16801-99-3Relevant 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 3'-O-(2-aminoethyl)-2'-deoxyuridines.
Abdel Aleem,Larsen,Pedersen,Nielsen
, p. 609 - 614 (2007/10/02)
Methyl 2-deoxy-3-O-[2-(formylamino)ethyl]-5-O-trityl-D-erythro- pentofuranoside (4) was obtained in a 3-O alkylation reaction by treatment with 2-chloroethylamine in DMF. Compound 4 afforded alpha nucleosides as the main products when condensed with uraci
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.
