Harrity, J.P.A., Mora, H., Sotorrios, L. et al. (5 more authors) (2018) Synthetic and Mechanistic Investigation of an Oxime Ether Electrocyclization Approach to Heteroaromatic Boronic Acid Derivatives. Chemistry - A European Journal, 24 (38). pp. 9530-9534.
Abstract
E-oxime ethers are found to be significantly more reactive in electrocyclizations than their Z-counterparts because of an available transition state stabilizing orbital interaction in the former case. The scope of this chemistry to deliver useful heterocyclic products is also described.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | This is the peer reviewed version of the following article: Harrity, J. ., Mora, H. , Sotorrios, L. , Ball-Jones, M. , Bialy, L. , Czechtizky, W. , Mendez, M. and Gomez-Bengoa, E. (2018), Synthetic and Mechanistic Investigation of an Oxime Ether Electrocyclization Approach to Heteroaromatic Boronic Acid Derivatives. Chem. Eur. J., which has been published in final form at https://doi.org/10.1002/chem.201802350. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving. |
Keywords: | electrocyclization; heteroaromic; boronic ester; stereochemistry |
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: | 15 May 2018 11:01 |
Last Modified: | 02 Dec 2020 08:39 |
Status: | Published |
Publisher: | Wiley |
Refereed: | Yes |
Identification Number: | 10.1002/chem.201802350 |
Related URLs: | |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:130779 |