On February 25, 2021, de Souza, Wanderson C.; Matsuo, Bianca T.; Matos, Priscilla M.; Correia, Jose Tiago M.; Santos, Marilia S.; Koenig, Burkhard; Paixao, Marcio W. published an article.Product Details of 157869-15-3 The title of the article was Photocatalyzed Intramolecular [2+2] Cycloaddition of N-Alkyl-N-(2-(1-arylvinyl)aryl)cinnamamides. And the article contained the following:
N-Alkyl-N-(2-(1-arylvinyl)aryl)cinnamamides were converted into natural product inspired scaffolds via iridium photocatalyzed intramol. [2+2] photocycloaddition The protocol had a broad substrate scope, while operating under mild reaction conditions. Tethering four components forming a trisubstituted cyclobutane core builds rapidly high mol. complexity. This approach allowed the design and synthesis of a variety of tetrahydrocyclobuta[c]quinolin-3(1H)-ones, in yields ranging between 20-99%, and with excellent regio- and diastereoselectivity. Moreover, it was demonstrated that the intramol. [2+2]-cycloaddition of 1,7-enynes-after fragmentation of the cyclobutane ring-leads to enyne-metathesis-like products. The experimental process involved the reaction of 2-((4-Methoxyphenyl)ethynyl)aniline(cas: 157869-15-3).Product Details of 157869-15-3
The Article related to alkyl arylvinyl arylcinnamamide preparation iridium diastereoselective regioselective photochem cycloaddition, diaryl alkyltetrahydrocyclobutaquinolinone preparation, catalysis, cycloaddition, dienes, energy transfer, photocatalysis and other aspects.Product Details of 157869-15-3
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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem