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Davis-Beirut Reaction: A Photochemical Brønsted Acid Catalyzed Route to N-Aryl 2H-Indazoles.

Authors :
Kraemer, Niklas
Kraemer, Niklas
Li, Clarabella J
Zhu, Jie S
Larach, Julio M
Tsui, Ka Yi
Tantillo, Dean J
Haddadin, Makhluf J
Kurth, Mark J
Kraemer, Niklas
Kraemer, Niklas
Li, Clarabella J
Zhu, Jie S
Larach, Julio M
Tsui, Ka Yi
Tantillo, Dean J
Haddadin, Makhluf J
Kurth, Mark J
Source :
Organic letters; vol 21, iss 15, 6058-6062; 1523-7060
Publication Year :
2019

Abstract

The Davis-Beirut reaction provides access to 2H-indazoles from aromatic nitro compounds. However, N-aryl targets have been traditionally challenging to access due to competitive alternate reaction pathways. Previously, the key nitroso imine intermediate was generated under alkaline conditions, but as reported here, the photochemistry of o-nitrobenzyl alcohols empowered Brønsted acid catalyzed conditions for accessing N-aryl targets. Anilines and alkyl amines give different outcomes under optimized conditions; the proposed mechanism was studied using quantum chemical calculations.

Details

Database :
OAIster
Journal :
Organic letters; vol 21, iss 15, 6058-6062; 1523-7060
Notes :
application/pdf, Organic letters vol 21, iss 15, 6058-6062 1523-7060
Publication Type :
Electronic Resource
Accession number :
edsoai.on1391604096
Document Type :
Electronic Resource