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NTIS 바로가기Journal of organic chemistry, v.83 no.1, 2018년, pp.185 - 193
Ishikawa, Fumihiro (State Key Laboratory of Natural Medicines and Department of Medicinal Chemistry, China Pharmaceutical University, Nanjing 210009,) , Jinno, Kazumi , Kinouchi, Eri , Ninomiya, Kiyofumi , Marumoto, Shinsuke , Xie, Weijia , Muraoka, Osamu , Morikawa, Toshio , Tanabe, Genzoh
A facile and highly diastereoselective approach toward the synthesis of potent salacinol-type α-glucosidase inhibitors, originally isolated from plants of the genus “Salacia”, was developed using the S-alkylation of thiosugars with epoxides in HFIP (∼90%, dr, α/β = &...
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