Literature DB >> 31247758

Vicarious Nucleophilic Chloromethylation of Nitroaromatics.

Viktor V Khutorianskyi1, Blanka Klepetářová1, P Beier1.   

Abstract

Nitroaromatics substituted with electron-acceptor or electron-donor groups undergo vicarious nucleophilic substitution with the lithium salt of dichloromethane to provide chloromethyl-substituted nitroaromatics in good to high yields. The methodology represents a new strategy for the synthesis of benzyl chlorides.

Entities:  

Year:  2019        PMID: 31247758     DOI: 10.1021/acs.orglett.9b01676

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Alkylation of Nitropyridines via Vicarious Nucleophilic Substitution.

Authors:  Damian Antoniak; Michał Barbasiewicz
Journal:  Org Lett       Date:  2022-01-03       Impact factor: 6.005

2.  How Do Aromatic Nitro Compounds React with Nucleophiles? Theoretical Description Using Aromaticity, Nucleophilicity and Electrophilicity Indices.

Authors:  Kacper Błaziak; Witold Danikiewicz; Mieczysław Mąkosza
Journal:  Molecules       Date:  2020-10-20       Impact factor: 4.411

  2 in total

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