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- W3177798413 endingPage "10581" @default.
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- W3177798413 abstract "The first and asymmetric total syntheses of two C11-oxygenated hetisine-type diterpenoid alkaloids, namely, (+)-davisinol and (+)-18-benzoyldavisinol, is described. The concise synthetic approach features a HAT-initiated transannular redox radical cyclization, an ODI-Diels-Alder cycloaddition, and an acylative kinetic resolution. By incorporating an efficient late-stage assembly of the azabicycle, our strategy would streamline the synthetic design of C20-diterpenoid alkaloids and pave the way for their modular syntheses." @default.
- W3177798413 created "2021-07-19" @default.
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- W3177798413 date "2021-07-09" @default.
- W3177798413 modified "2023-10-17" @default.
- W3177798413 title "Asymmetric Total Syntheses of (+)-Davisinol and (+)-18-Benzoyldavisinol: A HAT-Initiated Transannular Redox Radical Approach" @default.
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- W3177798413 doi "https://doi.org/10.1021/jacs.1c05703" @default.
- W3177798413 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34240855" @default.
- W3177798413 hasPublicationYear "2021" @default.
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