132575-43-0Relevant academic research and scientific papers
Fischer indole synthesis with selected 2,3-dideoxy-D-glycero-aldopentose derivatives. Conversion of d-xylose to (2S)-3-(indol-3-YL)propane-1,2-diol
Lajsic, Stevan,Cetkovic, Gordana,Popsavin, Mirjana,Popsavin, Velimir,Miljkovic, Dusan
, p. 298 - 304 (2007/10/03)
Two independent routes towards (2S)-3-(indol-3-yl)propane-1,2-diol (11) were achieved starting from 3,5-di-O-acetyl-1,2-O-cyclohexylidene-α-D-xylofuranose (1). Ethanethiolysis of 1 afforded acyclic diethyl dithioacetal 2 which was further O-deacetylated t
Novel dideoxynucleoside isosteres
Nair, Vasu,Lyons, Arthur G.,Purdy, David F.
, p. 8949 - 8968 (2007/10/02)
Novel 5-aza-7-deaza isosteres of the anti-HIV compounds, dideoxyinosine (ddI) and dideoxyguanosine (ddG), have been prepared by glycosylation of the corresponding isosteric bases with appropriately tailored dideoxyribose components. The glycosylation reac
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.
