Enantioselective C–H amidation of sulfondiimines for the synthesis of 1,2,4-benzothiadiazine-1-imines under cobalt catalysis

Enantioselective C–H amidation/cyclization reactions of sulfondiimines with dioxazolones to provide 1,2,4-benzothiadiazine-1-imines have been achieved by using a cobalt( iii ) catalyst and a pseudo C 2 -symmetric chiral carboxylic acid.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00355e
Citations
5
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
4.68

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article

Enantioselective C–H amidation of sulfondiimines for the synthesis of 1,2,4-benzothiadiazine-1-imines under cobalt catalysis

Kosuke Higashida, Takashi Endo, Tatsuhiko Yoshino, Asako Murata et al.
5 citations
Organic Chemistry Frontiers
Synthesis and Catalytic Reactions
4.68
article

Enantioselective C–H amidation of sulfondiimines for the synthesis of 1,2,4-benzothiadiazine-1-imines under cobalt catalysis

Kosuke Higashida, Takashi Endo, Tatsuhiko Yoshino, Asako Murata, Yuuki Hirata, Shigeki Matsunaga
article en
5 citations

Abstract

Enantioselective C–H amidation/cyclization reactions of sulfondiimines with dioxazolones to provide 1,2,4-benzothiadiazine-1-imines have been achieved by using a cobalt( iii ) catalyst and a pseudo C 2 -symmetric chiral carboxylic acid.

Organic Chemistry FrontiersVol. 12(15)
Hokkaido University (JP), Kyoto University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 6%
Synthesis and Catalytic Reactions
4.68
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