Please use this identifier to cite or link to this item: 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
Published version: http://dx.doi.org/10.1055/s-0041-1737966
Appears in Collections:Chemistry publications

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