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Preparation, analysis and characterization of (1R,3R,5S,7S)-4,4,7-trimethyl-8-azatricyclo[5.2.0.03,5]NONAN-9-one

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dc.contributor.author COJOCARI, Sergiu
dc.contributor.author SIDORENKO, Anatolie
dc.contributor.author MACAEV, Fliur
dc.date.accessioned 2024-04-29T09:28:36Z
dc.date.available 2024-04-29T09:28:36Z
dc.date.issued 2023
dc.identifier.citation COJOCARI, Sergiu, SIDORENKO, Anatolie, MACAEV, Fliur. Preparation, analysis and characterization of (1R,3R,5S,7S)-4,4,7-trimethyl-8-azatricyclo[5.2.0.03,5]NONAN-9-one. In: Natural sciences in the dialogue of generations: the nat. conf. with internat. particip., 14-15 Sept. 2023, Chişinău, Republica Moldova: Abstract Book, Chişinău 2023, p. 207. ISBN 978-9975-3430-9-1. en_US
dc.identifier.uri http://repository.utm.md/handle/5014/26966
dc.description.abstract It is well known that β-lactam are agents that interrupt bacterial formation via covalent binding to essential penicillin-binding proteins. The identification of the novel lactams, which not only improve the quality of therapy, but also reduce side effects on patients are still a major concern for medicinal chemists. In our work, the β-lactam 3 was synthesized by cycloaddition chlorosulfonyl isocyanate 2 to natural (+)-3-carene 1. en_US
dc.language.iso en en_US
dc.publisher Moldova State University en_US
dc.relation.ispartofseries The National Conference with international participation "Natural sciences in the dialogue of generations";14-15 Sept. 2023, Chişinău, Republica Moldova
dc.rights Attribution-NonCommercial-NoDerivs 3.0 United States *
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/3.0/us/ *
dc.subject lactams en_US
dc.title Preparation, analysis and characterization of (1R,3R,5S,7S)-4,4,7-trimethyl-8-azatricyclo[5.2.0.03,5]NONAN-9-one en_US
dc.type Article en_US


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