| Literature DB >> 14750802 |
Claude Spino1, Hadi Rezaei, Yves L Dory.
Abstract
Two electron-deficient dienes were reacted with a series of twelve electron-poor and electron-rich dienophiles to give, in some cases, the corresponding Diels-Alder adducts. Clear differences in the roles played by the two frontier orbital interactions emerged. It was demonstrated that in the case of normal Diels-Alder cycloadditions, the FMO theory could predict the relative reactivities between dienophiles, while in the case of inverse-electron demand Diels-Alder reactions, it could not. It was shown that the dissymmetry in electron-rich dienophiles increases their reactivities.Entities:
Year: 2004 PMID: 14750802 DOI: 10.1021/jo0353740
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354