75721-41-4Relevant academic research and scientific papers
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
Zylber, J.,Pontikis, R.,Merrien, A.,Merienne, C.,Baran-Marszak, M.,Gaudemer, A.
, p. 1579 - 1584 (1980)
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,
