Rhodium(III)‐Catalyzed (5+2) Annulation Reaction for the Synthesis of Nitro and Cyano Substituted Benzo[<i>b</i>]Oxepines

Abstract A Rh(III)‐catalyzed annulation reaction of 2‐(2‐nitrovinyl)phenols and disubstituted alkynes is developed to complete the first synthesis of biologically important 4‐nitro substituted benzo[ b ]oxepines. The same reaction conditions are also applied for the efficient synthesis of 4‐cyano substituted benzo[ b ]oxepines which have high biological significance. Some of the synthesized 4‐nitrobenzo[ b ]oxepines are easily transformed to triazole fused dibenzo[ b ]oxepines.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2024-09-17
DOI
https://doi.org/10.1002/ajoc.202400392
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.25

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article

Rhodium(III)‐Catalyzed (5+2) Annulation Reaction for the Synthesis of Nitro and Cyano Substituted Benzo[b]Oxepines

Pratiksha Bhorali, Supriya Khundrakpam, Deep J. Kalita
1 citations
Asian Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
0.25
article

Rhodium(III)‐Catalyzed (5+2) Annulation Reaction for the Synthesis of Nitro and Cyano Substituted Benzo[b]Oxepines

Pratiksha Bhorali, Supriya Khundrakpam, Deep J. Kalita
article en
1 citations

Abstract

Abstract A Rh(III)‐catalyzed annulation reaction of 2‐(2‐nitrovinyl)phenols and disubstituted alkynes is developed to complete the first synthesis of biologically important 4‐nitro substituted benzo[ b ]oxepines. The same reaction conditions are also applied for the efficient synthesis of 4‐cyano substituted benzo[ b ]oxepines which have high biological significance. Some of the synthesized 4‐nitrobenzo[ b ]oxepines are easily transformed to triazole fused dibenzo[ b ]oxepines.

Asian Journal of Organic ChemistryVol. 13(12)
North East Institute of Science and Technology (IN), Academy of Scientific and Innovative Research (IN)
Science and Engineering Research Board
Openalex Percentile: Top 48%
Catalytic C–H Functionalization Methods
0.25
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