Inexpensive and bench stable diarylmethylium tetrafluoroborates as organocatalysts in the light mediated hydrosulfonylation of unactivated alkenes-Reference-Cited by-同舟云学术

Inexpensive and bench stable diarylmethylium tetrafluoroborates as organocatalysts in the light mediated hydrosulfonylation of unactivated alkenes

Published:2023 Issue:10 Volume:14 Page:2721-2734
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Renzi Polyssena¹^ORCID,Azzi Emanuele¹^ORCID,Ascensio Sylvain¹,Parisotto Stefano¹^ORCID,Sordello Fabrizio¹^ORCID,Pellegrino Francesco¹^ORCID,Ghigo Giovanni¹^ORCID,Deagostino Annamaria¹^ORCID

Affiliation:

1. Department of Chemistry, University of Torino, Via Pietro Giuria, 7, 10125 Torino, Italy

Abstract

Can a cheap and bench stable salt catalyse the hydrosulfonylation of unactivated alkenes? Yes it does! Just mix a diarylmethylium tetrafluoroborate salt with a sulfinate salt, wait for the formation of the adduct and turn purple light on it.

Funder

Ministero dell'Università e della Ricerca

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/SC/D3SC00182B

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