《Thioether Ligand-Enabled Cationic Palladium(II)-Catalyzed Electrophilic C-H Arylation of α,β-Unsaturated Oxime Ethers》 was written by Yamada, Takahiro; Hashimoto, Yoshimitsu; Tanaka, Kosaku III; Morita, Nobuyoshi; Tamura, Osamu. Recommanded Product: 2495-35-4 And the article was included in Journal of Organic Chemistry in 2020. The article conveys some information:
The use of the cationic palladium(II) catalyst realized electrophilic C-H arylation of α,β-unsaturated O-SEM oximes with arylboronic acids. This Pd-catalyzed electrophilic C-H arylation is facilitated by employing alkyl aryl thioether ligands, and optimization of the ligand structure greatly improves the yield. The resulting α,β-unsaturated oximes would provide access to multisubstituted heterocyclic compounds The experimental part of the paper was very detailed, including the reaction process of Benzyl acrylate(cas: 2495-35-4Recommanded Product: 2495-35-4)
Benzyl acrylate(cas: 2495-35-4) is a reagent that can be used in the preparation of 2-(Phosphonomethyl)pentanedioic Acid, a selective glutamate carboxypeptidase 2 (GCP-II) inhibitor. It can also be used in the preparation of high refractive index polyacrylates.Recommanded Product: 2495-35-4
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