Cp*Co( <scp>iii</scp> )-catalyzed synthesis of isoquinolones <i>via</i> controlled annulation of primary arylamides with internal alkynes

In this study, we present the first cobalt(III)-catalyzed direct synthesis of isoquinolones from readily available primary arylamides and internal alkynes through a controlled oxidative C-H/N-H annulation reaction. This innovative protocol eliminates the need for expensive transition metal salts and external auxiliaries, producing the desired mono-annulated product exclusively while accommodating a wide range of substrates. Preliminary mechanistic studies highlight the critical role of copper oxide in facilitating the transformation. Additionally, peripheral modifications of the core isoquinolone rings have been performed to synthesize complex heterocyclic systems.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2024-11-13
DOI
https://doi.org/10.1039/d4ob01693a
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.50

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article

Cp*Co( iii )-catalyzed synthesis of isoquinolones via controlled annulation of primary arylamides with internal alkynes

Akanksha Singh Baghel, Amit Kumar, Saksham Mishra
2 citations
Organic & Biomolecular Chemistry
Catalytic C–H Functionalization Methods
0.50
article

Cp*Co( iii )-catalyzed synthesis of isoquinolones via controlled annulation of primary arylamides with internal alkynes

Akanksha Singh Baghel, Amit Kumar, Saksham Mishra
article en
2 citations

Abstract

In this study, we present the first cobalt(III)-catalyzed direct synthesis of isoquinolones from readily available primary arylamides and internal alkynes through a controlled oxidative C-H/N-H annulation reaction. This innovative protocol eliminates the need for expensive transition metal salts and external auxiliaries, producing the desired mono-annulated product exclusively while accommodating a wide range of substrates. Preliminary mechanistic studies highlight the critical role of copper oxide in facilitating the transformation. Additionally, peripheral modifications of the core isoquinolone rings have been performed to synthesize complex heterocyclic systems.

Organic & Biomolecular ChemistryVol. 23(2)
Indian Institute of Technology Patna (IN)
Council of Scientific and Industrial Research, India
Openalex Percentile: Top 38%
Catalytic C–H Functionalization Methods
0.50
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