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

DOI: 10.1016/S0040-4020(01)83125-2

Source and publish data:

Tetrahedron p. 1579 - 1584 (1980)

Update date:2022-08-04

Topics:

Authors:

Zylber, J.

Pontikis, R.

Merrien, A.

Merienne, C.

Baran-Marszak, M.

Gaudemer, A.

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Article abstract of DOI:10.1016/S0040-4020(01)83125-2

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,

Full text of DOI:10.1016/S0040-4020(01)83125-2

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