Batch and flow electrochemical synthesis of allyl sulfones <i>via</i> sulfonation of allyl trifluoroborates: a robust, regioselective, and scalable approach-Reference-Cited by-同舟云学术

Batch and flow electrochemical synthesis of allyl sulfones via sulfonation of allyl trifluoroborates: a robust, regioselective, and scalable approach

Published:2023 Issue:21 Volume:25 Page:8510-8515
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Mollari Leonardo¹,del Río-Rodríguez Roberto¹^ORCID,Fernández-Salas Jose A.¹²^ORCID,Alemán José¹²³^ORCID

Affiliation:

1. Departamento de Química Orgánica (módulo-1), Universidad Autónoma de Madrid, Cantoblanco, 28049-Madrid, Spain

2. Institute for Advanced Research in Chemical Sciences (IAdChem), Universidad Autónoma de Madrid, 28049-Madrid, Spain

3. Center for Innovation in Advanced Chemistry (ORFEO-CINQA), Universidad Autónoma de Madrid, 28049 Madrid, Spain

Abstract

A versatile and straightforward electrochemical system for the synthesis of allyl sulfones using readily accessible sulfinates and allyl trifluoroborate salts is presented.

Funder

Comunidad de Madrid

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/GC/D3GC02408C

Reference50 articles.

1. Evolving Organic Synthesis Fostered by the Pluripotent Phenylsulfone Moiety

2. Beyond classical sulfone chemistry: metal- and photocatalytic approaches for C–S bond functionalization of sulfones

3. Identification of 4-Substituted 1,2,3-Triazoles as Novel Oxazolidinone Antibacterial Agents with Reduced Activity against Monoamine Oxidase A

4. Cyclic Sulfones as Novel P3-Caps for Hepatitis C Virus NS3/4A (HCV NS3/4A) Protease Inhibitors: Synthesis and Evaluation of Inhibitors with Improved Potency and Pharmacokinetic Profiles

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