669082-61-5Relevant academic research and scientific papers
2,3-unsaturated allyl glycosides as glycosyl donors for selective α-glycosylation
Kumar, Brijesh,Aga, Mushtaq A.,Rouf, Abdul,Shah, Bhahwal A.,Taneja, Subhash C.
supporting information; experimental part, p. 3506 - 3510 (2011/06/26)
In the presence of NBS and a catalytic amount of a Lewis acid, 2,3-unsaturated allyl glycosides [6-(allyloxy)-3,6-dihydro-2-(hydroxymethyl)-2H- pyran-3-ol] have been successfully used as versatile glycosyl donors for the stereoselective α-glycosylation of
Direct Ferrier rearrangement on unactivated glycals catalyzed by indium(III) chloride
Nagaraj, Paramathevar,Ramesh, Namakkal G.
supporting information; experimental part, p. 3970 - 3973 (2009/10/04)
Anhydrous InCl3 has been shown to efficiently catalyze the Ferrier rearrangement by a direct allylic substitution of the hydroxyl group at C-3 position of glycals to afford the corresponding 2,3-unsaturated glycosides in high yields at ambient
