
Tetrahedron Letters p. 7957 - 7960 (1995)
Update date:2022-08-16
Topics:
Chen, Bang-Chi
Quinlan, Sandra L.
Stark, Derron R.
Reid, J. Gregory
Audia, Vicki H.
et al.
The anti-AIDS drug d4T is prepared in 75percent overall yiled starting from the readily available ribonucleoside 5-methyluridine (1).The key step in this new synthesis is the zinc-induced reductive elimination of the bromomesylate 4, which affords d4T without nucleoside bond cleavage.A facile procedure for the deprotection/isolation of this highly water soluble product is also described.
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