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
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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: |
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Depositing User: | Pure (York) | ||||
Date Deposited: | 23 Jan 2020 10:20 | ||||
Last Modified: | 07 Dec 2022 14:25 | ||||
Published Version: | https://doi.org/10.1021/acs.orglett.0c00053 | ||||
Status: | Published | ||||
Refereed: | Yes | ||||
Identification Number: | https://doi.org/10.1021/acs.orglett.0c00053 |