1453217-95-2

Upstream product

• 1091607-89-4 (R)-1-((3aR,5R,6R,6aR)-2,2-dimethyl-6-(naphthalen-2-ylmethoxy)tetrahydrofuro[3,2-d][1,3]dioxol-5-yl)ethane-1,2-diol 
• 956485-06-6 3-O-(2-naphthylmethyl)-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 2595-05-3 Diacetone D-glucose 
• 956485-07-7 ((3aR,6S,6aR)-2,2-dimethyl-6-(naphthalen-2-ylmethoxy)tetrahydrofuro[3,2-d][1,3]dioxole-5,5-diyl)dimethanol 
• 1057385-93-9 (3aR,5S,6R,6aR)-2,2-dimethyl-6-(naphthalen-2-ylmethoxy)tetrahydrofuro[3,2-d][1,3]dioxole-5-carbaldehyde 
• 1453217-78-1 (S)-1-((3aR,5S,6S,6aR)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyl-6-(naphthalen-2-ylmethoxy)tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)but-3-en-1-ol 
• 1453217-97-4 C₃₈H₅₄N₂O₇SSi₂ 
• 1453217-96-3 C₃₄H₅₂O₇Si₂ 
• 1453217-93-0 (3aR,4aS,5S,8aR,8bR)-5-((tert-butyldimethylsilyl)oxy)-4a-(((tert-butyldiphenylsilyl)oxy)methyl)-8a-hydroxy-2,2-dimethylhexahydro[1,3]dioxolo[4,5-b]benzofuran-7(4aH)-one 
• 1453217-94-1 C₃₄H₅₀O₇Si₂ 
• 1453217-91-8 1,2-O-isopropylidene-3-keto-4-C-(tert-butyldiphenylsilyl)oxymethyl-5-O-(tert-butyldimethylsilyl)-6-deoxy-6-C-vinyl-β-Lmannofuranose 
• 1453217-92-9 C₃₄H₅₂O₆Si₂ 
• 1453217-90-7 1,2-O-isopropylidene-3-O-(2-naphthylmethyl)-4-C-(tert-butyldiphenylsilyl)oxymethyl-5-O-(tert-butyldimethylsilyl)-6-deoxy-6-C-vinyl-β-L-mannofuranose 
• 956485-08-8 ((3aR,5R,6S,6aR)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyl-6-(naphthalen-2-ylmethoxy)tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methanol 

Downstream Products

• 1453218-00-2 (3aR,4aS,5S,8aR,8bR)-5,8a-bis(benzyloxy)-2,2-dimethyl-4a-((naphthalen-2-ylmethoxy)methyl)octahydro[1,3]dioxolo[4,5-b]benzofuran 
• 1453218-07-9 C₃₄H₃₆O₆ 
• 1453218-08-0 C₃₈H₄₀O₈ 
• 1453218-06-8 (2R,3R,3aR,7S,7aS)-3a,7-bis(benzyloxy)-2-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-7a-((naphthalen-2-ylmethoxy)methyl)octahydrobenzofuran-3-yl acetate 
• 1453218-10-4 C₃₉H₄₀N₂O₇ 
• 1453218-09-1 (2R,3R,3aR,7S,7aS)-3a,7-bis(benzyloxy)-2-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-7a-((naphthalen-2-ylmethoxy)methyl)octahydrobenzofuran-3-yl methanesulfonate 
• 1453218-12-6 C₃₉H₃₈N₂O₆ 
• 1453218-13-7 C₂₈H₃₀N₂O₆ 
• 1453218-11-5 ((5aR,6aS,7S,10aR,10bS)-7,10a-bis(benzyloxy)-3-methyl-2-oxo-7,8,9,10,10a,10b-hexahydro-2H-benzofuro[2′,3′:4,5]oxazolo[3,2-a]pyrimidin-6a(5aH)-yl)methyl methanesulfonate 
• 1453218-14-8 1-((2R,3S,3aR,7S,7aS)-3a,7-bis(benzyloxy)hexahydro-2H-3,7a-(epoxymethano)benzofuran-2-yl)-5-ethylpyrimidine-2,4(1H,3H)-dione 

Relevant academic research and scientific papers

TRICYCLIC NUCLEOSIDES AND OLIGOMERIC COMPOUNDS PREPARED THEREFROM

The present disclosure provides tricyclic nucleosides and oligomeric compounds prepared therefrom. More particularly, the tricyclic nucleosides provided herein comprise a tricyclic ribosyl sugar moiety having a bridge between the 4' and 2' ring carbon ato

A constrained tricyclic nucleic acid analogue of α-l-LNA: Investigating the effects of dual conformational restriction on duplex thermal stability

A constrained tricyclic analogue of α-l-LNA (2), which contains dual modes of conformational restriction about the ribose sugar moiety, has been synthesized and characterized by X-ray crystallography. Thermal denaturation experiments of oligonucleotide se