Related Products of 2213-63-0, New research progress on 2213-63-0 in 2021. Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. 2213-63-0, Name is 2,3-Dichloroquinoxaline, molecular formula is C8H4Cl2N2. In a Article，once mentioned of 2213-63-0
An original synthesis of the fused pyranoquinoxaline dithiolene ligand qpdt2- is discussed in detail. The most intriguing step is the introduction of the dithiolene moiety by Pd-catalyzed carbon-sulfur coupling. The corresponding MoIVO complex (Bu4N)2[MoO(qpdt)2] (2) underwent reversible protonation in a strongly acidic medium and remained stable under anaerobic conditions. Besides, 2 was found to be very sensitive towards oxygen, as upon oxidation it formed a planar dithiin derivative. Moreover, the qpdt2- ligand in the presence of [MoCl4(tBuNC)2] formed a tetracyclic structure. The products resulting from the unique reactivity of qpdt2- were characterized by X-ray diffraction, mass spectrometry, NMR spectroscopy, UV/Vis spectroscopy, and electrochemistry. Plausible mechanisms for the formation of these products are also proposed. Molybdopterin mimic: The synthesis of bio-inspired fused pyranoquinoxaline dithiolene ligand qpdt2- is discussed in detail. The most important step was introduction of the dithiolene moiety by Pd-catalyzed carbon-sulfur coupling. Reactions of MoIVO complex (Bu4N)2[MoO(qpdt)2], which mimics the active site of Mo enzymes, with protons, oxygen, and isocyanides led to new reactions and products (see scheme).
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Related Products of 2213-63-0. In my other articles, you can also check out more blogs about 2213-63-0
Reference：
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1507 | ChemSpider