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作 者:Samadhiya, Pushkal Sharma, Ritu Srivastava, Santosh K. Srivastava, Savitri D.
出 处:《Chinese Journal of Chemistry》2011年第8期1745-1752,共8页中国化学(英文版)
摘 要:Synthesis of N1-3-{(4-substitute daryl-3-chloro-2-oxo-azetidine)-iminocarbamyl}-propyl-6-nitroindazole 4a-- 4s was conducted by a conventional method. All the compounds were synthesized and characterized by IR, 1H NMR, 13C NMR, FAB-Mass techniques and chemical methods. All the final synthesized compounds were evaluated for their antimicrobial activity and antitubercular activity with MIC values against some selected microorganisms.Synthesis of N1-3-{(4-substitute daryl-3-chloro-2-oxo-azetidine)-iminocarbamyl}-propyl-6-nitroindazole 4a-- 4s was conducted by a conventional method. All the compounds were synthesized and characterized by IR, 1H NMR, 13C NMR, FAB-Mass techniques and chemical methods. All the final synthesized compounds were evaluated for their antimicrobial activity and antitubercular activity with MIC values against some selected microorganisms.
关 键 词:synthesis 6-nitroindazole 2-azetidinone biological activity
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