Solution-phase parallel synthesis of N,6-disubstituted isoquinuclidines as ibogaine analogs

Letters in Drug Design and Discovery

Volumn 2, Issue 1, 2005, Pages 51-54

  Levi, M S ^a   Khan, M O F ^a   Borne, R F ^a  

^a UNIVERSITY OF MISSISSIPPI   (United States)

Author keywords

Addiction; Anti addictive; Ibogaine; Isoquinuclidine; Parallel synthesis

Indexed keywords

1,2,3,4,5,6, HEXAHYDROAZEPINO[4,5 B]INDOLE; 3 CHLOROPERBENZOIC ACID; ALCOHOL; ANISOLE; BENZOPHENONE; CHLOROFORM; COCAINE; DIAMORPHINE; DIZOCILPINE; DOPAMINE 1 RECEPTOR; DOPAMINE 2 RECEPTOR; DOPAMINE TRANSPORTER; EPOXIDE; IBOGAINE; INDOLE DERIVATIVE; ISOQUINUCLIDINE; KAPPA OPIATE RECEPTOR; LITHIUM; MAGNESIUM SALT; MU OPIATE RECEPTOR; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; NORIBOGAINE; QUINUCLIDINE DERIVATIVE; SEROTONIN TRANSPORTER; TROPANE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CYCLIZATION; DRUG DEPENDENCE TREATMENT; DRUG RECEPTOR BINDING; DRUG STRUCTURE; DRUG SYNTHESIS; EPOXIDATION; GRIGNARD REACTION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; NEUROTOXICITY; OPPENAUER OXIDATION; POLYMERIZATION; PRIORITY JOURNAL; RING OPENING;

EID: 14344259038     PISSN: 15701808     EISSN: None     Source Type: Journal    
DOI: 10.2174/1570180053398217     Document Type: Article

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