Discovery of 26218-78-0

From this literature《Reductive couplings of 2-halopyridines without external ligand: phosphine-free nickel-catalyzed synthesis of symmetrical and unsymmetrical 2,2′-bipyridines》,we know some information about this compound(26218-78-0)Application In Synthesis of Methyl 6-bromonicotinate, but this is not all information, there are many literatures related to this compound(26218-78-0).

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 26218-78-0, is researched, SMILESS is C1=NC(=CC=C1C(=O)OC)Br, Molecular C7H6BrNO2Journal, Article, Journal of Organic Chemistry called Reductive couplings of 2-halopyridines without external ligand: phosphine-free nickel-catalyzed synthesis of symmetrical and unsymmetrical 2,2′-bipyridines, Author is Liao, Lian-Yan; Kong, Xing-Rui; Duan, Xin-Fang, the main research direction is bipyridine preparation; halopyridine reductive coupling nickel catalyst.Application In Synthesis of Methyl 6-bromonicotinate.

An unexpectedly facile synthetic approach for sym. and unsym. 2,2′-bipyridines through the Ni-catalyzed reductive couplings of 2-halopyridines was developed. The couplings were efficiently catalyzed by 5 mol % of NiCl2·6H2O without the use of external ligands. A variety of 2,2′-bipyridines including caerulomycin F have been efficiently synthesized.

From this literature《Reductive couplings of 2-halopyridines without external ligand: phosphine-free nickel-catalyzed synthesis of symmetrical and unsymmetrical 2,2′-bipyridines》,we know some information about this compound(26218-78-0)Application In Synthesis of Methyl 6-bromonicotinate, but this is not all information, there are many literatures related to this compound(26218-78-0).

Reference:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem