219661-90-2Relevant academic research and scientific papers
The stereoselective total synthesis of PF1163A
Kumar, Harish,Reddy, A. Srinivas,Reddy, B.V. Subba
supporting information, p. 1519 - 1522 (2014/03/21)
A stereoselective total synthesis of 13-membered macrocycle PF1163A, an antifungal agent, has been accomplished for the first time starting from d-xylose. This approach involves a diastereoselective allylation of lactal ether,3a reductive ring
Synthesis and antiviral evaluation of 2'-deoxy-4'-thio-L-nucleosides and their phosphotriester derivatives bearing S-acyl-2-thioethyl bioreversible phosphate-protecting groups
De Valette,Barascut,Imbach
, p. 2289 - 2310 (2007/10/03)
A new route to 2-deoxy-4-thio-L-ribofuranose and the synthesis of some 4'-thio-L-nucleosides are reported. Also, the bis(SATE) phosphotriester derivatives of 2'-deoxy-4'-thio-L-cytidine and -adenosine were synthesized and their biological activities are discussed.
