583826-59-9

Upstream product

• 583826-57-7 2-((2S,3S,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-thiazole 

Downstream Products

• 1053732-76-5 (2S,3S,4R,5R)-3,4-Bis-benzyloxy-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-2-carbaldehyde 
• 583826-62-4 (2S,3S,4S,5S)-3,4-Bis-benzyloxy-2-diisopropoxymethyl-5-iodomethyl-tetrahydro-furan 
• 583826-61-3 ((2R,3R,4S,5S)-3,4-Bis-benzyloxy-5-diisopropoxymethyl-tetrahydro-furan-2-yl)-methanol 
• 583826-60-2 2-[(2S,3S,4R,5R)-3,4-Bis-benzyloxy-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-thiazole 

Relevant academic research and scientific papers

A new synthetic approach to mycobacterial cell wall α-(1→5)-D-arabinofuranosyl C-oligosaccharides

Three designed arabinofuranose building blocks allowed the diastereoselective synthesis of a C-disaccharide and a C-trisaccharide by Wittig olefination. The latter compound represents the first example of all-carbon linked arabinofuranotriose analogue.