198020-80-3

Upstream product

• 358-23-6 trifluoromethylsulfonic anhydride 
• 192636-86-5 methyl 2-O-benzyl-4,6-O-benzylidene-β-D-(3-2H)glucopyranoside 
• 15038-71-8 methyl 2-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside 
• 68044-34-8 (4aR,6R,7S,8aR)-7-Benzyloxy-6-methoxy-2-phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-8-one 

Downstream Products

• 192636-86-5 methyl 2-O-benzyl-4,6-O-benzylidene-β-D-(3-2H)glucopyranoside 

Relevant academic research and scientific papers

α- And β-hydrogen eliminations in the reactions of some 3-O-triflylglycosides with (t)BuOK and pyridine

Previous papers [10-12] reported new reactions that occur when some carbohydrate triflates are treated with MeLi (or BuLi) in Et2O to give the C-methyl(butyl) or unsaturated compounds through elimination of the CH-hydrogen bearing a CF3SO3 group ( α-elimination) as a proton. This paper extends the previous work and describes the reactions for some 3-O-triflyl-D-gluco- and -allo-furanosides and -pyranosides with (t)BuOK and pyridine [instead of Me(Bu)Li], utilizing the corresponding 2- and 3-deuterated analogs. It was found that, when (t)BuOK was used, the 3-O-triflyl-D-glucopyranosides gave 2,3- and 3,4-unsaturated compounds through a-hydrogen elimination (a-elimination) followed by (possibly) C-3 carbene formation, while the 3-O-triflyl-D-allopyranosides gave mainly 2,3-unsaturated compounds through p-elimination. When pyridine was used, most of the compounds gave the corresponding 3-pyridinium derivatives through an SN2 process.