Synthesis of 3-substituted quinolines via transition-metal-catalyzed reductive cyclization of o-nitro baylis-hillman acetates

Journal of Organic Chemistry

Volumn 68, Issue 16, 2003, Pages 6427-6430

  O'Dell, David K ^a   Nicholas, Kenneth M ^a  

^a UNIVERSITY OF OKLAHOMA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

REDUCTIVE CYCLIZATION;

CARBON MONOXIDE; CATALYSIS; SYNTHESIS (CHEMICAL);

ORGANIC COMPOUNDS;

ACETIC ACID DERIVATIVE; METHYL 6 CHLOROQUINOLINE 3 CARBOXYLATE; METHYL 6,7 DIMETHOXYQUINOLINE 3 CARBOXYLATE; METHYL BENZO[H]QUINOLINE 3 CARBOXYLATE; METHYL[1,3]DIOXOLO[4,5 G]QUINOLINE 7 CARBOXYLATE; METHYLQUINOLINE 3 CARBOXYLATE; NITRO DERIVATIVE; QUINOLINE 3 CARBONITRILE; QUINOLINE DERIVATIVE; TRANSITION ELEMENT; UNCLASSIFIED DRUG;

AMINATION; ARTICLE; BAYLIS HILLMAN REACTION; CATALYST; CHEMICAL BOND; CHEMICAL REACTION; CYCLIZATION; DRUG SYNTHESIS; GAS CHROMATOGRAPHY; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; REACTION ANALYSIS; REDUCTION;

EID: 0042575704     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo034447c     Document Type: Article

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