| Literature DB >> 25247829 |
Noriko Okamoto1, Takuya Sueda, Reiko Yanada.
Abstract
Bi(OTf)3-catalyzed Meyer-Schuster rearrangement of electron-rich propargyl alcohols, followed by 1,4-addition of the resulting vinyl ketone, proceeded smoothly though Meyer-Schuster rearrangement of primary propargyl alcohols is rare. This tandem reaction can be extended to an intramolecular version, featuring a one-pot dihydroquinolone synthesis.Entities:
Mesh：
Substances：
Year: 2014 PMID： 25247829 DOI： 10.1021/jo5017663
Source DB: PubMed Journal: J Org Chem ISSN： 0022-3263 Impact factor: 4.354