DMD Oxidation of in-Situ-Generated σH Adducts Derived from Nitroarenes and the Carbanion of 2-Phenylpropionitrile to Phenols: The First Direct Substitution of a Nitro by a Hydroxy Group-Reference-Cited by-同舟云学术

DMD Oxidation of in-Situ-Generated σH Adducts Derived from Nitroarenes and the Carbanion of 2-Phenylpropionitrile to Phenols: The First Direct Substitution of a Nitro by a Hydroxy Group

Published:1998-05-30 Issue:13 Volume:63 Page:4390-4391
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Adam Waldemar¹,Ma̧kosza Mieczysław¹,Staliński Krzysztof¹,Zhao Cong-Gui¹

Affiliation:

1. Institute of Organic Chemistry, University of Würzburg, D-97074 Würzburg, Germany, and Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo980173v

Reference18 articles.

1. Electrophilic and nucleophilic aromatic substitution: Analogous and complementary processes

2. Vicarious nucleophilic substitution of hydrogen

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