Synthesis of highly substituted 2-perfluoroalkyl quinolines by electrophilic iodocyclization of perfluoroalkyl propargyl imines/amines

Organic and Biomolecular Chemistry

Volumn 7, Issue 1, 2009, Pages 85-93

  Likhar, Pravin R ^a   Subhas, Madavu Salian ^a   Roy, Sarabindu ^a   Kantam, Mannepalli Lakshmi ^a   Sridhar, Balasubramanian ^a   Seth, Ratanesh Kumar ^b   Biswas, Sukla ^b  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

^b NATIONAL INSTITUTE OF MALARIA RESEARCH   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIMALARIAL ACTIVITIES; CARBOXYLATION REACTIONS; EXCELLENT YIELDS; IODOCYCLIZATION; MILD REACTION CONDITIONS; PROPARGYL; SONOGASHIRA COUPLINGS; SYNTHESIS OF; TWO DIFFERENT METHODS;

ACETYLENE; AMINES; CARBOXYLATION; HYDROCARBONS; NITROGEN COMPOUNDS; ORGANIC COMPOUNDS;

AMINATION;

AMINE; ANTIMALARIAL AGENT; CARBON; IMINE; QUINOLINE DERIVATIVE;

ARTICLE; CHEMICAL MODEL; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; MASS SPECTROMETRY; METHODOLOGY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SYNTHESIS; TEMPERATURE; THIN LAYER CHROMATOGRAPHY; TIME; ULTRAVIOLET SPECTROPHOTOMETRY;

AMINES; ANTIMALARIALS; CARBON; CHROMATOGRAPHY, THIN LAYER; IMINES; MAGNETIC RESONANCE SPECTROSCOPY; MASS SPECTROMETRY; MODELS, CHEMICAL; MODELS, MOLECULAR; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; QUINOLINES; SPECTROPHOTOMETRY, ULTRAVIOLET; TEMPERATURE; TIME FACTORS;

EID: 57549085755     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b815398a     Document Type: Article

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