Mild Strategy for the Preparation of Alkyl Sulfonyl Fluorides from Alkyl Bromides and Alcohols Using Photoredox Catalysis and Flow Chemistry-Reference-Cited by-同舟云学术

Mild Strategy for the Preparation of Alkyl Sulfonyl Fluorides from Alkyl Bromides and Alcohols Using Photoredox Catalysis and Flow Chemistry

Published:2024-04-25 Issue:18 Volume:26 Page:3972-3976
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Gutiérrez-González Alejandro¹^ORCID,Karlsson Staffan²^ORCID,Leonori Daniele³^ORCID,Plesniak Mateusz P.¹^ORCID

Affiliation:

1. Medicinal Chemistry, Research and Early Development, Cardiovascular, Renal and Metabolism (CVRM), BioPharmaceuticals R&D, AstraZeneca Gothenburg, 431 83 Mölndal, Sweden

2. Early Chemical Development, Pharmaceutical Sciences, Biopharmaceuticals R&D, AstraZeneca Gothenburg, 431 83 Mölndal, Sweden

3. Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52056 Aachen, Germany

Funder

AstraZeneca

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c01216

Reference33 articles.

1. Pharmaceutical and medicinal significance of sulfur (SVI)-Containing motifs for drug discovery: A critical review

2. Crafting chemical space with sulfur functional groups

3. Sulfur(VI) Fluoride Exchange (SuFEx): Another Good Reaction for Click Chemistry

4. SuFEx Click Chemistry Enabled Late-Stage Drug Functionalization

5. Sulfonyl fluorides as targets and substrates in the development of new synthetic methods

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