Química Nova | |
Total syntheses of enokipodins | |
Macedo Jr., Fernando1  Universidade Estadual de Londrina, Londrina, Brasil1  Nascimento, Camila B.1  | |
关键词: enokipodins; quaternary center; enantioselective synthesis.; | |
DOI : 10.5935/0100-4042.20140157 | |
学科分类:化学(综合) | |
来源: Sociedade Brasileira de Quimica | |
【 摘 要 】
Enokipodins comprises a family of sesquiterpenes isolated from the mushroom Flammulina velutipes. These substances are attractive synthetic targets due to either their biological potential or structural characteristics. Since their isolation, about a decade ago, a considerable number of successful total syntheses have been published. Both via a racemic or enantioselective approach, these studies describe original and creative synthetic routes, particularly concerning the methodology used for constructing the benzylic quaternary center of these natural products. In this brief review, we discuss the reported total synthesis of enokipodins, focusing on the strategy adopted for the quaternary stereogenic center.
【 授权许可】
Unknown
【 预 览 】
Files | Size | Format | View |
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RO201912050596383ZK.pdf | 277KB | download |