Synthesis of\n1,2-Benzothiazine via Nickel-Catalyzed\nElectrochemical Intramolecular Amination

Constructing\na C–N bond by merging electrochemistry and\nnickel catalysis is considered a powerful strategy. Herein, we investigate\nhighly efficient intramolecular amination at room temperature with\nexcellent functional group tolerance. Mechanistic studies suggest\nthat the rapid ligand exchange may lead to the Ni<sup>I</sup>/Ni<sup>III</sup> catalytic cycle. This method not only provides a new perspective\nfor intramolecular amination but also offers a novel approach for\nconstructing the benzothiazine scaffold.

Publication Details

Journal
Figshare
Published
2024-10-07
DOI
https://doi.org/10.1021/acs.orglett.4c03222.s001
Primary Topic
Radical Photochemical Reactions
Type
article
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article

Synthesis of\n1,2-Benzothiazine via Nickel-Catalyzed\nElectrochemical Intramolecular Amination

Figshare
Radical Photochemical Reactions
article

Synthesis of\n1,2-Benzothiazine via Nickel-Catalyzed\nElectrochemical Intramolecular Amination

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Abstract

Constructing\na C–N bond by merging electrochemistry and\nnickel catalysis is considered a powerful strategy. Herein, we investigate\nhighly efficient intramolecular amination at room temperature with\nexcellent functional group tolerance. Mechanistic studies suggest\nthat the rapid ligand exchange may lead to the Ni<sup>I</sup>/Ni<sup>III</sup> catalytic cycle. This method not only provides a new perspective\nfor intramolecular amination but also offers a novel approach for\nconstructing the benzothiazine scaffold.

Figshare
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Radical Photochemical Reactions
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Synthesis of\n1,2-Benzothiazine via Nickel-Catalyzed\nElectrochemical Intramolecular Amination · Figshare (2024) | TGRS Research Map | TGRS