New deoxynojirimycin derivatives as potent inhibitors of intestinal α-glucohydrolases
摘要:
New N-alkyl, alkenyl and benzyl substituted DNJ derivatives incorporating a silicon atom in the substituent were synthesised. Kinetic parameters (K-i, t(1/2)) for inhibition of rat intestinal alpha-glucohydrolases as well as human lysosomal alpha-glucosidases were measured. New DNJ derivatives are potent and selective inhibitors of intestinal alpha-glucohydrolases. (C) 1997, Elsevier Science Ltd.
DOI:
10.1016/s0960-894x(97)00012-7
作为产物:
描述:
3-氯丙基二甲基苯基硅烷 、 碘化钠 在
乙醚 、 水 、 Sodium sulfate-III 作用下,
以
丙酮 为溶剂,
反应 24.0h,
以to afford pure dimethyl(3-iodopropyl)phenylsilane as a slightly yellow oil (12.5 g, 93%)的产率得到dimethyl(3-iodopropyl)phenylsilane