2010
DOI: 10.5155/eurjchem.1.3.236-245.54
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1,2,4-Triazine Chemistry Part I: Orientation of cyclization reactions of functionalized 1,2,4-triazine derivatives

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Cited by 25 publications
(5 citation statements)
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“…Abdel-Rahman et al [10] synthesized various 1,2,4-triazine derivatives as pharmacological, medicinal and antimicrobial agents based upon these results 2-(3′-phenyl-6′-oxo-5′-arylidene- (11) was synthesized from the interaction between compound 3 with oxazol-5-one (9) in aqueous ethanol to give the acid hydrazide 10 followed by ring closure reaction in warmed aqueous K2CO3 (Scheme-IV).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Abdel-Rahman et al [10] synthesized various 1,2,4-triazine derivatives as pharmacological, medicinal and antimicrobial agents based upon these results 2-(3′-phenyl-6′-oxo-5′-arylidene- (11) was synthesized from the interaction between compound 3 with oxazol-5-one (9) in aqueous ethanol to give the acid hydrazide 10 followed by ring closure reaction in warmed aqueous K2CO3 (Scheme-IV).…”
Section: Resultsmentioning
confidence: 99%
“…On the other hand, pyrazoles showed a very important medicinal and pharmacological properties [4]. Various heterocyclic nitrogen systems such as phathalazine [5] and 1,2,4-triazine derivatives reported as antimicrobial, anti HIV, anticancer and molluscicidal agents against snail [6][7][8][9][10]. Upon these observations, the present work tends to combination of these heterocyclic in one novel systems in view of their antibacterial in the compare with antibiotics.…”
Section: Introductionmentioning
confidence: 99%
“…In addition, introduction fluorine atoms to pyrazolopyrimidine enhance and improve their pharmacological properties [8] [9]. Abdel Rahman et al [10] [11] [12], reported that the orientation of cyclization reactions of functionalized amino and/or hydrazine bearing heterocyclic moieties depends on the effect of substituents, solvent pH, temper-International Journal of Organic Chemistry ature, chemoselective orientation heterocycleization and regioselectivity of electrocyclization as well as preferring the cite of closure as this work focused on N'-heteroaryl guanidine 4 as electron donors towards various electron-acceptors reagents in view of their fungicidal effects.…”
Section: Introductionmentioning
confidence: 99%
“…1,2,4-Triazines play an essential task in various biological routes and in synthesis of drugs. Therefore, a lot of heterocyclic systems attitude 1,2,4triazines are found to have significant pharmacological effects [6][7][8][9][10][11][12][13] . That targets have anti-AIDS 14,15 , antiviral 16 , anticancer [17][18][19][20] , antimicrobial [21][22][23][24] , antitumor 25 , antithelmintic drugs 26 .…”
Section: Introductionmentioning
confidence: 99%