Palladium-catalyzed carbonylative synthesis of quinazolines: Silane act as better nucleophile than amidine
Author:
Funder
ZSTU
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Process Chemistry and Technology,Catalysis
Reference51 articles.
1. Palladium-Catalyzed Carbonylation Reactions of Aryl Halides and Related Compounds
2. Palladium-catalyzed carbonylative coupling reactions between Ar–X and carbon nucleophiles
3. Oxidative Carbonylation as a Powerful Tool for the Direct Synthesis of Carbonylated Heterocycles
4. Synthesis of Heterocycles via Palladium-Catalyzed Carbonylations
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1. Synthesis of 2-arylquinazolines by Chan–Evans–Lam coupling of 2-formylphenylboronic acids with amidines;Chemistry of Heterocyclic Compounds;2024-04
2. Recent approaches for the synthesis of heterocycles from amidines via a metal catalyzed C–H functionalization reaction;Organic & Biomolecular Chemistry;2024
3. Visible light-induced one-pot three-component synthesis of quinazolines under catalyst-free condition;Molecular Catalysis;2023-07
4. Transition-metal-catalyzed synthesis of quinazolines: A review;Frontiers in Chemistry;2023-03-16
5. Synthesis of quinazoline by decarboxylation of 2-aminobenzylamine and α-keto acid under visible light catalysis;Organic & Biomolecular Chemistry;2022
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