Synthetic Approaches to Tetracyclic Indolines as Versatile Building Blocks of Diverse Indole Alkaloids

• Published in: Chemistry : a European journal Vol. 24; no. 54; pp. 14302 - 14315
• Main Authors: Wang, Yanshi, Xie, Fukai, Lin, Bin, Cheng, Maosheng, Liu, Yongxiang
• Format: Journal Article
• Language: English
• Published: Germany Wiley Subscription Services, Inc 25.09.2018
• Subjects: Alkaloids; Biodiversity; building blocks; Carbazole; Carbazoles; Chemical reactions; Chemistry; Construction; cyclization; Heterocyclic compounds; Indoles; Organic chemistry; Palladium; Scaffolds; tetracyclic; total synthesis; building blocks; total synthesis; cyclization; tetracyclic; alkaloids
• ISSN: 0947-6539; 1521-3765; 1521-3765
• DOI: 10.1002/chem.201800775

Indole alkaloids bearing the tetracyclic indoline scaffolds of 1H‐pyrrolo[2,3‐d]carbazole have shown fascinating chemical diversity and significant biological activities. The development of efficient synthetic methodologies for such a tetracyclic scaffold remains highly desirable in both synthetic chemistry and medicinal chemistry. This review outlines key strategies for the construction of the tetracyclic indoline scaffolds in total syntheses of many indole alkaloids. The key strategies include nucleophilic additions, Diels–Alder reactions, radical cyclizations, and palladium‐catalyzed coupling reactions. The representative examples and their applications in the total syntheses are described here and discussed in depth. Tetracyclic indolines have acted as versatile building blocks for the syntheses of diverse indole alkaloids through half a century. There is a wide range of synthetic strategies for the common frameworks, which could be classified into nucleophilic additions, Diels–Alder reactions, radical cyclizations, palladium‐catalyzed coupling reactions, etc. The representative examples and their applications in the total syntheses are described here and discussed in depth.