
Tetrahedron Letters p. 2379 - 2382 (1992)
Update date:2022-09-26
Topics:
Nikiforov, Theo T.
Conolly, Bernard A.
The title compound was prepared in four steps and 62percent yield from thymidine.After incorporation into synthetic oligodeoxynucleotides, the S-(2-cyanoethyl) group was removed by treatment with DBU in CH3CN to give products containing 4-thiothymidine residues.
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Doi:10.1021/np300544a
(2012)Doi:10.3184/174751914X14102462623785
(2014)Doi:10.1016/0008-6215(92)84132-C
(1992)Doi:10.1039/c5ob00847f
(2015)Doi:10.1007/s10600-013-0441-3
(2013)Doi:10.1039/j39660001950
(1966)