Novel 2-aryl-3,4,5-trihydroxypiperidines: Synthesis and glycosidase inhibition

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摘要 Threepairsofnovel2-aryl-3,4,5-trihydroxypiperidines(6–8andtheirenantiomers),thepiperidineanaloguesofthepyrrolidinealkaloidsradicamineAandradicamineB,werepreparedfromsixmemberedcyclicnitronesthroughaconcisetwo-stepprocedure,i.e.,Grignardreagentadditionanddeprotection.Thesenovelpolyhydroxylatedpiperidineiminosugarswereassayedagainst10typesofenzymes.Onlycompound8exhibitedweakinhibition(IC501080mmol/L)againstb-galactosidasefromratintestinallactases.
机构地区 不详
出版日期 2013年12月22日(中国期刊网平台首次上网日期,不代表论文的发表时间)
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