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Gyimesi-Forrás K, Akasaka K, Lämmerhofer M, et al. Enantiomer separation of a powerful chiral auxiliary, 2-methoxy-2-(1-naphthyl)propionic acid by liquid chromatography using chiral anion exchanger-type stationary phases in polar-organic mode; investigation of molecular recognition aspects. Chirality. 2005;17:S134-42doi: 10.1002/chir.20123.
Gyimesi-Forrás, K., Akasaka, K., Lämmerhofer, M., Maier, N. M., Fujita, T., Watanabe, M., Harada, N., & Lindner, W. (2005). Enantiomer separation of a powerful chiral auxiliary, 2-methoxy-2-(1-naphthyl)propionic acid by liquid chromatography using chiral anion exchanger-type stationary phases in polar-organic mode; investigation of molecular recognition aspects. Chirality, 17S134-42. https://doi.org/10.1002/chir.20123
Gyimesi-Forrás, Krisztina, et al. "Enantiomer separation of a powerful chiral auxiliary, 2-methoxy-2-(1-naphthyl)propionic acid by liquid chromatography using chiral anion exchanger-type stationary phases in polar-organic mode; investigation of molecular recognition aspects." Chirality vol. 17 (2005): S134-42. doi: https://doi.org/10.1002/chir.20123
Gyimesi-Forrás K, Akasaka K, Lämmerhofer M, Maier NM, Fujita T, Watanabe M, Harada N, Lindner W. Enantiomer separation of a powerful chiral auxiliary, 2-methoxy-2-(1-naphthyl)propionic acid by liquid chromatography using chiral anion exchanger-type stationary phases in polar-organic mode; investigation of molecular recognition aspects. Chirality. 2005;17:S134-42. doi: 10.1002/chir.20123. PMID: 15806575.
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