Abstract:
Nitration of 1,2,2,3-tetrasubstituted 5-triphenylmethylbenzimidazolines using an Ag+/NO2−system shows an unexpected (for benzimidazolines) orientation of the nitro group into position 7, which may be due to the strong steric influence of the rather bulky triphenylmethyl substituent.
Document Type:
Article
Language: English
Citation:
A. S. Morkovnik, “Steric control in the ion radical nitration of 5-triphenylmethylbenzimidazolines using a silver/nitrite system”, Mendeleev Commun., 7:5 (1997), 175–176
Linking options:
https://www.mathnet.ru/eng/mendc4843
https://www.mathnet.ru/eng/mendc/v7/i5/p175
This publication is cited in the following 1 articles:
A. S. MORKOVNIK, “ChemInform Abstract: Steric Control in the Ion Radical Nitration of 5‐Triphenylmethylbenzimidazolines Using a Silver/Nitrite System.”, ChemInform, 29:9 (1998)
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