Diazotization of Aminopyridines in the Presence of Camphorsulfonic Acid. Synthesis and Some Properties of Pyridinyl Camphorsulfonates / A. N. Sanzhiev, E. A . Krasnokutskaya, K. D. Erin, V. D. Filimonov

Set Level: Russian Journal of Organic ChemistryCoauthor: Sanzhiev, A. N., chemist, Associate Scientist of Tomsk Polytechnic University, 1993-, Aldar Nikolaevich;Krasnokutskaya, E. A ., organic chemist, Professor of Tomsk Polytechnic University, Doctor of chemical sciences, 1966-, Elena Aleksandrovna;Erin, K. D., chemical engineer, Engineer of Tomsk Polytechnic University, 1995-, Kirill Dmitrievich;Filimonov, V. D., Russian chemist, Professor of the TPU, 1945-, Viktor DmitrievichCorporate Author (Secondary): Национальный исследовательский Томский политехнический университет, Инженерная школа новых производственных технологий, Научно-образовательный центр Н. М. КижнераLanguage: английский.Abstract: Diazotization of 2-, 3-, and 4-aminopyridines in the presence of both racemic camphor-10-sulfonic acid and its pure enantiomers led to the formation of the corresponding pyridyl camphorsulfonates in moderate yields. Pyridyl camphorsulonates were found to be more reactive in alkaline alcoholysis than analogous pyridyl trifluoromethanesulfonates and pyridyl p-toluenesulfonates..Bibliography: [References: 17 tit.].Audience: .Subject: электронный ресурс | труды учёных ТПУ | aminopyridines | pyridyl sulfonates | pyridyl camphorsulfonates | camphor-10-sulfonic acid | alcoholysis | аминопиридины | пиридинилсульфонаты | пиридинилкамфорсульфонаты | алкоголиз Online Resources:Click here to access online
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[References: 17 tit.]

Diazotization of 2-, 3-, and 4-aminopyridines in the presence of both racemic camphor-10-sulfonic acid and its pure enantiomers led to the formation of the corresponding pyridyl camphorsulfonates in moderate yields. Pyridyl camphorsulonates were found to be more reactive in alkaline alcoholysis than analogous pyridyl trifluoromethanesulfonates and pyridyl p-toluenesulfonates.

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