Abstract
The detailed processes in the Claisen rearrangement were observed. The process was vibrationally excited in the electronic ground state by a stimulated Raman process using a 5-fs pulse. The Claisen rearrangement was found to follow a three-step pathway. At first, the C4-O bond is weakened to generate a bisallyl-like intermediate. Next, the formation of a weak C 1-C6 bond results in the generation of an aromatic-like intermediate. Finally, C4-O breaking and C1-C6 formation occur simultaneously to generate the product.
Original language | English |
---|---|
Pages (from-to) | 374-375 |
Number of pages | 2 |
Journal | Chemistry Letters |
Volume | 39 |
Issue number | 4 |
DOIs | |
State | Published - 19 Apr 2010 |