253683-37-3

Upstream product

• 1552-12-1 1,5-cis,cis-cyclooctadiene 
• 51097-60-0 (Z)-oct-4-enedial 
• 56506-08-2 (Z)-oct-4-ene-1,8-diol 
• 100-39-0 benzyl bromide 

Downstream Products

• 253683-23-7 8-O-benzyl-4-(Z)-octenyl-2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

Br?nsted Acid-Catalyzed Enantioselective Iodocycloetherification Enabled by Triphenylphosphine Selenide Cocatalysis

Enantioselective iodocycloetherifications can be conducted using sterically highly demanding BINOL-based phosphoric acid diesters as catalyst. To achieve highly enantioselective reactions, cocatalysis by triphenylphosphine selenide is necessary. With coca

Solid-phase oligosaccharide synthesis: preparation of complex structures using a novel linker and different glycosylating agents.

[formula: see text] A beta-(1-->4)-linked trisaccharide was prepared in 53% yield on a polymer support using glycosyl phosphates and released by cross-metathesis of a novel linker to reveal the anomeric n-pentenyl glycoside. Heptasaccharide 33 was prepared in 9% yield in 14 steps.