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https://hdl.handle.net/2440/136595
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Type: | Journal article |
Title: | Ring Forming Approaches to para-Quinones: Toward a General Diels-Alder Disconnection |
Author: | Budwitz, J.E. Newton, C.G. |
Citation: | Synlett: accounts and rapid communications in synthetic organic chemistry, 2022; 33(15):1473-1480 |
Publisher: | Thieme Publishing |
Issue Date: | 2022 |
ISSN: | 0936-5214 1437-2096 |
Statement of Responsibility: | Jessica E. Budwitz, Christopher G. Newton |
Abstract: | para-Quinones feature extensively as targets and/or intermediates throughout a number of chemical and biological subdisciplines, highlighting the importance of efficient preparative methods. This Synpacts article provides an overview of ring forming approaches to para-hydroquinones and para-benzoquinones, concluding with our recent contribution concerning the development of 2,5-bis(tert-butyldimethylsilyloxy)furans as vicinal bisketene equivalents in the Diels–Alder reaction. |
Keywords: | Diels–Alder; cycloaddition; annulation; hydroquinone; benzoquinone; furan |
Description: | Article published online: 27 June 2022 |
Rights: | © 2022. Thieme. All rights reserved |
DOI: | 10.1055/s-0041-1737966 |
Grant ID: | http://purl.org/au-research/grants/arc/DE180100462 |
Appears in Collections: | Chemistry publications |
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