740817-18-9 1-O-acetyl-2,3,4-tri-O-benzyl-1-C-(2-thiazolyl)-α-L-fucopyranose 

Downstream Products

• 740817-14-5 (1S)-2,6-anhydro-3,4,5-tri-O-benzyl-7-deoxy-1-C-phenyl-1-C-(2-thiazolyl)-L-glycero-D-manno-heptitol 
• 740817-16-7 3,7-anhydro-4,5,6-tri-O-benzyl-8-deoxy-2-C-phenyl-aldehydo-L-threo-D-ido-octose 
• 740817-17-8 methyl 3,7-anhydro-4,5,6-tri-O-benzyl-8-deoxy-2-C-phenyl-L-threo-D-ido-octonate 
• 740817-21-4 (1S)-2,6-anhydro-1,3,4,5-tetra-O-benzyl-7-deoxy-1-C-phenyl-1-C-(2-thiazolyl)-L-glycero-D-manno-heptitol 

Relevant academic research and scientific papers

Concise and practical synthesis of C-glycosyl ketones from sugar benzothiazoles and their transformation into chiral tertiary alcohols

A collection of 13 unsymmetrical ketones, each one featuring a sugar (D-glucosyl, D-galactosyl, D-mannosyl, and L-fucosyl) and an aglycone moiety (phenyl, 2-thiazolyl, TMS-ethynyl, allyl, and 1-propenyl) was prepared by a uniform route based on the use of

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