129678-64-4

Upstream product

• 130468-30-3 1-<3-deoxy-3-C-(4,5-dihydro-5-methyl-1,3,5-dithiazin-2-yl)-β-D-arabino-pentofuranosyl>thymine 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 130351-53-0 1-[(2R,3S,4S,5S)-3-Hydroxy-4-(5-methyl-[1,3,5]dithiazinan-2-yl)-5-trityloxymethyl-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidine-2,4-dione 
• 115913-84-3 1-(2,3-epoxy-5-O-trityl-β-D-lyxo-pentofuranosyl)thymine 
• 6302-94-9 5-methyl-[1,3,5]dithiazinane 

Downstream Products

• 129678-53-1 1-<5-O-(tert-butyldiphenylsilyl)-3-deoxy-3-C-formyl-β-D-arabino-pentofuranosyl>thymine 
• 719302-91-7 1-[5-O-(tert-butyldiphenylsilyl)-3-deoxy-3-C-(4,5-dihydro-5-methyl-1,3,5-dithiazin-2-yl)-2-O-(trifluoromethanesulfonyl)-β-D-arabino-pentofuranosyl]thymine 
• 130351-67-6 1-(3-deoxy-3-C-formyl-β-D-lyxo-pentofuranosyl)thymine 3',5'-O-hemiacetal 
• 130351-55-2 1-<3-deoxy-3-C-(hydroxymethyl)-β-D-arabino-pentofuranosyl>thymine 
• 129707-48-8 1-<5-O-(tert-butyldiphenylsilyl)-3-deoxy-3-C-(hydroxymethyl)-β-D-arabino-pentofuranosyl>thymine 
• 129678-70-2 1-<5-O-(tert-butyldiphenylsilyl)-3-deoxy-3-C-formyl-2-O-(4-methoxytetrahydropyran-4-yl)-β-D-arabino-pentofuranosyl>thymine 
• 129678-72-4 1-<5-O-(tert-butyldiphenylsilyl)-3-deoxy-3-C-(difluoromethyl)-2-O-(4-methoxytetrahydropyran-4-yl)-β-D-arabino-pentofuranosyl>thymine 
• 719302-96-2 C₅₅H₆₉N₅O₁₁Si₂ 
• 719302-97-3 C₅₄H₆₆FN₅O₁₀Si₂ 
• 719303-01-2 C₄₃H₄₇F₂N₅O₁₁ 
• 719303-00-1 C₄₄H₅₀FN₅O₁₂ 
• 719302-92-8 1-[5-O-(tert-butyldiphenylsilyl)-2,3-dideoxy-3-C-(4,5-dihydro-5-methyl-1,3,5-dithiazin-2-yl)-2-fluoro-β-D-ribo-pentofuranosyl]thymine 
• 129678-68-8 1-<5-O-(tert-butyldiphenylsilyl)-3-deoxy-3-C-(4,5-dihydro-5-methyl-1,3,5-dithiazin-2-yl)-2-O-(4-methoxytetrahydropyran-4-yl)-β-D-arabino-pentofuranosyl>thymine 

Relevant academic research and scientific papers

Synthesis of 2′-Substituted MMI Linked Nucleosidic Dimers: An Optimization Study in Search of High Affinity Oligonucleotides for Use in Antisense Constructs

The synthesis of a series of methylene(methylimino) (MMI) linked oligodeoxyribonucleotide dimers modified at the 2′-position with fluoro and/or methoxy groups and their incorporation into different sequences has been accomplished. From these dimers, bis 2

Synthesis of antiviral activity of 3'-deoxy-3'-C-hydroxymethyl nucleosides

A series of 3'-branched-chain sugar nucleosides, in particular 3'-deoxy-3'-C-hydroxymethyl nucleosides, have been synthesized and evaluated as antiviral agents. Reaction of 1-(2,3-epoxy-5-O-trityl-β-D-lyxo-pentafuranosyl) derivatives 12 and 13, of uracil