Al-Saedy, M.A.E. and Harrity, J.P.A. (2016) Synthesis and Stabilities of 3-Borylated Indoles. Synlett, 27 (11). pp. 1674-1676. ISSN 0936-5214
Abstract
We report herein that 3-pinacol boronic esters undergo facile protodeborylation in the presence of palladium catalysts and base, and this contributes significantly to the generation of nonborylated indole byproducts in the B2Pin2-mediated palladium-catalysed borylative cyclization of 2-alkynylanilides. Suginome’s reagent provides an alternative method to access 3-borylated indoles as these compounds are less susceptible to protodeborylation.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2016 Georg Thieme Verlag Stuttgart · New York. This is an author produced version of a paper subsequently published in Synlett. Uploaded in accordance with the publisher's self-archiving policy. |
Keywords: | Palladium; cyclisation; indoles; boronic ester; protodeborylation |
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: | 20 Apr 2016 10:59 |
Last Modified: | 17 Apr 2017 22:25 |
Published Version: | http://dx.doi.org/10.1055/s-0035-1561944 |
Status: | Published |
Publisher: | Georg Thieme Verlag |
Refereed: | Yes |
Identification Number: | 10.1055/s-0035-1561944 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:98137 |