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- W2398840382 endingPage "5536" @default.
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- W2398840382 abstract "An efficient and novel strategy for the enantioselective syntheses of various iboga alkaloids has been developed. The salient features include a gold-catalyzed oxidation of a terminal alkyne followed by cyclization, a Stevens rearrangement and a tandem sequence that combines the gold-catalyzed oxidation, cyclization and [1,2]-shift. The catharanthine analogs provided by our approach were further converted to the vinca alkaloid vinblastine and its analogs, which confirmed the remarkable sensitivity of the cytotoxicity to the C20' substituent of vinblastine." @default.
- W2398840382 created "2016-06-24" @default.
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- W2398840382 creator A5074942308 @default.
- W2398840382 date "2016-01-01" @default.
- W2398840382 modified "2023-10-01" @default.
- W2398840382 title "Enantioselective synthesis of Iboga alkaloids and vinblastine via rearrangements of quaternary ammoniums" @default.
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- W2398840382 doi "https://doi.org/10.1039/c6sc00932h" @default.
- W2398840382 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6021789" @default.
- W2398840382 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30034694" @default.
- W2398840382 hasPublicationYear "2016" @default.
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