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- W2019019962 abstract "An efficient stereoselective synthesis of dendrobate alkaloid (+)-241D and its C-4 epimer was achieved from the inexpensive, commercially available starting material decanal (10) in an overall yield of 21.9% and 21.1%, respectively. This synthesis utilizes the key steps of Maruoka asymmetric allylation, one-pot epoxidation followed by nucleophilic addition of an organomagnesium reagent (Forsyth’s protocol) and subsequent functional group transformations." @default.
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- W2019019962 date "2010-02-01" @default.
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- W2019019962 title "Stereoselective synthesis of dendrobate alkaloid (+)-241D and its C-4 epimer" @default.
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- W2019019962 doi "https://doi.org/10.1016/j.tetlet.2009.12.111" @default.
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