B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-catalyzed TMSOTf-assisted intermolecular redox-neutral cyclization of <i>N</i>,<i>N</i>-dialkyl arylamines and allylic esters

We report a one-pot intermolecular redox-neutral cyclization of N , N -dialkylanilines and allylic esters for tetrahydroquinoline synthesis under metal-free and oxidant-free conditions.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00863h
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

B(C6F5)3-catalyzed TMSOTf-assisted intermolecular redox-neutral cyclization of N,N-dialkyl arylamines and allylic esters

Cuifen Lu, Chao Ma, Junqi Nie, Shuo Peng et al.
Organic Chemistry Frontiers
Organoboron and organosilicon chemistry
article

B(C6F5)3-catalyzed TMSOTf-assisted intermolecular redox-neutral cyclization of N,N-dialkyl arylamines and allylic esters

Cuifen Lu, Chao Ma, Junqi Nie, Shuo Peng, Wenjing Wang, Qingchun Wang, Sheng‐Chao Huang
article en

Abstract

We report a one-pot intermolecular redox-neutral cyclization of N , N -dialkylanilines and allylic esters for tetrahydroquinoline synthesis under metal-free and oxidant-free conditions.

Organic Chemistry FrontiersVol. 12(21)
China Three Gorges University (CN), Chemical Synthesis Lab (SG), Hubei University (CN)
Openalex Percentile: Top 87%
Organoboron and organosilicon chemistry
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