1198465-44-9

Upstream product

• 1198465-29-0 (6Z)-3,6-anhydro-1,2:4,5-bis-O-(1-methylethylidene)-7-bromo-7-deoxy-7-(3-nitrophenyl)-L-gluco-hept-6-enitol 
• 82101-74-4 methyl (E)-3-(tributylstannyl)acrylate 
• 13331-27-6 m-nitrobenzene boronic acid 

Relevant academic research and scientific papers

Tetrasubstituted C-glycosylidenes and C-glycosyl compounds from Di-and Monobromo-substituted exo-glycals

Efficient methods for functionalization of readily available exo-glycals have been developed. Sequential palladium-catalysed cross-coupling of dibromo-substituted exo-glycals was first explored and allowed the formation of new disubstituted exo-glycals as

Efficient access to disubstituted exo-glycals. Application to the preparation of C-glycosyl compounds

Efficient methods of preparation of disubstituted exo-glycals by palladium cross-coupling reaction on the readily available dibromo exo-glycal and methoxycarbonyl exo-glycal have been developed. Hydrogenation of these new monosubstituted and disubstituted