First-principles study of the reaction mechanism governing the SNAr of the dimethylamine on 2-methoxy-5-nitrothiophenes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s00214-019-2519-x.pdf
Reference75 articles.
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4. Naredla RR, Raja EK, Klumpp DA (2013) Preparation of aryl-substituted 2-oxyindoles by superelectrophilic chemistry. Tetrahedron Lett 54:3245–3247. https://doi.org/10.1016/j.tetlet.2013.04.011
5. Dell’Erba C, Guareschi A, Spinelli D (1967) Selenophene series. III. Substituent effect on the rate of reaction of various 2-bromo-3-nitro-5-X-selenophenes with piperidine in ethanol. J Heterocycl Chem 4(3):438–440. https://doi.org/10.1002/jhet.5570040331
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