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• W2783450153 abstract "The first enantioselective total synthesis of (−)-petromindole, an architecturally distinct congener of indole diterpene family, has been achieved. Key features of this synthetic route include the scalable and concise synthesis of tricyclic allylic alcohol from enantiopure Wieland–Mischer ketone derivative, and TMSOTf-mediated, highly efficient biomimetic C-4 cyclization of indole derivative for the rapid construction of a hexacyclic skeleton of petromindole." @default.
• W2783450153 created "2018-01-26" @default.
• W2783450153 creator A5042259011 @default.
• W2783450153 creator A5058956249 @default.
• W2783450153 date "2018-01-16" @default.
• W2783450153 modified "2023-09-25" @default.
• W2783450153 title "Biomimetic Enantioselective Total Synthesis of (−)-Petromindole" @default.
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• W2783450153 doi "https://doi.org/10.1021/acs.orglett.7b03768" @default.
• W2783450153 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29336573" @default.
• W2783450153 hasPublicationYear "2018" @default.
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