Literature DB >> 31403305

Catalytic Amination of β-(Hetero)arylethyl Ethers by Phosphazene Base t-Bu-P4.

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


  2 in total

1.  LiCl-promoted amination of β-methoxy amides (γ-lactones).

Authors:  Ru Zhao; Bing-Lin Zeng; Wen-Qiang Jia; Hong-Yi Zhao; Long-Ying Shen; Xiao-Jian Wang; Xian-Dao Pan
Journal:  RSC Adv       Date:  2020-09-21       Impact factor: 4.036

2.  Highly Efficient Darzens Reactions Mediated by Phosphazene Bases under Mild Conditions.

Authors:  Carmine Lops; Paolo Pengo; Lucia Pasquato
Journal:  ChemistryOpen       Date:  2022-10       Impact factor: 2.630

  2 in total

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