| Literature DB >> 31147660 |
Michaelyn C Lux1, Melissa L Boby2, Joshua L Brooks3, Derek S Tan4.
Abstract
Bicyclic ether scaffolds are found in a variety of natural products and are of interest in probe and drug discovery. A palladium-catalyzed cascade reaction has been developed to provide efficient access to these scaffolds from readily available linear diene-diol substrates. A Pd redox-relay process is used strategically to transmit reactivity between an initial oxypalladative cyclization and a subsequent π-allyl-Pd cyclization at remote sites. The reaction affords a variety of bicyclic ether scaffolds with complete diastereoselectivity for cis-ring fusion.Entities:
Year: 2019 PMID: 31147660 PMCID: PMC6601619 DOI: 10.1039/c9cc03775f
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222