280574-35-8

Upstream product

• 64775-10-6 ((3aR,5S,6aR)-2,2-dimethyl-6-methylene-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methanol 
• 3254-16-8 3,4,6-tri-O-acetyl-[1,2-O-(1-methoxyethylidene)]-α-D-glucopyranose 
• 103931-45-9 5-O-(tert-butyldimethylsilyl)-1,2-O-isopropylidene-α-D-erythro-pentofuranos-3-ulose 
• 280574-32-5 phenyl 3,4,6-tri-O-p-methoxybenzyl-1-seleno-β-D-glucopyranoside 
• 280574-39-2 3,4,6-tri-O-p-methoxybenzyl-1,2-O-(1-methoxyethylidene)-α-D-glucopyranose 
• 146035-66-7 3-deoxy-3-methylene-5-O-<(tert-butyldimethyl)silyl>-1,2-O-isopropylidene-α-D-ribofuranose 
• 29073-91-4 (3aR,5R,6S,7S,7aR)-5-Hydroxymethyl-2-methoxy-2-methyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-6,7-diol 

Downstream Products

• 280574-37-0 3-deoxy-3-(4,5,7-tri-O-p-methoxybenzyl-2,6-anhydro-1-deoxy-D-glycero-D-ido-heptitol-1-yl)-1,2-O-(1-methylethylidene)-α-D-ribo-pentofuranose 

Relevant academic research and scientific papers

Synthesis of the C-glycosidic analog of adenophostin A, a potent IP3 receptor agonist, using a temporary silicon-tethered radical coupling reaction as the key step

Synthesis of the C-glycosidic analog (3) of adenophostin A, a very potent IP3 receptor agonist, was achieved using a temporary silicon-tethered reductive radical coupling reaction as the key step. Radical reaction of the silaketal substrate 6 with Bu3SnH/AIBN in benzene occurred stereoselectively, and subsequent desilylation gave the desired C-glycosidic disaccharide 7 with the (3α,1'α-configuration as the major product. Compound 7 was converted into the target 3 via the introduction of an adenine base by a Vorbruggen glycosylation reaction. (C) 2000 Elsevier Science Ltd.

Synthesis of the C-glycosidic analogue of adenophostin A and its uracil congener as potential IP3 receptor ligands. Stereoselective construction of the C-glycosidic structure by a temporary silicon-tethered radical coupling reaction

Synthesis of the C-glycosidic analogue 9 of adenophostin A, a very potent IP3 receptor agonist, and its uracil congener 10 was achieved via a temporary silicon-tethered radical coupling reaction as the key step. Phenyl 3,4,6-tri-O-(p-methoxyben