Solution-Phase Parallel Synthesis of N-Arylisoquinuclidines

被引:0
|
作者
Borne, Ronald F. [2 ,3 ]
Levi, Mark S. [1 ]
Khan, M. O. Faruk [4 ]
Wilson, Norman H. [5 ]
机构
[1] Univ Arkansas Med Sci, Dept Pharmacol & Toxicol, Little Rock, AR 72205 USA
[2] Univ Mississippi, Sch Pharm, Dept Med Chem, University, MS 38677 USA
[3] Univ Mississippi, Sch Pharm, Lab Appl Drug Design & Synth, University, MS 38677 USA
[4] SW Oklahoma State Univ, Coll Pharm, Weatherford, OK 73096 USA
[5] Univ Edinburgh, Sch Biomed Sci, Edinburgh, Midlothian, Scotland
关键词
Addiction; Ibogaine; Isoquinuclidine; Parallel synthesis; Anti-addictive; IBOGAINE ANALOGS;
D O I
10.2174/157018009787158517
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The naturally-occurring alkaloid ibogaine, found in the West African shrub Tabernanthe iboga, possesses the ability to diminish self-administration of substances of abuse, such as cocaine, heroin and alcohol. The presence of the isoquinuclidine ring system in the structure of ibogaine became the lead for the design of a 16-member library of N-aryl isoquinuclidines, where pyridine, pyrimidine and quinoline ring systems were attached directly to the bicyclic nitrogen. A solution-phase method for their synthesis is described.
引用
收藏
页码:78 / 81
页数:4
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