
Межи внутримолекулярная гетероциклизация карбонильных соединений и их тиокарбамидных производных алициклического строения в зависимости от условий активации нуклеофильных центров осуществляется регионаправленно с образованием неизвестных ранее аннелированных и спиросочленённых соединений пиразолинового, тиазолового, тиадиазолинового рядов, перспективных в плане изучения биологической активности.
Interand intramolecular heterocyclisation carbonyl compounds and them thiacarbamd derivatives an alicyclic structure depending of activation of nucleophilic centers it is carried out regiodirectly with formation of unknown earlier annelic and spirocyclic compounds thiazolic and thiadiazolic lines, perspective by way of studying biological activity.
α, β-НЕПРЕДЕЛЬНЫЕ КЕТОНЫ, β-АМИНОКЕТОНЫ, ТИОКАРБАМИДЫ, ГЕТЕРОЦИКЛИЗАЦИЯ, ПИРАЗОЛИНЫ, ТИАЗОЛЫ, 4-ТИАДИАЗОЛИНЫ, β-UNSATURATED KETONES, β-AMINOKETONES
α, β-НЕПРЕДЕЛЬНЫЕ КЕТОНЫ, β-АМИНОКЕТОНЫ, ТИОКАРБАМИДЫ, ГЕТЕРОЦИКЛИЗАЦИЯ, ПИРАЗОЛИНЫ, ТИАЗОЛЫ, 4-ТИАДИАЗОЛИНЫ, β-UNSATURATED KETONES, β-AMINOKETONES
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