In 2019,ACS Catalysis included an article by Hemric, Brett N.; Chen, Andy W.; Wang, Qiu. Recommanded Product: 1779-49-3. The article was titled 《Copper-Catalyzed 1,2-Amino Oxygenation of 1,3-Dienes: A Chemo-, Regio-, and Site-Selective Three-Component Reaction with O-Acylhydroxylamines and Carboxylic Acids》. The information in the text is summarized as follows:
A three-component reaction for 1,2-amino oxygenation of 1,3-dienes has been achieved using O-acyl hydroxylamines and carboxylic acids. The reaction occurs through copper-catalyzed amination of olefins followed by nucleophilic addition of carboxylic acids, offering high levels of chemo-, regio-, and site-selectivity. The method is effective for both terminal and internal 1,3-dienes, including those bearing multiple, unsym. substituents. The amino oxygenation conditions also exhibited remarkable selectivity toward 1,3-dienes over alkenes, good tolerance of sensitive functional groups, and reliable scalability. In the experiment, the researchers used Methyltriphenylphosphonium bromide(cas: 1779-49-3Recommanded Product: 1779-49-3)
Methyltriphenylphosphonium bromide(cas: 1779-49-3) is an organophosphorus compound, with potential use as a precursor and a solvent in organic synthesis. And it is used widely for methylenation via the Wittig reaction.Recommanded Product: 1779-49-3
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary