153186-18-6

Upstream product

• 115693-78-2 1,2:5,6-di-O-isopropylidene-3-O-(4-methoxybenzyl)-α-D-glucofuranose 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 824-94-2 p-methoxybenzyl chloride 

Downstream Products

• 851393-61-8 (1R,3SR,4S,7R)-3-methoxy-7-(p-methoxybenzyloxy)-1-(p-methoxybenzyloxymethyl)-2,5-dioxabicyclo[2.2.1]heptane 
• 676126-64-0 (2S,3R,4R)-4-hydroxy-3-(p-methoxybenzyloxy)-4-(p-methoxybenzyloxymethyl)tetrahydrofuran-2-carbaldehyde 
• 676126-71-9 (1R,3S,4R,7R)-7-(p-methoxybenzyloxy)-1-(p-methoxybenzyloxymethyl)-3-phenyl-2,5-dioxabicyclo[2.2.1]heptane 
• 676126-67-3 (2S,3R,4R)-4-hydroxy-2-(phenylcarbonyl)-3-(p-methoxybenzyloxy)-4-(p-methoxybenzyloxymethyl)tetrahydrofuran 
• 676126-69-5 (2R,3R,4R)-4-hydroxy-2-[(R)-hydroxy(phenyl)methyl]-3-(p-methoxybenzyloxy)-4-(p-methoxybenzyloxymethyl)tetrahydrofuran 
• 676126-65-1 (2R,3R,4R)-4-hydroxy-2-[(S)-hydroxy(phenyl)methyl]-3-(p-methoxybenzyloxy)-4-(p-methoxybenzyloxymethyl)tetrahydrofuran 
• 676126-72-0 (1R,3S,4R,7R)-7-(p-methoxybenzyloxy)-1-(p-methoxybenzyloxymethyl)-3-(1-pyrenyl)-2,5-dioxabicyclo[2.2.1]heptane 
• 676126-68-4 (2S,3R,4R)-4-hydroxy-2-(1-pyrenylcarbonyl)-3-(p-methoxybenzyloxy)-4-(p-methoxybenzyloxymethyl)tetrahydrofuran 
• 676126-66-2 (2R,3R,4R)-4-hydroxy-2-[(S)-hydroxy(1-pyrenyl)methyl]-3-(p-methoxybenzyloxy)-4-(p-methoxybenzyloxymethyl)tetrahydrofuran 
• 676126-70-8 (2R,3R,4R)-4-hydroxy-2-[(R)-hydroxy(1-pyrenyl)methyl]-3-(p-methoxybenzyloxy)-4-(p-methoxybenzyloxymethyl)tetrahydrofuran 
• 153186-20-0 3,5-O-(p-methoxybenzylidene)-4-C-iodomethyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 153186-19-7 3,5-O-(p-methoxybenzylidene)-4-C-hydroxymethyl-1,2-O-isopropylidene-α-D-xylofuranose 

Relevant academic research and scientific papers

Oligodeoxynucleotides containing α-L-ribo configured LNA-type C-aryl nucleotides

Synthesis of 2′-O,4′-C-methylene-α-L-ribofuranosyl derivatives containing phenyl and 1-pyrenyl aglycons, i.e., novel α-L-ribo configured LNA-type C-aryl nucleosides, has been accomplished. Key synthetic steps included stereoselective Grignard reactions on