New learning discoveries about 17739-45-6

In some applications, this compound(17739-45-6)Recommanded Product: 2-(2-Bromoethoxy)tetrahydro-2H-pyran is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Zhu, Bin-Bin; Ye, Wen-Bo; He, Zhi-Tao; Zhang, Shu-Sheng; Feng, Chen-Guo; Lin, Guo-Qiang researched the compound: 2-(2-Bromoethoxy)tetrahydro-2H-pyran( cas:17739-45-6 ).Recommanded Product: 2-(2-Bromoethoxy)tetrahydro-2H-pyran.They published the article 《Regioselective Tandem C-H Alkylation/Coupling Reaction of ortho-Iodophenylethylenes via C,C-Pallada(II)cycles》 about this compound( cas:17739-45-6 ) in ACS Catalysis. Keywords: styrene iodo regioselective diastereoselective alkylation nucleophilic substitution palladacycle pyridone. We’ll tell you more about this compound (cas:17739-45-6).

Five-membered C,C-pallada(II)cycles are a unique class of diorganopalladium species with favorable stability and an electron-rich nature, leading to efficient sequential reactions with diverse electrophiles and nucleophiles. Specifically, the development of aryl-alkenyl-palladacycle-based transformations could provide an attractive approach with regio- and stereocontrol for the construction of multifunctionalized arylethylenes. However, currently, the C,C-pallada(II)cycle formation relies on a rigid skeleton or steric congestion in the backbone to promote cyclopalladation, and the formation of aryl-alkenyl-palladacycle without an α-substituent has not been achieved. Furthermore, reactions that could discriminate between the two sp2 carbon centers of such C(sp2),C(sp2)-palladacycle remain elusive. Herein, a regioselective three-component tandem alkylation/coupling reaction applicable for a variety of non-, α-, or β-substituted and α,β-disubstituted ortho-iodophenylethylenes is reported. Electron-rich 2-pyridone ligands are employed to enable the cyclopalladation process leading to aryl-alkenyl-palladacycle intermediates, of which the two C-Pd bonds are discriminated toward alkylation by their inherent steric and electronic differences. Good linear free-energy relationships between regio-/chemoselectivities and Hammett σ values are observed

In some applications, this compound(17739-45-6)Recommanded Product: 2-(2-Bromoethoxy)tetrahydro-2H-pyran is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Pyridazine – Wikipedia,
Pyridazine | C4H4N2 – PubChem