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- W2952379551 abstract "The first enantioselective total syntheses of architecturally interesting prenylated pyrroloindole alkaloids, (−)-pseudophrynamines 272A (3d) and 270 (3b), have been achieved starting from enantioenriched 2-oxindoles having all-carbon quaternary stereocenters. A common strategy involving a thio-urea catalyzed aldol reaction is employed for the total synthesis of both spiro(pyrrolidinyl-oxindole) and hexahydropyrrolo[2,3-b]indole alkaloids." @default.
- W2952379551 created "2019-06-27" @default.
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- W2952379551 date "2016-04-01" @default.
- W2952379551 modified "2023-09-23" @default.
- W2952379551 title "ChemInform Abstract: Unified Approach to the Spiro(pyrrolidinyl-oxindole) and Hexahydropyrrolo[2,3-b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A." @default.
- W2952379551 cites W2306203053 @default.
- W2952379551 doi "https://doi.org/10.1002/chin.201617121" @default.
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