854654-33-4

Upstream product

• 854654-29-8 (3,7-anhydro-8-O-tert-butyldiphenylsilyl-1,2,6-trideoxy-4,5-di-O-isopropylidene-D-glycero-D-galacto-oct-1-enitol-6-yl)-2',3',4',6'-tetra-O-benzyl-α-D-glucopyranoside 
• 854654-31-2 (3,7-anhydro-1,2,6-trideoxy-4,5-di-O-isopropylidene-D-glycero-D-galacto-oct-1-enitol-6-yl)-2',3',4',6'-tetra-O-benzyl-α-D-glucopyranoside 
• 98-59-9 p-toluenesulfonyl chloride 
• 854654-27-6 3,7-anhydro-8-O-tert-butyldiphenylsilyl-1,2-dideoxy-4,5-di-O-isopropylidene-D-glycero-D-galacto-oct-1-enitol 

Downstream Products

• 854654-37-8 (3,7-anhydro-1,2,6,8-tetradeoxy-4,5-di-O-isopropylidene-D-galacto-octo-1,7-dienitol-6-yl)-2',3',4',6'-tetra-O-benzyl-α-D-glucopyranoside 
• 854654-35-6 (3,7-anhydro-8-bromo-1,2,6,8-tetradeoxy-4,5-di-O-isopropylidene-D-glycero-D-galacto-oct-1-enitol-6-yl)-2',3',4',6'-tetra-O-benzyl-α-D-glucopyranoside 

Relevant academic research and scientific papers

Alternative approaches towards glycosylated eight-membered ring compounds employing Claisen rearrangement of mono and disaccharide allyl vinyl ether precursors

Highly functionalized eight-membered rings having a glycosidic residue were synthesized in two different ways involving either glycosylation of a sugar-derived cyclooctenone with high stereocontrol as well as a Claisen rearrangement of a disaccharide deri