Oxime Palladacycles: Stable and Efficient Catalysts for Carbon-Carbon Coupling Reactions

Overview

Journal Org Lett

Publisher American Chemical Society

Specialties Biochemistry
Chemistry

Date 2000 Jul 13

PMID 10891167

Citations 5

Authors

ALONSO

Najera

PACHECO

Affiliations

Soon will be listed here.

Abstract

Oxime palladacycles are thermally stable complexes not sensitive to air or moisture, easily prepared from very cheap materials, which can be used as versatile and very efficient catalysts for different carbon-carbon bond-forming reactions.

Citing Articles

Spirocyclic derivatives as antioxidants: a review.

Acosta-Quiroga K, Rojas-Pena C, Nerio L, Gutierrez M, Polo-Cuadrado E RSC Adv. 2022; 11(36):21926-21954.

PMID: 35480788 PMC: 9034179. DOI: 10.1039/d1ra01170g.

Mesoporous Palladium N,N'-Bis(3-Allylsalicylidene)o-Phenylenediamine-Methyl Acrylate Resins as Heterogeneous Catalysts for the Heck Coupling Reaction.

Mella C, Torres C, Pecchi G, Campos C Materials (Basel). 2019; 12(16).

PMID: 31426313 PMC: 6721152. DOI: 10.3390/ma12162612.

Chloro({2-[mesityl(quinolin-8-yl-κN)boryl]-3,5-dimethyl-phenyl}methyl-κC)palladium(II) as a catalyst for Heck reactions.

Tamang S, Hoefelmeyer J Molecules. 2015; 20(7):12979-91.

PMID: 26193250 PMC: 6332355. DOI: 10.3390/molecules200712979.

Low Pressure Vinylation of Aryl and Vinyl Halides via Heck-Mizoroki Reactions Using Ethylene.

Smith C, RajanBabu T Tetrahedron. 2010; 66(5):1102-1110.

PMID: 20676383 PMC: 2910319. DOI: 10.1016/j.tet.2009.11.017.

2-Pyridinealdoxime, a new ligand for a Pd-precatalyst: application in solid-phase-assisted Suzuki-Miyaura reaction.

Solodenko W, Brochwitz C, Wartchow R, Hashem M, Dawood K, Vaultier M Mol Divers. 2005; 9(4):333-9.

PMID: 16311810 DOI: 10.1007/s11030-005-7457-y.