The Experts below are selected from a list of 6 Experts worldwide ranked by ideXlab platform
Katalin Marthi - One of the best experts on this subject based on the ideXlab platform.
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Optical resolution of 1-(1-naphthyl)ethylamine by its dicarboxylic Acid Derivatives: Structural features of the Oxalic Acid Derivative diastereomeric salt pair.
Chirality, 2009Co-Authors: Laura Bereczki, Petra Bombicz, József Bálint, Gabriella Egri, József Schindler, György Pokol, Elemér Fogassy, Katalin MarthiAbstract:Optical resolution methods were established for racemic 1-(1-naphthyl) ethylamine. The resolving agents were synthesized by N-derivatizing (R)-1-(1-naphthyl) ethylamine with dicarboxylic Acids. Oxalic, malonic, and succinic Acid Derivatives were found to be suitable resolving agents. These resolutions are parallel to a series of optical resolutions of 1-phenylethylamine which had been previously performed by our research group using similar Derivative resolving agents (Balint et al., Tetrahedron: Asymmetry 2001;12:1511–1518.) The comparison of the results of the enantiomer separations is performed. The diastereomeric salts formed with (R)-N-[1-(1-naphthyl)ethyl]oxalamic Acid were investigated by single crystal X-ray diffraction. The crystal structures were compared with the previously published structures of the diastereomers of the phenyl-substituted analogue, namely (R)- and (S)-1-phenylethylammonium (R)-N-(1-phenylethyl)oxalamates (Balint et al., Tetrahedron: Asymmetry 2001;12:1511–1518.) Chirality, 2009. © 2008 Wiley-Liss, Inc.
Laura Bereczki - One of the best experts on this subject based on the ideXlab platform.
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Optical resolution of 1-(1-naphthyl)ethylamine by its dicarboxylic Acid Derivatives: Structural features of the Oxalic Acid Derivative diastereomeric salt pair.
Chirality, 2009Co-Authors: Laura Bereczki, Petra Bombicz, József Bálint, Gabriella Egri, József Schindler, György Pokol, Elemér Fogassy, Katalin MarthiAbstract:Optical resolution methods were established for racemic 1-(1-naphthyl) ethylamine. The resolving agents were synthesized by N-derivatizing (R)-1-(1-naphthyl) ethylamine with dicarboxylic Acids. Oxalic, malonic, and succinic Acid Derivatives were found to be suitable resolving agents. These resolutions are parallel to a series of optical resolutions of 1-phenylethylamine which had been previously performed by our research group using similar Derivative resolving agents (Balint et al., Tetrahedron: Asymmetry 2001;12:1511–1518.) The comparison of the results of the enantiomer separations is performed. The diastereomeric salts formed with (R)-N-[1-(1-naphthyl)ethyl]oxalamic Acid were investigated by single crystal X-ray diffraction. The crystal structures were compared with the previously published structures of the diastereomers of the phenyl-substituted analogue, namely (R)- and (S)-1-phenylethylammonium (R)-N-(1-phenylethyl)oxalamates (Balint et al., Tetrahedron: Asymmetry 2001;12:1511–1518.) Chirality, 2009. © 2008 Wiley-Liss, Inc.
Petra Bombicz - One of the best experts on this subject based on the ideXlab platform.
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Optical resolution of 1-(1-naphthyl)ethylamine by its dicarboxylic Acid Derivatives: Structural features of the Oxalic Acid Derivative diastereomeric salt pair.
Chirality, 2009Co-Authors: Laura Bereczki, Petra Bombicz, József Bálint, Gabriella Egri, József Schindler, György Pokol, Elemér Fogassy, Katalin MarthiAbstract:Optical resolution methods were established for racemic 1-(1-naphthyl) ethylamine. The resolving agents were synthesized by N-derivatizing (R)-1-(1-naphthyl) ethylamine with dicarboxylic Acids. Oxalic, malonic, and succinic Acid Derivatives were found to be suitable resolving agents. These resolutions are parallel to a series of optical resolutions of 1-phenylethylamine which had been previously performed by our research group using similar Derivative resolving agents (Balint et al., Tetrahedron: Asymmetry 2001;12:1511–1518.) The comparison of the results of the enantiomer separations is performed. The diastereomeric salts formed with (R)-N-[1-(1-naphthyl)ethyl]oxalamic Acid were investigated by single crystal X-ray diffraction. The crystal structures were compared with the previously published structures of the diastereomers of the phenyl-substituted analogue, namely (R)- and (S)-1-phenylethylammonium (R)-N-(1-phenylethyl)oxalamates (Balint et al., Tetrahedron: Asymmetry 2001;12:1511–1518.) Chirality, 2009. © 2008 Wiley-Liss, Inc.
József Bálint - One of the best experts on this subject based on the ideXlab platform.
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Optical resolution of 1-(1-naphthyl)ethylamine by its dicarboxylic Acid Derivatives: Structural features of the Oxalic Acid Derivative diastereomeric salt pair.
Chirality, 2009Co-Authors: Laura Bereczki, Petra Bombicz, József Bálint, Gabriella Egri, József Schindler, György Pokol, Elemér Fogassy, Katalin MarthiAbstract:Optical resolution methods were established for racemic 1-(1-naphthyl) ethylamine. The resolving agents were synthesized by N-derivatizing (R)-1-(1-naphthyl) ethylamine with dicarboxylic Acids. Oxalic, malonic, and succinic Acid Derivatives were found to be suitable resolving agents. These resolutions are parallel to a series of optical resolutions of 1-phenylethylamine which had been previously performed by our research group using similar Derivative resolving agents (Balint et al., Tetrahedron: Asymmetry 2001;12:1511–1518.) The comparison of the results of the enantiomer separations is performed. The diastereomeric salts formed with (R)-N-[1-(1-naphthyl)ethyl]oxalamic Acid were investigated by single crystal X-ray diffraction. The crystal structures were compared with the previously published structures of the diastereomers of the phenyl-substituted analogue, namely (R)- and (S)-1-phenylethylammonium (R)-N-(1-phenylethyl)oxalamates (Balint et al., Tetrahedron: Asymmetry 2001;12:1511–1518.) Chirality, 2009. © 2008 Wiley-Liss, Inc.
Gabriella Egri - One of the best experts on this subject based on the ideXlab platform.
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Optical resolution of 1-(1-naphthyl)ethylamine by its dicarboxylic Acid Derivatives: Structural features of the Oxalic Acid Derivative diastereomeric salt pair.
Chirality, 2009Co-Authors: Laura Bereczki, Petra Bombicz, József Bálint, Gabriella Egri, József Schindler, György Pokol, Elemér Fogassy, Katalin MarthiAbstract:Optical resolution methods were established for racemic 1-(1-naphthyl) ethylamine. The resolving agents were synthesized by N-derivatizing (R)-1-(1-naphthyl) ethylamine with dicarboxylic Acids. Oxalic, malonic, and succinic Acid Derivatives were found to be suitable resolving agents. These resolutions are parallel to a series of optical resolutions of 1-phenylethylamine which had been previously performed by our research group using similar Derivative resolving agents (Balint et al., Tetrahedron: Asymmetry 2001;12:1511–1518.) The comparison of the results of the enantiomer separations is performed. The diastereomeric salts formed with (R)-N-[1-(1-naphthyl)ethyl]oxalamic Acid were investigated by single crystal X-ray diffraction. The crystal structures were compared with the previously published structures of the diastereomers of the phenyl-substituted analogue, namely (R)- and (S)-1-phenylethylammonium (R)-N-(1-phenylethyl)oxalamates (Balint et al., Tetrahedron: Asymmetry 2001;12:1511–1518.) Chirality, 2009. © 2008 Wiley-Liss, Inc.
