
Tetrahedron p. 2719 - 2728 (1995)
Update date:2022-08-12
Topics:
Pickering
Malhi
Coe
Walker
The preparation of 4'-methyloxycarbamyl-3'-deoxythymidine from chiral amino acid precursors is described. The route chosen employs a hitherto unreported electrochemical oxidation of a suitably protected derivative of trans-4-hydroxy-L-proline, to obtain the key intermediate compound. Conventional condensation methodology is then used to arrive at the target nucleoside.
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Doi:10.1021/jm00158a026
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(1982)Doi:10.1039/c8nj00606g
(2018)Doi:10.1016/j.bmc.2018.05.036
(2018)Doi:10.1039/d0cy01603a
(2020)Doi:10.1016/S0040-4039(00)90615-4
(1967)