New explortion of 3-Bromo-10H-phenothiazine

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Reference of 3939-23-9, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about Reference of 3939-23-9

Reference of 3939-23-9, 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, 3939-23-9, molcular formula is C12H8BrNS, introducing its new discovery.

Potassium carbonate-mediated tandem C-S and C-N coupling reaction for the synthesis of phenothiazines under transition-metal-free and ligand-free conditions

An efficient potassium carbonate-mediated tandem C-S and C-N coupling reaction between N-(2-iodophenyl)acetamides and 2-halo-benzenethiols has been developed. This protocol affords a simple and efficient approach for the construction of phenothiazine derivatives without the need for addition of transition-metal catalyst or ligand for the first time. Furthermore, the reaction can be easily performed on a large scale.

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Reference£º
Thiazine – an overview | ScienceDirect Topics,
Thiazine | C4H5NS – PubChem