316353-08-9

Upstream product

• 3173-56-6 benzyl isothiocyanate 
• 316352-68-8 thioethyl 3,4,6-tri-O-(tert-butyldimethylsilyl)-β-D-glucopyranose 
• 121654-00-0 3,4,6-tris-O-tert-butyldimethylsilyl-1,2-anhydro-α-D-glucopyranose 

Downstream Products

• 316353-10-3 thioethyl 2-O-benzylcarbamoyl-β-D-glucopyranose 
• 316353-16-9 Isopropyl-carbamic acid (2S,3R,4S,5R,6R)-3-benzylcarbamoyloxy-2-ethylsulfanyl-5-hydroxy-6-hydroxymethyl-tetrahydro-pyran-4-yl ester 
• 316353-12-5 thioethyl 2-O-benzylcarbamoyl-4,6-O-(4-methoxybenzylidene)-β-D-glucopyranose 
• 316353-20-5 2-bromoethyl 2-O-benzylcarbamoyl-3-O-isopropylcarbamoyl-β-D-glucopyranose 
• 316353-13-6 thioethyl 2-O-benzylcarbamoyl-3-O-isopropylcarbamoyl-4,6-O-(4-methoxybenzylidene)-β-D-glucopyranose 
• 316353-14-7 thioethyl 2-O-benzylcarbamoyl-3-O-isopropylcarbamoyl-6-O-(4-methoxybenzyl)-β-D-glucopyranose 
• 316353-18-1 thioethyl 4-O-benzyl-2-O-benzylcarbamoyl-3-O-isopropylcarbamoyl-6-O-(4-methoxybenzyl)-β-D-glucopyranose 

Relevant academic research and scientific papers

Development of an efficient, regio- and stereoselective route to libraries based on the β-D-glucose scaffold

The design and execution of an efficient synthetic route for the sequential functionalization of the five hydroxyl substituents of β-D-glucose has been achieved. This strategy, based on the stereoselective glycosidation of thioglycosides, provides a new approach for the parallel construction of a wide variety β-D-glucose analogues and as such holds promise for solid-support library syntheses.