Abstract
Kinetic studies of the pyridine catalyzed reaction between phenylmethanesulfochloride and phenols in non-aqueous media have provided quantitative estimates for the effect of reactant structure, catalyst and reaction medium polarity on competing reaction routes. For the first time a “sulfene” mechanism in pyridine catalyzed processes of alkanesulfonyl transport has been discovered. Criteria for its realization are suggested.
Abstract
Изучена кинетика катализируемой пиридинами реакции фенилметансульфохлорида с фенолами в неводных средах. количественно оценено влияние строения рергента, катализатора и полярности среды на конкурирующие маршруты реакции. Впервые обнаружен “сульфеновый” механизм в катализируемых пиридинами процессах алкансульфонильного транспорта и определены критерии его реализации.
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Skrypnik, Y.G., Lyashchuk, S.N. Kinetic studies of pyridine catalyzed alkanesulfornylation of phenols. React Kinet Catal Lett 43, 283–288 (1991). https://doi.org/10.1007/BF02064686
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DOI: https://doi.org/10.1007/BF02064686