volume 3, issue 3, P337-339 2012
DOI: 10.5155/eurjchem.3.3.337-339.609
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Abstract: A formal stereoselective synthesis of Herbarumin III has been accomplished starting from butanal involving Maruoka asymmetric allylation, diastereoselective iodine-induced electrophilic cyclization and conversion of iodocarbonate into syn-epoxy alcohol as the key steps.Nonenolide Phytotoxic effect Syn-epoxy alcohol Maruoka allylation Trimethylsulfonium iodide Diastereoselective iodine-induced electrophilic cyclization

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