Artykuły w czasopismach na temat „Cage-amine”
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Long, Augustin, Olivier Perraud, Erwann Jeanneau, Christophe Aronica, Jean-Pierre Dutasta i Alexandre Martinez. "A hemicryptophane with a triple-stranded helical structure". Beilstein Journal of Organic Chemistry 14 (24.07.2018): 1885–89. http://dx.doi.org/10.3762/bjoc.14.162.
Pełny tekst źródłaKoutsantonis, George A., Gareth L. Nealon, Craig E. Buckley, Mark Paskevicius, Laurent Douce, Jack M. Harrowfield i Alasdair W. McDowall. "Wormlike Micelles from a Cage Amine Metallosurfactant". Langmuir 23, nr 24 (listopad 2007): 11986–90. http://dx.doi.org/10.1021/la701283b.
Pełny tekst źródłaMa, Michelle T., Margaret S. Cooper, Rowena L. Paul, Karen P. Shaw, John A. Karas, Denis Scanlon, Jonathan M. White, Philip J. Blower i Paul S. Donnelly. "Macrobicyclic Cage Amine Ligands for Copper Radiopharmaceuticals: A Single Bivalent Cage Amine Containing Two Lys3-bombesin Targeting Peptides". Inorganic Chemistry 50, nr 14 (18.07.2011): 6701–10. http://dx.doi.org/10.1021/ic200681s.
Pełny tekst źródłaModak, Ritwik, Bijnaneswar Mondal, Prodip Howlader i Partha Sarathi Mukherjee. "Self-assembly of a “cationic-cage” via the formation of Ag–carbene bonds followed by imine condensation". Chemical Communications 55, nr 47 (2019): 6711–14. http://dx.doi.org/10.1039/c9cc02341k.
Pełny tekst źródłaRivera, Augusto, Martı́n E. Núñez, Martha S. Morales-Rı́os i Pedro Joseph-Nathan. "Preparation of cage amine 1,3,6,8-tetraazatricyclo[4.3.1.13,8]undecane". Tetrahedron Letters 45, nr 41 (październik 2004): 7563–65. http://dx.doi.org/10.1016/j.tetlet.2004.08.123.
Pełny tekst źródłaHong, Dae Ho, Brian J. Knight, Vincent J. Catalano i Leslie J. Murray. "Isolation of chloride- and hydride-bridged tri-iron and -zinc clusters in a tris(β-oxo-δ-diimine) cyclophane ligand". Dalton Transactions 48, nr 26 (2019): 9570–75. http://dx.doi.org/10.1039/c9dt00799g.
Pełny tekst źródłaSmith, Paul H., Zelideth E. Reyes, Chi Woo Lee i Kenneth N. Raymond. "Characterization of a series of lanthanide amine cage complexes". Inorganic Chemistry 27, nr 23 (listopad 1988): 4154–65. http://dx.doi.org/10.1021/ic00296a015.
Pełny tekst źródłaKlein, Liv B., Thorbjørn J. Morsing, Ruth A. Livingstone, Dave Townsend i Theis I. Sølling. "The effects of symmetry and rigidity on non-adiabatic dynamics in tertiary amines: a time-resolved photoelectron velocity-map imaging study of the cage-amine ABCO". Physical Chemistry Chemical Physics 18, nr 14 (2016): 9715–23. http://dx.doi.org/10.1039/c5cp07910a.
Pełny tekst źródłaGeue, RJ, P. Osvath, AM Sargeson, KR Acharya, SB Noor, TNG Row i K. Venkatesan. "The Reaction of a Nitro-Capped Cobalt(III) Cage Complex With Base: the Crystal Structure of a Contracted Cage Complex, and the Mechanism of Its Formation". Australian Journal of Chemistry 47, nr 3 (1994): 511. http://dx.doi.org/10.1071/ch9940511.
Pełny tekst źródłaAcharyya, Koushik, i Partha Sarathi Mukherjee. "Shape and size directed self-selection in organic cage formation". Chemical Communications 51, nr 20 (2015): 4241–44. http://dx.doi.org/10.1039/c5cc00075k.
Pełny tekst źródłaChen, Gong-Jun, Chao-Qun Chen, Xue-Tian Li, Hui-Chao Ma i Yu-Bin Dong. "Cu3L2 metal–organic cages for A3-coupling reactions: reversible coordination interaction triggered homogeneous catalysis and heterogeneous recovery". Chemical Communications 54, nr 82 (2018): 11550–53. http://dx.doi.org/10.1039/c8cc07208f.
Pełny tekst źródłaSargeson, Alan M., i Peter A. Lay. "Dependence of the Properties of Cobalt(III) Cage Complex as a Function of the Derivatization of Amine Substituents". Australian Journal of Chemistry 62, nr 10 (2009): 1280. http://dx.doi.org/10.1071/ch09368.
Pełny tekst źródłaPinto, Andrea, Giulia Spigolon, Raquel Gavara, Cristiano Zonta, Giulia Licini i Laura Rodríguez. "Tripodal gold(i) polypyridyl complexes and their Cu+ and Zn2+ heterometallic derivatives. Effects on luminescence". Dalton Transactions 49, nr 41 (2020): 14613–25. http://dx.doi.org/10.1039/d0dt02564j.
Pełny tekst źródłaMdzinarishvili, Alexander, Werner J. Geldenhuys, Thomas J. Abbruscato, Ulrich Bickel, Jochen Klein i Cornelis J. Van der Schyf. "NGP1-01, a lipophilic polycyclic cage amine, is neuroprotective in focal ischemia". Neuroscience Letters 383, nr 1-2 (lipiec 2005): 49–53. http://dx.doi.org/10.1016/j.neulet.2005.03.042.
Pełny tekst źródłaClark, IJ, II Creaser, LM Engelhardt, JM Harrowfield, ER Krausz, GM Moran, AM Sargeson i AH White. "Synthesis, Structure and Redox Properties of Nickel Complexes of Cage Amine Ligands". Australian Journal of Chemistry 46, nr 1 (1993): 111. http://dx.doi.org/10.1071/ch9930111.
Pełny tekst źródłaComba, Peter, Lutz M. Engelhardt, Jack MacB Harrowfield, Geoffrey A. Lawrance, Lisandra L. Martin, Alan M. Sargeson i Allan H. White. "Synthesis and characterization of a stable hexa-amine vanadium(IV) cage complex". Journal of the Chemical Society, Chemical Communications, nr 3 (1985): 174. http://dx.doi.org/10.1039/c39850000174.
Pełny tekst źródłaPaterson, Brett M., Gojko Buncic, Lachlan E. McInnes, Peter Roselt, Carleen Cullinane, David S. Binns, Charmaine M. Jeffery, Roger I. Price, Rodney J. Hicks i Paul S. Donnelly. "Bifunctional 64Cu-labelled macrobicyclic cage amine isothiocyanates for immuno-positron emission tomography". Dalton Transactions 44, nr 11 (2015): 4901–9. http://dx.doi.org/10.1039/c4dt02983f.
Pełny tekst źródłaEdward, John T., Francis L. Chubb, Denis FR Gilson, Rosemary C. Hynes, Françoise Sauriol i Alain Wiesenthal. "Article". Canadian Journal of Chemistry 77, nr 5-6 (1.06.1999): 1057–65. http://dx.doi.org/10.1139/v99-118.
Pełny tekst źródłaLing, Irene, Alexandre N. Sobolev, Rauzah Hashim i Jack M. Harrowfield. "Stereochemistry of cage amine complexes – probing the ligand conformational flexibility with hydrogen bonds". CrystEngComm 16, nr 48 (2014): 11058–63. http://dx.doi.org/10.1039/c4ce01980f.
Pełny tekst źródłaMorozov, Boris S., Siva S. R. Namashivaya, Marina A. Zakharko, Aleksandr S. Oshchepkov i Evgeny A. Kataev. "Anthracene‐Based Amido−Amine Cage Receptor for Anion Recognition under Neutral Aqueous Conditions". ChemistryOpen 9, nr 2 (4.12.2019): 171–75. http://dx.doi.org/10.1002/open.201900309.
Pełny tekst źródłaMorozov, Boris S., Siva S. R. Namashivaya, Marina A. Zakharko, Aleksandr S. Oshchepkov i Evgeny A. Kataev. "Anthracene‐Based Amido−Amine Cage Receptor for Anion Recognition under Neutral Aqueous Conditions". ChemistryOpen 9, nr 2 (30.01.2020): 99. http://dx.doi.org/10.1002/open.202000009.
Pełny tekst źródłaYao, Yuan, Jingya Li, Yanyan Zhou, Ting Gao, Hongfeng Li i Pengfei Yan. "Turn-on luminescence detection of biogenic amine with an Eu(III) tetrahedron cage". Dyes and Pigments 192 (sierpień 2021): 109441. http://dx.doi.org/10.1016/j.dyepig.2021.109441.
Pełny tekst źródłaSapchenko, Sergey A., Danil N. Dybtsev i Vladimir P. Fedin. "Cage amines in the metal–organic frameworks chemistry". Pure and Applied Chemistry 89, nr 8 (26.07.2017): 1049–64. http://dx.doi.org/10.1515/pac-2016-1206.
Pełny tekst źródłaQiu, Gege, Djamel Eddine Khatmi, Alexandre Martinez i Paola Nava. "Rationalization of chirality transfer and fast conformational changes in a tris(2-pyridylmethyl)amine-based cage". RSC Advances 11, nr 23 (2021): 13763–68. http://dx.doi.org/10.1039/d1ra01761f.
Pełny tekst źródłaHarrowfield, Jack M., George A. Koutsantonis, Nigel A. Lengkeek, Brian W. Skelton i Allan H. White. "Structural and Electrochemical Studies of Co(III) Cage Amine Complexes with Pendent Thienylmethylamino Groups". Inorganic Chemistry 49, nr 7 (5.04.2010): 3152–61. http://dx.doi.org/10.1021/ic9019603.
Pełny tekst źródłaDiaz, Martin, Jojo Jaballas, Dan Tran, Hans Lee, Joachin Arias i Thomas Onak. "Interaction of Trimethylamine andcloso-1,6-C2B7H9. Evidence for an “Open” Cage C2B7H9/Amine Adduct". Inorganic Chemistry 35, nr 16 (styczeń 1996): 4536–40. http://dx.doi.org/10.1021/ic960254e.
Pełny tekst źródłaKawakami, Yoshiteru, Kazuo Yamaguchi, Tsutomu Yokozawa, Takanori Serizawa, Minoru Hasegawa i Yoshio Kabe. "Higher Polyhedral Silsesquioxane (POSS) Cage by Amine-catalyzed Condensation of Silanols and Related Siloxanes". Chemistry Letters 36, nr 6 (5.06.2007): 792–93. http://dx.doi.org/10.1246/cl.2007.792.
Pełny tekst źródłaQiu, Gege, Paola Nava, Alexandre Martinez i Cédric Colomban. "A tris(benzyltriazolemethyl)amine-based cage as a CuAAC ligand tolerant to exogeneous bulky nucleophiles". Chemical Communications 57, nr 18 (2021): 2281–84. http://dx.doi.org/10.1039/d0cc08005e.
Pełny tekst źródłaOsvath, P., i AM Sargeson. "Ring Opening and Rearrangement of a Nitro-Capped Cobalt(III) Cage Complex With an N3S3 Donor Set". Australian Journal of Chemistry 47, nr 5 (1994): 807. http://dx.doi.org/10.1071/ch9940807.
Pełny tekst źródłaPaterson, Brett M., Peter Roselt, Delphine Denoyer, Carleen Cullinane, David Binns, Wayne Noonan, Charmaine M. Jeffery i in. "PET imaging of tumours with a64Cu labeled macrobicyclic cage amine ligand tethered to Tyr3-octreotate". Dalton Trans. 43, nr 3 (2014): 1386–96. http://dx.doi.org/10.1039/c3dt52647j.
Pełny tekst źródłaŠtíbr, Bohumil. "Acyl chloride carbon insertion into dicarbaborane cages – new route to tricarbollide cages". Pure and Applied Chemistry 87, nr 2 (1.02.2015): 135–42. http://dx.doi.org/10.1515/pac-2014-0937.
Pełny tekst źródłaQiu, Gege, Cédric Colomban, Nicolas Vanthuyne, Michel Giorgi i Alexandre Martinez. "Chirality transfer in a cage controls the clockwise/anticlockwise propeller arrangement of the tris(2-pyridylmethyl)amine ligand". Chemical Communications 55, nr 94 (2019): 14158–61. http://dx.doi.org/10.1039/c9cc07244f.
Pełny tekst źródłaVasylevskyi, Serhii, Anja Holzheu i Katharina M. Fromm. "Solid-state structure and antimicrobial and cytotoxicity studies of a cucurbit[6]uril-like Cu6 L 4 constructed from 3,5-bis[(1H-tetrazol-5-yl)methyl]-4H-1,2,4-triazol-4-amine". Acta Crystallographica Section C Structural Chemistry 74, nr 11 (18.10.2018): 1413–19. http://dx.doi.org/10.1107/s2053229618013670.
Pełny tekst źródłaLockman, J. A., W. J. Geldenhuys, M. R. Jones-Higgins, J. D. Patrick, D. D. Allen i C. J. Van der Schyf. "NGP1-01, a multi-targeted polycyclic cage amine, attenuates brain endothelial cell death in iron overload conditions". Brain Research 1489 (grudzień 2012): 133–39. http://dx.doi.org/10.1016/j.brainres.2012.10.029.
Pełny tekst źródłaBudi Hartono, Sandy, ShiZhang Qiao, Kevin Jack, Bradley P. Ladewig, Zhengping Hao i GaoQing (Max) Lu. "Improving Adsorbent Properties of Cage-like Ordered Amine Functionalized Mesoporous Silica with Very Large Pores for Bioadsorption". Langmuir 25, nr 11 (2.06.2009): 6413–24. http://dx.doi.org/10.1021/la900023p.
Pełny tekst źródłaLay, PA, J. Lydon, AWH Mau, P. Osvath, AM Sargeson i WHF Sasse. "The Synthesis and Properties of Cobalt Cage Complexes With N3S3 Donor Sets". Australian Journal of Chemistry 46, nr 5 (1993): 641. http://dx.doi.org/10.1071/ch9930641.
Pełny tekst źródłaGoez, Martin, Isabell Frisch i Ingo Sartorius. "Electron and hydrogen self-exchange of free radicals of sterically hindered tertiary aliphatic amines investigated by photo-CIDNP". Beilstein Journal of Organic Chemistry 9 (26.02.2013): 437–46. http://dx.doi.org/10.3762/bjoc.9.46.
Pełny tekst źródłaMorozov, Boris S., Siva S. R. Namashivaya, Marina A. Zakharko, Aleksandr S. Oshchepkov i Evgeny A. Kataev. "Front Cover: Anthracene‐Based Amido−Amine Cage Receptor for Anion Recognition under Neutral Aqueous Conditions (ChemistryOpen 2/2020)". ChemistryOpen 9, nr 2 (28.01.2020): 97. http://dx.doi.org/10.1002/open.202000010.
Pełny tekst źródłaYoun, Yeobum, Jiwoong Seol, Minjun Cha, Yun-Ho Ahn i Huen Lee. "Structural Transition Induced by CH4 Enclathration and Cage Expansion with Large Guest Molecules Occurring in Amine Hydrate Systems". Journal of Chemical & Engineering Data 59, nr 6 (19.05.2014): 2004–12. http://dx.doi.org/10.1021/je500167n.
Pełny tekst źródłaDeryabin, Dmitry G., Olga K. Davydova, Zulfiya ZH Yankina, Alexey S. Vasilchenko, Sergei A. Miroshnikov, Alexey B. Kornev, Anastasiya V. Ivanchikhina i Pavel A. Troshin. "The Activity of [60]Fullerene Derivatives Bearing Amine and Carboxylic Solubilizing Groups againstEscherichia coli: A Comparative Study". Journal of Nanomaterials 2014 (2014): 1–9. http://dx.doi.org/10.1155/2014/907435.
Pełny tekst źródłaGahan, LR, TW Hambley i PC Healy. "Dithiocarbamates as Innocent Anions: The Synthesis and Structural Properties of (8-Methyl-3,6,10,13,16,19-hexaazabicyclo[6.6.6]-icosan-1-amine)cobalt(Ii I) Tris(N,N-diethyldithiocarbamate), [Co(AMMEsar)][Et2dtc]3". Australian Journal of Chemistry 41, nr 5 (1988): 635. http://dx.doi.org/10.1071/ch9880635.
Pełny tekst źródłaMa, Michelle T., Oliver C. Neels, Delphine Denoyer, Peter Roselt, John A. Karas, Denis B. Scanlon, Jonathan M. White, Rodney J. Hicks i Paul S. Donnelly. "Gallium-68 Complex of a Macrobicyclic Cage Amine Chelator Tethered to Two Integrin-Targeting Peptides for Diagnostic Tumor Imaging". Bioconjugate Chemistry 22, nr 10 (19.10.2011): 2093–103. http://dx.doi.org/10.1021/bc200319q.
Pełny tekst źródłaYao, Yuan, Yanyan Zhou, Tianyu Zhu, Ting Gao, Hongfeng Li i Pengfei Yan. "Eu(III) Tetrahedron Cage as a Luminescent Chemosensor for Rapidly Reversible and Turn-On Detection of Volatile Amine/NH3". ACS Applied Materials & Interfaces 12, nr 13 (9.03.2020): 15338–47. http://dx.doi.org/10.1021/acsami.9b21425.
Pełny tekst źródłaMa, Michelle T., John A. Karas, Jonathan M. White, Denis Scanlon i Paul S. Donnelly. "A new bifunctional chelator for copper radiopharmaceuticals: a cage amine ligand with a carboxylate functional group for conjugation to peptides". Chemical Communications, nr 22 (2009): 3237. http://dx.doi.org/10.1039/b903426a.
Pełny tekst źródłaHarrowfield, JM, Y. Kim, BW Skelton i AH White. "Mixed Transition Metal/Lanthanide Complexes: Structural Characterization of Solids Containing Cage Amine Chromium(III) Cations and Tris(dipicolinato)lanthanide Anions". Australian Journal of Chemistry 48, nr 4 (1995): 807. http://dx.doi.org/10.1071/ch9950807.
Pełny tekst źródłaPulido, Angeles, Ming Liu, Paul Reiss, Anna Slater, Sam Chong, Marc Little, Tom Hasell, Mike Briggs, Andrew Cooper i Graeme Day. "Towards computer-guided tuning of the crystal packing of porous organic cages". Acta Crystallographica Section A Foundations and Advances 70, a1 (5.08.2014): C667. http://dx.doi.org/10.1107/s2053273314093322.
Pełny tekst źródłaMagerstadt, M., R. Bruce King, M. G. Newton, N. E. Tonks i C. E. Ringold. "Preparation of a novel sulfur-nitrogen cage compound by the transamination of bis(dimethylamino) sulfide with a macrocyclic tetra(secondary amine)". Journal of the American Chemical Society 108, nr 4 (luty 1986): 850–51. http://dx.doi.org/10.1021/ja00264a055.
Pełny tekst źródłaLiu, Ming, Marc A. Little, Kim E. Jelfs, James T. A. Jones, Marc Schmidtmann, Samantha Y. Chong, Tom Hasell i Andrew I. Cooper. "Acid- and Base-Stable Porous Organic Cages: Shape Persistence and pH Stability via Post-synthetic “Tying” of a Flexible Amine Cage". Journal of the American Chemical Society 136, nr 21 (13.05.2014): 7583–86. http://dx.doi.org/10.1021/ja503223j.
Pełny tekst źródłaSpringborg, Johan, Ulla Pretzmann, Carl Erik Olsen, Kim Simonsen, György Liptay, Katrin Trautwein-Fritz, Joseph Stackhouse i in. "An Inert Proton Coordinated Inside the Tetrahedral Cage [3 6]Adamanzane. Synthesis of the Inside Monoprotonated Amine 1,5,9,13-Tetraazatricyclo[7.7.3.3(5,13)]docosane." Acta Chemica Scandinavica 50 (1996): 294–98. http://dx.doi.org/10.3891/acta.chem.scand.50-0294.
Pełny tekst źródłaAlt, Karen, Brett M. Paterson, Katie Ardipradja, Christine Schieber, Gojko Buncic, Bock Lim, Stan S. Poniger i in. "Single-Chain Antibody Conjugated to a Cage Amine Chelator and Labeled with Positron-Emitting Copper-64 for Diagnostic Imaging of Activated Platelets". Molecular Pharmaceutics 11, nr 8 (14.07.2014): 2855–63. http://dx.doi.org/10.1021/mp500209a.
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