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Synthesis of Highly Functionalized Bismacycles via Post-Transmetallation Modification of Aryboronic Acids

Sivanandan, Sudheesh T.; Guiry, Patrick J.; Owen, Benjamin; Ball, Liam

Synthesis of Highly Functionalized Bismacycles via Post-Transmetallation Modification of Aryboronic Acids Thumbnail


Authors

Patrick J. Guiry

Benjamin Owen

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LIAM BALL Liam.Ball@nottingham.ac.uk
Associate Professor



Abstract

Bismacycles featuring a sulfone-bridged scaffold have recently been developed as versatile and convenient electrophilic arylating agents. Here, we report that the exocyclic aryl group, which is ultimately transferred to a nucleophilic coupling partner, can be functionalized through cross-coupling, heteroatom substitutions, oxidations and reductions, and protecting group manipulations. This “postsynthetic modification” approach provides concise and divergent access to complex aryl bismacycles. The utility of the functionalized bismacycles in electrophilic arylation of C−H and O−H bonds is demonstrated.

Journal Article Type Article
Acceptance Date Jun 9, 2023
Online Publication Date Jul 12, 2023
Publication Date Jul 21, 2023
Deposit Date Jul 3, 2023
Publicly Available Date Jul 18, 2023
Journal Journal of Organic Chemistry
Print ISSN 0022-3263
Electronic ISSN 1520-6904
Peer Reviewed Peer Reviewed
Volume 88
Issue 14
Pages 9730-9736
DOI https://doi.org/10.1021/acs.joc.3c00361
Public URL https://nottingham-repository.worktribe.com/output/22656521
Publisher URL https://pubs.acs.org/doi/10.1021/acs.joc.3c00361

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