| Literature DB >> 33044791 |
Naresh Bhuma1, Ludivine Lebedel1, Hiroki Yamashita2, Yutaka Shimizu2, Zahra Abada1,3, Ana Ardá4,5, Jérôme Désiré1, Bastien Michelet1, Agnès Martin-Mingot1, Ali Abou-Hassan3, Masahiro Takumi2, Jérôme Marrot6, Jesús Jiménez-Barbero4,5, Aiichiro Nagaki2, Yves Blériot1, Sébastien Thibaudeau1.
Abstract
The transformation of glycals into 2,3-unsaturated glycosyl derivatives, reported by Ferrier in 1962, is supposed to involve an α,β unsaturated glycosyl cation, an elusive ionic species that has still to be observed experimentally. Herein, while combination of TfOH and flow conditions failed to observe this ionic species, its extended lifetime in superacid solutions allowed its characterization by NMR-based structural analysis supported by DFT calculations. This allyloxycarbenium ion was further exploited in the Ferrier rearrangement to afford unsaturated nitrogen-containing C-aryl glycosides and C-alkyl glycosides under superacid and flow conditions, respectively.Entities:
Keywords: C-glycoside; Ferrier rearrangement; glycosylation; oxycarbenium; superelectrophiles
Year: 2020 PMID: 33044791 DOI: 10.1002/anie.202010175
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336