| Literature DB >> 31403305 |
Masanori Shigeno1, Ryutaro Nakamura1, Kazutoshi Hayashi1, Kanako Nozawa-Kumada1, Yoshinori Kondo1.
Abstract
We describe the catalytic amination of β-(hetero)arylethyl ethers with amines using the organic superbase t-Bu-P4 to obtain β-(hetero)arylethylamines. The reaction has a broad substrate scope and allows the transformations of electron-deficient and electron-neutral β-(hetero)arylethyl ethers with various amines including pyrrole, N-alkylaniline, diphenylamine, aniline, indole, and indoline derivatives. Mechanistic studies indicate a two-reaction pathway of MeOH elimination from the substrate to form a (hetero)arylalkene followed by the hydroamination of the alkene.Entities:
Year: 2019 PMID: 31403305 DOI: 10.1021/acs.orglett.9b02309
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005