219653-06-2

Upstream product

• 278168-48-2 Methanesulfonic acid (2R,3S,5R)-2-({[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-methyl)-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 
• 102368-13-8 1,1'-Thiocarbonyldi-2(1H)-pyridone 
• 209255-51-6 5'-monomethoxytritylamino-3'-amino-2',3',5'-trideoxythymidine 
• 14470-28-1 mono-4-methoxytrityl chloride 
• 209255-49-2 1-[(2R,4S,5R)-4-Azido-5-({[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-methyl)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidine-2,4-dione 
• 209255-47-0 (1R,9R,10R)-10-({[(4-Methoxy-phenyl)-diphenyl-methyl]-amino}-methyl)-4-methyl-8,11-dioxa-2,6-diaza-tricyclo[7.2.1.0^2,7]dodeca-3,6-dien-5-one 
• 118849-15-3 5'-N-(4-methoxytrityl)-5'-amino-5'-deoxy-thymidine 
• 25152-20-9 5'-amino-5'-deoxythymidine 

Relevant academic research and scientific papers

Solid-phase synthesis of oligomeric deoxynucleic-thiourea (DNT) and deoxynucleic S-methylthiourea (DNmt): A neutral/polycationic analogue of DNA

A solid-phase synthesis for oligomeric DNmt is reported. Synthesis proceeds in 3'-5' direction and involves coupling of a protected 3'-isothiocyanate with the corresponding 5'-amine of the growing oligo chain. The difference in oligomeric thiourea/S-methy