@article{oai:niigata-u.repo.nii.ac.jp:00002603,
 author = {Tayama, Eiji and Sato, Ryota and Takedachi, Keisuke and Iwamoto, Hajime and Hasegawa, Eietsu},
 issue = {24},
 journal = {Tetrahedron, Tetrahedron},
 month = {Jun},
 note = {Selective amine de-alkylation enables the conversion of Sommelet–Hauser rearrangement products into 2-aryl-2-bromoacetic acid derivatives. These compounds are valuable synthetic intermediates in the synthesis of α-aryl-α-amino or α-aryl-β-amino acid derivatives. The method presented herein is a formal de-N,N-dialkylation of Sommelet–Hauser rearrangement products.},
 pages = {4710--4718},
 title = {A formal method for the de-N,N-dialkylation of Sommelet-Hauser rearrangement products},
 volume = {68},
 year = {2012}
}