| Literature DB >> 33459485 |
Hai Huang1, Tianyu Zhang1, Jianwei Sun1,2.
Abstract
Mild oxetane opening by soft carbon nucleophiles has been developed for efficient C-C bond formation. In the presence of LiNTf2 or TBSNTf2 as catalyst, silyl ketene acetals were found to be effective nucleophiles to generate a wide range of highly oxygenated molecules, which are key substructure in natural products like polyketides. Furthermore, intramolecular oxetane opening by a styrene-based carbon nucleophile via a Prins-type process was also achieved with Sc(OTf)3 as catalyst, leading to efficient formation of the useful 2,3-dihydrobenzo[b]oxepine skeleton.Entities:
Keywords: C−C bond formation; Lewis acids; oxetane; ring opening; strained molecules
Year: 2020 PMID: 33459485 DOI: 10.1002/anie.202013062
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336