Diels-Alder reactivities of strained and unstrained cycloalkenes with normal and inverse-electron-demand dienes: activation barriers and distortion/interaction analysis.
The Diels-Alder reactions of the cycloalkenes, cyclohexene through cyclopropene, with a series of dienes--1,3-dimethoxybutadiene, cyclopentadiene, 3,6-dimethyltetrazine, and 3,6-bis(trifluoromethyl)tetrazine--were studied with quantum mechanical calculations and compared with experimental values whe...
Main Authors: | Liu, F, Paton, R, Kim, S, Liang, Y, Houk, K |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2013
|
Similar Items
-
Experimental Diels-Alder reactivities of cycloalkenones and cyclic dienes explained through transition-state distortion energies.
by: Paton, R, et al.
Published: (2011) -
Hyperconjugative Antiaromaticity Activates 4 H -Pyrazoles as Inverse-Electron-Demand Diels–Alder Dienes
by: Levandowski, Brian, et al.
Published: (2020) -
Origins of stereoselectivity in the trans Diels-Alder paradigm.
by: Paton, R, et al.
Published: (2010) -
Diels-Alder exo selectivity in terminal-substituted dienes and dienophiles: experimental discoveries and computational explanations.
by: Lam, Y, et al.
Published: (2009) -
Diels–Alder Adducts of Morphinan-6,8-Dienes and Their Transformations
by: János Marton, et al.
Published: (2022-04-01)