71508-05-9

Upstream product

• 77128-72-4 N-(9-fluorenylmethoxycarbonyl)-O-methyl-L-tyrosine 
• 65109-11-7 2',5'-bis-O-(tert-butyldimethylsilyl)adenosine 
• 1273196-83-0 9-[3-bromo-5-O-tert-butyldiphenylsilyl-3-deoxy-2-O-(N-vinylcarbamoyl)-β-D-xylofuranosyl]adenine 
• 1273196-85-2 C₂₉H₃₂N₆O₄Si 
• 1273196-87-4 3'-amino-5'-O-(tert-butyldiphenylsilyl)-3-deoxyadenosine 
• 1273196-89-6 5'-O-(tert-butyldiphenylsilyl)-3'-[N-(9-fluorenyl)methoxycarbonyl-O-methyl-L-tyrosyl]amido-3'-deoxyadenosine 
• 2627-64-7 9-(2,3-anhydro-β-D-ribofuranosyl)adenine 
• 125084-70-0 9-<2,3-anhydro-5-O-<(tert-butyl)diphenylsilyl>-β-D-ribofuranosyl>adenine 
• 125084-68-6 9-<3-bromo-5-O-<(tert-butyl)diphenylsilyl>-3-deoxy-β-D-xylofuranosyl>adenine 
• 58-61-7 adenosine 
• 118525-25-0 9-[2',5'-bis-(O-tert-butyldimethylsilyl)-β-D-xylofuranosyl]-9H-adenine 
• 86734-95-4 9-(2,5-di-O-tert-butyldimethylsilyl-β-D-erythro-pentofuran-3-ulosyl)adenosine 

Relevant academic research and scientific papers

Shorter puromycin analog synthesis by means of an efficient Staudinger-Vilarrasa coupling

An efficient Staudinger-Vilarrasa coupling generates amides from azides and 1-hydroxybenzotriazole esters of amino- or hydroxy acid derivatives in very high isolated yields and purity. New puromycin analogs, mostly putative biosynthetic intermediates, wer

A practical route to 3′-amino-3′-deoxyadenosine derivatives and puromycin analogues

3′-Aminoacylamino-3′-deoxyadenosines, analogues of the antibiotic puromycin, have been synthesized from adenosine. They key 3′-azido derivative 10 was obtained through a 3′-oxidation/reduction/substitution procedure. A modified purification protocol on a

High-yield immobilization of a puromycin analogue for the solid support synthesis of aminoacyl-tRNA fragments

(Matrix presented) An efficient procedure for the immobilization of 3′-deoxy-3′-(O-methyltyrosyl)aminoadenosine was developed. A poly(ethylene glycol)-derived diacid linker/spacer was attached to aminomethyl polystyrene. Coupling of the 2′-hydroxy instead

The shortest synthetic route to puromycin analogues using a modified robins approach

We are reporting on the utility of commercial vinyl isocyanate for a practical synthetic route from adenosine to N6-bis-demethylpuromycin in seven steps and 65% overall yield. A clean one-pot conversion of 3′-bromo-2′-carbamoyl derivative 8 to

Facile and rapid access to inosine puromycin analogues through the use of adenylate deaminase

To study the ribosomal peptidyl transfer, puromycin analogues are of interest in which adenine has been replaced by hypoxanthine. We synthesized inosine puromycin analogues from 3′-azidodeoxyadenosine derivatives using adenylate deaminase for the quantita