Utilization of High-Throughput Experimentation (HTE) and ChemBeads Toward the Development of an Aryl Bromide and Benzyl Bromide Photoredox Cross-Electrophile Coupling-Reference-Cited by-同舟云学术

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Utilization of High-Throughput Experimentation (HTE) and ChemBeads Toward the Development of an Aryl Bromide and Benzyl Bromide Photoredox Cross-Electrophile Coupling

Published:2024-03-18 Issue:12 Volume:26 Page:2420-2424
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Glogowski Michal P.¹^ORCID,Cercizi Noel¹,Lynch-Colameta Tessa¹,Ridgers Lance H.¹,Phelan James P.¹^ORCID,Rowley Ann M.¹^ORCID,Rauch Martin P.¹^ORCID

Affiliation:

1. GSK, 1250 South Collegeville Road, Collegeville, Pennsylvania 19426, United States

Funder

GlaxoSmithKline

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c00577

Reference24 articles.

1. Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis

2. Merging photoredox with nickel catalysis: Coupling of α-carboxyl sp 3 -carbons with aryl halides

3. Single-electron transmetalation in organoboron cross-coupling by photoredox/nickel dual catalysis

4. ART─An Amino Radical Transfer Strategy for C(sp²)–C(sp³) Coupling Reactions, Enabled by Dual Photo/Nickel Catalysis

5. N -(Acyloxy)phthalimides as Redox-Active Esters in Cross-Coupling Reactions

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