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- W2057353118 abstract "An efficient strategy for the stereocontrolled synthesis of (−)-bulgecinine hydrochloride 1 was accomplished by utilizing a Wittig Horner olefination, stereoselective reduction of the double bond and intramolecular N-alkylation to furnish the target." @default.
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- W2057353118 date "2006-11-01" @default.
- W2057353118 modified "2023-09-27" @default.
- W2057353118 title "Stereoselective synthesis of (−)-bulgecinine hydrochloride and its C-2 epimer from l-ascorbic acid" @default.
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- W2057353118 doi "https://doi.org/10.1016/j.tetasy.2006.10.033" @default.
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