Diastereoselective Synthesis of (Aryloxy)phosphoramidate Prodrugs was written by Arbelo Roman, Cristina;Wasserthal, Philip;Balzarini, Jan;Meier, Chris. And the article was included in European Journal of Organic Chemistry in 2011.Recommanded Product: 76186-04-4 This article mentions the following:
The first diastereoselective synthesis of aryloxyphosphoramidate prodrugs of 3′-deoxy-2′,3′-didehydrothymidine monophosphate (d4TMP) was recently reported. The synthetic approach utilized the chiral auxiliary (S)-4-isopropylthiazolidine-2-thione. For this strategy, a stereochem. pure phosphorodiamidate intermediate was needed. The diastereoselective formation of this key compound was investigated by using different phenols and
(S)-4-Isopropylthiazolidine-2-thione (cas: 76186-04-4) belongs to thiazolidine derivatives. Thiazolidine motifs are very intriguing heterocyclic five-membered moieties present in diverse natural and bioactive compounds having sulfur at the first position and nitrogen at the third position. In addition, the use of thiazolidines as an inhibitor of tyrosyl-DNA phosphodiesterase Iand influenza neuraminidase, pro-drugs for the treatment of cystinosis, radioprotective against γ-irradiation and as S1P1 receptor agonist has also been reported.Recommanded Product: 76186-04-4
Referemce:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com