Maduli, E.J.M., Edeson, S.J., Swanson, S. et al. (2 more authors) (2015) 2-Iodoisatogens: Versatile Intermediates for the Synthesis of Nitrogen Heterocycles. Organic Letters, 17 (2). 390 - 392. ISSN 1523-7060
Abstract
A Cu-promoted cyclization of 2-nitrophenyl iodoacetylenes provides a direct route to a range of 2-iodoisatogens. These compounds represent useful intermediates for the late-stage elaboration of the C–I bond to furnish isatins and a range of alternative heterocyclic products.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2014 American Chemical Society. This is an author produced version of a paper subsequently published in Organic Letters. Uploaded in accordance with the publisher's self-archiving policy. |
Dates: |
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Institution: | The University of Sheffield |
Academic Units: | The University of Sheffield > Faculty of Science (Sheffield) > Department of Chemistry (Sheffield) |
Depositing User: | Symplectic Sheffield |
Date Deposited: | 01 Oct 2015 15:42 |
Last Modified: | 23 Mar 2018 10:45 |
Published Version: | http://dx.doi.org/10.1021/ol503487f |
Status: | Published |
Publisher: | American Chemical Society |
Refereed: | Yes |
Identification Number: | 10.1021/ol503487f |
Related URLs: | |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:90393 |