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- W2019296059 endingPage "10503" @default.
- W2019296059 startingPage "10487" @default.
- W2019296059 abstract "A direct approach to the synthesis of indolizidine and quinolizidine scaffolds of iminosugars is described. The presented strategy is based on a one-pot sugar lactam reduction with Schwartz’s reagent followed by a diastereoselective Mannich/Michael tandem reaction of the resulting sugar imine with Danishefsky’s diene. The stereochemical course of the investigated reaction has been explained in detail. The obtained bicyclic products are attractive building blocks for the synthesis of various naturally occurring polyhydroxylated alkaloids and their derivatives." @default.
- W2019296059 created "2016-06-24" @default.
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- W2019296059 creator A5018671619 @default.
- W2019296059 date "2014-10-30" @default.
- W2019296059 modified "2023-10-17" @default.
- W2019296059 title "Synthesis of Polyhydroxylated Quinolizidine and Indolizidine Scaffolds from Sugar-Derived Lactams via a One-Pot Reduction/Mannich/Michael Sequence" @default.
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