Related Articles:

Practical Synthesis of Optically Active Fluorine-substituted. ALPHA.-Phenylethylamines by Retardation of Hydrogenolytic Cleavage at Benzylic Position

[Kanai, Masatomi; Yasumoto, Manabu; Kuriyama, Yokusu; Inomiya, Kenjin; Katsuhara, Yutaka; Higashiyama, Kimio; Ishii, Akihiro Chemistry Letters, 2004 , vol. 33, # 11 p. 1424 - 1425]

A facile method for the asymmetric synthesis of enantiomerically pure 1-(2-fluorophenyl)-ethylamine [1]

[Bringmann, G.; Geisler, J.-P. Journal of Fluorine Chemistry, 1990 , vol. 49, # 1 p. 67 - 73]

Practical Synthesis of Optically Active Fluorine-substituted. ALPHA.-Phenylethylamines by Retardation of Hydrogenolytic Cleavage at Benzylic Position

[Chemistry Letters, , vol. 33, # 11 p. 1424 - 1425]

Practical Synthesis of Optically Active Fluorine-substituted. ALPHA.-Phenylethylamines by Retardation of Hydrogenolytic Cleavage at Benzylic Position

[Chemistry Letters, , vol. 33, # 11 p. 1424 - 1425]

Asymmetric Synthesis of Nonracemic Primary Amines via Spiroborate-Catalyzed Reduction of Pure (E)-and (Z)-O-Benzyloximes: Applications toward the Synthesis of …

[Journal of Organic Chemistry, , vol. 78, # 11 p. 5314 - 5327]