Using the phospha-Michael reaction for making phosphonium phenolate zwitterions

Matthias R. Steiner, Max Schmallegger, Larissa Donner, Johann A. Hlina, Christoph Marschner, Judith Baumgartner and Christian Slugovc
Beilstein J. Org. Chem. 2024, 20, 41–51. https://doi.org/10.3762/bjoc.20.6

Supporting Information

Accession codes CCDC 2287962 and 2287963 contain the supplementary crystallographic data for 2a and 2f, respectively. These data can be obtained free of charge via https://www.ccdc.cam.ac.uk/data_request/cif, or by emailing data_request@ccdc.cam.ac.uk, or by contacting Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44 1223 336033.

Supporting Information File 1: Experimental procedures, plot of the solid-state structure of 2f, crystallographic data, NMR spectra, UV–vis spectra and experimental and simulated time conversion plots for the zwitterion formation.
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Using the phospha-Michael reaction for making phosphonium phenolate zwitterions
Matthias R. Steiner, Max Schmallegger, Larissa Donner, Johann A. Hlina, Christoph Marschner, Judith Baumgartner and Christian Slugovc
Beilstein J. Org. Chem. 2024, 20, 41–51. https://doi.org/10.3762/bjoc.20.6

How to Cite

Steiner, M. R.; Schmallegger, M.; Donner, L.; Hlina, J. A.; Marschner, C.; Baumgartner, J.; Slugovc, C. Beilstein J. Org. Chem. 2024, 20, 41–51. doi:10.3762/bjoc.20.6

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Scholarly Works

  • Steiner, M. R.; Marschner, C.; Baumgartner, J.; Hlina, J. A.; Slugovc, C. Synthesis, characterization and stability of phosphonium phenolate zwitterions derived from a (diphenylphosphino)phenol derivative and oxiranes. Monatshefte für Chemie - Chemical Monthly 2024, 155, 715–723. doi:10.1007/s00706-024-03216-1
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