Theoretical Studies on Pentadienyl Cation Electrocyclizations

Author(s): Rebecca L. Davis, Dean J. Tantillo

Journal Name: Current Organic Chemistry

Volume 14 , Issue 15 , 2010

Become EABM
Become Reviewer
Call for Editor


Pentadienyl cation electrocyclizations have played key roles in the syntheses of many complex organic molecules. Herein, theoretical studies on the mechanisms of pentadienyl cation electrocyclizations are reviewed and general principles applicable to the design of such reactions are highlighted.

Keywords: Pentadienyl, carbocation, electrocyclization, Nazarov, quantum chemistry, Cyclopentene rings, Post-Hartree-Fock, Density functional theory, Highest occupied molecular orbital (HOMO), Conrotation, Torquoselectivity, C2 rotation, Houk's torquoselectivity model, Lewis acid activation, Trauner's systems, Vinyl allenes, Hammond Postulate, The Bell-Evans-Polanyi Principle, Zwitterionic species, Piancatelli reaction, Substituents at C3, Brønsted acids, Metal Promoted Cyclizations

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2010
Page: [1561 - 1577]
Pages: 17
DOI: 10.2174/138527210793563297
Price: $58

Article Metrics

PDF: 6