Computational Studies on the Electrocyclizations of
1-Amino-1,3,5-hexatrienes
Vildan Adar Guner
K. N. Houk
Ian W. Davies
10.1021/jo048540s.s001
https://acs.figshare.com/articles/journal_contribution/Computational_Studies_on_the_Electrocyclizations_of_1_Amino_1_3_5_hexatrienes/3315979
Electrocyclizations of 1,3,5-hexatrienes containing up to four electron-donating and/or electron
withdrawing substituents have been studied computationally using the hybrid density functional,
B3LYP. Electron donating substituents at positions C-1 and C-5 decrease activation barriers by
0.3 to 2.3 kcal/mol. Introducing of an electron-withdrawing group, CO<sub>2</sub>Me, at C-4 further decreases
the activation energy by 7 kcal/mol. Electron-withdrawing groups (NO<sub>2</sub>, SO<sub>2</sub>Ph and CN<sup>+</sup>Me<sub>2</sub>) at
C-2 have a profound effect of 17−25 kcal/mol on the activation energy.
2004-11-12 00:00:00
decrease activation barriers
CO
substituent
B 3LYP Electron
Electrocyclization
activation energy
kcal