Abstract
The aim of the current work is to synthesize the new heterocyclic pentacyclic condensed systems that combine benzothiophen and benzimidazole/triazole into one molecule. The dibenzothiophene was taken as an initial compound and by consistent “extension” was annihilated the imidazole and triazole nucleuses. As a result two new pentacyclic systems were produced: 3H-, 7H-diimidazole[4,5-b][5,4-g] dibenzothiophene-5,5-dioxide and 3H-, 7H-ditriazole[4,5-b][5,4-g] dibenzothiophene-5,5-dioxide with the promising antimi-crobial activity. Their spectral characteristics were studied.
Highlights
The world medical practice confirms that the microorganisms and viruses are becoming more and more dangerous to humans
The dibenzothiophene was taken as an initial compound and by consistent “extension” was annihilated the imidazole and triazole nucleuses
The pathogenic and conditionally pathogenic strains of bacteria causing the infection processes are characterized by a large number of genetic resistance as well as residence in adverse conditions
Summary
The world medical practice confirms that the microorganisms and viruses are becoming more and more dangerous to humans. It is impossible to create a vaccine against all infectious diseases. The pathogenic and conditionally pathogenic strains of bacteria causing the infection processes are characterized by a large number of genetic resistance as well as residence in adverse conditions. These genetic monsters represent the products of selection at those massively used antimicrobial and antiviral drugs. The synthesis of new compounds and their antimicrobial and antiviral activities study become very important
Sign-in/Register to view highlights & summary Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
