Abstract
A central idea in organic chemistry for the past 50 years is that cyclopropenyl anion is antiaromatic. A correlation between cycloalkene acidities and allylic bond angles reveals that energetically this is not case, cyclopropenyl anion is nonaromatic.
Original language | English (US) |
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Pages (from-to) | 7370-7372 |
Number of pages | 3 |
Journal | Journal of Organic Chemistry |
Volume | 78 |
Issue number | 14 |
DOIs | |
State | Published - Jul 19 2013 |