Cobalt- and Iron-Catalyzed Redox Condensation of o-Substituted Nitrobenzenes with Alkylamines: A Step- and Redox-Economical Synthesis of Diazaheterocycles-Reference-Cited by-同舟云学术

Cobalt- and Iron-Catalyzed Redox Condensation of o-Substituted Nitrobenzenes with Alkylamines: A Step- and Redox-Economical Synthesis of Diazaheterocycles

Published:2013-11-14 Issue:24 Volume:15 Page:6218-6221
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Nguyen Thanh Binh¹,Le Bescont Julie¹,Ermolenko Ludmila¹,Al-Mourabit Ali¹

Affiliation:

1. Centre de Recherche de Gif-sur-Yvette, Institut de Chimie des Substances Naturelles, CNRS, 91198 Gif-sur-Yvette Cedex, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol403064z

Reference33 articles.

1. Palladium-Catalyzed One-Pot Diarylamine Formation from Nitroarenes and Cyclohexanones

2. Ruthenium‐Catalyzed One‐Pot Aromatic Secondary Amine Formation from Nitroarenes and Alcohols

3. Direct One‐Pot Reductive N‐Alkylation of Nitroarenes by using Alcohols with Supported Gold Catalysts

4. Iron-Catalyzed One-Pot 2,3-Diarylquinazolinone Formation from 2-Nitrobenzamides and Alcohols

5. Iron-Catalyzed 2-Arylbenzoxazole Formation from o-Nitrophenols and Benzylic Alcohols

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