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- W2014967422 abstract "While there are a few reports for the asymmetric allylation of imines, the addition of allyl substrates to cyclic imines remains a challenge. Using conditions similar to a report by Shibasaki and co-workers (J. Am. Chem. Soc. 2002, 124, 6536-6537), the authors obtained their desired product in 91% yield and 71% ee. One recrystallization with (-)-dibenzoyl-l-tartaric acid afforded their compound with 97% ee. This compound was then carried on to complete the synthesis of (-)-Emetine." @default.
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- W2014967422 date "2006-06-01" @default.
- W2014967422 modified "2023-10-18" @default.
- W2014967422 title "(-)-Emetine Synthesis via Asymmetric Allylation of Cyclic Imines" @default.
- W2014967422 doi "https://doi.org/10.1055/s-2006-941818" @default.
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