Correction: Amine–borane complex-initiated SF5Cl radical addition on alkenes and alkynes

  1. Audrey Gilbert1,
  2. Pauline Langowski1,
  3. Marine Delgado2,
  4. Laurent Chabaud2ORCID Logo,
  5. Mathieu Pucheault2 and
  6. Jean-François Paquin1ORCID Logo

1Départment de chimie, Université Laval, Québec, QC, G1V 0A6, Canada
2Institut des Sciences Moléculaires - Groupe ORGA - UMR 5255, Université de Bordeaux, 351 Cours de la libération, 33405 Talence, France

  1. Corresponding author email

Guest Editor: D. O'Hagan
Beilstein J. Org. Chem. 2021, 17, 1725–1726. https://doi.org/10.3762/bjoc.17.120
Received 08 Jul 2021, Accepted 16 Jul 2021, Published 23 Jul 2021

Keywords: amine–borane complex; pentafluorosulfanyl chloride; pentafluorosulfanyl substituent; radical addition; radical initiation

The stereochemistry of some alkene products (2i–k) in Scheme 4 of the original publication was misattributed. The corrected structures are shown in Scheme 1.

[1860-5397-17-120-i1]

Scheme 1: Corrected Scheme 4 of the original article. Scope of the Et3B and the DICAB-initiated SF5Cl additions on alkynes. Unless noted otherwise, isolated yields are reported. aYield estimated by 19F NMR analysis of the crude mixture using 2-fluoro-4-nitrotoluene as an internal standard.

A corrected version of Supporting Information File 1 is also part of this Correction. The new Supporting Information File 1 is the complete file with the corrections marked in yellow color.

Finally, the Table of Content graphic was also corrected. The corrected version of the original graphical abstract is shown in Scheme 2.

[1860-5397-17-120-i2]

Scheme 2: Corrected graphical abstract of the original publication.

We apologize for any inconvenience caused.

Supporting Information

Supporting Information File 1: General information, synthetic procedures, additional optimization results, NMR spectra for known compounds (1H, 19F) and full characterization of all new compounds.
Format: PDF Size: 2.6 MB Download

© 2021 Gilbert et al.; licensee Beilstein-Institut.
This is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the author(s) and source are credited and that individual graphics may be subject to special legal provisions.
The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)

 
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