| Literature DB >> 29115009 |
Xiaoming Chen1, Hai-Jun Zhang1, Xinkan Yang2, Houqiang Lv2, Xiaoru Shao1, Cheng Tao2, Huifei Wang1, Bin Cheng2, Yun Li2, Jingjing Guo2, Jing Zhang1, Hongbin Zhai1,2,3.
Abstract
(-)-Daphnilongeranin B and (-)-daphenylline are two hexacyclic Daphniphyllum alkaloids, each containing a complex cagelike backbone. Described herein are the first asymmetric total synthesis of (-)-daphnilongeranin B and a bioinspired synthesis of (-)-daphenylline with an unusual E ring embedded in a cagelike framework. The key features include an intermolecular [3+2] cycloaddition, a late-stage aldol cyclization to install the F ring of daphnilongeranin B, and a bioinspired cationic rearrangement leading to the tetrasubstituted benzene ring of daphenylline.Entities:
Keywords: [3+2] cycloaddition; alkaloids; asymmetric total synthesis; natural products; rearrangement
Year: 2017 PMID: 29115009 DOI: 10.1002/anie.201709762
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336