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- W2951796756 abstract "Abstract A novel and efficient process is described for the total synthesis of a dihydroxypyrrolidine alkaloid, (−)-codonopsinine in 33% overall yield. The synthetic strategy is based on the stereoselective reduction of an α-hydroxypyrrolidine intermediate, elaborated through asymmetric deoxygenation of a homochiral quaternary α-hydroxylactam." @default.
- W2951796756 created "2019-06-27" @default.
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- W2951796756 date "2010-08-04" @default.
- W2951796756 modified "2023-09-27" @default.
- W2951796756 title "ChemInform Abstract: Total Synthesis of Natural (-)-Codonopsinine Employing Stereoselective Reduction of Quaternary α-Hydroxypyrrolidine." @default.
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- W2951796756 doi "https://doi.org/10.1002/chin.199644236" @default.
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