Laboratory of applied chemistry problems (Laboratory of OKI N5)

About the laboratory

1967 When the preparation of 3(5)-substituted pyrazoles from diacetylene and hydrazine hydrate was discovered, the laboratory was named the Nitrogen-Containing Monomers Laboratory. 20 candidate and 4 doctoral dissertations were defended on these topics.

Hovhannes Sargsi Attaryan
position: head of OKI N5 laboratory
scientific degree: doctor of chemical sciences, professor
e-mail: hovelenatt@mail.ru
Karine Samsoni Badalyan
position: senior researcher
scientific degree: candidate of chemical sciences
Email: karinebadalyan1947@gmail.com
Markosyan Anna Jivani
position: researcher
scientific degree: candidate of chemical sciences
e-mail: a_markart@mail.ru
Hasmik Nveri Khachatryan
position: scientific researcher
degree: candidate of chemical sciences
Email: hasmikjasmin1@gmail.com
Robert Mamikoni Hakobyan
position: researcher
scientific degree: candidate of chemical sciences
e-mail: varayakb@gmail.com
Bolyan Lilya Alberti
position: junior researcher
Email: lilyabolyan@gmail.com
Ashkharuhi Ghevondi Aleksanyan
position: teacher. researcher
e-mail: aleksanyan1994@bk.ru
Sukoyan Astghik Hakobi
Email: astghik.sukoyan@gmail.com
position: teacher. researcher
Bichakhchyan Lilit Ashoti
e-mail: lilitbicakhchyan@mail.ru
position: teacher. researcher
Kharatyan Levon Aliki
e-mail: levonxaratyan17@mail.ru
position: senior laboratory assistant
Grant

18T-2Е151 – “Research in the field of technologically simulated reactions of vinylacetylene and some of its derivatives” ( 2018-2020 )
15T-1D348 – “Convenient and ecologically clean environment for carrying out nucleophilic reactions” ( 2016-2018 )
EIF 2020 (Enterprise Incubator Fund)/ “Synthesis of chitosan and its new derivatives”

Since 2010, the laboratory has been renamed “Laboratory of Applied Chemistry Problems” and deals with technologically simulated reactions, focusing on the synthesis of nitrogen-containing heterocycles.

Multidisciplinary researches are now being carried out in the direction of obtaining new heterocyclic substituted butenolides, their transformations, as well as the wide application of the aza-Michael reaction.

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