57731-92-7

Upstream product

• 57731-88-1 N⁶,N⁶-dibenzoyl-5'-deoxy-5'-iodo-2',3'-O-isopropylideneadenosine 
• 138840-71-8 5'-Anisyltelluro-5'-deoxy-2',3'-O-isopropylidene-6-N,N'-dibenzoyl-adenosine 
• 75765-67-2 O-isopropylidene-2',3' N,N'-dibenzoyl-6 dihydro-7,8 cyclo-5',8 desoxy-5 adenosine 
• 40982-79-4 N⁶,N⁶-dibenzoyl-5'-O-mesyl-2',3'-O-isopropylidene adenosine 
• 57731-93-8 (8Ξ)-N⁶,N⁶-dibenzoyl-O^2',O^3'-isopropylidene-7,8-dihydro-8,5'-cyclo-5'-deoxy-adenosine 

Relevant academic research and scientific papers

Synthesis of 5′,8-cyclopurine and of 5′,6-cyclodihydropyrimidine nucleosides using intramolecular radical cyclisation based on the aryl telluride radical exchange process

The synthesis of C-cyclopurine and C-cyclodihydropyrimidine nucleosides has been effected using 5′-aryltelluronucleosides. Generation of methyl radicals from the photolysis of the acetyl derivative of N-hydroxy-2-thiopyridone permitted, by radical exchang

SYNTHESE DE LA CYCLO-5'-8 DESOXY-5' ADENOSINE: STEREOCHIMIE ET MECHANISME DE LA CYCLISATION D'UN DERIVE DE L'IODO-5' ADENOSINE PAR LE ZINC

N,N'-Dibenzoyl 2',3'-O-isopropylidene 5'-deoxy 5'-iodo adenosine can efficiently transformed into the corresponding 5',8-cyclo-7,8-dihydronucleoside by zinc in pyridine.Only one diastereoisomer is obtained.By spin decoupling and NOE techniques at 250 MHz,