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• W1758780643 abstract "A stereoselective total synthesis of Stagonolide F (98% ee) is described employing asymmetric α-aminooxylation, Jorgensen’s asymmetric epoxidation, Brown asymmetric allylation, Steglich esterification and ring closing metathesis as key steps. The use of organocatalytic α-aminooxylation and Jorgensen’s asymmetric epoxidation of aldehydes for the introduction of chirality makes this approach more attractive." @default.
• W1758780643 created "2016-06-24" @default.
• W1758780643 creator A5026183074 @default.
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• W1758780643 date "2015-11-01" @default.
• W1758780643 modified "2023-10-17" @default.
• W1758780643 title "An efficient organocatalytic route for asymmetric total synthesis of Stagonolide F" @default.
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• W1758780643 doi "https://doi.org/10.1016/j.tetlet.2015.09.082" @default.
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