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 |
|---|---|
| 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: | 17 Sep 2025 01:48 |
| 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 |

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