## Abstract Rate data are reported for the reactions of 2‐chloro‐5‐nitropyridine **2a**, 2‐chloro‐3‐nitropyridine **2b**, and the corresponding 2‐phenoxy derivatives **2c** with __n__‐butylamine, pyrrolidine and piperidine and **2d** with __n__‐butylamine and pyrrolidine in dimethyl sulfoxide (DMSO
✦ LIBER ✦
Erratum: “Nucleophilic heteroaromatic substitution: Kinetics of the reactions of nitropyridines with aliphatic amines in dipolar aprotic solvents”, Int J Chem Kinet 2008, 40, 125
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 39 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
line 14: 1-phenoxy should read 2-phenoxy. Page 129, paragraph 3, line 10: the slope of the plot should read the slopes of the plots. Page 134, paragraph 2, lines 2-4: The reaction of pyrrolidine with 2c in acetonitrile is not base-catalyzed whereas that in DMSO is catalyzed should read The reaction of pyrrolidine with 2c in acetonitrile is base-catalyzed whereas that in DMSO is not catalyzed.
📜 SIMILAR VOLUMES
Nucleophilic heteroaromatic substitution
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Chukwuemeka Isanbor; Thomas A. Emokpae
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Article
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2008
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John Wiley and Sons
🌐
English
⚖ 256 KB