Cascade reaction based synthetic strategies targeting biologically intriguing indole polycycles

被引:76
作者
Ciulla, Maria Gessica [1 ]
Zimmermann, Stefan [1 ,2 ]
Kumar, Kamal [1 ]
机构
[1] Max Planck Inst Mol Physiol, Abt Chem Biol, Otto Hahn Str 11, D-44227 Dortmund, Germany
[2] Tech Univ Dortmund, Fak Chem & Chem Biol, Otto Hahn Str 6, D-44221 Dortmund, Germany
关键词
INTRAMOLECULAR DIELS-ALDER/1,3-DIPOLAR CYCLOADDITION; ONE-POT SYNTHESIS; NATURAL-PRODUCTS; DIELS-ALDER; DOMINO REACTIONS; DIVERGENT SYNTHESIS; BRANCHING CASCADES; CATALYTIC APPROACH; AZOMETHINE YLIDES; SYNTHESIS YIELDS;
D O I
10.1039/c8ob02620c
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Indole polycycles are common structural frameworks of biologically intriguing small molecules of natural and synthetic origin and therefore remain interesting and challenging synthetic targets. Cascade reactions wherein a number of reactions occur in a sequential manner in the same reaction apparatus are highly efficient chemical processes which quickly build up molecular complexity. Synthetic approaches based on cascade reactions are highly useful as they tend to avoid multiple reaction work-up steps as well as purifications of all intermediary products. Therefore, in the last decade, a number of cascade reaction based approaches to build various molecular scaffolds of biological interest have been reported. However, a relatively smaller number of cascade reaction based synthetic strategies have targeted the indole polycycles. In this article, we have summarized some interesting cascade reaction based synthesis designs leading to complex indole polycycles including some biologically intriguing and natural product inspired indole frameworks.
引用
收藏
页码:413 / 431
页数:19
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