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Inter- and intramolecular heterocyclisation carbonyl compounds and them thiacarbam derivatives an alicyclic structure depending of activation of nucleophilic centers it is carried out regiodirectly with formation of unknown earlier annelic and spitoycitic compounds thiazolic and thiadiazolic lines, perspective by way of studying biological activity.

Tetrahydroquinolines are important structural fragments of many biologically active compounds exhibiting antifungal, antitumor, antiviral and neurotropic properties. This paper presents methods for the synthesis of N-substituted tetrahydroquinoline-6-carbaldehydes and a study of the possibility of their olefi nation using the Wittig and Horner – Wadsworth – Emmons methods. As a result of the interaction of N-alkyl- and N-acylhydroquinolines with the Vilsmeier – Haack complex, N-substituted tetrahydroquinoline-6-carbaldehydes have been obtained in yields of 77–85%.

Приведены данные по получению замещенных гексагидротетразолохиназолинов на основе
кросс-сопряженных диеноновых производных циклогексана и 5-амино-1,2,3,4-тетразола.
Обсуждены вопросы по регионаправленности реакций и строению полученных веществ.
 

Studied «one-pot» reaction of 3,4-dihydronaphthalene-1 (2H)-one with aromatic aldehydes and (thio)urea in conditions of modified Biginelli reaction under thermal and microwave exposure. Showed a reduction reaction time and increasing the yield of the desired products benzohinazolinonsderivatives with microwave activation starting compounds.