Artículos de revistas sobre el tema "Spirocyclic molecules"
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Fominova, Kateryna, Taras Diachuk, Dmitry Granat, Taras Savchuk, Vladyslav Vilchynskyi, Oleksiy Svitlychnyi, Vladyslav Meliantsev et al. "Oxa-spirocycles: synthesis, properties and applications". Chemical Science 12, n.º 34 (2021): 11294–305. http://dx.doi.org/10.1039/d1sc03615g.
Texto completoBenabdallah, Mohammed, Oualid Talhi, Fatiha Nouali, Nouredine Choukchou-Braham, Khaldoun Bachari y Artur M. S. Silva. "Advances in Spirocyclic Hybrids: Chemistry and Medicinal Actions". Current Medicinal Chemistry 25, n.º 31 (16 de octubre de 2018): 3748–67. http://dx.doi.org/10.2174/0929867325666180309124821.
Texto completoPaquette, Leo A. "Spirocyclic Restriction of Nucleosides". Australian Journal of Chemistry 57, n.º 1 (2004): 7. http://dx.doi.org/10.1071/ch03267.
Texto completoShen, Guo-Liang, Jing Sun y Chao-Guo Yan. "Construction of dispirocyclohexyl-3,3′-bisoxindole and dispirocyclopentyl-3,3′-bisoxindole via domino cycloaddition reactions of N-benzylbenzimidazolium salts with 2-(2-oxoindolin-3-ylidene)acetates". RSC Advances 5, n.º 6 (2015): 4475–83. http://dx.doi.org/10.1039/c4ra13760d.
Texto completoKappen, Lizzy S., Yiqing Lin, Graham B. Jones y Irving H. Goldberg. "Probing DNA Bulges with Designed Helical Spirocyclic Molecules†". Biochemistry 46, n.º 2 (enero de 2007): 561–67. http://dx.doi.org/10.1021/bi061744d.
Texto completoG. Keller, Sascha, Mako Kamiya y Yasuteru Urano. "Recent Progress in Small Spirocyclic, Xanthene-Based Fluorescent Probes". Molecules 25, n.º 24 (16 de diciembre de 2020): 5964. http://dx.doi.org/10.3390/molecules25245964.
Texto completoHolovatiuk, V. M., O. A. Brazhko y V. I. Kashkovsky. "ВИВЧЕННЯ ГОСТРОЇ ТОКСИЧНОСТІ ТА АНАЛГЕТИЧНОЇ АКТИВНОСТІ НОВИХ СПІРОЦИКЛІЧНИХ ПОХІДНИХ ПІРАЗОЛІДИН-3,5-ДІОНУ". Biological Bulletin of Bogdan Chmelnitskiy Melitopol State Pedagogical University 6, n.º 3 (4 de noviembre de 2016): 149–53. http://dx.doi.org/10.15421/201681.
Texto completoInnocenti, Riccardo, Elena Lenci, Gloria Menchi y Andrea Trabocchi. "Combination of multicomponent KA2 and Pauson–Khand reactions: short synthesis of spirocyclic pyrrolocyclopentenones". Beilstein Journal of Organic Chemistry 16 (12 de febrero de 2020): 200–211. http://dx.doi.org/10.3762/bjoc.16.23.
Texto completoChernyshov, Vladimir V., Yuri V. Gatilov, Olga I. Yarovaya, Igor P. Koskin, Spartak S. Yarovoy, Konstantin A. Brylev y Nariman F. Salakhutdinov. "The first example of the stereoselective synthesis and crystal structure of a spirobicycloquinazolinone based on (–)-fenchone and anthranilamide". Acta Crystallographica Section C Structural Chemistry 75, n.º 12 (26 de noviembre de 2019): 1675–80. http://dx.doi.org/10.1107/s2053229619015766.
Texto completoLinden, Anthony, Grzegorz Mlostoń, Paulina Grzelak y Heinz Heimgartner. "Chemo- and regioselective [3 + 2]-cycloadditions of thiocarbonyl ylides: crystal structures of trans-8-benzoyl-1,1,3,3-tetramethyl-7-trifluoromethyl-5-thiaspiro[3.4]octan-2-one and trans-3-benzoyl-2,2-diphenyl-4-(trifluoromethyl)tetrahydrothiophene". Acta Crystallographica Section E Crystallographic Communications 74, n.º 12 (6 de noviembre de 2018): 1705–9. http://dx.doi.org/10.1107/s2056989018015335.
Texto completoThompson, Kirstie A., Ronita Mathias, Daeok Kim, Jihoon Kim, Neel Rangnekar, J. R. Johnson, Scott J. Hoy et al. "N-Aryl–linked spirocyclic polymers for membrane separations of complex hydrocarbon mixtures". Science 369, n.º 6501 (16 de julio de 2020): 310–15. http://dx.doi.org/10.1126/science.aba9806.
Texto completoSwamy, K. C. Kumara, Roberta O. Day, Joan M. Holmes y Robert R. Holmes. "Pentacoordinated molecules. 81. Conformational preferences of spirocyclic pentaoxyphosphoranes varying in ring size". Journal of the American Chemical Society 112, n.º 16 (agosto de 1990): 6095–103. http://dx.doi.org/10.1021/ja00172a028.
Texto completoLanger, Peter. "Synthesis of Purines and Related Molecules by Cyclization Reactions of Heterocyclic Enamines". Synlett 33, n.º 05 (22 de octubre de 2021): 440–57. http://dx.doi.org/10.1055/s-0040-1719845.
Texto completoPappin, Brighid B., Stephan M. Levonis, Peter C. Healy, Milton J. Kiefel, Michela I. Simone y Todd A. Houston. "Crystallization-induced amide bond formation creates a boron-centered spirocyclic system". Heterocyclic Communications 23, n.º 3 (27 de junio de 2017): 167–69. http://dx.doi.org/10.1515/hc-2017-0023.
Texto completoZaytseva, Elena y Dmitrii Mazhukin. "Spirocyclic Nitroxides as Versatile Tools in Modern Natural Sciences: From Synthesis to Applications. Part I. Old and New Synthetic Approaches to Spirocyclic Nitroxyl Radicals". Molecules 26, n.º 3 (28 de enero de 2021): 677. http://dx.doi.org/10.3390/molecules26030677.
Texto completoPaquette, Leo A., George A. O'Doherty, Benjamin L. Miller, Robin D. Rogers, Arnold L. Rheingold y Steven L. Geib. "Isodicyclopentadienes and related molecules. 48. Stereochemically uniform mode of iron carbonyl complexation to spirocyclic isodicyclopentadienes". Organometallics 8, n.º 9 (septiembre de 1989): 2167–72. http://dx.doi.org/10.1021/om00111a012.
Texto completoHans, Johannes, Roberta O. Day y Robert R. Holmes. "Pentacoordinated molecules. 89. Hydrogen-bonded chain and dimer formations of spirocyclic tetraoxyphosphoranes possessing phosphorinane chair conformations". Inorganic Chemistry 30, n.º 20 (octubre de 1991): 3928–36. http://dx.doi.org/10.1021/ic00020a028.
Texto completoHolmes, Robert R., Soheila Shafieezad, V. Chandrasekhar, Arjun C. Sau, Joan M. Holmes y Roberta O. Day. "Pentacoordinated molecules. 70. New five- and six-coordinated anionic tin(IV) complexes. Molecular structure of spirocyclic stannates with mixed ligands". Journal of the American Chemical Society 110, n.º 4 (febrero de 1988): 1168–74. http://dx.doi.org/10.1021/ja00212a027.
Texto completoHolmes, Robert R., Roberta O. Day, V. Chandrasekhar y Joan M. Holmes. "Pentacoordinated molecules. 61. Synthesis and molecular structure of five-coordinated spirocyclic anionic silicates containing tert-butyl groups. Hydrogen-bonding effects". Inorganic Chemistry 24, n.º 13 (junio de 1985): 2009–15. http://dx.doi.org/10.1021/ic00207a012.
Texto completoHolmes, Robert R., Roberta O. Day, Arjun C. Sau y Joan M. Holmes. "Pentacoordinated molecules. 63. Distortion coordinate for nonrigid five-coordinated germanium. Synthesis and molecular structure of spirocyclic anionic methylgermanates varying in ring composition". Inorganic Chemistry 25, n.º 5 (febrero de 1986): 600–606. http://dx.doi.org/10.1021/ic00225a005.
Texto completoHolmes, Robert R., K. C. Kumara Swamy, Joan M. Holmes y Roberta O. Day. "Pentacoordinated molecules. 84. Conformational effects of ring fusion and heteroatom substitution in six-membered rings of spirocyclic oxyphosphoranes". Inorganic Chemistry 30, n.º 5 (marzo de 1991): 1052–62. http://dx.doi.org/10.1021/ic00005a033.
Texto completoHANS, J., R. O. DAY y R. R. HOLMES. "ChemInform Abstract: Pentacoordinated Molecules. Part 89. Hydrogen-Bonded Chain and Dimer Formations of Spirocyclic Tetraoxyphosphoranes Possessing Phosphorinane Chair Conformations." ChemInform 23, n.º 3 (22 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199203214.
Texto completoDietz, Jochen, Ulrich Müller, Volker Müller y Kurt Dehnicke. "Die Kristallstrukturen von (NEt4+)2[Se52- · 1/2 Se6·Se7] und von (NPr4)2Se11 / The Crystal Structures of (NEt4+)2[Se52- · 1/2 Se6 · Se7] and (NPr4)2Se11". Zeitschrift für Naturforschung B 46, n.º 10 (1 de octubre de 1991): 1293–99. http://dx.doi.org/10.1515/znb-1991-1003.
Texto completoHolmes, Robert R., Roberta O. Day, Arjun C. Sau, Charles A. Poutasse y Joan M. Holmes. "Pentacoordinated molecules. 58. Stereochemically nonrigid five-coordinated germanates. Synthesis and structure of hydroxy- and halo-containing spirocyclic germanium(IV) complexes". Inorganic Chemistry 24, n.º 2 (enero de 1985): 193–99. http://dx.doi.org/10.1021/ic00196a015.
Texto completoVillabona, Marc, Marina Benet, Silvia Mena, Rabih O. Al-Kaysi, Jordi Hernando y Gonzalo Guirado. "Multistimuli-Responsive Fluorescent Switches Based on Spirocyclic Meisenheimer Compounds: Smart Molecules for the Design of Optical Probes and Electrochromic Materials". Journal of Organic Chemistry 83, n.º 16 (13 de junio de 2018): 9166–77. http://dx.doi.org/10.1021/acs.joc.8b01211.
Texto completoHOLMES, R. R., K. C. K. SWAMY, J. M. HOLMES y R. O. DAY. "ChemInform Abstract: Pentacoordinated Molecules. Part 84. Conformational Effects of Ring Fusion and Heteroatom Substitution in Six-Membered Rings of Spirocyclic Oxyphosphoranes." ChemInform 22, n.º 25 (23 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199125208.
Texto completoDay, Roberta O., K. C. Kumara Swamy, Lisa Fairchild, Joan M. Holmes y Robert R. Holmes. "Pentacoordinated molecules. 85. Influence of hydrogen bonding on the formation of boat and chair conformations of six-membered rings in spirocyclic tetraoxyphosphoranes". Journal of the American Chemical Society 113, n.º 5 (febrero de 1991): 1627–35. http://dx.doi.org/10.1021/ja00005a028.
Texto completoYang, Jun, Bo-Wen Pan, Lin Chen, Ying Zhou y Xiong-Li Liu. "Recent advances in organocatalytic cascade reactions for enantioselective synthesis of chiral spirolactone skeletons". Chemical Synthesis 3, n.º 1 (2023): 7. http://dx.doi.org/10.20517/cs.2022.38.
Texto completoKumar, Nakul, Gajendra Kumar Inwati, Emad M. Ahmed, Chhagan Lal, Bharat Makwana, Virendra K. Yadav, Saiful Islam, Hyun-Jo Ahn, Krishna K. Yadav y Byong-Hun Jeon. "Modified 7-Chloro-11H-indeno[1,2-b]quinoxaline Heterocyclic System for Biological Activities". Catalysts 12, n.º 2 (11 de febrero de 2022): 213. http://dx.doi.org/10.3390/catal12020213.
Texto completoDAY, R. O., K. C. K. SWAMY, L. FAIRCHILD, J. M. HOLMES y R. R. HOLMES. "ChemInform Abstract: Pentacoordinated Molecules. Part 85. Influence of Hydrogen Bonding on the Formation of Boat and Chair Conformations of Six-Membered Rings in Spirocyclic Tetraoxyphosphoranes." ChemInform 22, n.º 24 (23 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199124184.
Texto completoYadav, J. S., B. V. Subba Reddy, V. Hari Krishna, T. Swamy y GG KS Narayana Kumar. "Iodine-promoted Prins-cyclization of ketones — A facile synthesis of spirocyclic-4-iodo-tetrahydropyrans and 5,6-dihydro-2H-pyrans". Canadian Journal of Chemistry 85, n.º 6 (1 de junio de 2007): 412–15. http://dx.doi.org/10.1139/v07-048.
Texto completoLukin, Alexei, Kristina Komarova, Lyubov Vinogradova, Elizaveta Rogacheva, Lyudmila Kraeva y Mikhail Krasavin. "Synthesis and Antibacterial Evaluation of Ciprofloxacin Congeners with Spirocyclic Amine Periphery". International Journal of Molecular Sciences 24, n.º 2 (4 de enero de 2023): 954. http://dx.doi.org/10.3390/ijms24020954.
Texto completoMaassarani, Fida, Michel Pfeffer y Guy Le Borgne. "Reaction of cyclopalladated compounds Part 16. Stepwise insertion of one, two, and three alkyne molecules into the palladium-carbon bond of a six-membered palladocycle. One-pot synthesis of spirocyclic compounds". Organometallics 6, n.º 10 (octubre de 1987): 2043–53. http://dx.doi.org/10.1021/om00153a003.
Texto completoKitschke, Philipp, Ana-Maria Preda, Alexander A. Auer, Sebastian Scholz, Tobias Rüffer, Heinrich Lang y Michael Mehring. "Spirocyclic tin salicyl alcoholates – a combined experimental and theoretical study on their structures, 119Sn NMR chemical shifts and reactivity in thermally induced twin polymerization". Dalton Transactions 48, n.º 1 (2019): 220–30. http://dx.doi.org/10.1039/c8dt03695k.
Texto completoBrindisi, Margherita, Sandra Gemma, Sanil Kunjir, Luisa Di Cerbo, Simone Brogi, Silvia Parapini, Sarah D'Alessandro et al. "Synthetic spirocyclic endoperoxides: new antimalarial scaffolds". MedChemComm 6, n.º 2 (2015): 357–62. http://dx.doi.org/10.1039/c4md00454j.
Texto completoYuan, Hongdong, Chongrong Tang, Shikuan Su, Lei Cui, Xueshun Jia, Chunju Li y Jian Li. "A bicyclization reaction with two molecular allenyl ketones and isocyanides: synthesis of a lactone-containing azaspirocycle derivative". Chemical Communications 55, n.º 50 (2019): 7231–34. http://dx.doi.org/10.1039/c9cc02785h.
Texto completoKour, Smit, Sandeep Rana, Smitha Kizhake, Dragana Lagundžin, David Klinkebiel, Jayapal Reddy Mallareddy, Tom Huxford, Nicholas T. Woods y Amarnath Natarajan. "Stapling proteins in the RELA complex inhibits TNFα-induced nuclear translocation of RELA". RSC Chemical Biology 3, n.º 1 (2022): 32–36. http://dx.doi.org/10.1039/d1cb00183c.
Texto completoBiţă, Andrei, Ion Romulus Scorei, Nagendra Rangavajla, Ludovic Everard Bejenaru, Gabriela Rău, Cornelia Bejenaru, Maria Viorica Ciocîlteu et al. "Diester Chlorogenoborate Complex: A New Naturally Occurring Boron-Containing Compound". Inorganics 11, n.º 3 (9 de marzo de 2023): 112. http://dx.doi.org/10.3390/inorganics11030112.
Texto completoPesquet, Anthony, Hamid Marzag, Michael Knorr, Carsten Strohmann, Ata Martin Lawson, Alina Ghinet, Joëlle Dubois, Farce Amaury, Adam Daïch y Mohamed Othman. "Access to 3-spiroindolizines containing an isoindole ring through intra-molecular arylation of spiro-N-acyliminium species: a new family of potent farnesyltransferase inhibitors". Organic & Biomolecular Chemistry 17, n.º 10 (2019): 2798–808. http://dx.doi.org/10.1039/c8ob02612b.
Texto completoSong, Kunpeng, Yinjie Wang, Fang Ruan, Weiwei Yang y Jiping Liu. "Synthesis of a Novel Spirocyclic Inflatable Flame Retardant and Its Application in Epoxy Composites". Polymers 12, n.º 11 (29 de octubre de 2020): 2534. http://dx.doi.org/10.3390/polym12112534.
Texto completoKotha, Sambasivarao y Kalyaneswar Mandal. "Metathetic approach to naphthoxepin and spirocyclic molecular frameworks". Tetrahedron Letters 45, n.º 7 (febrero de 2004): 1391–94. http://dx.doi.org/10.1016/j.tetlet.2003.12.075.
Texto completoSawhney, Gifty, Javeed Ur Rasool, Diksha Saroch, Mumin Ozturk, Frank Brombacher, Bilal Ahmad, Asha Bhagat, Asif Ali, Suraj P. Parihar y Zabeer Ahmed. "Arteannuin-B and (3-Chlorophenyl)-2-Spiroisoxazoline Derivative Exhibit Anti-Inflammatory Effects in LPS-Activated RAW 264.7 Macrophages and BALB/c Mice-Induced Proinflammatory Responses via Downregulation of NF-κB/P38 MAPK Signaling". Molecules 27, n.º 22 (20 de noviembre de 2022): 8068. http://dx.doi.org/10.3390/molecules27228068.
Texto completoKhuzin, Artur A., Dim I. Galimov y Liliya L. Khuzina. "Photochromic and Luminescent Properties of a Salt of a Hybrid Molecule Based on C60 Fullerene and Spiropyran—A Promising Approach to the Creation of Anticancer Drugs". Molecules 28, n.º 3 (22 de enero de 2023): 1107. http://dx.doi.org/10.3390/molecules28031107.
Texto completoQu, Haijun, Xuejian Li, Fan Mo y Xufeng Lin. "Efficient synthesis of dihydropyrimidinones via a three-component Biginelli-type reaction of urea, alkylaldehyde and arylaldehyde". Beilstein Journal of Organic Chemistry 9 (11 de diciembre de 2013): 2846–51. http://dx.doi.org/10.3762/bjoc.9.320.
Texto completoMaddirala, Amarendar Reddy y Peter R. Andreana. "Methyl isocyanide as a convertible functional group for the synthesis of spirocyclic oxindole γ-lactams via post-Ugi-4CR/transamidation/cyclization in a one-pot, three-step sequence". Beilstein Journal of Organic Chemistry 14 (18 de abril de 2018): 875–83. http://dx.doi.org/10.3762/bjoc.14.74.
Texto completoBöhm, Stanislav, Michal Hocek, Jan Němeček, Vladimír Havlíček y Josef Kuthan. "Preparation and Spectroscopic Properties of Spirocyclic 1-Methyl-2,4,4,6-tetraaryl-1,4-dihydropyridines". Collection of Czechoslovak Chemical Communications 59, n.º 5 (1994): 1105–14. http://dx.doi.org/10.1135/cccc19941105.
Texto completoLukyanov, Boris, Gennadii Vasilyuk, Eugene Mukhanov, Leonid Ageev, Maria Lukyanova, Yury Alexeenko, Serguei Besugliy y Valeri Tkachev. "Multifunctional Spirocyclic Systems". International Journal of Photoenergy 2009 (2009): 1–6. http://dx.doi.org/10.1155/2009/689450.
Texto completoShetgaonkar, Samata E., Shiva Prasad Kollur, Renjith Raveendran Pillai, Karthick Thangavel, Sanja J. Armaković, Stevan Armaković, Chandan Shivamallu et al. "Investigation of Pharmaceutical Importance of 2H-Pyran-2-One Analogues via Computational Approaches". Symmetry 13, n.º 9 (3 de septiembre de 2021): 1619. http://dx.doi.org/10.3390/sym13091619.
Texto completoGarcia-Yuste, Santiago, Konrad W. Hellmann, Lutz H. Gade, Ian J. Scowen y Mary McPartlin. "Bis[1,3-bis(diphenylmethylsilylamido)propane]zirconium: A Spirocyclic Complex Containing a Sterically Demanding Chelating Amido Ligand". Zeitschrift für Naturforschung B 54, n.º 10 (1 de octubre de 1999): 1260–64. http://dx.doi.org/10.1515/znb-1999-1007.
Texto completoLivendahl, M., J. Jamroskovic, M. Hedenström, T. Görlich, N. Sabouri y E. Chorell. "Synthesis of phenanthridine spiropyrans and studies of their effects on G-quadruplex DNA". Organic & Biomolecular Chemistry 15, n.º 15 (2017): 3265–75. http://dx.doi.org/10.1039/c7ob00300e.
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