奥弗曼重排反应 (Chinese Wikipedia)

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Larry E. Overman. A general method for the synthesis of amines by the rearrangement of allylic trichloroacetimidates. 1,3 Transposition of alcohol and amine functions. J. Am. Chem. Soc. 1976, 98: 2901–2910. doi:10.1021/ja00426a038.
Overman, L. E. Allylic and propargylic imidic esters in organic synthesis. Accounts of Chemical Research. 1980, 13: 218–224. doi:10.1021/ar50151a005.
Overman, L. E. Thermal and mercuric ion catalyzed [3,3]-sigmatropic rearrangement of allylic trichloroacetimidates. 1,3 Transposition of alcohol and amine functions. Journal of the American Chemical Society. 1974, 96: 597–599. doi:10.1021/ja00809a054.
Chen, Y. K.; Lurain, A. E.; Walsh, P. J. A General, Highly Enantioselective Method for the Synthesis of D and L α-Amino Acids and Allylic Amines. Journal of the American Chemical Society. 2002, 124: 12225–12231. doi:10.1021/ja027271p.
Anderson, C. E.; Overman, L. E. J. Am. Chem. Soc. 2003, 125, 12412–12413. (doi:10.1021/ja037086r)

Organic Syntheses, Coll. Vol. 6, p.507; Vol. 58, p.4 (Article （页面存档备份，存于互联网档案馆）)
Asymmetric Overman Rearrangement Organic Syntheses, Vol. 82, p.134 (2005). (Article （页面存档备份，存于互联网档案馆）)

Organic Syntheses, Coll. Vol. 6, p.507; Vol. 58, p.4 (Article （页面存档备份，存于互联网档案馆）)
Asymmetric Overman Rearrangement Organic Syntheses, Vol. 82, p.134 (2005). (Article （页面存档备份，存于互联网档案馆）)