An efficient new route towards biologically active isocryptolepine and γ-carboline derivatives using an intramolecular thermal electrocyclization strategy

Tetrahedron Letters

Volumn 52, Issue 28, 2011, Pages 3686-3688

  Hingane, Dattatray G ^a   Kusurkar, Radhika S ^a  

^a UNIVERSITY OF PUNE   (India)

Author keywords

Carboline; 5 Methyl 11H indolo 3,2 c quinoline 5 inium iodide; Antiplasmodial; Intramolecular electrocyclisation; Isocryptolepine

Indexed keywords

11H INDOLO[3,2 C]QUINOLINE; 5 METHYL 11H INDOLO[3,2 C]QUINOLINE 5 INIUMIODIDE; ANTINEOPLASTIC AGENT; CRYPTOLEPINE DERIVATIVE; GAMMA CARBOLINE DERIVATIVE; ISOCRYPTOLEPINE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CYCLIZATION; DRUG STRUCTURE; DRUG SYNTHESIS; ELECTROCHEMISTRY; INFRARED SPECTROSCOPY; INTRAMOLECULAR THERMAL ELECTROCYCLIZATION; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 79958297460     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.05.049     Document Type: Article

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