Nickel‐Catalyzed Transannulation Reaction of 1,2,3,4‐Benzothiatriazin‐1,1(2<i>H</i>)‐dioxide with Alkyne and the Detailed Investigation of Reaction Mechanism

Abstract Herein, we provide two nickel complexes and a series of control experiments to study the mechanism of the nickel‐catalyzed transannulation reaction of 1,2,3,4‐benzo‐thiatriazin‐1,1(2 H )‐dioxide with aryne and alkyne in detail. In addition, we provide a new protocol for the cycloaddition of 1,2,3,4‐benzothiatriazin‐1,1(2 H )‐dioxide with alkyne on the basis of a similar reaction pathway.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-03-14
DOI
https://doi.org/10.1002/adsc.202500231
Citations
1
Primary Topic
Phenothiazines and Benzothiazines Synthesis and Activities
Type
article
Field-Weighted Citation Impact
0.81
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article

Nickel‐Catalyzed Transannulation Reaction of 1,2,3,4‐Benzothiatriazin‐1,1(2H)‐dioxide with Alkyne and the Detailed Investigation of Reaction Mechanism

Vijaykumar H. Thorat, Jen‐Chieh Hsieh, Ya-Chu Chuang, Chung-Hung Hsieh
1 citations
Advanced Synthesis & Catalysis
Phenothiazines and Benzothiazines Synthesis and Activities
0.81
article

Nickel‐Catalyzed Transannulation Reaction of 1,2,3,4‐Benzothiatriazin‐1,1(2H)‐dioxide with Alkyne and the Detailed Investigation of Reaction Mechanism

Vijaykumar H. Thorat, Jen‐Chieh Hsieh, Ya-Chu Chuang, Chung-Hung Hsieh
article en
1 citations

Abstract

Abstract Herein, we provide two nickel complexes and a series of control experiments to study the mechanism of the nickel‐catalyzed transannulation reaction of 1,2,3,4‐benzo‐thiatriazin‐1,1(2 H )‐dioxide with aryne and alkyne in detail. In addition, we provide a new protocol for the cycloaddition of 1,2,3,4‐benzothiatriazin‐1,1(2 H )‐dioxide with alkyne on the basis of a similar reaction pathway.

Advanced Synthesis & CatalysisVol. 367(11)
Tamkang University (TW), National Tsing Hua University (TW)
Openalex Percentile: Top 30%
Phenothiazines and Benzothiazines Synthesis and Activities
0.81
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