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Synthesis of 2-aryl quinazolinones via iron-catalyzed cross-dehydrogenative coupling (CDC) between N–H and C–H bonds

https://doi.org/10.1039/d0ob00866d
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Kosmotropes Perturbation and Ambiphilic Dual Activation: Responsible Features for the Construction of C‐N Bond towards the Synthesis of Quinazolin‐4(3 H )‐ones in Water
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Metal‐Free Graphene Oxide Promoted a Novel Multicomponent Reaction for the Synthesis of 3‐Substituted Quinazolinones Using DMSO as One Carbon Synthon
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Identification of chemokine receptor CCR4 antagonist
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Synthesis of novel 4,6-disubstituted quinazoline derivatives, their anti-inflammatory and anti-cancer activity (cytotoxic) against U937 leukemia cell lines☆
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Synthesis and in vitro antitumor activities of novel 4-anilinoquinazoline derivatives
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The chemistry of recently isolated naturally occurring quinazolinone alkaloids
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Synthesis of quinazolinones from anthranilamides and aldehydes via metal-free aerobic oxidation in DMSO
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En Route to Intermolecular Cross-Dehydrogenative Coupling Reactions
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Acceptorless Dehydrogenative Coupling of o-Aminobenzamides with the Activation of Methanol as a C1 Source for the Construction of Quinazolinones
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Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion
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Cross-Dehydrogenative Coupling (CDC): Exploring C−C Bond Formations beyond Functional Group Transformations
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Catalytic Dehydrogenative Cross-Coupling: Forming Carbon−Carbon Bonds by Oxidizing Two Carbon−Hydrogen Bonds
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Iron Catalysis in Organic Synthesis
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6-Alkylamino- and 2,3-Dihydro-3‘-methoxy-2-phenyl-4-quinazolinones and Related Compounds: Their Synthesis, Cytotoxicity, and Inhibition of Tubulin Polymerization
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Studies on organosulfur compounds. XII. Syntheses and pharmacological activities of 2-heterocyclic substituted 4(3H)-quinazolinones.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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