Publikation: The Reaction of alpha-Chlorocarbenium Salts with Nitriles : Formation of Chloro-Substituted 2-Azoniaallene Salts
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1989
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Synthesis. 1989, 1989(12), S. 918-922. ISSN 0039-7881. eISSN 1437-210X. Verfügbar unter: doi: 10.1055/s-1989-27430
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Diaryl or arylchloro substituted α-chlorocarbenium salts react with benzonitriles or dimethylcyanamide to afford chloro substituted 2-azoniaallene salts 10a, b, 11c. An X-ray structural analysis confirms the constitution of one of these salts (11c). Substitution of the chlorine atoms in 1,3-dichloro-1,3-diphenyl-2-azoniaallene hexachloroantimonate (10a) by the nucleophiles water, p-cresol, p-toluidine, diethylamine, hydrazine, methyl-, phenyl-, 2.4,6-trichlorophenylhydrazine, hydroxylamine, N-phenylhydroxylamine, 1,3-dimethylurea, and ethyl allophanate have been carried out affording heterocycles and open-chain compounds 13-21.
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JOCHIMS, Johannes, Helmut FISCHER, Atef HAMED, Tran HUU-PHUOC, Josef HOFMANN, 1989. The Reaction of alpha-Chlorocarbenium Salts with Nitriles : Formation of Chloro-Substituted 2-Azoniaallene Salts. In: Synthesis. 1989, 1989(12), S. 918-922. ISSN 0039-7881. eISSN 1437-210X. Verfügbar unter: doi: 10.1055/s-1989-27430BibTex
@article{Jochims1989React-23551,
title={The Reaction of alpha-Chlorocarbenium Salts with Nitriles : Formation of Chloro-Substituted 2-Azoniaallene Salts},
year={1989},
doi={10.1055/s-1989-27430},
number={12},
volume={1989},
issn={0039-7881},
journal={Synthesis},
pages={918--922},
author={Jochims, Johannes and Fischer, Helmut and Hamed, Atef and Huu-Phuoc, Tran and Hofmann, Josef}
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<dcterms:abstract xml:lang="eng">Diaryl or arylchloro substituted α-chlorocarbenium salts react with benzonitriles or dimethylcyanamide to afford chloro substituted 2-azoniaallene salts 10a, b, 11c. An X-ray structural analysis confirms the constitution of one of these salts (11c). Substitution of the chlorine atoms in 1,3-dichloro-1,3-diphenyl-2-azoniaallene hexachloroantimonate (10a) by the nucleophiles water, p-cresol, p-toluidine, diethylamine, hydrazine, methyl-, phenyl-, 2.4,6-trichlorophenylhydrazine, hydroxylamine, N-phenylhydroxylamine, 1,3-dimethylurea, and ethyl allophanate have been carried out affording heterocycles and open-chain compounds 13-21.</dcterms:abstract>
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