Rossi-Ashton, James A, Clarke, Aimee K, Taylor, Richard J K orcid.org/0000-0002-5880-2490 et al. (1 more author) (2020) Modular Synthesis of Polycyclic Alkaloid Scaffolds via an Enantioselective Dearomative Cascade. Organic Letters. 1175–1181. ISSN 1523-7052
Abstract
The polycyclic core of the akuammiline alkaloids can be synthesized from simple tryptamine and tryptophol derivatives via a Ag(I)-catalyzed enantioselective dearomative cyclization cascade sequence. The complex tetracyclic scaffolds are prepared via a rapid, versatile, three-step modular synthesis from simple commercially available indole derivatives in high yields and enantiomeric excess (up to 99% yield and >99% ee).
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2020 American Chemical Society. |
Dates: |
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Institution: | The University of York |
Academic Units: | The University of York > Faculty of Sciences (York) > Chemistry (York) |
Funding Information: | Funder Grant number EPSRC EP/R013748/1 |
Depositing User: | Pure (York) |
Date Deposited: | 23 Jan 2020 10:20 |
Last Modified: | 11 Apr 2025 23:21 |
Published Version: | https://doi.org/10.1021/acs.orglett.0c00053 |
Status: | Published |
Refereed: | Yes |
Identification Number: | 10.1021/acs.orglett.0c00053 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:155905 |