One-pot synthesis of pyrrolo[3,2-f]-and pyrrolo[2,3-h]quinoline derivatives: Observation of an unexpected mechanistic pathway

Synlett

Volumn 23, Issue 5, 2012, Pages 717-722

  Ramesh, Subburethinam ^a   Nagarajan, Rajagopal ^a  

^a UNIVERSITY OF HYDERABAD   (India)

Author keywords

5 aminoindole; Lewis acid; one pot synthesis; pyrroloquinoline

Indexed keywords

1,2,3 TRIMETHYL 1H 5 INDOLAMINE; 1,2,3 TRIMETHYL 7,9 DIPHENYL 3H PYRROLO[3,2 F]QUINOLINE; 5 AMINOINDOLE DERIVATIVE; 7,8,9 TRIMETHYL 2,4 DIPHENYL 7H PYRROLO[2,3 H]QUINOLINE; ACETYLENE DERIVATIVE; BENZALDEHYDE DERIVATIVE; DIPHENYLACETYLENE; LEWIS ACID; O NITROPHENYLACETYLENE; PHENYLACETYLENE; PYRROLO[2,3 H]QUINOLINE DERIVATIVE; PYRROLO[3,2 F]QUINOLINE DERIVATIVE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

BIOLOGICAL ACTIVITY; CATALYSIS; CATALYST; CHEMICAL BINDING; CONTROLLED STUDY; CYCLOADDITION; DRUG STRUCTURE; ELECTRON TRANSPORT; ONE POT SYNTHESIS; PROCESS OPTIMIZATION; REVIEW; SUBSTITUTION REACTION; TEMPERATURE; X RAY CRYSTALLOGRAPHY;

EID: 84858077125     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0031-1290565     Document Type: Review

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