Liddon, John T R orcid.org/0000-0002-5287-9817, James, Michael J. orcid.org/0000-0003-2591-0046, Clarke, Aimee K. et al. (3 more authors) (2016) Catalyst-driven scaffold diversity : selective synthesis of spirocycles, carbazoles and quinolines from indolyl ynones. Chemistry : A European Journal. 8777–8780. ISSN 1521-3765
Abstract
Medicinally relevant spirocyclic indolenines, carbazoles and quinolines can each be directly synthesised selectively from common indolyl ynone starting materials by catalyst variation. The high yielding, divergent reactions all proceed via an initial dearomatising spirocyclisation reaction to generate an intermediate vinyl metal species which then rearranges selectively by careful choice of catalyst and reaction conditions.
Metadata
Authors/Creators: |
|
---|---|
Copyright, Publisher and Additional Information: | © 2016, The publisher. This is an author-produced version of the published paper. Uploaded in accordance with the publisher’s self-archiving policy. Further copying may not be permitted; contact the publisher for details |
Keywords: | carbazoles, catalysis, diversity, quinolines, spirocycles, Stereoisomerism, Spiro Compounds/chemical synthesis, Indoles/chemistry, Carbazoles/chemical synthesis, Mesylates/chemistry, Quinolines/chemical synthesis |
Dates: |
|
Institution: | The University of York |
Academic Units: | The University of York > Faculty of Sciences (York) > Chemistry (York) |
Depositing User: | Pure (York) |
Date Deposited: | 17 May 2016 10:03 |
Last Modified: | 09 Mar 2023 00:12 |
Published Version: | https://doi.org/10.1002/chem.201601836 |
Status: | Published |
Refereed: | Yes |
Identification Number: | https://doi.org/10.1002/chem.201601836 |
Related URLs: |
Downloads
Filename: Liddon_et_al_2016_Chemistry_A_European_Journal.pdf
Description: Liddon_et_al-2016-Chemistry_-_A_European_Journal
Filename: John_Liddon_paper_version_8_revised_for_transfer_to_CEJ.docx
Description: John Liddon paper version 8- revised for transfer to CEJ