Harrity, J.P.A., Brown, A. and Comas-Barcelo, J. (2017) A Mild and Regiospecific Synthesis of Pyrazoleboranes. Chemistry - A European Journal , 23 (22). pp. 5228-5231. ISSN 0947-6539
Abstract
Alkynylboranes show unprecedented reactivity in their [4 + 2] cycloaddition of sydnones offering access to fully substituted pyrazoles within a few hours at room temperature. This method delivers synthetically valuable pyrazoleboranes with complete control of regioselectivity, and these intermediates can be further elaborated through functionalization of the C-B bond.
Metadata
| Item Type: | Article |
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| Authors/Creators: |
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| Copyright, Publisher and Additional Information: | © 2017 Wiley. This is an author produced version of a paper subsequently published in Chemistry - A European Journal . Uploaded in accordance with the publisher's self-archiving policy. |
| Keywords: | cycloaddition; sydnone; alkynylborane; regioselective; pyrazole |
| 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 ECHONET - 316379 |
| Depositing User: | Symplectic Sheffield |
| Date Deposited: | 22 Mar 2017 15:15 |
| Last Modified: | 13 Jul 2023 11:41 |
| Status: | Published |
| Publisher: | Wiley |
| Refereed: | Yes |
| Identification Number: | 10.1002/chem.201701019 |
| Related URLs: | |
| Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:113892 |
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