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Author Correction: Modular diastereoselective synthesis of hindered cyclobutane amino nitriles through triplet nitrene-mediated ring expansion
Correction to: Nature Chemistry https://doi.org/10.1038/s41557-026-02156-z, published online 1 June 2026. In the version of the article initially published, the reference “Liang, Y. et al. Nitrene equivalent mediated metal-free ring expansions of alkylidenecyclopropanes and an alkylidenecyclobutane. Org. Lett. 8, 5877–5879 (2006)” was missing and has now been added as ref. 40 to the second paragraph of the “Strategies” section, in the sentence beginning “In contrast to the aryl-substituted ACPs”.
Modular diastereoselective synthesis of hindered cyclobutane amino nitriles through triplet nitrene-mediated ring expansion
Abstract Cyclobutane amino nitriles (CBANs), as a class of sterically hindered α,α-disubstituted unnatural amino acid derivatives, have garnered notable interest in pharmaceutical research due to their capacity to enhance molecule potency, metabolic stability and selectivity. However, the advancement and exploration of the chemical space of CBANs are impeded by general synthetic strategies, particularly for sterically more hindered vicinal tetrasubstituted derivatives.
Total Syntheses of Polycyclic Diterpenes Phomopsene, Methyl Phomopsenonate, and iso-Phomopsene via Reorganization of C-C Single Bonds
Download Hi-Res ImageDownload to MS-PowerPointCite This:J. Am. Chem. Soc. 2023, XXXX, XXX CCDC 2267214, 2267606–2267613, and 2278859 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/data_request/cif, or by emailing data_request@ccdc.cam.ac.uk, or by contacting The Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44 1223 336033.
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