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Astha M. Dwivedi, Rajesh G. Gonnade, Suban K. Sahoo, Ashutosh V. Bedekar, “Separation of isomers of chiral thiourea derivatives via spontaneous resolution and rationale of molecular recognition”, CrystEngComm, 2025
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Jin Xu, Yunna Xue, Qi Zhang, Xiangyang Zhang, “Phase equilibrium behaviors of chiral threonine: Phase diagrams, solubility, and thermodynamic model correlations”, Journal of Molecular Liquids, 395 (2024), 123829
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Toms Rekis, “Crystallization of chiral molecular compounds: what can be learned from the Cambridge Structural Database?”, Acta Crystallogr B Struct Sci Cryst Eng Mater, 76:3 (2020), 307
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Alexander A. Bredikhin, Zemfira A. Bredikhina, “Stereoselective Crystallization as a Basis for Single‐Enantiomer Drug Production”, Chem Eng & Technol, 40:7 (2017), 1211
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Zemfira A. Bredikhina, Alexey V. Kurenkov, Dmitry B. Krivolapov, Alexander A. Bredikhin, “Stereoselective crystallization of 3-(2,6-dimethylphenoxy)propane-1,2-diol: preparation of the single-enantiomer drug mexiletine”, Tetrahedron: Asymmetry, 26:10-11 (2015), 577
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Robert R. Fayzullin, Heike Lorenz, Zemfira A. Bredikhina, Alexander A. Bredikhin, Andreas Seidel-Morgenstern, “Solubility and Some Crystallization Properties of Conglomerate Forming Chiral Drug Guaifenesin in Water”, Journal of Pharmaceutical Sciences, 103:10 (2014), 3176
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Patricia Écija, Luca Evangelisti, Montserrat Vallejo, Francisco J. Basterretxea, Alberto Lesarri, Fernando Castaño, Walther Caminati, Emilio J. Cocinero, “Conformational Flexibility of Mephenesin”, J. Phys. Chem. B, 118:20 (2014), 5357
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Alexander A. Bredikhin, Dmitry V. Zakharychev, Zemfira A. Bredikhina, Aidar T. Gubaidullin, Robert R. Fayzullin, “Crystal structure and phase behavior of the tolyl glycerol ethers. From the conglomerate former to the chirality-driven nanogelator”, CrystEngComm, 14:1 (2012), 211
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Rohit Singh, Robert Vince, “2-Azabicyclo[2.2.1]hept-5-en-3-one: Chemical Profile of a Versatile Synthetic Building Block and its Impact on the Development of Therapeutics”, Chem. Rev., 112:8 (2012), 4642
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A. A. Bredikhin, Z. A. Bredikhina, D. V. Zakharychev, “Crystallization of chiral compounds: thermodynamical, structural and practical aspects”, Mendeleev Commun., 22:4 (2012), 171–180
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Mehdi Hatami, Khalil Farhadi, Assem Abdollahpour, “Using dispersive liquid–liquid microextraction and liquid chromatography for determination of guaifenesin enantiomers in human urine”, J of Separation Science, 34:21 (2011), 2933
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Alexander A. Bredikhin, Igor A. Litvinov, Dmitry B. Krivolapov, Bulat R. Fattahov, Aidar T. Gubaidullin, Flyura S. Akhatova, Zemfira A. Bredikhina, “Chirality driven crystallization behavior of ortho, meta, and para-cyanophenyl glycerol ethers”, Journal of Molecular Structure, 981:1-3 (2010), 163
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Alexander A. Bredikhin, Aidar T. Gubaidullin, Zemfira A. Bredikhina, “Absolute configuration and crystal packing chirality for three conglomerate-forming ortho-halogen substituted phenyl glycerol ethers”, Journal of Molecular Structure, 975:1-3 (2010), 323
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Alexander A. Bredikhin, Aidar T. Gubaidullin, Zemfira A. Bredikhina, Dmitry B. Krivolapov, Alexander V. Pashagin, Igor A. Litvinov, “Absolute configuration and crystal packing for three chiral drugs prone to spontaneous resolution: Guaifenesin, methocarbamol and mephenesin”, Journal of Molecular Structure, 920:1-3 (2009), 377
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Alexander A. Bredikhin, Zemfira A. Bredikhina, Flyura S. Akhatova, Dmitry V. Zakharychev, Elena V. Polyakova, “From racemic compounds through metastable to stable racemic conglomerates: crystallization features of chiral halogen and cyano monosubstituted phenyl glycerol ethers”, Tetrahedron: Asymmetry, 20:18 (2009), 2130
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Alexander A. Bredikhin, Zemfira A. Bredikhina, Victorina G. Novikova, Alexander V. Pashagin, Dmitry V. Zakharychev, Aidar T. Gubaidullin, “Three different types of chirality‐driven crystallization within the series of uniformly substituted phenyl glycerol ethers”, Chirality, 20:10 (2008), 1092
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Z. A. Bredikhina, V. G. Novikova, Yu. Ya. Efremov, D. R. Sharafutdinova, A. A. Bredikhin, “4(2)-Methoxyphenyl glycerol ethers in the synthesis of nonracemic di-O,O-acylglycerols”, Russ Chem Bull, 57:11 (2008), 2320
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D. V. Zakharychev, A. A. Bredikhin, “Crystallization of chiral compounds 4. Simple physical model for reconstruction of post-eutectic DSC traces for melting of binary enantiomeric mixtures”, Russ Chem Bull, 56:7 (2007), 1337
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Alexander A. Bredikhin, Zemfira A. Bredikhina, Dmitry V. Zakharychev, Larisa V. Konoshenko, “Spontaneous resolution among chiral glycerol derivatives: crystallization features of ortho-alkoxysubstituted phenyl glycerol ethers”, Tetrahedron: Asymmetry, 18:16 (2007), 1964
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D. V. Zakharychev, S. N. Lazarev, Z. A. Bredikhina, A. A. Bredikhin, “Crystallization of chiral compounds 3. 3-phenoxypropane-1,2-diol and 3-(2-halophenoxy)propane-1,2-diols”, Russ Chem Bull, 55:2 (2006), 230