Mora-Radó, H., Bialy, L., Czechtizky, W. et al. (2 more authors) (2016) An Alkyne Diboration/6π-Electrocyclization Strategy for the Synthesis of Pyridine Boronic Acid Derivatives. Angewandte Chemie International Edition, 55 (19). pp. 5834-5836. ISSN 1433-7851
Abstract
A new and efficient synthesis of pyridine-based heteroaromatic boronic acid derivatives is reported through a novel diboration/6π-electrocyclization strategy. This method delivers a range of functionalized heterocycles from readily available starting materials.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. This is an author produced version of a paper subsequently published in Angewandte Chemie International Edition. Uploaded in accordance with the publisher's self-archiving policy. |
Keywords: | Boronic esters; diboration; electrocyclic reactions; nitrogen heterocycles; synthetic methods |
Dates: |
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Institution: | The University of Sheffield |
Academic Units: | The University of Sheffield > Faculty of Science (Sheffield) > Department of Chemistry (Sheffield) |
Funding Information: | Funder Grant number EUROPEAN COMMISSION - FP6/FP7 COSSHNET - 606734 |
Depositing User: | Symplectic Sheffield |
Date Deposited: | 20 Apr 2016 08:29 |
Last Modified: | 14 Apr 2017 03:06 |
Published Version: | http://dx.doi.org/10.1002/anie.201601084 |
Status: | Published |
Publisher: | Wiley |
Refereed: | Yes |
Identification Number: | 10.1002/anie.201601084 |
Related URLs: | |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:98421 |