Annellation of triazole and tetrazole systems onto pyrrolo[2,3-d] pyrimidines: Synthesis of tetrazolo[1,5-c]-pyrrolo[3,2-e]-pyrimidines and triazolo[1,5-c]pyrrolo-[3,2-e]pyrimidines as potential antibacterial agents

Molecules

Volumn 7, Issue 7, 2002, Pages 554-565

  Dave, Chaitanya G ^a   Shah, Rina D ^a  

^a M G SCIENCE INSTITUTE   (India)

Author keywords

Antibacterial activity; Pyrrolo 2,3 d pyrimidines; Tetrazolopyrrolopyrimidines; Triazolopyrrolopyrimidines

Indexed keywords

7 (3 CHLORO 4 FLUOROPHENYL) 9 (4 CHLOROPHENYL)TETRAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7 (3 CHLORO 4 FLUOROPHENYL) 9 (4 METHOXYPHENYL)TETRAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7 (3 CHLORO 4 FLUOROPHENYL) 9 PHENYL 7H TETRAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7 (4 CHLOROPHENYL) 9 PHENYL 7H TETRAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7 (4 CHLOROPHENYL) 9 PHENYL 7H TRIAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7 (4 FLUOROPHENYL) 9 (4 CHLOROPHENYL) 7H TETRAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7 (4 FLUOROPHENYL) 9 (4 METHOXYPHENYL)TETRAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7 (4 FLUOROPHENYL) 9 PHENYLTETRAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7 (4 PHENYL) 9 (4 CHLOROPHENYL) 7H TETRAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7 (4 PHENYL) 9 (4 CHLOROPHENYL) 7H TRIAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7 PHENYL 9 (4 METHOXYPHENYL)TETRAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7 PHENYL 9 (4 METHOXYPHENYL)TRIAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7,9 BIS(4 CHLOROPHENYL) 7H TETRAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7,9 BIS(4 CHLOROPHENYL) 7H TRIAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7,9 BIS(4 METHOXYPHENYL)TETRAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7,9 BIS(4 METHOXYPHENYL)TRIAZOLO[1,5 C] 7H PYRROLO[3,2 E]PYRIMIDINE; 7,9 DIPHENYLTETRAZOLO[1,5 C]PYRROLO 7H [3,2 E]PYRIMIDINE; AMPICILLIN; PYRIMIDINE DERIVATIVE; TRIAZOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ARTICLE; CHEMICAL REACTION; DRUG SCREENING; DRUG SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; SCREENING TEST; SUBSTITUTION REACTION;

EID: 3242806698     PISSN: 14203049     EISSN: None     Source Type: Journal    
DOI: 10.3390/70700554     Document Type: Article

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