During our studies of carbocation rearrangements we have encountered many reactions that can be described as both concerted and asynchronous. Such reactions involve no intermediates (they are concerted) but they do involve several "events" that do not occur simultaneously (these events occur asynchronously). An example is shown above. The reaction shown is an example of a hiscotropic reaction in which a hydrogen shifts over two carbons and a 3-membered ring opens in a process with a single transition state structure. As you can see from the structures along the reaction coordinate, however, migration of the hydrogen precedes ring-opening. Such processes are sometimes tied to potential energy surfaces with unsusual features such as flat plateaues and bifurcations. We have found that concerted asynchronous reactions may also be common occurrences in the processes used by Nature to construct complex terpene natural products. Key papers:
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