@article{oai:niigata-u.repo.nii.ac.jp:00002233,
 author = {Tayama, Eiji and Orihara, Kiwako and Kimura, Hiroshi},
 issue = {20},
 journal = {Organic and Biomolecular Chemistry, Organic and Biomolecular Chemistry},
 month = {Aug},
 note = {The Stevens rearrangement of N-allylic α-aryl amino acid-derived ammonium salts and the Sommelet–Hauser rearrangement of N-benzylic α-alkyl amino acid-derived ammonium salts are shown to proceed with remarkably high levels of diastereoselectivity.  The methods presented in this work provide new routes to optically active α-quaternary α-aryl amino acid derivatives.},
 pages = {3673--3680},
 title = {New synthetic routes to optically active α-quaternary α-aryl amino acid derivatives via the diastereoselective Stevens and Sommelet–Hauser rearrangements},
 volume = {6},
 year = {2008}
}