167641-89-6Relevant academic research and scientific papers
Radical Mediated Synthesis of 3'-α-C-allenyl-2',3'-dideoxythymidine as a non-polar analogue of AZT
Becouarn, Stephan,Czernecki, Stanislas,Valery, Jean-Marc
, p. 873 - 876 (1995)
The 1,2-propadienyl (allenyl) group was selectively introduced at the 3'-α-C position by free radical C-C bond formation reaction involving triphenylprop-2-ynylstannane and protected 2',3'-dideoxy-3'-halogenothymidine.
Radical mediated synthesis of 3'-α-C-allenyl-2',3'-dideoxythymidine as a non-polar analogue of AZT
Becouarn,Czernecki,Valery
, p. 307 - 309 (2007/10/02)
The synthesis of the novel modified nucleoside (1) exhibiting the 1,2- propadienyl [allenyl] group at the 3'-α-position is described. The 3'-C-C bond was formed by radical reaction between triphenylprop 2-ynylstannane (2) and the 3'-bromo(iodo)-2',3'-dide
