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 |
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