122621-07-2Relevant articles and documents
Radical mediated synthesis of 3'-α-C-allenyl-2',3'-dideoxythymidine as a non-polar analogue of AZT
Becouarn,Czernecki,Valery
, p. 307 - 309 (1995)
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
Synthesis of 2'-Deoxyribonucleosides: ?-3',5'-Di-O-benzoylthymidine [ Thymidine, 3',5'-dibenzoate ]
Prudhomme, Daniel R.,Park, Minnie,Wang, Zhiwei,Buck, Jason R.,Rizzo, Carmelo J.,Chambournier, Gilles,Djung, Jane,Hart, David J.
, p. 162 - 162 (2017/09/30)
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STEREOSELECTIVITIES IN THE COUPLING REACTION BETWEEN SILYLATED PYRIMIDINE BASES AND 1-HALO-2,3-DIDEOXYRIBOSE
Kawakami, Hiroshi,Ebata, Takashi,Koseki, Koshi,Matsumoto, Katsuya,Matsushita, Hajime,et al.
, p. 2041 - 2054 (2007/10/02)
Coupling reactions between 1-chloro-2,3-dideoxyribose and silylated pyrimidines have been examined from the point of stereoselectivity.When the reaction was carried out in chloroform, the selectivity was in the anomeric ratio of α:β = 4:6.On the other hand, the presence of tertiary amine raises the selectivity to α:β = 3:7.