Abstract
In a series of publications [2, 3] the synthesis of styryltetrazoles, containing substituents with strong electron-acceptor properties (F, NO2, CN, CO2H) in the aryl fragment based on cross-coupling of С-, Nvinyltetrazole with halobenzenes by Heck reaction is described. However no information exists on the synthesis of similar compounds containing electrondonor substituents. The electronic effect of the substituent in the aromatic fragment may significantly affect the efficiency of this reaction. The nature of the halogen present in the haloarene and the composition of the catalytic system are also of fundamental importance [4–7].
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