| Literature DB >> 20963218 |
Pierrick Nun1, Sylvain Gaillard, Albert Poater, Luigi Cavallo, Steven P Nolan.
Abstract
Substituted indenes can be prepared after a sequence [1,3] O-acyl shift-hydroarylation-[1,3] O-acyl shift. Each step is catalyzed by a cationic NHC-Gold(I) species generated in situ after reaction between [(IPr)AuOH] and HBF(4)·OEt(2). This interesting silver-free way is fully supported by a computational study justifying the formation of each intermediate.Entities:
Year: 2010 PMID: 20963218 DOI: 10.1039/c0ob00758g
Source DB: PubMed Journal: Org Biomol Chem ISSN: 1477-0520 Impact factor: 3.876