| Literature DB >> 31339615 |
Xiao-Wei Liang1, Yunlong Zhao1, Xu-Ge Si1, Meng-Meng Xu1, Jia-Hao Tan1, Zhi-Mao Zhang1, Cheng-Gong Zheng1, Chao Zheng2, Quan Cai1.
Abstract
An enantioselective chemical synthesis of arene cis-dihydrodiols has been realized from 2-pyrones through sequential ytterbium-catalyzed asymmetric inverse-electron-demand Diels-Alder (IEDDA) reaction of 2-pyrones and retro-Diels-Alder extrusion of CO2 . By using this strategy, a series of substituted arene cis-dihydrodiols can be obtained efficiently with high enantioselectivity (>99 % ee in many cases). Based on this strategy, efficient and concise asymmetric total syntheses of (+)-MK7607 and 1-epi-(+)-MK7607 were accomplished.Entities:
Keywords: Diels-Alder reaction; asymmetric catalysis; dihydrodiols; retro-Diels-Alder reactions; total synthesis
Year: 2019 PMID: 31339615 DOI: 10.1002/anie.201908284
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336