Pure and Applied Chemistry

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• Roux Christèle, Candy Mathieu, Pons Jean-Marc, Chuzel Olivier, Bressy Cyril: Stereocontrol of All-Carbon Quaternary Centers through Enantioselective Desymmetrization of Meso Primary Diols by Organocatalyzed Acyl Transfer. Angew. Chem. 2014, 126, 785. <http://dx.doi.org/10.1002/ange.201308268>
• Roux Christèle, Candy Mathieu, Pons Jean-Marc, Chuzel Olivier, Bressy Cyril: Stereocontrol of All-Carbon Quaternary Centers through Enantioselective Desymmetrization of Meso Primary Diols by Organocatalyzed Acyl Transfer. Angew. Chem. Int. Ed. 2014, 53, 766. <http://dx.doi.org/10.1002/anie.201308268>
• Greco Cristina, Marini Alberto, Frezza Elisa, Ferrarini Alberta: From the Molecular Structure to Spectroscopic and Material Properties: Computational Investigation of a Bent-Core Nematic Liquid Crystal. ChemPhysChem 2014, n/a. <http://dx.doi.org/10.1002/cphc.201301030>
• Nolsøe Jens M. J., Hansen Trond V.: Asymmetric Iodolactonization: An Evolutionary Account. Eur. J. Org. Chem. 2014, n/a. <http://dx.doi.org/10.1002/ejoc.201301400>
• Lomas John S.: 1 H NMR spectra of butane-1,4-diol and other 1,4-diols: DFT calculation of shifts and coupling constants. Magn. Reson. Chem. 2014, 52, 87. <http://dx.doi.org/10.1002/mrc.4039>
• Fujita Shinsaku: Three aspects of an absolute configuration on the basis of the stereoisogram approach and revised terminology on related stereochemical concepts. J Math Chem 2014. <http://dx.doi.org/10.1007/s10910-014-0326-0>
• Fries Patrick, Müller Melanie Kim, Hartung Jens: Stereoselective synthesis of side chain-functionalized tetrahydropyrans from 5-hexenols. Tetrahedron 2014, 70, 1336. <http://dx.doi.org/10.1016/j.tet.2013.12.019>
• Kempter Irina, Frensch Britta, Kopf Thomas, Kluge Ralph, Csuk René, Svoboda Ingrid, Fuess Hartmut, Hartung Jens: Synthesis and structural characterization of the isomuscarines. Tetrahedron 2014, 70, 1918. <http://dx.doi.org/10.1016/j.tet.2013.12.085>
• Han Lu-Lu, Li Zhong-Hui, Chen Jiang-Shan, Wang Xing-Po, Sun Di: Solution and Mechanochemical Syntheses of Two Novel Cocrystals: Ligand Length Modulated Interpenetration of Hydrogen-Bonded 2D 63-hcb Networks Based on a Robust Trimeric Heterosynthon. Crystal Growth & Design 2014, 14, 1221. <http://dx.doi.org/10.1021/cg4017454>
• Cruz-Cabeza Aurora J., Bernstein Joel: Conformational Polymorphism. Chem. Rev. 2014, 114, 2170. <http://dx.doi.org/10.1021/cr400249d>
• Dickson Callum J., Madej Benjamin D., Skjevik Åge A., Betz Robin M., Teigen Knut, Gould Ian R., Walker Ross C.: Lipid14: The Amber Lipid Force Field. J. Chem. Theory Comput. 2014, 10, 865. <http://dx.doi.org/10.1021/ct4010307>
• Johnstone Timothy C., Lippard Stephen J.: The Chiral Potential of Phenanthriplatin and Its Influence on Guanine Binding. J. Am. Chem. Soc. 2014, 136, 2126. <http://dx.doi.org/10.1021/ja4125115>
• Condon David E., Yildirim Ilyas, Kennedy Scott D., Mort Brendan C., Kierzek Ryszard, Turner Douglas H.: Optimization of an AMBER Force Field for the Artificial Nucleic Acid, LNA, and Benchmarking with NMR of L(CAAU). J. Phys. Chem. B 2014, 118, 1216. <http://dx.doi.org/10.1021/jp408909t>
• Hong Sung-Gil, Kim Han Sol, Kim Jungbae: Highly Stabilized Lipase in Polyaniline Nanofibers for Surfactant-Mediated Esterification of Ibuprofen. Langmuir 2014, 30, 911. <http://dx.doi.org/10.1021/la404189e>
• Weber Fabian, Brückner Reinhard: Conformational Analysis of δ-Lactones by DFT Calculations: The Parent Compound and its Monomethyl and Selected Dimethyl Derivatives. Chem. Eur. J. 2013, 19, 1288. <http://dx.doi.org/10.1002/chem.201202988>
• Núñez Irene, Merino Estíbaliz, Lecea Mercedes, Pieraccini Silvia, Spada Gian Piero, Rosini Carlo, Mazzeo Giuseppe, Ribagorda María, Carreño M. Carmen: Control of the Helical Chirality of Enantiopure Sulfinyl (Z )-Azobenzene-Based Photoswitches. Chem. Eur. J. 2013, 19, 3397. <http://dx.doi.org/10.1002/chem.201203243>
• Zask Arie, Murphy John, Ellestad George A.: Biological Stereoselectivity of Atropisomeric Natural Products and Drugs. Chirality 2013, 25, 265. <http://dx.doi.org/10.1002/chir.22145>
• Gerlach Hans: Chirality: A Relational Geometric-Physical Property. Chirality 2013, 25, 684. <http://dx.doi.org/10.1002/chir.22216>
• Lomas John S.: 1 H NMR spectra of ethane-1,2-diol and other vicinal diols in benzene: GIAO/DFT shift calculations. Magn. Reson. Chem. 2013, 51, 32. <http://dx.doi.org/10.1002/mrc.3899>
• Lomas John S.: 1 H NMR spectra of alkane-1,3-diols in benzene: GIAO/DFT shift calculations. Magn. Reson. Chem. 2013, 51, 469. <http://dx.doi.org/10.1002/mrc.3973>
• Pogodin Sergey, Assadi Naela, Agranat Israel: Conformational space of tetrakis(2-naphthalenyl)ethene: a naphthologous AIE luminogen. Struct Chem 2013, 24, 1747. <http://dx.doi.org/10.1007/s11224-013-0331-0>
• Grulich Michal, Štěpánek Václav, Kyslík Pavel: Perspectives and industrial potential of PGA selectivity and promiscuity. Biotechnology Advances 2013, 31, 1458. <http://dx.doi.org/10.1016/j.biotechadv.2013.07.005>
• Jacobsen Elisabeth Egholm, el-Behairy Mohammed Farrag, Skattebøl Lars, Anthonsen Thorleif: Enantiopure dihalocyclopropyl alcohols and esters by lipase catalyzed kinetic resolution. Journal of Biotechnology 2013, 168, 284. <http://dx.doi.org/10.1016/j.jbiotec.2013.08.030>
• Johnstone Timothy C., Lippard Stephen J.: Conformational isomerism of trans-[Pt(NH2C6H11)2I2] and the classical Wernerian chemistry of [Pt(NH2C6H11)4]X2 (X=Cl, Br, I). Polyhedron 2013, 52, 565. <http://dx.doi.org/10.1016/j.poly.2012.08.010>
• Ostrowski Sławomir, Jamróz Michał H., Dobrowolski Jan Cz.: A study on the stability, chirality, and theoretical spectra of the heterofullerenes C69X (X=N, P, As, B, Si, Ge). Tetrahedron: Asymmetry 2013, 24, 1097. <http://dx.doi.org/10.1016/j.tetasy.2013.07.022>
• Stilinović Vladimir, Kaitner Branko: Structural and Thermodynamic Insight into Solid State Phase Transition Mechanism of a 1,3,3′-Triketone. Crystal Growth & Design 2013, 13, 1703. <http://dx.doi.org/10.1021/cg400016z>
• Bulacu Monica, Goga Nicolae, Zhao Wei, Rossi Giulia, Monticelli Luca, Periole Xavier, Tieleman D. Peter, Marrink Siewert J.: Improved Angle Potentials for Coarse-Grained Molecular Dynamics Simulations. J. Chem. Theory Comput. 2013, 9, 3282. <http://dx.doi.org/10.1021/ct400219n>
• Dicks Andrew P.: A Supplement to the “Historical Origins of Stereochemical Line and Wedge Symbolism”. J. Chem. Educ. 2013, 90, 1109. <http://dx.doi.org/10.1021/ed400249y>
• Poger David, Mark Alan E.: The Relative Effect of Sterols and Hopanoids on Lipid Bilayers: When Comparable Is Not Identical. J. Phys. Chem. B 2013, 117, 16129. <http://dx.doi.org/10.1021/jp409748d>
• Lago Ana Belén, Carballo Rosa, Rodríguez-Hermida Sabina, Vázquez-López Ezequiel M.: Control over the preparation of two pH-dependent Cu(ii) supramolecular isomers based on 1,3,5-benzenetricarboxylic acid and the bis(4-pyridylthio)methane ligand. CrystEngComm 2013, 15, 1563. <http://dx.doi.org/10.1039/c2ce26652k>
• Yuan Shuai, Wang Hua, Wang Deng-Xu, Lu Hai-Feng, Feng Sheng-Yu, Sun Di: Reactant ratio-modulated six new copper(i)–iodide coordination complexes based on diverse [CumIm] aggregates and biimidazole linkers: syntheses, structures and temperature-dependent luminescence properties. CrystEngComm 2013, 15, 7792. <http://dx.doi.org/10.1039/c3ce41021h>
• Lago Ana Belén, Carballo Rosa, Fabelo Oscar, Fernández-Hermida Nuria, Lloret Francesc, Vázquez-López Ezequiel M.: Metallosupramolecular compounds based on Cu(ii)/oxalate/twisted NSSN ligands showing a new in situ S–C bond cleavage. CrystEngComm 2013, 15, 10550. <http://dx.doi.org/10.1039/c3ce41525b>
• Gupta Pankaj, Mahajan Neha, Taneja Subhash Chandra: Recent advances in the stereoselective synthesis of 1,3-diols using biocatalysts. Catal. Sci. Technol. 2013, 3, 2462. <http://dx.doi.org/10.1039/c3cy00125c>
• Sun Di, Xu Meng-Zhen, Liu Shan-Shan, Yuan Shuai, Lu Hai-Feng, Feng Sheng-Yu, Sun Dao-Feng: Eight Zn(ii) coordination networks based on flexible 1,4-di(1H-imidazol-1-yl)butane and different dicarboxylates: crystal structures, water clusters, and topologies. Dalton Trans. 2013, 42, 12324. <http://dx.doi.org/10.1039/c3dt51114f>
• Yuan Shuai, Liu Shan-Shan, Lu Hai-Feng, Xu Meng-Zhen, Sun Di: A two-dimensional silver–iodide organic network constructed from a unique [Ag6I6] hexagonal prism-based one-dimensional column motif. Acta Crystallogr C Cryst Struct Commun 2013, 69, 216. <http://dx.doi.org/10.1107/S0108270113002916>
• Seidel Rüdiger, Goddard Richard, Oppel Iris: Structural Diversity of Metallosupramolecular Assemblies Based on the Bent Bridging Ligand 4,4′-Dithiodipyridine †. Polymers 2013, 5, 527. <http://dx.doi.org/10.3390/polym5020527>
• Krasnov Victor P., Gruzdev Dmitry A., Levit Galina L.: Nonenzymatic Acylative Kinetic Resolution of Racemic Amines and Related Compounds. Eur J Org 2012, 2012, 1471. <http://dx.doi.org/10.1002/ejoc.201101489>
• Lomas John S.: 1H NMR study of the hetero-association of unsaturated alcohols with pyridine. J. Phys. Org. Chem. 2012, 25, 620. <http://dx.doi.org/10.1002/poc.1953>
• Lomas John S., Maurel François: GIAO/DFT calculations of relative conformer energies and 1H NMR shifts of unsaturated alcohols in benzene. J. Phys. Org. Chem. 2012, 25, 628. <http://dx.doi.org/10.1002/poc.1954>
• Fujita Shinsaku: Stereoisograms of trigonal bipyramidal compounds: II. RS-stereogenicity/RS-stereoisomerism versus stereogenicity/stereoisomerism, leading to a revised interpretation of Berry’s pseudorotation. J Math Chem 2012, 50, 1815. <http://dx.doi.org/10.1007/s10910-012-0007-9>
• Fujita Shinsaku: Importance of the proligand-promolecule model in stereochemistry. II. The stereoisogram approach to stereoisomeric features of prismane derivatives. J Math Chem 2012, 50, 2168. <http://dx.doi.org/10.1007/s10910-012-0024-8>
• Fujita Shinsaku: Importance of the proligand-promolecule model in stereochemistry. I. The unit-subduced-cycle-index (USCI) approach to geometric features of prismane derivatives. J Math Chem 2012, 50, 2202. <http://dx.doi.org/10.1007/s10910-012-0025-7>
• Siodła Tomasz, Hoffmann Marcin, Koroniak Henryk: Photoisomerization of fluorinated 1,3-dimethyl-5-propenyl uracils. J Photochem Photobiol A Chem 2012, 231, 60. <http://dx.doi.org/10.1016/j.jphotochem.2012.01.010>
• Hao Hong-Jun, Sun Di, Liu Fu-Jing, Huang Rong-Bin, Zheng Lan-Sun: Dicarboxylate-controlled three Zn(II) coordination polymers incorporating flexible 1,2-bis(imidazol-1′-yl)ethane ligand: Syntheses, structures, thermal stabilities and photoluminescent properties. J Mole Struct 2012, 1012, 131. <http://dx.doi.org/10.1016/j.molstruc.2011.12.030>
• Kartal Zeki, T��rk Tu��ba, Smol���yakov Alexander F., Dolgushin Fedor M., Ginzburg Allan G., Bashilov Vasily V., Antipin Mikhail Yu., Luo Geng-Geng, Wu Dong-Liang, Liu Li, Wu Sheng-Hui, Li Dong-Xu, Xiao Zi-Jing, Dai Jing-Cao: FT-IR spectroscopic and thermal study of M(1,6-hexanedithiol)Ni(CN)4���2(1,4-dioxane) clathrate (M=Mn, Co, Ni and Cd). Journal of Molecular Structure 2012, 1014, 74. <http://dx.doi.org/10.1016/j.molstruc.2012.02.003>
• Fujita Shinsaku: Extended pseudoasymmetry and geometric prochirality clarifying the scope of the concepts of holantimers and stereoisograms. Tetrahedron: Asymmetry 2012, 23, 623. <http://dx.doi.org/10.1016/j.tetasy.2012.04.020>
• Zhou Wanding, Nakhleh Luay: Quantifying and Assessing the Effect of Chemical Symmetry in Metabolic Pathways. J. Chem. Inf. Model. 2012, 52, 2684. <http://dx.doi.org/10.1021/ci300259u>
• Knight Fergus R., Randall Rebecca A. M., Athukorala Arachchige Kasun S., Wakefield Lucy, Griffin John M., Ashbrook Sharon E., Bühl Michael, Slawin Alexandra M. Z., Woollins J. Derek: Noncovalent Interactions in Peri-Substituted Chalconium Acenaphthene and Naphthalene Salts: A Combined Experimental, Crystallographic, Computational, and Solid-State NMR Study. Inorg. Chem. 2012, 51, 11087. <http://dx.doi.org/10.1021/ic301627y>
• Fokin Andrey A., Chernish Lesya V., Gunchenko Pavel A., Tikhonchuk Evgeniya Yu., Hausmann Heike, Serafin Michael, Dahl Jeremy E. P., Carlson Robert M. K., Schreiner Peter R.: Stable Alkanes Containing Very Long Carbon–Carbon Bonds. J. Am. Chem. Soc. 2012, 134, 13641. <http://dx.doi.org/10.1021/ja302258q>
• Rogachev Andrey Yu., Wen Xiao-Dong, Hoffmann Roald: Jailbreaking Benzene Dimers. S J Am Chem Soc 2012, 134, 8062. <http://dx.doi.org/10.1021/ja302597r>
• Wehle Marko, Vilotijevic Ivan, Lipowsky Reinhard, Seeberger Peter H., Varon Silva Daniel, Santer Mark: Mechanical Compressibility of the Glycosylphosphatidylinositol (GPI) Anchor Backbone Governed by Independent Glycosidic Linkages. J. Am. Chem. Soc. 2012, 134, 18964. <http://dx.doi.org/10.1021/ja302803r>
• Newhouse Timothy R., Li Xin, Blewett Megan M., Whitehead Clare M. C., Corey E. J.: A Tetradentate Ligand for the Enantioselective Ti(IV)-Promoted Oxidation of Sulfides to Sulfoxides: Origin of Enantioselectivity. J. Am. Chem. Soc. 2012, 134, 17354. <http://dx.doi.org/10.1021/ja305991k>
• Knoll Wolfgang, Kaneno Daisuke, Bobek Michael M., Brecker Lothar, Rosenberg Murray G., Tomoda Shuji, Brinker Udo H.: Intra- and Intermolecular Reaction Selectivities of γ-Substituted Adamantanylidenes. J Org Chern 2012, 77, 1340. <http://dx.doi.org/10.1021/jo202132c>
• Dai Fangna, Sun Di, Sun Wenming, Liu Yun-Qi, Sun Daofeng: Conformation variation of tris(2-carboxyethyl)isocyanuric acid induced by cocrystallized N-heterocyclic organic molecules. CrysEngComm 2012, 14, 1376. <http://dx.doi.org/10.1039/c1ce06209c>
• Aschenbach Lara K., Knight Fergus R., Randall Rebecca A. M., Cordes David B., Baggott Alex, Bühl Michael, Slawin Alexandra M. Z., Woollins J. Derek: Onset of three-centre, four-electron bonding in peri-substituted acenaphthenes: A structural and computational investigation. DALTON T 2012, 41, 3141. <http://dx.doi.org/10.1039/c1dt11697e>
• Li Yun-Hua, Sun Di, Hao Hong-Jun, Zhao Yang, Huang Rong-Bin, Zheng Lan-Sun: Three novel organosilver(I) coordination networks constructed from diallylmelamine and polycarboxylates incorporating silver-vinyl bonding. DALTON T 2012, 41, 2289. <http://dx.doi.org/10.1039/c1dt11866h>
• Seal Prasenjit, Papajak Ewa, Yu Tao, Truhlar Donald G.: Statistical thermodynamics of 1-butanol, 2-methyl-1-propanol, and butanal. Journal Chemical Physics 2012, 136, 034306. <http://dx.doi.org/10.1063/1.3674995>
• Papajak Ewa, Seal Prasenjit, Xu Xuefei, Truhlar Donald G.: Thermochemistry of radicals formed by hydrogen abstraction from 1-butanol, 2-methyl-1-propanol, and butanal. J. Chem. Phys. 2012, 137, 104314. <http://dx.doi.org/10.1063/1.4742968>
• Sun Di, Yan Zhi-Hao: A novel one-dimensional silver cylinder stabilized by mixed 2-mercaptobenzoic acid and ethylenediamine ligands. Acta Crystallogr C Cryst Struct Commun 2012, 68, m229. <http://dx.doi.org/10.1107/S0108270112031125>
• Fujita Shinsaku: Symmetry-Itemized Enumeration of Cubane Derivatives as Three-Dimensional Entities by the Elementary-Superposition Method of the USCI Approach. Bull. Chem. Soc. Jpn. 2012, 85, 811. <http://dx.doi.org/10.1246/bcsj.20120009>
• Zimmer Lucie E., Sparr Christof, Gilmour Ryan: Konformative Fluoreffekte in der Organokatalyse: eine neuartige Strategie zum molekularen Design. angew chemie 2011, 123, 12062. <http://dx.doi.org/10.1002/ange.201102027>
• Nakanishi Waka, Matsuno Taisuke, Ichikawa Junji, Isobe Hiroyuki: Illusory Molecular Expression of “Penrose Stairs” by an Aromatic Hydrocarbon. Angew Chem 2011, 123, 6172. <http://dx.doi.org/10.1002/ange.201102210>
• Zimmer Lucie E., Sparr Christof, Gilmour Ryan: Fluorine Conformational Effects in Organocatalysis: An Emerging Strategy for Molecular Design. Angew Chem Int E 2011, 50, 11860. <http://dx.doi.org/10.1002/anie.201102027>
• Nakanishi Waka, Matsuno Taisuke, Ichikawa Junji, Isobe Hiroyuki: Illusory Molecular Expression of “Penrose Stairs” by an Aromatic Hydrocarbon. Angew Chem Int Ed 2011, 50, 6048. <http://dx.doi.org/10.1002/anie.201102210>
• de Diego Heidi Lopez, Bond Andrew D., Dancer Robert James: Formation of solid solutions between racemic and enantiomeric citalopram oxalate. Chirality 2011, 23, 408. <http://dx.doi.org/10.1002/chir.20943>
• Lohr Andreas, Würthner Frank: Chiral Amplification, Kinetic Pathways, and Morphogenesis of Helical Nanorods upon Self-assembly of Dipolar Merocyanine Dyes. Isr. J. Chem. 2011, 51, 1052. <http://dx.doi.org/10.1002/ijch.201100023>
• Can Nafiz O.: HPLC determination of cefprozil in tablets using monolithic and C18 silica columns. J Sep Science 2011, n/a. <http://dx.doi.org/10.1002/jssc.201100170>
• Fujita Shinsaku: Theory of organic stereoisomerism in harmony with molecular symmetry. J Math Chem 2011, 49, 95. <http://dx.doi.org/10.1007/s10910-010-9732-0>
• Luo Geng-Geng, Wu Dong-Liang, Liu Li, Xia Jiu-Xu, Li Dong-Xu, Dai Jing-Cao, Xiao Zi-Jing: A discrete water hexamer with a new planar tetrameric water moiety trapped in the crystal host of [Ag(azelate)(4,4′-bipyridine)]·(H2O)3. J Mole Struct 2011, 1005, 172. <http://dx.doi.org/10.1016/j.molstruc.2011.08.046>
• Sun Di, Li Yun-Hua, Hao Hong-Jun, Liu Fu-Jing, Wen Yi-Mei, Huang Rong-Bin, Zheng Lan-Sun: Solvent-Controlled Rare Case of a Triple Helical Molecular Braid Assembled from Proton-Transferred Sebacic Acid. Growth Des 2011, 11, 3323. <http://dx.doi.org/10.1021/cg2006953>
• Hao Hong-Jun, Sun Di, Liu Fu-Jing, Huang Rong-Bin, Zheng Lan-Sun: Discrete Octamer Water Cluster and 1D T5(2) Water Tape Trapped in Two Luminescent Zn(II)/1,2-Bis(imidazol-1′-yl)ethane/Dicarboxylate Hosts: From 2D (4,4) Net to 3D 5-Fold Interpenetrated Diamond Network. Growth Des 2011, 11, 5475. <http://dx.doi.org/10.1021/cg201067q>
• Díaz-Urrutia Christian, Baker R. Tom, Wu Ruilian, Silks L. A. “Pete”, Hanson Susan K., Sedai Baburam: Comparison of Copper and Vanadium Homogeneous Catalysts for Aerobic Oxidation of Lignin Models. ACS Catal 2011, 1, 794. <http://dx.doi.org/10.1021/cs200149v>
• Dorofeeva Olga V., Mitin Alexander V., Altova Ekaterina P., Karasev Nikolai M., Nabiev Orudzh G., Vilkov Lev V., Oberhammer Heinz: Anomeric effect in N-azidomethylpyrrolidine: gas-phase electron diffraction and theoretical study. Phys Chem Chem Phys 2011, 13, 1490. <http://dx.doi.org/10.1039/c0cp00894j>
• Ramesh Veera V. E., Roy Arup, Vijayadas Kuruppanthara N., Kendhale Amol M., Prabhakaran Panchami, Gonnade Rajesh, Puranik Vedavati G., Sanjayan Gangadhar J.: Conformationally rigid aromatic amino acids as potential building blocks for abiotic foldamers. Org Biomol Chem 2011, 9, 367. <http://dx.doi.org/10.1039/c0ob00593b>
• Sakamoto Masami, Fujita Kazuyuki, Yagishita Fumitoshi, Unosawa Atsushi, Mino Takashi, Fujita Tsutomu: Kinetic resolution of racemic amines using provisional molecular chirality generated by spontaneous crystallization. Chem Commun 2011, 47, 4267. <http://dx.doi.org/10.1039/c1cc00081k>
• Jiang Feilong, Zhang Shuquan, Ma Jie, Li Xingjun, Hong Maochun, Bu Yang: Topological variability of Zn(ii) and Co(ii) 3D coordination polymers obtained through solvothermal in situ disulfide cleavage. CrystEngCommun 2011, 13, 6323. <http://dx.doi.org/10.1039/c1ce05592e>
• Sun Di, Li Yun-Hua, Hao Hong-Jun, Liu Fu-Jing, Zhao Yang, Huang Rong-Bin, Zheng Lan-Sun: Syntheses, structures and photoluminescent properties of a series of Ag(i) coordination architectures based on 2,4-diamino-6-methyl-1,3,5-triazine and dicarboxylates: from a 0D discrete molecule to a 3D infinite network. CrystEngCommun 2011, 13, 6431. <http://dx.doi.org/10.1039/c1ce05683b>
• Pérez J., Carrascosa R., García L., Barandika G., Calderón-Casado A., Pérez E., Serrano J. L., Santana M. D.: Coordination to metal centers: A tool to fix high energy conformations in organic molecules. Application to 2,4,4-trimethyl-1,5,9-triazacyclododec-1-ene and related macrocycles. DALTON T 2011, 40, 9504. <http://dx.doi.org/10.1039/c1dt11281c>
• Ding Lei, Lin Lirong, Liu Chengyong, Li Hongkun, Qin Anjun, Liu Yan, Song Ling, Zhang Hui, Tang Ben Zhong, Zhao Yufen: Concentration effects in solid-state CD spectra of chiral atropisomeric compounds. New J Chem 2011, 35, 1781. <http://dx.doi.org/10.1039/c1nj20185a>
• Bentley Ronald: Chiral: A confusing etymology. Chirality 2010, 22, 1. <http://dx.doi.org/10.1002/chir.20699>
• Poger David, Van Gunsteren Wilfred F., Mark Alan E.: A new force field for simulating phosphatidylcholine bilayers. J Comput Chem 2010, 31, 1117. <http://dx.doi.org/10.1002/jcc.21396>
• Hussaini Syed R.: Interconversion of Fischer and zig-zag projections learning stereochemistry with the help of hands. Reson 2010, 15, 351. <http://dx.doi.org/10.1007/s12045-010-0029-1>
• Marinho Maria Vanda, Visentin Lorenzo do Canto, de Souza Márcia Cristina, Diniz Renata, Krambrock Klaus, Yoshida Maria Irene, Machado Flávia C.: Syntheses, crystal structures and electron paramagnetic resonance studies of CoII- and MnII-coordination polymers with the twisted ligand di(4-pyridyl)disulfide in double bridge fashion. J Polyhedron 2010, 29, 2657. <http://dx.doi.org/10.1016/j.poly.2010.06.004>
• Couzijn Erik P. A., Slootweg J. Chris, Ehlers Andreas W., Lammertsma Koop: Stereomutation of Pentavalent Compounds: Validating the Berry Pseudorotation, Redressing Ugi’s Turnstile Rotation, and Revealing the Two- and Three-Arm Turnstiles. J Am Chem Soc 2010, 132, 18127. <http://dx.doi.org/10.1021/ja105306s>
• Amoedo Almudena, Carballo Rosa, García-Martínez Emilia, Lago Ana Belén, Vázquez-López Ezequiel M.: Molecular metallocycles, acyclic metallodimers and 2D coordination polymers containing the twisted ligand bis(pyrimidin-2-ylthio)methane. Dalton Trans 2010, 39, 2385. <http://dx.doi.org/10.1039/b915942h>
• Belén Lago Ana, Amoedo Almudena, Carballo Rosa, García-Martínez Emilia, Vázquez-López Ezequiel M.: Metal coordination and in situ S–C bond cleavage of the bis(2-pyridylthio)methane ligand. Dalton Trans 2010, 39, 10076. <http://dx.doi.org/10.1039/c0dt00560f>
• Gao Hongmei, Zhang Guiqiu, Meng Lin, Chen Dezhan: Chiral discrimination in hydrogen-bonded complexes of 2-fluorooxirane with hydrogen peroxide. Molec Phys 2010, 108, 2073. <http://dx.doi.org/10.1080/00268976.2010.505207>
• McIldowie M.J., Mocerino M., Ogden M.I.: A brief review of C _n -symmetric calixarenes and resorcinarenes. Supramol Chem 2010, 22, 13. <http://dx.doi.org/10.1080/10610270902980663>
• Komatsu Naoki: Stereochemistry of Carbon Nanotubes. Jpn J Appl Phys 2010, 49, 02BC01. <http://dx.doi.org/10.1143/JJAP.49.02BC01>
• Anderson Marcus, Wilcox Katie, Guericke Mike, Chu Han, Wilson Mark V., Wilson Erin, Lucas Kerry, Holmes Andrea E.: Enantiodiscrimination of methamphetamine by circular dichroism using a porphyrin tweezer. Chirality 2009, NA. <http://dx.doi.org/10.1002/chir.20752>
• Garten Sarit, Biedermann P. Ulrich, Topiol Sid, Agranat Israel: Electrostatic chiral distinction: Tetrahedral model dimers. Chirality 2009, n/a. <http://dx.doi.org/10.1002/chir.20813>
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