One-pot assembly of functionalized (<em>m</em>-terphenyl-4'-yl)isoquinolines from 1-methylisoquinoline and electrophilic acylacetylenes

The relative reactivity of deprotonated CH<sub>3</sub> group and nitrogen atom of 1-methylisoquinoline towards electrophilic triple bond crucially depends on the acetylene structure and the reaction conditions. 1-Acyl-2-arylacetylenes react with 1-methylisoquinoline in a 2 : 1 molar ratio (34 mol in trace to 11

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Publication Details

Journal
Mendeleev Communications
Published
2025-01-01
DOI
https://doi.org/10.71267/mencom.7695
Citations
1
Primary Topic
Synthesis and Characterization of Pyrroles
Type
article
Field-Weighted Citation Impact
0.94
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article

One-pot assembly of functionalized (m-terphenyl-4'-yl)isoquinolines from 1-methylisoquinoline and electrophilic acylacetylenes

А. В. Афонин, Lina P. Nikitina, Igor А. Ushakov, Kseniya V. Belyaeva et al.
1 citations
Mendeleev Communications
Synthesis and Characterization of Pyrroles
0.94
article

One-pot assembly of functionalized (m-terphenyl-4'-yl)isoquinolines from 1-methylisoquinoline and electrophilic acylacetylenes

А. В. Афонин, Lina P. Nikitina, Igor А. Ushakov, Kseniya V. Belyaeva, Б. А. Трофимов, Alexander V. Vashchenko, Veronika S. Saliy
article en
1 citations

Abstract

The relative reactivity of deprotonated CH<sub>3</sub> group and nitrogen atom of 1-methylisoquinoline towards electrophilic triple bond crucially depends on the acetylene structure and the reaction conditions. 1-Acyl-2-arylacetylenes react with 1-methylisoquinoline in a 2 : 1 molar ratio (34 mol in trace to 11

Mendeleev CommunicationsVol. 35(4)
A.E. Favorsky Irkutsk Institute of Chemistry (RU)
Openalex Percentile: Top 26%
Synthesis and Characterization of Pyrroles
0.94
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