192637-01-7

Upstream product

• 358-23-6 trifluoromethylsulfonic anhydride 
• 192636-99-0 methyl 2-O-benzyl-4,6-O-benzylidene-α-D-(3-2H)allopyranoside 
• 157809-94-4 (4aR,6S,7S,8aR)-7-Benzyloxy-6-methoxy-2-phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-8-one 
• 15038-71-8 methyl 2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 

Downstream Products

• 192636-99-0 methyl 2-O-benzyl-4,6-O-benzylidene-α-D-(3-2H)allopyranoside 

Relevant academic research and scientific papers

α-Hydrogen elimination in some 3- and 4-triflates of α-D- glycopyranosides

In previous papers [A. El Nemr and T. Tsuchiya, Tetrahedron Lett., 36 (1995) 7665-7668; A. El Nemr, T. Tsuchiya, and Y. Kobayashi, Carbohydr. Res., 293 (1996) 31-59] we reported new reactions that occur when some carbohydrate triflates are treated with MeLi (or BuLi) in ether, giving C-methyl (or butyl) or unsaturated compounds. Both reactions may be explained by α-hydrogen elimination in the triflates. This paper is an extension of the previous work and describes the mechanism of unsaturation of some 3- or 4-triflylates of α-D-glycopyranosides. By using deuterated analogs, it was found that methyl 2-O-benzyl-4,6-O-benzylidene-3-O-triflyl-α-D-glucopyranoside gives the 2,3- and 3,4-unsaturated compounds through a-hydrogen elimination, and the corresponding allopyranoside gives the 2,3-unsaturated compound through α- and β- (for 14) and α-hydrogen eliminations (for 19). Carbene formation is proposed as the key intermediate for the former eliminations, and a 1 → 2 proton-shift is proposed as the key reaction for the latter.