Green synthesis of some bioactive heterocyclic compounds from natural precursors
نویسنده
چکیده
3.
منابع مشابه
Synthesis of some new tetrahydropyrimidine derivatives as possible antibacterial agents
Heterocyclic compounds containing a pyrimidine nucleus are of special interests due to their applications in medicinal chemistry as they are the basic skeleton of several bioactive compounds such as antifungal, antibacterial, antitumor and antitubercular. As a part of our research in the synthesis of pyrimidine derivatives containing biological activities, some new tetrahydropyrimidine derivati...
متن کاملSynthesis of some new tetrahydropyrimidine derivatives as possible antibacterial agents
Heterocyclic compounds containing a pyrimidine nucleus are of special interests due to their applications in medicinal chemistry as they are the basic skeleton of several bioactive compounds such as antifungal, antibacterial, antitumor and antitubercular. As a part of our research in the synthesis of pyrimidine derivatives containing biological activities, some new tetrahydropyrimidine derivati...
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Thiazines are a group of heterocyclic organic compounds that are still largely unexplored for their pharmacological activities. There are different available methods for the synthesis of thiazine derivatives in the literature. In this review, we discuss available methods of thiazine preparation through green synthesis methods. Beside their synthesis, many thiazine derivatives are biologically a...
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Introduction In recent years, a new approach called “Green Chemistry” emerged in the field of organic chemistry, to prevent or minimize contamination from the laboratory bench up to industrial production. It purpose is to avoid residue formation, saving time and costs. One of the strategies proposed for the existing products involves designing alternative synthesis steps that do not use toxic s...
متن کاملSynthesis of Some New Heterocyclic Compounds with Potential Biological Activity
A series of new 2-arylimino-3-aryl-5-[5?-(3,4-dichlorophenyl)-2?-furylidene]-4-thiazolidinones (3a-l) have been synthesised by the condensation of 5-(3,4-dichlorophenyl)-2-furaldehyde 1 with 2-arylimino-3-aryl-5H-4-thiazolidinones 2 in glacial acetic acid. The physical and spectral data of the synthesised compounds are determined. The synthesised compounds have been screened for their in vitro ...
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تاریخ انتشار 2013