Synthesis of 2,5-Diaryl-1,5-dienes from Allylic Bromides Using Visible-Light Photoredox Catalysis
Author:
Affiliation:
1. Department of Chemistry, 1102 Natural Sciences II, University of California, Irvine, California 92697-2025, United States
Funder
Division of Chemistry
National Institutes of Health
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.5b01962
Reference78 articles.
1. Photoredox catalysis by [Ru(bpy)3]2+ to trigger transformations of organic molecules. Organic synthesis using visible-light photocatalysis and its 20th century roots
2. Visible light photoredox catalysis: applications in organic synthesis
3. Shining Light on Photoredox Catalysis: Theory and Synthetic Applications
4. Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis
5. Synthetic applications of photoredox catalysis with visible light
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1. Photoredox Selective Homocoupling of Propargyl Bromides;The Journal of Organic Chemistry;2022-11-01
2. Enantioselective Reductive Homocoupling of Allylic Acetates Enabled by Dual Photoredox/Palladium Catalysis: Access to C2-Symmetrical 1,5-Dienes;Journal of the American Chemical Society;2021-08-05
3. Synthesis of Six-Membered Spiro Azacyclic Oxindole Derivatives via a One-Pot Process of Umpolung Allylation/Aza-Prins Cyclization;Organic Letters;2021-02-09
4. Visible Light‐Triggered β‐Allylation of Indoles Using Baylis‐Hillman Bromides;Asian Journal of Organic Chemistry;2020-06-23
5. Sulfur-Mediated Allylic C–H Arylation, Epoxidation, and Aziridination;The Journal of Organic Chemistry;2019-07-09
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