A silver(I)-catalyzed reaction of 2-alkynylbenzaldoxime with arylsulfonyl chloride
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference42 articles.
1. Generation of 1-aroxyisoquinolines via a silver-catalyzed reaction of 2-alkynylbenzaldoxime with phenol in the presence of p -toluenesulfonyl chloride
2. For selected examples:
3. [Pd(PPh3)2(saccharinate)2]—general catalyst for Suzuki–Miyaura, Negishi cross-coupling and C–H bond functionalization of coumaryl and pyrone substrates
4. A versatile palladium catalyst system for Suzuki–Miyaura coupling of alkenyl tosylates and mesylates
5. Facile synthesis of 4-acetyl-coumarins, -thiocoumarin and -quinolin-2(1H)-one via very high α-regioselective Heck coupling on tosylates
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1. Design of polymer-based nanoreactors for efficient acid/base cascade catalysis: A comparative study of site isolation strategies;Journal of Molecular Structure;2023-08
2. Advances and applications of 2-alkynylbenzaldoxime as a valuable synthetic framework for synthesizing N-heterocycles;Tetrahedron;2023-07
3. Silver‐Catalyzed Cyclizations;Silver Catalysis in Organic Synthesis;2018-12-21
4. Highly efficient AgNO3 -catalyzed approach to 2-(benzo[d ]azol-2-yl)phenols from salicylaldehydes with 2-aminothiophenol, 2-aminophenol and benzene-1,2-diamine;Applied Organometallic Chemistry;2018-02-08
5. Tandem Silver-Catalyzed Cyclization/Nucleophilic Functionalization of 2-Alkynylindole-3-carbaldehyde Oximes to Afford New 2,4-Disubstituted γ-Carbolines;European Journal of Organic Chemistry;2016-09-21
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