A REGIO AND STEREOSELECTIVE SYNTHESIS OF 2',2'',3',4'-TETRADEUTERIO-2'-DEOXY NUCLEOSIDES

DOI: 10.1016/S0040-4020(01)83465-7

Source and publish data:

Tetrahedron p. 4227 - 4234 (1987)

Update date:2022-08-05

Topics:

Authors:

Pathak, T.

Chattopadhyaya, J.

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Article abstract of DOI:10.1016/S0040-4020(01)83465-7

Methyl β-D-arabinopyranoside (1) has been stereoselectively deuterated, by the treatment of deuterated Raney Ni in D2O, to give the 2,3,4-trideutereo-β-D-arabinopyranoside 2 in 33percent yield.It was then converted to 3,4-isopropylidene derivative 3b in 9

Full text of DOI:10.1016/S0040-4020(01)83465-7

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