Synthesis and fucosidase inhibitory study of unnatural pyrrolidine alkaloid 4-epi-(+)-codonopsinine.

J Org Chem

Institut de Chimie Moléculaire de Reims, UFR Sciences, CNRS, BP 1039, 51687 Reims Cedex 2, France.

Published: May 2011

The total synthesis of enantiopure 4-epi-(+)-codonopsinine was achieved in 10 steps starting from D-ribose as a chiral building block. The key step involved a highly stereoselective nucleophilic addition of a Grignard reagent to a protected ribosylamine. Synthesis of the N-desmethyl derivative and its p-tolyl analogue was also accomplished, and the compounds were assayed against α-fucosidase.

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http://dx.doi.org/10.1021/jo200176uDOI Listing

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