Ligand-Induced Regioselectivity in Metal-Catalyzed Aryne Reactions Using Borylaryl Triflates as Aryne Precursors
Author:
Affiliation:
1. University of Minnesota, Department of Chemistry, Minneapolis, Minnesota 55455, USA
Funder
University of Minnesota
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.organomet.3c00103
Reference70 articles.
1. A Comprehensive History of Arynes in Natural Product Total Synthesis
2. Leveraging Fleeting Strained Intermediates to Access Complex Scaffolds
3. Conjugated Trimeric Scaffolds Accessible from Indolyne Cyclotrimerizations: Synthesis, Structures, and Electronic Properties
4. π-Extension of heterocycles via a Pd-catalyzed heterocyclic aryne annulation: π-extended donors for TADF emitters
5. A platform for on-the-complex annulation reactions with transient aryne intermediates
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1. Nickel binding enables isolation and reactivity of previously inaccessible 7-aza-2,3-indolynes;Science;2024-04-26
2. Ligand-Controlled Regioinduction in a PHOX-Ni Aryne Complex;ACS Organic & Inorganic Au;2023-11-02
3. Insights into the Regioselectivity of Metal-Catalyzed Aryne Reactions;Synlett;2023-09-18
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