Original and rapid access to new alkaloid analogues of neocryptolepine: Synthesis of substituted 6-methyl-6H-indolo[2,3-b]quinolines via TDAE strategy

Synlett

Volumn , Issue 20, 2005, Pages 3047-3050

  Amiri Attou, Ouassila ^a   Terme, Thierry ^a   Vanelle, Patrice ^a  

^a AIX MARSEILLE UNIVERSITY   (France)

Author keywords

1 methyl isatin; Alkaloids; Indolo 2,3 b quinoline; Reduction; TDAE

Indexed keywords

1 METHYLISATIN; 6 METHYL 6H INDOLO[2,3 B]QUINOLINE; ALKALOID; ALPHA HYDROXY LACTAM; INDOLE DERIVATIVE; ISATIN DERIVATIVE; LACTAM DERIVATIVE; NEOCRYPTOLEPINE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTIPROTOZOAL ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CRYPTOLEPIS; CYCLIZATION; DEHYDRATION; DNA CONFORMATION; DNA REPLICATION; DRUG CYTOTOXICITY; ELECTRON TRANSPORT; PROTON NUCLEAR MAGNETIC RESONANCE; REDUCTION; SYNTHESIS;

EID: 29744458599     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-921916     Document Type: Article

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