38642-74-9, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 38642-74-9, molcular formula is C13H8N2S, introducing its new discovery.
Method for synthesizing N – aryl phenothiazine compounds (by machine translation)
The invention discloses a method for synthesizing N – aryl phenothiazine compounds, which belongs to the technical field of organic chemistry. In order to indole compounds 1 and phenothiazine 2 as reaction raw material, cuprous bromide as a catalyst, in a polar aprotic solvent, under the air atmosphere of the reaction, the obtained N – aryl substituted phenothiazine compounds 3. The invention using air as the oxidizing agent, with green, economic, and environmental protection, the use of the indole and phenothiazine between dehydrogenation C (sp2 ) – H/N – H cross-coupling, constructing the model C – N key, widens the N – aryl phenothiazine compound synthesis method. (by machine translation)
Because enzymes can increase reaction rates by enormous factors and tend to be very specific, 38642-74-9, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 38642-74-9
Reference£º
Thiazine – an overview | ScienceDirect Topics,
Thiazine | C4H5NS – PubChem