《Decarboxylative Conjunctive Cross-coupling of Vinyl Boronic Esters using Metallaphotoredox Catalysis》 was written by Mega, Riccardo S.; Duong, Vincent K.; Noble, Adam; Aggarwal, Varinder K.. Recommanded Product: 2495-35-4 And the article was included in Angewandte Chemie, International Edition in 2020. The article conveys some information:
Photochem. decarboxylation, arylation and borylation of carboxylic acids and α-amino acids catalyzed by 1,2,3,5-tetracarbazolyl. The synthesis of complex alkyl boronic esters through conjunctive cross-coupling of vinyl boronic esters with carboxylic acids and aryl iodides is described. The reaction proceeds under mild metallaphotoredox conditions and involves an unprecedented decarboxylative radical addition/cross-coupling cascade of vinyl boronic esters. Excellent functional-group tolerance is displayed, and application of a range of carboxylic acids, including secondary α-amino acids, and aryl iodides provides efficient access to highly functionalized alkyl boronic esters. The decarboxylative conjunctive cross-coupling was also applied to the synthesis of sedum alkaloids. After reading the article, we found that the author used 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
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics