Статті в журналах з теми "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, no. 34 (2021): 11294–305. http://dx.doi.org/10.1039/d1sc03615g.
Повний текст джерелаBenabdallah, Mohammed, Oualid Talhi, Fatiha Nouali, Nouredine Choukchou-Braham, Khaldoun Bachari, and Artur M. S. Silva. "Advances in Spirocyclic Hybrids: Chemistry and Medicinal Actions." Current Medicinal Chemistry 25, no. 31 (October 16, 2018): 3748–67. http://dx.doi.org/10.2174/0929867325666180309124821.
Повний текст джерелаPaquette, Leo A. "Spirocyclic Restriction of Nucleosides." Australian Journal of Chemistry 57, no. 1 (2004): 7. http://dx.doi.org/10.1071/ch03267.
Повний текст джерелаShen, Guo-Liang, Jing Sun, and 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, no. 6 (2015): 4475–83. http://dx.doi.org/10.1039/c4ra13760d.
Повний текст джерелаKappen, Lizzy S., Yiqing Lin, Graham B. Jones, and Irving H. Goldberg. "Probing DNA Bulges with Designed Helical Spirocyclic Molecules†." Biochemistry 46, no. 2 (January 2007): 561–67. http://dx.doi.org/10.1021/bi061744d.
Повний текст джерелаG. Keller, Sascha, Mako Kamiya, and Yasuteru Urano. "Recent Progress in Small Spirocyclic, Xanthene-Based Fluorescent Probes." Molecules 25, no. 24 (December 16, 2020): 5964. http://dx.doi.org/10.3390/molecules25245964.
Повний текст джерелаHolovatiuk, V. M., O. A. Brazhko та 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, № 3 (4 листопада 2016): 149–53. http://dx.doi.org/10.15421/201681.
Повний текст джерелаInnocenti, Riccardo, Elena Lenci, Gloria Menchi, and Andrea Trabocchi. "Combination of multicomponent KA2 and Pauson–Khand reactions: short synthesis of spirocyclic pyrrolocyclopentenones." Beilstein Journal of Organic Chemistry 16 (February 12, 2020): 200–211. http://dx.doi.org/10.3762/bjoc.16.23.
Повний текст джерелаChernyshov, Vladimir V., Yuri V. Gatilov, Olga I. Yarovaya, Igor P. Koskin, Spartak S. Yarovoy, Konstantin A. Brylev, and 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, no. 12 (November 26, 2019): 1675–80. http://dx.doi.org/10.1107/s2053229619015766.
Повний текст джерелаLinden, Anthony, Grzegorz Mlostoń, Paulina Grzelak, and 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, no. 12 (November 6, 2018): 1705–9. http://dx.doi.org/10.1107/s2056989018015335.
Повний текст джерелаThompson, 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, no. 6501 (July 16, 2020): 310–15. http://dx.doi.org/10.1126/science.aba9806.
Повний текст джерелаSwamy, K. C. Kumara, Roberta O. Day, Joan M. Holmes, and Robert R. Holmes. "Pentacoordinated molecules. 81. Conformational preferences of spirocyclic pentaoxyphosphoranes varying in ring size." Journal of the American Chemical Society 112, no. 16 (August 1990): 6095–103. http://dx.doi.org/10.1021/ja00172a028.
Повний текст джерелаLanger, Peter. "Synthesis of Purines and Related Molecules by Cyclization Reactions of Heterocyclic Enamines." Synlett 33, no. 05 (October 22, 2021): 440–57. http://dx.doi.org/10.1055/s-0040-1719845.
Повний текст джерелаPappin, Brighid B., Stephan M. Levonis, Peter C. Healy, Milton J. Kiefel, Michela I. Simone, and Todd A. Houston. "Crystallization-induced amide bond formation creates a boron-centered spirocyclic system." Heterocyclic Communications 23, no. 3 (June 27, 2017): 167–69. http://dx.doi.org/10.1515/hc-2017-0023.
Повний текст джерелаZaytseva, Elena, and 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, no. 3 (January 28, 2021): 677. http://dx.doi.org/10.3390/molecules26030677.
Повний текст джерелаPaquette, Leo A., George A. O'Doherty, Benjamin L. Miller, Robin D. Rogers, Arnold L. Rheingold, and Steven L. Geib. "Isodicyclopentadienes and related molecules. 48. Stereochemically uniform mode of iron carbonyl complexation to spirocyclic isodicyclopentadienes." Organometallics 8, no. 9 (September 1989): 2167–72. http://dx.doi.org/10.1021/om00111a012.
Повний текст джерелаHans, Johannes, Roberta O. Day, and Robert R. Holmes. "Pentacoordinated molecules. 89. Hydrogen-bonded chain and dimer formations of spirocyclic tetraoxyphosphoranes possessing phosphorinane chair conformations." Inorganic Chemistry 30, no. 20 (October 1991): 3928–36. http://dx.doi.org/10.1021/ic00020a028.
Повний текст джерелаHolmes, Robert R., Soheila Shafieezad, V. Chandrasekhar, Arjun C. Sau, Joan M. Holmes, and 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, no. 4 (February 1988): 1168–74. http://dx.doi.org/10.1021/ja00212a027.
Повний текст джерелаHolmes, Robert R., Roberta O. Day, V. Chandrasekhar, and 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, no. 13 (June 1985): 2009–15. http://dx.doi.org/10.1021/ic00207a012.
Повний текст джерелаHolmes, Robert R., Roberta O. Day, Arjun C. Sau, and 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, no. 5 (February 1986): 600–606. http://dx.doi.org/10.1021/ic00225a005.
Повний текст джерелаHolmes, Robert R., K. C. Kumara Swamy, Joan M. Holmes, and Roberta O. Day. "Pentacoordinated molecules. 84. Conformational effects of ring fusion and heteroatom substitution in six-membered rings of spirocyclic oxyphosphoranes." Inorganic Chemistry 30, no. 5 (March 1991): 1052–62. http://dx.doi.org/10.1021/ic00005a033.
Повний текст джерелаHANS, J., R. O. DAY, and R. R. HOLMES. "ChemInform Abstract: Pentacoordinated Molecules. Part 89. Hydrogen-Bonded Chain and Dimer Formations of Spirocyclic Tetraoxyphosphoranes Possessing Phosphorinane Chair Conformations." ChemInform 23, no. 3 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199203214.
Повний текст джерелаDietz, Jochen, Ulrich Müller, Volker Müller, and 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, no. 10 (October 1, 1991): 1293–99. http://dx.doi.org/10.1515/znb-1991-1003.
Повний текст джерелаHolmes, Robert R., Roberta O. Day, Arjun C. Sau, Charles A. Poutasse, and 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, no. 2 (January 1985): 193–99. http://dx.doi.org/10.1021/ic00196a015.
Повний текст джерелаVillabona, Marc, Marina Benet, Silvia Mena, Rabih O. Al-Kaysi, Jordi Hernando, and 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, no. 16 (June 13, 2018): 9166–77. http://dx.doi.org/10.1021/acs.joc.8b01211.
Повний текст джерелаHOLMES, R. R., K. C. K. SWAMY, J. M. HOLMES, and 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, no. 25 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199125208.
Повний текст джерелаDay, Roberta O., K. C. Kumara Swamy, Lisa Fairchild, Joan M. Holmes, and 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, no. 5 (February 1991): 1627–35. http://dx.doi.org/10.1021/ja00005a028.
Повний текст джерелаYang, Jun, Bo-Wen Pan, Lin Chen, Ying Zhou, and Xiong-Li Liu. "Recent advances in organocatalytic cascade reactions for enantioselective synthesis of chiral spirolactone skeletons." Chemical Synthesis 3, no. 1 (2023): 7. http://dx.doi.org/10.20517/cs.2022.38.
Повний текст джерелаKumar, Nakul, Gajendra Kumar Inwati, Emad M. Ahmed, Chhagan Lal, Bharat Makwana, Virendra K. Yadav, Saiful Islam, Hyun-Jo Ahn, Krishna K. Yadav, and Byong-Hun Jeon. "Modified 7-Chloro-11H-indeno[1,2-b]quinoxaline Heterocyclic System for Biological Activities." Catalysts 12, no. 2 (February 11, 2022): 213. http://dx.doi.org/10.3390/catal12020213.
Повний текст джерелаDAY, R. O., K. C. K. SWAMY, L. FAIRCHILD, J. M. HOLMES, and 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, no. 24 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199124184.
Повний текст джерелаYadav, J. S., B. V. Subba Reddy, V. Hari Krishna, T. Swamy, and 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, no. 6 (June 1, 2007): 412–15. http://dx.doi.org/10.1139/v07-048.
Повний текст джерелаLukin, Alexei, Kristina Komarova, Lyubov Vinogradova, Elizaveta Rogacheva, Lyudmila Kraeva, and Mikhail Krasavin. "Synthesis and Antibacterial Evaluation of Ciprofloxacin Congeners with Spirocyclic Amine Periphery." International Journal of Molecular Sciences 24, no. 2 (January 4, 2023): 954. http://dx.doi.org/10.3390/ijms24020954.
Повний текст джерелаMaassarani, Fida, Michel Pfeffer, and 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, no. 10 (October 1987): 2043–53. http://dx.doi.org/10.1021/om00153a003.
Повний текст джерелаKitschke, Philipp, Ana-Maria Preda, Alexander A. Auer, Sebastian Scholz, Tobias Rüffer, Heinrich Lang, and 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, no. 1 (2019): 220–30. http://dx.doi.org/10.1039/c8dt03695k.
Повний текст джерелаBrindisi, 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, no. 2 (2015): 357–62. http://dx.doi.org/10.1039/c4md00454j.
Повний текст джерелаYuan, Hongdong, Chongrong Tang, Shikuan Su, Lei Cui, Xueshun Jia, Chunju Li, and Jian Li. "A bicyclization reaction with two molecular allenyl ketones and isocyanides: synthesis of a lactone-containing azaspirocycle derivative." Chemical Communications 55, no. 50 (2019): 7231–34. http://dx.doi.org/10.1039/c9cc02785h.
Повний текст джерелаKour, Smit, Sandeep Rana, Smitha Kizhake, Dragana Lagundžin, David Klinkebiel, Jayapal Reddy Mallareddy, Tom Huxford, Nicholas T. Woods та Amarnath Natarajan. "Stapling proteins in the RELA complex inhibits TNFα-induced nuclear translocation of RELA". RSC Chemical Biology 3, № 1 (2022): 32–36. http://dx.doi.org/10.1039/d1cb00183c.
Повний текст джерелаBiţă, 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, no. 3 (March 9, 2023): 112. http://dx.doi.org/10.3390/inorganics11030112.
Повний текст джерелаPesquet, Anthony, Hamid Marzag, Michael Knorr, Carsten Strohmann, Ata Martin Lawson, Alina Ghinet, Joëlle Dubois, Farce Amaury, Adam Daïch, and 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, no. 10 (2019): 2798–808. http://dx.doi.org/10.1039/c8ob02612b.
Повний текст джерелаSong, Kunpeng, Yinjie Wang, Fang Ruan, Weiwei Yang, and Jiping Liu. "Synthesis of a Novel Spirocyclic Inflatable Flame Retardant and Its Application in Epoxy Composites." Polymers 12, no. 11 (October 29, 2020): 2534. http://dx.doi.org/10.3390/polym12112534.
Повний текст джерелаKotha, Sambasivarao, and Kalyaneswar Mandal. "Metathetic approach to naphthoxepin and spirocyclic molecular frameworks." Tetrahedron Letters 45, no. 7 (February 2004): 1391–94. http://dx.doi.org/10.1016/j.tetlet.2003.12.075.
Повний текст джерелаSawhney, Gifty, Javeed Ur Rasool, Diksha Saroch, Mumin Ozturk, Frank Brombacher, Bilal Ahmad, Asha Bhagat, Asif Ali, Suraj P. Parihar та 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, № 22 (20 листопада 2022): 8068. http://dx.doi.org/10.3390/molecules27228068.
Повний текст джерелаKhuzin, Artur A., Dim I. Galimov, and 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, no. 3 (January 22, 2023): 1107. http://dx.doi.org/10.3390/molecules28031107.
Повний текст джерелаQu, Haijun, Xuejian Li, Fan Mo, and Xufeng Lin. "Efficient synthesis of dihydropyrimidinones via a three-component Biginelli-type reaction of urea, alkylaldehyde and arylaldehyde." Beilstein Journal of Organic Chemistry 9 (December 11, 2013): 2846–51. http://dx.doi.org/10.3762/bjoc.9.320.
Повний текст джерелаMaddirala, Amarendar Reddy, та 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 квітня 2018): 875–83. http://dx.doi.org/10.3762/bjoc.14.74.
Повний текст джерелаBöhm, Stanislav, Michal Hocek, Jan Němeček, Vladimír Havlíček, and Josef Kuthan. "Preparation and Spectroscopic Properties of Spirocyclic 1-Methyl-2,4,4,6-tetraaryl-1,4-dihydropyridines." Collection of Czechoslovak Chemical Communications 59, no. 5 (1994): 1105–14. http://dx.doi.org/10.1135/cccc19941105.
Повний текст джерелаLukyanov, Boris, Gennadii Vasilyuk, Eugene Mukhanov, Leonid Ageev, Maria Lukyanova, Yury Alexeenko, Serguei Besugliy, and Valeri Tkachev. "Multifunctional Spirocyclic Systems." International Journal of Photoenergy 2009 (2009): 1–6. http://dx.doi.org/10.1155/2009/689450.
Повний текст джерелаShetgaonkar, 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, no. 9 (September 3, 2021): 1619. http://dx.doi.org/10.3390/sym13091619.
Повний текст джерелаGarcia-Yuste, Santiago, Konrad W. Hellmann, Lutz H. Gade, Ian J. Scowen, and Mary McPartlin. "Bis[1,3-bis(diphenylmethylsilylamido)propane]zirconium: A Spirocyclic Complex Containing a Sterically Demanding Chelating Amido Ligand." Zeitschrift für Naturforschung B 54, no. 10 (October 1, 1999): 1260–64. http://dx.doi.org/10.1515/znb-1999-1007.
Повний текст джерелаLivendahl, M., J. Jamroskovic, M. Hedenström, T. Görlich, N. Sabouri, and E. Chorell. "Synthesis of phenanthridine spiropyrans and studies of their effects on G-quadruplex DNA." Organic & Biomolecular Chemistry 15, no. 15 (2017): 3265–75. http://dx.doi.org/10.1039/c7ob00300e.
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