Vicarious Nucleophilic Substitution of (Chloroalkyl)heterocycles with Nitroarenes | Zendy

Florio Saverio | Zendy; Lorusso Patrizia | Zendy; Luisi Renzo | Zendy; Granito Catia | Zendy; Ronzini Ludovico | Zendy; Troisi Luigino | Zendy

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Vicarious Nucleophilic Substitution of (Chloroalkyl)heterocycles with Nitroarenes

Author(s) -

Florio Saverio,

Lorusso Patrizia,

Luisi Renzo,

Granito Catia,

Ronzini Ludovico,

Troisi Luigino

Publication year - 2004

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.200300806

Subject(s) - chemistry , benzothiazole , thiazole , carbanion , nucleophilic substitution , nucleophile , medicinal chemistry , substitution reaction , potassium , substitution (logic) , organic chemistry , stereochemistry , catalysis , programming language , computer science

The vicarious nucleophilic substitution of potassium carbanions of the (chloromethyl)pyridines 1a and 1b , (chloromethyl)benzothiazole 1c , (chloromethyl)thiazole 1d , (chloroethyl)thiazole 1e and (chloroethyl)benzothiazole 1f with nitroarenes, leading to nitrobenzyl heterocycles 2 and 4 − 14 has been studied. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)

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