| Literature DB >> 28152222 |
Yi-An Guo1, Meng Zhao1, Zhengshuang Xu1, Tao Ye1.
Abstract
The total synthesis of four actinoranone stereoisomers led to unambiguous assignment of relative and absolute stereochemistry of the natural product. Key features of the convergent, fully stereocontrolled route include the use of a Negishi carbozirconation/iodination, a Friedel-Crafts cyclization, a Felkin-controlled addition reaction, a Mitsunobu reaction, and a late-stage C-H oxidation.Entities:
Keywords: actinoranone; meroterpenoid; natural products; stereochemistry; total synthesis
Mesh:
Substances:
Year: 2017 PMID: 28152222 DOI: 10.1002/chem.201700476
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236