105454-46-4Relevant academic research and scientific papers
Enantiospecific synthesis of the heparanase inhibitor (+)-trachyspic acid and stereoisomers from a common precursor
Zammit, Steven C.,Ferro, Vito,Hammond, Edward,Rizzacasa, Mark A.
, p. 2826 - 2834 (2008/03/14)
The total synthesis of natural (+)-trachyspic acid and its enantiomer is described starting from a common 2-deoxy-d-ribose derivative. The synthesis of the corresponding C3 epimers from the same starting material is also described. Each stereoisomer was a
Synthesis of erythro and threo furanoid glycals from 1- and 2-phenylselenenyl-carbohydrate derivatives
Bravo, Fernando,Kassou, Mohamed,Diaz, Yolanda,Castillon, Sergio
, p. 83 - 97 (2007/10/03)
Differently protected erythro and threo furanoid glycals were synthesized by selenoxide elimination when phenyl 1-selenoglycosides were treated in oxidizing conditions (tBuOOH, Ti(OiPr)4, Et2iPrN). Th
2-deoxyuridines and riboside precursors
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, (2008/06/13)
A process is provided for the preparation of certain 2-deoxyuridines including the steps forming a substituted alkyl 5-O-"protected"-2-deoxyribofuranoside, hydrocarbylating the latter compound, and condensing the hydrocarbylated compound in the presence o
3-Azido-2,3-dideoxy-D-erythropentose:A Precursor for 3'-Azido-3'-deoxythymidine (AZT)
Gurjar, M. K.,Ashok, B.,Rao, A. V. Rama
, p. 905 (2007/10/02)
3-Azido-2,3-dideoxy-D-erythropentose, a precursor for AIDS drug AZT, has been synthesised from D-xylose.
