79535-83-4

Upstream product

• 42506-03-6 pixyl chloride 
• 79527-11-0 6-N-(m-chlorobenzoyl)-2'-deoxyadenosine 

Downstream Products

• 79527-45-0 C₆₃H₅₅Cl₂N₁₀O₁₁P 
• 79527-44-9 Phosphoric acid (2R,3S,5R)-5-[6-(3-chloro-benzoylamino)-purin-9-yl]-3-hydroxy-tetrahydro-furan-2-ylmethyl ester (2R,3S,5R)-5-[6-(3-chloro-benzoylamino)-purin-9-yl]-2-(9-phenyl-9H-xanthen-9-yloxymethyl)-tetrahydro-furan-3-yl ester 2-chloro-phenyl ester 
• 79526-72-0 C₄₁H₃₇Br₃Cl₃N₇O₁₄P₂ 
• 79535-65-2 C₆₀H₄₉Br₃Cl₃N₇O₁₅P₂ 
• 79527-47-2 C₆₃H₅₅Cl₂N₁₀O₁₂P 

Relevant academic research and scientific papers

2-(TRIMETHYLSILYL)ETHYL CHLOROFORMATE: A CONVENIENT REAGENT FOR PROTECTION OF HYDROXYL FUNCTION

2-(Trimethylsilyl)ethyl chloroformate reacts with alcohols to give carbonates in high yield. n-Bu4NF in THF(0.2M) solution for 10 min or ZnBr2 or ZnCl2 in CH3NO2 for 10 min regenerate the alcohol at 20 deg C.

A General Approach to the Chemical Synthesis of Oligodeoxyribonucleotides

A general procedure for the synthesis of oligodeoxynucleotides has been described using 9-phenylxanthen-9-yl as a 5'-protecting group.The building blocks 9 and 11, all sixteen of them in each category (Tables 2 and 3), have been unambiguously synthesized