305834-13-3

Upstream product

• 305834-12-2 methyl 2,3,4-tri-O-benzyl-β-D-allo-pyranoside 
• 2595-05-3 Diacetone D-glucose 
• 100-39-0 benzyl bromide 
• 18469-06-2 methyl β-D-allo-pyranoside 

Downstream Products

• 177913-75-6 (2R,3R,4R)-2,3,4-Tris-benzyloxy-hex-5-enal 
• 1261294-50-1 bis(methyl 2,3,4-tri-O-benzyl-6-deoxy-β-D-allopyranosid-6-yl) sulfide 
• 1261294-43-2 methyl 6-S-acetyl-2,3,4-tri-O-benzyl-6-deoxy-β-D-allopyranoside 
• 1310825-95-6 (3R,4R,5S,6R)-6-[(N-benzyl)amino]-3,4,5-tris-(benzyloxy)-1,8-nonadiene 
• 1310825-96-7 (3R,4R,5S,6R)-6-[(N-benzyl-N-(benzyloxycarbonyl))amino]-3,4,5-tris-(benzyloxy)-1,8-nonadiene 
• 1310825-97-8 (3R,4R,5S,6R)-6-[(N-benzyl-N-(benzyloxycarbonyl))amino]-3,4,5-tris(benzyloxy)-cycloheptene 
• 1310825-98-9 (1RS,2R,3S,4S,5R)-5-[(N-benzyl-N-(benzyloxycarbonyl))amino]-2,3,4-tris(benzyloxy)-cycloheptanol 
• 1310825-99-0 (2S,3S,4S,5R)-5-[(N-benzyl-N-(benzyloxycarbonyl))amino]-2,3,4-tris(benzyloxy)-cycloheptanone 
• 195245-30-8 3,4,5-tri-O-benzyl-1,2,6-trideoxy-6-iodo-L-ribo-hex-1-enitol 
• 139014-28-1 3,4,5-tri-O-benzyl-1,2-dideoxy-L-ribo-hex-1-enitol 

Relevant academic research and scientific papers

First total synthesis of 3-Epi-calystegin B2

A straightforward chiral pool synthesis for a non-natural calystegin, 3-epi-B2, is described. Key steps of this synthesis include an ultrasound-assisted Zn-mediated tandem ring opening reaction followed by a Grubbs' catalyst-mediated ring closu

Efficient synthesis of (6-deoxy-glycopyranosid-6-yl) sulfone derivatives and their effect on Ca2+-ATPase

Synthesis of a series of novel (6-deoxy-glycopyranosid-6-yl) sulfone derivatives has been achieved using a general synthetic strategy. Yields were excellent in every case. The synthetic compounds were evaluated for their biological potential against Casu

The cobalt-catalyzed oxygenative radical route from hexopyranosides to carbapentofuranoses

Cobalt-catalyzed radical cyclization/oxygenation of various 6-iodohex-1-enitols gave in one step the carbocyclic analogs of pentofuranoses. The reaction was run under very mild conditions and gave moderate to good yields of carbapentofuranoses within a few hours. All the possible 6-iodohex-1-enitol stereoisomers were prepared, and the influence of relative configurations and protecting groups was studied.