Three Step Synthesis of Fully and Differently Arylated Pyridines,European Journal of Organic Chemistry

当前位置： X-MOL 学术 › Eur. J. Org. Chem. › 论文详情

Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)

Three Step Synthesis of Fully and Differently Arylated Pyridines
European Journal of Organic Chemistry ( IF 2.5 ) Pub Date : 2020-01-17 , DOI: 10.1002/ejoc.201901663
Mao Arita ₁ , Soichi Yokoyama _{1,

2} , Haruyasu Asahara _{1,

2,

3} , Nagatoshi Nishiwaki _{1,

2}

Affiliation

Condensation of β‐(2‐pyridyl)enamine and α,β‐unsaturated ketone in the presence of FeCl₃ under air afforded highly substituted pyridines. Synthesis of differently substituted pentaarylpyridines was consequently achieved via only three steps from commercially available reagents with simple experimental manipulations.