Zeitschriftenartikel zum Thema „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, Nr. 34 (2021): 11294–305. http://dx.doi.org/10.1039/d1sc03615g.
Benabdallah, Mohammed, Oualid Talhi, Fatiha Nouali, Nouredine Choukchou-Braham, Khaldoun Bachari und Artur M. S. Silva. „Advances in Spirocyclic Hybrids: Chemistry and Medicinal Actions“. Current Medicinal Chemistry 25, Nr. 31 (16.10.2018): 3748–67. http://dx.doi.org/10.2174/0929867325666180309124821.
Paquette, Leo A. „Spirocyclic Restriction of Nucleosides“. Australian Journal of Chemistry 57, Nr. 1 (2004): 7. http://dx.doi.org/10.1071/ch03267.
Shen, Guo-Liang, Jing Sun und 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, Nr. 6 (2015): 4475–83. http://dx.doi.org/10.1039/c4ra13760d.
Kappen, Lizzy S., Yiqing Lin, Graham B. Jones und Irving H. Goldberg. „Probing DNA Bulges with Designed Helical Spirocyclic Molecules†“. Biochemistry 46, Nr. 2 (Januar 2007): 561–67. http://dx.doi.org/10.1021/bi061744d.
G. Keller, Sascha, Mako Kamiya und Yasuteru Urano. „Recent Progress in Small Spirocyclic, Xanthene-Based Fluorescent Probes“. Molecules 25, Nr. 24 (16.12.2020): 5964. http://dx.doi.org/10.3390/molecules25245964.
Holovatiuk, V. M., O. A. Brazhko und 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, Nr. 3 (04.11.2016): 149–53. http://dx.doi.org/10.15421/201681.
Innocenti, Riccardo, Elena Lenci, Gloria Menchi und Andrea Trabocchi. „Combination of multicomponent KA2 and Pauson–Khand reactions: short synthesis of spirocyclic pyrrolocyclopentenones“. Beilstein Journal of Organic Chemistry 16 (12.02.2020): 200–211. http://dx.doi.org/10.3762/bjoc.16.23.
Chernyshov, Vladimir V., Yuri V. Gatilov, Olga I. Yarovaya, Igor P. Koskin, Spartak S. Yarovoy, Konstantin A. Brylev und 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, Nr. 12 (26.11.2019): 1675–80. http://dx.doi.org/10.1107/s2053229619015766.
Linden, Anthony, Grzegorz Mlostoń, Paulina Grzelak und 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, Nr. 12 (06.11.2018): 1705–9. http://dx.doi.org/10.1107/s2056989018015335.
Thompson, 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, Nr. 6501 (16.07.2020): 310–15. http://dx.doi.org/10.1126/science.aba9806.
Swamy, K. C. Kumara, Roberta O. Day, Joan M. Holmes und Robert R. Holmes. „Pentacoordinated molecules. 81. Conformational preferences of spirocyclic pentaoxyphosphoranes varying in ring size“. Journal of the American Chemical Society 112, Nr. 16 (August 1990): 6095–103. http://dx.doi.org/10.1021/ja00172a028.
Langer, Peter. „Synthesis of Purines and Related Molecules by Cyclization Reactions of Heterocyclic Enamines“. Synlett 33, Nr. 05 (22.10.2021): 440–57. http://dx.doi.org/10.1055/s-0040-1719845.
Pappin, Brighid B., Stephan M. Levonis, Peter C. Healy, Milton J. Kiefel, Michela I. Simone und Todd A. Houston. „Crystallization-induced amide bond formation creates a boron-centered spirocyclic system“. Heterocyclic Communications 23, Nr. 3 (27.06.2017): 167–69. http://dx.doi.org/10.1515/hc-2017-0023.
Zaytseva, Elena, und 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, Nr. 3 (28.01.2021): 677. http://dx.doi.org/10.3390/molecules26030677.
Paquette, Leo A., George A. O'Doherty, Benjamin L. Miller, Robin D. Rogers, Arnold L. Rheingold und Steven L. Geib. „Isodicyclopentadienes and related molecules. 48. Stereochemically uniform mode of iron carbonyl complexation to spirocyclic isodicyclopentadienes“. Organometallics 8, Nr. 9 (September 1989): 2167–72. http://dx.doi.org/10.1021/om00111a012.
Hans, Johannes, Roberta O. Day und Robert R. Holmes. „Pentacoordinated molecules. 89. Hydrogen-bonded chain and dimer formations of spirocyclic tetraoxyphosphoranes possessing phosphorinane chair conformations“. Inorganic Chemistry 30, Nr. 20 (Oktober 1991): 3928–36. http://dx.doi.org/10.1021/ic00020a028.
Holmes, Robert R., Soheila Shafieezad, V. Chandrasekhar, Arjun C. Sau, Joan M. Holmes und 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, Nr. 4 (Februar 1988): 1168–74. http://dx.doi.org/10.1021/ja00212a027.
Holmes, Robert R., Roberta O. Day, V. Chandrasekhar und 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, Nr. 13 (Juni 1985): 2009–15. http://dx.doi.org/10.1021/ic00207a012.
Holmes, Robert R., Roberta O. Day, Arjun C. Sau und 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, Nr. 5 (Februar 1986): 600–606. http://dx.doi.org/10.1021/ic00225a005.
Holmes, Robert R., K. C. Kumara Swamy, Joan M. Holmes und Roberta O. Day. „Pentacoordinated molecules. 84. Conformational effects of ring fusion and heteroatom substitution in six-membered rings of spirocyclic oxyphosphoranes“. Inorganic Chemistry 30, Nr. 5 (März 1991): 1052–62. http://dx.doi.org/10.1021/ic00005a033.
HANS, J., R. O. DAY und R. R. HOLMES. „ChemInform Abstract: Pentacoordinated Molecules. Part 89. Hydrogen-Bonded Chain and Dimer Formations of Spirocyclic Tetraoxyphosphoranes Possessing Phosphorinane Chair Conformations.“ ChemInform 23, Nr. 3 (22.08.2010): no. http://dx.doi.org/10.1002/chin.199203214.
Dietz, Jochen, Ulrich Müller, Volker Müller und 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, Nr. 10 (01.10.1991): 1293–99. http://dx.doi.org/10.1515/znb-1991-1003.
Holmes, Robert R., Roberta O. Day, Arjun C. Sau, Charles A. Poutasse und 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, Nr. 2 (Januar 1985): 193–99. http://dx.doi.org/10.1021/ic00196a015.
Villabona, Marc, Marina Benet, Silvia Mena, Rabih O. Al-Kaysi, Jordi Hernando und 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, Nr. 16 (13.06.2018): 9166–77. http://dx.doi.org/10.1021/acs.joc.8b01211.
HOLMES, R. R., K. C. K. SWAMY, J. M. HOLMES und 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, Nr. 25 (23.08.2010): no. http://dx.doi.org/10.1002/chin.199125208.
Day, Roberta O., K. C. Kumara Swamy, Lisa Fairchild, Joan M. Holmes und 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, Nr. 5 (Februar 1991): 1627–35. http://dx.doi.org/10.1021/ja00005a028.
Yang, Jun, Bo-Wen Pan, Lin Chen, Ying Zhou und Xiong-Li Liu. „Recent advances in organocatalytic cascade reactions for enantioselective synthesis of chiral spirolactone skeletons“. Chemical Synthesis 3, Nr. 1 (2023): 7. http://dx.doi.org/10.20517/cs.2022.38.
Kumar, Nakul, Gajendra Kumar Inwati, Emad M. Ahmed, Chhagan Lal, Bharat Makwana, Virendra K. Yadav, Saiful Islam, Hyun-Jo Ahn, Krishna K. Yadav und Byong-Hun Jeon. „Modified 7-Chloro-11H-indeno[1,2-b]quinoxaline Heterocyclic System for Biological Activities“. Catalysts 12, Nr. 2 (11.02.2022): 213. http://dx.doi.org/10.3390/catal12020213.
DAY, R. O., K. C. K. SWAMY, L. FAIRCHILD, J. M. HOLMES und 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, Nr. 24 (23.08.2010): no. http://dx.doi.org/10.1002/chin.199124184.
Yadav, J. S., B. V. Subba Reddy, V. Hari Krishna, T. Swamy und 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, Nr. 6 (01.06.2007): 412–15. http://dx.doi.org/10.1139/v07-048.
Lukin, Alexei, Kristina Komarova, Lyubov Vinogradova, Elizaveta Rogacheva, Lyudmila Kraeva und Mikhail Krasavin. „Synthesis and Antibacterial Evaluation of Ciprofloxacin Congeners with Spirocyclic Amine Periphery“. International Journal of Molecular Sciences 24, Nr. 2 (04.01.2023): 954. http://dx.doi.org/10.3390/ijms24020954.
Maassarani, Fida, Michel Pfeffer und 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, Nr. 10 (Oktober 1987): 2043–53. http://dx.doi.org/10.1021/om00153a003.
Kitschke, Philipp, Ana-Maria Preda, Alexander A. Auer, Sebastian Scholz, Tobias Rüffer, Heinrich Lang und 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, Nr. 1 (2019): 220–30. http://dx.doi.org/10.1039/c8dt03695k.
Brindisi, 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, Nr. 2 (2015): 357–62. http://dx.doi.org/10.1039/c4md00454j.
Yuan, Hongdong, Chongrong Tang, Shikuan Su, Lei Cui, Xueshun Jia, Chunju Li und Jian Li. „A bicyclization reaction with two molecular allenyl ketones and isocyanides: synthesis of a lactone-containing azaspirocycle derivative“. Chemical Communications 55, Nr. 50 (2019): 7231–34. http://dx.doi.org/10.1039/c9cc02785h.
Kour, Smit, Sandeep Rana, Smitha Kizhake, Dragana Lagundžin, David Klinkebiel, Jayapal Reddy Mallareddy, Tom Huxford, Nicholas T. Woods und Amarnath Natarajan. „Stapling proteins in the RELA complex inhibits TNFα-induced nuclear translocation of RELA“. RSC Chemical Biology 3, Nr. 1 (2022): 32–36. http://dx.doi.org/10.1039/d1cb00183c.
Biţă, 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, Nr. 3 (09.03.2023): 112. http://dx.doi.org/10.3390/inorganics11030112.
Pesquet, Anthony, Hamid Marzag, Michael Knorr, Carsten Strohmann, Ata Martin Lawson, Alina Ghinet, Joëlle Dubois, Farce Amaury, Adam Daïch und 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, Nr. 10 (2019): 2798–808. http://dx.doi.org/10.1039/c8ob02612b.
Song, Kunpeng, Yinjie Wang, Fang Ruan, Weiwei Yang und Jiping Liu. „Synthesis of a Novel Spirocyclic Inflatable Flame Retardant and Its Application in Epoxy Composites“. Polymers 12, Nr. 11 (29.10.2020): 2534. http://dx.doi.org/10.3390/polym12112534.
Kotha, Sambasivarao, und Kalyaneswar Mandal. „Metathetic approach to naphthoxepin and spirocyclic molecular frameworks“. Tetrahedron Letters 45, Nr. 7 (Februar 2004): 1391–94. http://dx.doi.org/10.1016/j.tetlet.2003.12.075.
Sawhney, Gifty, Javeed Ur Rasool, Diksha Saroch, Mumin Ozturk, Frank Brombacher, Bilal Ahmad, Asha Bhagat, Asif Ali, Suraj P. Parihar und 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, Nr. 22 (20.11.2022): 8068. http://dx.doi.org/10.3390/molecules27228068.
Khuzin, Artur A., Dim I. Galimov und 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, Nr. 3 (22.01.2023): 1107. http://dx.doi.org/10.3390/molecules28031107.
Qu, Haijun, Xuejian Li, Fan Mo und Xufeng Lin. „Efficient synthesis of dihydropyrimidinones via a three-component Biginelli-type reaction of urea, alkylaldehyde and arylaldehyde“. Beilstein Journal of Organic Chemistry 9 (11.12.2013): 2846–51. http://dx.doi.org/10.3762/bjoc.9.320.
Maddirala, Amarendar Reddy, und 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 (18.04.2018): 875–83. http://dx.doi.org/10.3762/bjoc.14.74.
Böhm, Stanislav, Michal Hocek, Jan Němeček, Vladimír Havlíček und Josef Kuthan. „Preparation and Spectroscopic Properties of Spirocyclic 1-Methyl-2,4,4,6-tetraaryl-1,4-dihydropyridines“. Collection of Czechoslovak Chemical Communications 59, Nr. 5 (1994): 1105–14. http://dx.doi.org/10.1135/cccc19941105.
Lukyanov, Boris, Gennadii Vasilyuk, Eugene Mukhanov, Leonid Ageev, Maria Lukyanova, Yury Alexeenko, Serguei Besugliy und Valeri Tkachev. „Multifunctional Spirocyclic Systems“. International Journal of Photoenergy 2009 (2009): 1–6. http://dx.doi.org/10.1155/2009/689450.
Shetgaonkar, 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, Nr. 9 (03.09.2021): 1619. http://dx.doi.org/10.3390/sym13091619.
Garcia-Yuste, Santiago, Konrad W. Hellmann, Lutz H. Gade, Ian J. Scowen und Mary McPartlin. „Bis[1,3-bis(diphenylmethylsilylamido)propane]zirconium: A Spirocyclic Complex Containing a Sterically Demanding Chelating Amido Ligand“. Zeitschrift für Naturforschung B 54, Nr. 10 (01.10.1999): 1260–64. http://dx.doi.org/10.1515/znb-1999-1007.
Livendahl, M., J. Jamroskovic, M. Hedenström, T. Görlich, N. Sabouri und E. Chorell. „Synthesis of phenanthridine spiropyrans and studies of their effects on G-quadruplex DNA“. Organic & Biomolecular Chemistry 15, Nr. 15 (2017): 3265–75. http://dx.doi.org/10.1039/c7ob00300e.