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Chromatographic resolution of enantiomers: Selective review
Charles H. Lochmuller, Rex W. Souter
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http://dx.doi.org/10.1016/S0021-9673(00)95302-02. Chirality. -1997. - V.9. - №.2. - P.99. - 102
Davankov, V.A.
The nature of chiral recognition: Is it a three-point interaction?
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http://dx.doi.org/10.1002/(SICI)1520-636X(1997)9:2<99::AID-CHIR3>3.0.CO;2-BLipka-Belloli, E., Guelzim, A., Yous, S., Lefebvre, J., Descamps-Francois, C., Capet, F., Vaccher, C.
Melatonin receptor agents: Synthesis, resolution by HPLC on polysaccharides chiral stationary phases, absolute configuration, and pharmacology of the enantiomers of (±)-N-[2-(7-fluoro-1,2,3,4- tetrahydronaphthalen-1-yl)ethyl]acetamide
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http://dx.doi.org/10.1002/chir.10204. Nature - 1948. - V.162. - №.4129. - P.963-963
Ogston, A.G.
Interpretation of Experiments on Metabolic processes, using Isotopic Tracer Elements
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http://dx.doi.org/10.1038/162963b0Bentley, R.
Ogston and the development of prochirality theory
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http://dx.doi.org/10.1038/276673a0