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Oxidative nucleophilic substitution of hydrogen in nitroarenes with phenylacetonitrile derivatives

✍ Scribed by Mieczyslaw Ma̧kosza; Krzysztof Staliński

Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
836 KB
Volume
54
Category
Article
ISSN
0040-4020

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✦ Synopsis

Tertiary carbanions generated from a-substituted phenylacetonitriles in liquid ammonia add to nitrobenzenes in the para position to form the corresponding oH-adducts which are transformed, depending on the starting nitriles and the reaction conditions, to products of oxidative nucleophilic substitution of hydrogen, ONSH or vicarious nucleophilic substitution, VNS.

📜 SIMILAR VOLUMES

ChemInform Abstract: Nucleophilic Substi
ChemInform Abstract: Nucleophilic Substitution of Hydrogen in Activated Nitroarenes by Phenylacetonitrile Carbanion.
✍ V. Yu. Orlov; Ya. V. Sokovikov; A. D. Kotov; A. A. Starikov 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

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