| Literature DB >> 29624769 |
Yanshi Wang1,2, Fukai Xie1,2,3, Bin Lin1,2, Maosheng Cheng1,2, Yongxiang Liu1,2,3.
Abstract
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.Entities:
Keywords: alkaloids; building blocks; cyclization; tetracyclic; total synthesis
Year: 2018 PMID: 29624769 DOI: 10.1002/chem.201800775
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236