Will they co-crystallize?
暂无分享,去创建一个
Jerome G. P. Wicker | Richard I. Cooper | Lorraine M. Crowley | S. P. Stokes | Simon E. Lawrence | Oliver Robshaw | Edmund J. Little | S. P. Stokes | S. Lawrence | R. Cooper | L. Crowley | Oliver Robshaw | Edmund J. Little
[1] A. Beatty,et al. A high-yielding supramolecular reaction. , 2002, Journal of the American Chemical Society.
[2] Eleanor J. Gardiner,et al. Validation of a Computational Cocrystal Prediction Tool: Comparison of Virtual and Experimental Cocrystal Screening Results , 2014 .
[3] H. Titi,et al. Hydrogen bonding and pi-pi interactions in 1-benzofuran-2,3-dicarboxylic acid and its 1:1 cocrystals with pyridine, phenazine and 1,4-phenylenediamine. , 2009, Acta crystallographica. Section C, Crystal structure communications.
[4] Peter T. A. Galek,et al. Knowledge-based model of hydrogen-bonding propensity in organic crystals. , 2007, Acta crystallographica. Section B, Structural science.
[5] Jerome G. P. Wicker,et al. Will it crystallise? Predicting crystallinity of molecular materials , 2015 .
[6] Å. Rasmuson,et al. Estimation of Melting Temperature of Molecular Cocrystals Using Artificial Neural Network Model , 2017 .
[7] László Fábián,et al. Cambridge Structural Database Analysis of Molecular Complementarity in Cocrystals , 2009 .
[8] D. Braga,et al. Using Salt Cocrystals to Improve the Solubility of Niclosamide , 2015 .
[9] M. C. Etter. A new role for hydrogen-bond acceptors in influencing packing patterns of carboxylic acids and amides , 1982 .
[10] Christer B. Aakeröy,et al. Building co-crystals with molecular sense and supramolecular sensibility , 2005 .
[11] G. Desiraju,et al. Combinatorial Exploration of the Structural Landscape of Acid–Pyridine Cocrystals , 2014 .
[12] Gaël Varoquaux,et al. Scikit-learn: Machine Learning in Python , 2011, J. Mach. Learn. Res..
[13] C. Hunter,et al. Quantifying intermolecular interactions: guidelines for the molecular recognition toolbox. , 2004, Angewandte Chemie.
[14] T. Lu,et al. Enhancing the Hygroscopic Stability of S-Oxiracetam via Pharmaceutical Cocrystals , 2012 .
[15] Orn Almarsson,et al. Crystal engineering of novel cocrystals of a triazole drug with 1,4-dicarboxylic acids. , 2003, Journal of the American Chemical Society.
[16] Christer B. Aakeröy,et al. Using cocrystals to systematically modulate aqueous solubility and melting behavior of an anticancer drug. , 2009, Journal of the American Chemical Society.
[17] S. P. Stokes,et al. Utilizing Sulfoxide...Iodine Halogen Bonding for Cocrystallization , 2012 .
[18] Aeri Park,et al. The salt-cocrystal continuum: the influence of crystal structure on ionization state. , 2007, Molecular pharmaceutics.
[19] I. Bruno,et al. Cambridge Structural Database , 2002 .
[20] G. Perlovich. Thermodynamic characteristics of cocrystal formation and melting points for rational design of pharmaceutical two-component systems , 2015 .
[21] Margaret C. Etter,et al. Hydrogen bonds as design elements in organic chemistry , 1991 .
[22] Xiaochuan Wang,et al. Five Energetic Cocrystals of BTF by Intermolecular Hydrogen Bond and π-Stacking Interactions , 2013 .
[23] Jeanette T. Dunlap,et al. Crystal engineering approach to forming cocrystals of amine hydrochlorides with organic acids. Molecular complexes of fluoxetine hydrochloride with benzoic, succinic, and fumaric acids. , 2004, Journal of the American Chemical Society.
[24] T. Friščić,et al. Experimental and database studies of three-centered halogen bonds with bifurcated acceptors present in molecular crystals, cocrystals and salts , 2011 .
[25] Christer B Aakeröy,et al. Cocrystal or salt: does it really matter? , 2007, Molecular pharmaceutics.
[26] D. Allan,et al. The formation of paracetamol (acetaminophen) adducts with hydrogen-bond acceptors. , 2002, Acta crystallographica. Section B, Structural science.
[27] Kevin S. Eccles,et al. Co-crystallisation through halogen bonding with racemic or enantiopure sulfinamides , 2013 .
[28] Colin R. Groom,et al. Knowledge-based approaches to co-crystal design , 2014 .
[29] P. Karamertzanis,et al. Can the Formation of Pharmaceutical Cocrystals Be Computationally Predicted? I. Comparison of Lattice Energies , 2009 .
[30] Benjamin M. Scott,et al. How robust is the hydrogen-bonded amide ‘ladder’ motif? , 2007 .
[31] Andrew P. Bradley,et al. The use of the area under the ROC curve in the evaluation of machine learning algorithms , 1997, Pattern Recognit..
[32] Gautam R Desiraju,et al. Crystal engineering: from molecule to crystal. , 2013, Journal of the American Chemical Society.
[33] William Jones,et al. Improving Mechanical Properties of Crystalline Solids by Cocrystal Formation: New Compressible Forms of Paracetamol , 2009 .
[34] Aurora J. Cruz-Cabeza,et al. Acid–base crystalline complexes and the pKa rule , 2012 .
[35] J. Hanley,et al. The meaning and use of the area under a receiver operating characteristic (ROC) curve. , 1982, Radiology.
[36] A. Klamt,et al. Rational coformer or solvent selection for pharmaceutical cocrystallization or desolvation. , 2012, Journal of pharmaceutical sciences.
[37] A. Powell,et al. Crystal design approaches for the synthesis of paracetamol co-crystals , 2012 .