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Diastereoselective Synthesis of Salacinol-Type α-Glucosidase Inhibitors

Journal 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

Abstract AI-Helper 아이콘AI-Helper

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 = &...

참고문헌 (31)

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