86710-51-2

Upstream product

• 68892-41-1 5'-O-dimethoxytrityl-N-isobutyryldeoxyguanosine 
• 123-76-2 levulinic acid 
• 591-12-8 5-methyl-2-furanone 

Downstream Products

• 93134-54-4 Phosphoric acid (2R,3S,5R)-5-(6-benzoylamino-purin-9-yl)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-yl ester (2R,3S,5R)-3-hydroxy-5-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-tetrahydro-furan-2-ylmethyl ester methyl ester 
• 93134-56-6 C₅₀H₅₇N₁₀O₁₄P 
• 93134-47-5 C₅₁H₅₈N₇O₁₆P 
• 93134-55-5 C₅₂H₅₅N₈O₁₄P 
• 93134-57-7 C₄₆H₅₂N₇O₁₄P 
• 656249-33-1 C₅₇H₆₄N₁₁O₁₅PS 
• 656249-32-0 C₅₇H₆₄N₁₁O₁₅P 
• 90678-70-9 2-N-isobutyryl-6-O-(cyanoethyl)-5'-O-dimethoxytrityl-3'-O-levulinyl-2'-deoxyguanosine 
• 93134-41-9 N²-isobutyryl-3'-O-levulinyl-2'-deoxyguanosine 

Relevant academic research and scientific papers

Oligodeoxyribonucleotide phosphorothioates: Substantial reduction of (N- 1)-mer content through the use of trimeric phosphoramidite synthons

Use of fully protected trimeric phosphoramidite synthons in the synthesis of oligonucleotide phosphorothioate shows a substantial reduction (>85%) in (n-1)-mer content as compared to oligomers synthesized through coupling of standard phosphoramidite monom

2,2,5,5-Tetramethylpyrrolidin-3-one-1-sulfinyl group for 5′-hydroxyl protection of deoxyribonucleoside phosphoramidites in the solid-phase preparation of DNA oligonucleotides

Several nitrogen-sulfur reagents have been investigated as potential 5′-hydroxyl protecting groups for deoxyribonucleoside phosphoramidites to improve the synthesis of oligonucleotides on glass microarrays. Out of the nitrogen-sulfur-based protecting grou

Improvements in Oligodeoxyribonucleotide Synthesis: Methyl N,N-Dialkylphosphoramidite Dimer Units for Solid Support Phosphite Methodology

Two procedures for the synthesis of methyl N,N-dialkylphosphoramidite dinucleotides (dimer units) compatible with the current solid support phosphite methodology of oligodeoxynucleotide synthesis are described for the first time.In the first procedure a c