| Literature DB >> 19760715 |
José Barluenga1, Amadeo Fernández, Alejandro Diéguez, Félix Rodríguez, Francisco J Fañanás.
Abstract
An efficient method for the synthesis of [3.3.1]bicyclic compounds from easily available alkynol derivatives has been developed. The reaction is based on a gold- or platinum-catalyzed tandem process that involves an intramolecular hydroalkoxylation of a triple bond followed by a Prins-type cyclization. The reaction has been carried out with differently substituted alkynol derivatives and oxygen-, nitrogen-, and carbon-centered nucleophiles. The incorporation of halogen atoms as nucleophiles and elimination reactions has also been studied. Enantiomerically pure [3.3.1]bicyclic systems were easily synthesized from the chiral pool.Entities:
Year: 2009 PMID: 19760715 DOI: 10.1002/chem.200900856
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236