New Resolution Technologies Controlled by Chiral Discrimination Mechanisms von Sakai, Kenichi, Sakurai, Rumiko, Nohira, Hiroyuki

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Dielectrically Controlled Enantiomeric Resolution (DCR) of (R)- and (S)-2-Methylpyrrolidine by (R,R)-Tartaric Acid von Sakurai, Rumiko, Yuzawa, Atsushi, Sakai, Kenichi, Hirayama, Noriaki

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Practical resolution of 1-phenyl-2-(4-methylphenyl)ethylamine using a single resolving agent controlled by the dielectric constant of the solvent von Sakai, Kenichi, Sakurai, Rumiko, Nohira, Hiroyuki, Tanaka, Rumiko, Hirayama, Noriaki

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Molecular Mechanisms of Dielectrically Controlled Resolution (DCR) von Sakai, Kenichi, Sakurai, Rumiko, Hirayama, Noriaki

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Optical Rotation Study on Solvent Dependence of Diastereomeric Salt Discrimination Properties von Taniguchi, Kayoko, Sakurai, Rumiko, Sakai, Kenichi, Yasutake, Mikio, Hirose, Takuji

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Molecular mechanism of dielectrically controlled optical resolution (DCR) von Sakai, Kenichi, Sakurai, Rumiko, Akimoto, Toshio, Hirayama, Noriaki

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Resolution of 3-(methylamino)-1-(2-thienyl)propan-1-ol, a new key intermediate for duloxetine, with ( S)-mandelic acid von Sakai, Kenichi, Sakurai, Rumiko, Yuzawa, Atsushi, Kobayashi, Yuka, Saigo, Kazuhiko

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Racemic [1 SR,2 RS,( RS)]- N-cyano(phenyl)methyl-1-aminoindan-2-ol: crystal structure and reactivity towards thermal epimerization in the solid state von Sakurai, Rumiko, Itoh, Osamu, Uchida, Akira, Hattori, Tetsutaro, Miyano, Sotaro, Yamaura, Masanori

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Dielectrically controlled resolution (DCR) of 3-aminopiperidine via diastereomeric salt formation with N-tosyl-(S)-phenylalanine von Sakurai, Rumiko, Sakai, Kenichi, Kodama, Koichi, Yamaura, Masanori

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Practical resolution of 3-aminopyrrolidine via diastereomeric salt formation with ( S)-2-methoxy-2-phenylacetic acid von Sakurai, Rumiko, Yuzawa, Atsushi, Sakai, Kenichi

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Molecular mechanism of DCR phenomenon observed in ( RS)-1-cyclohexylethylamine–mandelic acid resolution system von Sakai, Kenichi, Sakurai, Rumiko, Hirayama, Noriaki

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Solvent-induced chirality control in the enantioseparation of 1-phenylethylamine via diastereomeric salt formation von Kodama, Koichi, Kimura, Yuria, Shitara, Hiroaki, Yasutake, Mikio, Sakurai, Rumiko, Hirose, Takuji

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Chiral discrimination controlled by the solvent dielectric constant von Sakai, Kenichi, Sakurai, Rumiko, Hirayama, Noriaki

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Resolution of 1-cyclohexylethylamine via diastereomeric salt formation with enantiopure 2-phenylacetic acids von Sakai, Kenichi, Yokoyama, Masami, Sakurai, Rumiko, Hirayama, Noriaki

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Practical continuous resolution of α-amino-ε-caprolactam by diastereomeric salt formation using a single resolving agent with a solvent switch method von Sakai, Kenichi, Sakurai, Rumiko, Yuzawa, Atsushi, Hirayama, Noriaki

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Epimerization of Diastereomeric α-Amino Nitriles to Single Stereoisomers in the Solid State von Sakurai, Rumiko, Suzuki, Shuji, Hashimoto, Junichi, Baba, Manabu, Itoh, Osamu, Uchida, Akira, Hattori, Tetsutaro, Miyano, Sotaro, Yamaura, Masanori

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Resolution of racemic cis-1-amino-2-indanol by diastereomeric salt formation with ( S)-2-phenylpropionic acid von Sakurai, Rumiko, Sakai, Kenichi

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Conformational Analysis of Diastereomeric α-Amino Nitriles von SAKURAI, Rumiko, UCHIDA, Akira, HATTORI, Tetsutaro, YAMAURA, Masanori

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Conformational Analysis of Diastereomeric [alpha]-Amino Nitriles von SAKURAI, Rumiko, UCHIDA, Akira, HATTORI, Tetsutaro, YAMAURA, Masanori

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Conformational Analysis of Diastereomeric α-Amino Nitriles von SAKURAI, Rumiko, UCHIDA, Akira, HATTORI, Tetsutaro, YAMAURA, Masanori

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