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Stereoselective Synthesis of Vicinal Diamines

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引用

Reetz, M. T., Jaeger, R., Drewlies, R., & Hübel, M. (1991). Stereoselective Synthesis of Vicinal Diamines. Angewandte Chemie, International Edition in English, 30(1), 103-106. doi:10.1002/anie.199101031.


引用: https://hdl.handle.net/21.11116/0000-000E-7B28-C
要旨
α-Amino aldimines such as 1, which are readily accessible from amino acids, react with alkyllithium and -cerium compounds in a chelation-controlled manner to give the vicinal diamines 2 in optical yields of up to 90%. However, if the donor strength of the aldimine nitrogen atom is weakened by the electron-withdrawing tosyl group, the chelation effect is suppressed and reaction with Grignard reagents gives preferentially the stereoisomeric adducts with opposite relative configuration. Bn = benzyl.