Effective Synthetic Strategies for the Construction of Isoquinoline Scaffold found in Biologically Active Natural Products

被引:17
|
作者
Haider, Saqlain [1 ]
Chittiboyina, Amar G. [1 ]
Khan, Ikhlas A. [1 ,2 ]
机构
[1] Univ Mississippi, Sch Pharm, Natl Ctr Nat Prod Res, University, MS 38677 USA
[2] Univ Mississippi, Sch Pharm, Dept BioMol Sci, Div Pharmacognosy, University, MS 38677 USA
关键词
Biologically active natural products; tetrahydroisoquinolines; morphine; Bischler Napieralski Reaction; Pictet-Spengler Reaction; natural alkaloids; AEROCOLONIGENES SUBSP ANTIBIOTICA; FORMAL TOTAL-SYNTHESIS; PROTOBERBERINE ALKALOIDS; MACROCYCLIC LACTONES; ASYMMETRIC-SYNTHESIS; CYCLIZATION; (-)-LEMONOMYCIN; CYCLOADDITION; (+/-)-CODEINE; CONVERGENT;
D O I
10.2174/1385272821666171005150423
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Background: Alkaloids are a diverse group of naturally occurring secondary metabolites which exhibit various pharmacological properties. They have been synthesized via various synthetic routes in order to study their medicinal efficacy and structure activity relationships. Methodology: Keeping in view the pharmaceutical significance of this class of compounds, the present review has been written with a focus on the synthetic approaches used for efficient construction of isoquinoline scaffolds in natural alkaloids including crispine A, emetine, erythrocarine, jamatine, annosqualine, morphine, lemonomycin, papaverine, berberine, and codeine. Conclusion: The main goal behind the compilation of these schemes is to inspire organic chemists and help reinvigorate the development of novel strategies for the synthesis of isoquinoline alkaloids and their derivatives in the future.
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页码:148 / 164
页数:17
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