What is it about?
The reaction proceeded in good yield to afford the desired alpha-aryl azetidinic acid esters without any detectable amount of the competitive [1,2] Stevens rearrangement products. The ring-strain of four-membered N-heterocycles unstabilizes an ammonium enolate form and enables the efficient genaration of a carbanionic ylide, which is a desired intermediate for the Sommelet–Hauser rearrangement. This effect would enhance the rate of the Sommelet–Hauser rearrangement. As a further synthetic application, the asymmetric rearrangement involving N-to-C chirality transmission followed by the regio- and stereo-controlled nucleophilic ring-openings of the products were demonstrated. The corresponding acyclic quaternary alpha-aryl amino acid esters were obtained with excellent enantio-purities by these successive stereoselective transmissions.
Why is it important?
Although the Sommelet–Hauser rearrangement still has structural limitations, our method provides efficient access to various types of -aryl amino acid derivatives. This study will expand the synthetic scope and utility of not only the Sommelet–Hauser rearrangement but also analogous sigmatropic rearrangements.
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This page is a summary of: Ring-Strain Effects in Base-Induced Sommelet-Hauser Rearrangement: Application to Successive Stereocontrolled Transformations, European Journal of Organic Chemistry, June 2016, Wiley, DOI: 10.1002/ejoc.201600611.
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