epohelmin-b has been researched along with allyl-bromide* in 1 studies
1 other study(ies) available for epohelmin-b and allyl-bromide
Article | Year |
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Asymmetric syntheses of epohelmins A and B by In-mediated allylation.
A diastereoselective new approach for the synthesis of trans-4-hydroxy-5-allyl-2-pyrrolidinone 9 has been developed through In-mediated allylation of α-chiral aldimine 8 with allyl bromide. The stereochemistry at the C-2 stereogenic center of 9 was controlled by both the α-OTBS substitution and the sulfinamide moiety. The utility of this asymmetric allylation is demonstrated by the asymmetric syntheses of epohelmins A (4) and B (10). Topics: Allyl Compounds; Bridged Bicyclo Compounds, Heterocyclic; Pyrrolidinones; Stereoisomerism; Sulfonium Compounds | 2016 |