Effects of Substituents in the 3-Position on the [2 + 2] Pentadienyl Cation Electrocyclization1
- 1 July 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 62 (15) , 5110-5115
- https://doi.org/10.1021/jo9703313
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Identification of multiple transition structures on the potential energy hypersurface for [2+2] electrocyclization of the pentadienyl cation bearing a phosphorus in the 3-positionJournal of Molecular Graphics, 1995
- Theoretical studies of the Nazarov cyclization 3. Torquoselectivity and hyperconjugation in the Nazarov cyclization. The effects of inner versus outer .beta.-methyl and .beta.-silyl groupsThe Journal of Organic Chemistry, 1993
- Theoretical studies of the Nazarov cyclization. 2. The effect of .beta.-silyl and .beta.-methyl groupsThe Journal of Organic Chemistry, 1991
- Structure and inversion barrier of phosphirene and 1,2-dihydrophosphete. An ab initio studyThe Journal of Organic Chemistry, 1991
- Theoretical Studies of the Nazarov Cyclization 1. 1,4-Pentadien-3-one.Tetrahedron Letters, 1991
- Theoretical predictions of torquoselectivity in pentadienyl cation electrocyclizationsThe Journal of Organic Chemistry, 1989
- Not the enolate Claisen rearrangement. A surprising route to the “right-wing” of indanomycin (X-14547A)Tetrahedron Letters, 1986
- Self-consistent molecular orbital methods 25. Supplementary functions for Gaussian basis setsThe Journal of Chemical Physics, 1984
- Self-consistent molecular orbital methods. 21. Small split-valence basis sets for first-row elementsJournal of the American Chemical Society, 1980
- Note on an Approximation Treatment for Many-Electron SystemsPhysical Review B, 1934