Silver‐Catalyzed Synthesis of Substituted Carbazoles through a Tandem Intramolecular Hydroamination/Cyclization Sequence | Zendy

Purnachandar Dalovai | Zendy; Suneel Kanaparthy | Zendy; Sridhar Balasubramanian | Zendy; Karunakar Galla V. | Zendy

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Silver‐Catalyzed Synthesis of Substituted Carbazoles through a Tandem Intramolecular Hydroamination/Cyclization Sequence

Author(s) -

Purnachandar Dalovai,

Suneel Kanaparthy,

Sridhar Balasubramanian,

Karunakar Galla V.

Publication year - 2017

Publication title -

asian journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.846

H-Index - 44

eISSN - 2193-5815

pISSN - 2193-5807

DOI - 10.1002/ajoc.201700379

Subject(s) - hydroamination , chemistry , carbazole , intramolecular force , catalysis , tandem , combinatorial chemistry , sequence (biology) , medicinal chemistry , organic chemistry , materials science , composite material , biochemistry

A silver‐catalyzed synthesis of substituted carbazoles from 2‐(6‐substituted‐3‐hexanol‐1,5‐diynyl)anilines has been achieved. In this transformation, new C−C and C−N bonds were formed through a hydroamination reaction, followed by cyclization. The carbazole derivatives were obtained in good‐to‐excellent yields in a one‐pot synthesis at ambient temperature.

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