Jump to main content
Jump to site search

Issue 22, 2000
Previous Article Next Article

A density functional theory study of π-facial stereoselectivity in intramolecular Diels–Alder reactions

Author affiliations

Abstract

B3LYP/6-31G(d) theory has been used to construct a transition structure model which correctly accounts for the observed π-diastereofacial selectivity in intramolecular Diels-Alder reactions induced by allylic substituents attached to the diene.

Back to tab navigation

Supplementary files

Publication details

The article was received on 08 Aug 2000, accepted on 27 Sep 2000 and first published on 31 Oct 2000


Article type: Communication
DOI: 10.1039/B006486F
Citation: Chem. Commun., 2000,0, 2215-2216

  •   Request permissions

    A density functional theory study of π-facial stereoselectivity in intramolecular Diels–Alder reactions

    M. N. Paddon-Row and M. S. Sherburn, Chem. Commun., 2000, 0, 2215
    DOI: 10.1039/B006486F

Search articles by author

Spotlight

Advertisements