Статті в журналах з теми "Carbocyclic ring compounds"
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Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Carbocyclic ring compounds".
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Yavari, Issa, and Aliyeh Khajeh-Khezri. "Recent Advances in the Synthesis of Hetero- and Carbocyclic Compounds and Complexes Based on Acenaphthylene-1,2-dione." Synthesis 50, no. 20 (August 16, 2018): 3947–73. http://dx.doi.org/10.1055/s-0037-1610209.
Повний текст джерелаLautens, Mark, Dino Alberico, Cyril Bressy, Yuan-Qing Fang, Brian Mariampillai, and Thorsten Wilhelm. "Palladium-catalyzed ring-forming reactions: Methods and applications." Pure and Applied Chemistry 78, no. 2 (January 1, 2006): 351–61. http://dx.doi.org/10.1351/pac200678020351.
Повний текст джерелаBanwell, MG. "New Methods for the Synthesis of Troponoid Compounds." Australian Journal of Chemistry 44, no. 1 (1991): 1. http://dx.doi.org/10.1071/ch9910001.
Повний текст джерелаSaborit, Gisela V., Carlos Cativiela, Ana I. Jiménez, Josep Bonjoch, and Ben Bradshaw. "Synthesis of cis-hydrindan-2,4-diones bearing an all-carbon quaternary center by a Danheiser annulation." Beilstein Journal of Organic Chemistry 14 (October 9, 2018): 2597–601. http://dx.doi.org/10.3762/bjoc.14.237.
Повний текст джерелаHalliday, Jill I., Mary Chebib, and Malcolm D. McLeod. "Synthesis and Biological Evaluation of a New Family of Constrained Azabicyclic Homocholine Analogues." Australian Journal of Chemistry 63, no. 5 (2010): 808. http://dx.doi.org/10.1071/ch10024.
Повний текст джерелаMikaia, Anzor. "Protocol for structure determination of unknowns by EI mass spectrometry. II. Diagnostic ions in one ring alicyclic, heterocyclic, and aromatic compounds." Journal of Physical and Chemical Reference Data 52, no. 2 (June 1, 2023): 021501. http://dx.doi.org/10.1063/5.0140771.
Повний текст джерелаSivakrishna, Balija, Sehbanul Islam, Amarendra Panda, Maddi Saranya, Manas K. Santra, and Shantanu Pal. "Synthesis and Anticancer Properties of Novel Truncated Carbocyclic Nucleoside Analogues." Anti-Cancer Agents in Medicinal Chemistry 18, no. 10 (January 23, 2019): 1425–31. http://dx.doi.org/10.2174/1871520618666180322120533.
Повний текст джерелаTakahashi, Hidetoshi, Kazuhiro Yoshida, and Akira Yanagisawa. "Synthesis of Carbocyclic Aromatic Compounds Using Ruthenium-Catalyzed Ring-Closing Enyne Metathesis." Journal of Organic Chemistry 74, no. 10 (May 15, 2009): 3632–40. http://dx.doi.org/10.1021/jo900456g.
Повний текст джерелаPaquette, Leo A. "Book Review, Carbocyclic Three-Membered Ring Compounds, Houben-Weyl, Methods of Organic Chemistry." Synthesis 1998, no. 02 (February 1998): 225. http://dx.doi.org/10.1055/s-1998-4511.
Повний текст джерелаPaquette, Leo A. "Book Review, Carbocyclic Four-Membered Ring Compounds, Houben-Weyl, Methods of Organic Chemistry." Synthesis 1998, no. 02 (February 1998): 226. http://dx.doi.org/10.1055/s-1998-4512.
Повний текст джерелаLiboska, Radek, Milena Masojídková, and Ivan Rosenberg. "Carbocyclic Phosphonate-Based Nucleotide Analogs Related to PMEA. I. Racemic trans-Configured Derivatives." Collection of Czechoslovak Chemical Communications 61, no. 2 (1996): 313–32. http://dx.doi.org/10.1135/cccc19960313.
Повний текст джерелаHwu, Jih Ru, and John M. Wetzel. "Silicon-promoted ring contractions in the formation of carbocyclic spiro compounds. Total synthesis of (-)-solavetivone." Journal of Organic Chemistry 57, no. 3 (January 1992): 922–28. http://dx.doi.org/10.1021/jo00029a025.
Повний текст джерелаLiu, Wei, Wenjun Zhang, Hongbo Jin, Qingbo Zhang, Yuchan Chen, Xiaodong Jiang, Guangtao Zhang, et al. "Genome Mining of Marine-Derived Streptomyces sp. SCSIO 40010 Leads to Cytotoxic New Polycyclic Tetramate Macrolactams." Marine Drugs 17, no. 12 (November 25, 2019): 663. http://dx.doi.org/10.3390/md17120663.
Повний текст джерелаYan, Ning, Yongmei Du, Xinmin Liu, Hongbo Zhang, Yanhua Liu, and Zhongfeng Zhang. "A Review on Bioactivities of Tobacco Cembranoid Diterpenes." Biomolecules 9, no. 1 (January 16, 2019): 30. http://dx.doi.org/10.3390/biom9010030.
Повний текст джерелаHWU, J. R., and J. M. WETZEL. "ChemInform Abstract: Silicon-Promoted Ring Contractions in the Formation of Carbocyclic Spiro Compounds. Total Synthesis of (-)-Solavetivone." ChemInform 23, no. 26 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199226254.
Повний текст джерелаSchmiedel, Volker Martin, and Hans-Ulrich Reissig. "Alkoxyallenes as Starting Materials for the Syntheses of Natural Products." Current Organic Chemistry 23, no. 27 (January 15, 2020): 2976–3003. http://dx.doi.org/10.2174/1385272824666191218115731.
Повний текст джерелаZaki, Magdi E. A., Sami A. Al-Hussain, Aamal A. Al-Mutairi, Vijay H. Masand, Abdul Samad, and Rahul D. Jawarkar. "Mechanistic Analysis of Chemically Diverse Bromodomain-4 Inhibitors Using Balanced QSAR Analysis and Supported by X-ray Resolved Crystal Structures." Pharmaceuticals 15, no. 6 (June 14, 2022): 745. http://dx.doi.org/10.3390/ph15060745.
Повний текст джерелаGirisha, Marisiddaiah, Hemmige S. Yathirajan, Jerry P. Jasinski, and Christopher Glidewell. "Different acid–base behaviour of a pyrazole and an isoxazole with organic acids: crystal and molecular structures of the salt 3-(4-fluorophenyl)-1H-pyrazolium 2,4,6-trinitrophenolate and of the cocrystal 4-amino-N-(3,4-dimethyl-1,2-oxazol-5-yl)benzenesulfonamide–3,5-dinitrobenzoic acid (1/1)." Acta Crystallographica Section C Structural Chemistry 72, no. 8 (July 12, 2016): 612–18. http://dx.doi.org/10.1107/s2053229616010494.
Повний текст джерелаWojtasik, Katarzyna, Monika Pokladko-Kowar, and Ewa Gondek. "Optimization of Bulk Heterojunction Photovoltaic Structures with Heterocyclic Derivatives." Crystals 13, no. 5 (April 27, 2023): 734. http://dx.doi.org/10.3390/cryst13050734.
Повний текст джерелаKudrevich, Svetlana V., Johan E. Van Lier, Maria G. Galpern, and Evgeny A. Luk'yanets. "Substituted tetra-2,3-pyrazinoporphyrazines. Part I. Angular annelation of tetra-2,3-quinoxalinoporphyrazine." Canadian Journal of Chemistry 74, no. 4 (April 1, 1996): 508–15. http://dx.doi.org/10.1139/v96-055.
Повний текст джерелаChen, Xuefei, Min Xu, Jin Lü, Jianguo Xu, Yemin Wang, Shuangjun Lin, Zixin Deng, and Meifeng Tao. "Biosynthesis of Tropolones inStreptomycesspp.: Interweaving Biosynthesis and Degradation of Phenylacetic Acid and Hydroxylations on the Tropone Ring." Applied and Environmental Microbiology 84, no. 12 (April 13, 2018): e00349-18. http://dx.doi.org/10.1128/aem.00349-18.
Повний текст джерелаAksenov, A. V., N. A. Aksenov, A. S. Lyakhovnenko, A. B. Kumshaeva, and I. V. Aksenova. "Novel three-component reaction of perimidines with 1,3,5-triazines and carbonyl compounds in polyphosphoric acid. an efficient method for peri-annelation of a carbocyclic and pyridine ring." Chemistry of Heterocyclic Compounds 48, no. 4 (July 2012): 634–41. http://dx.doi.org/10.1007/s10593-012-1037-8.
Повний текст джерелаAksenov, A. V., N. A. Aksenov, A. S. Lyakhovnenko, A. B. Kumshaeva, and I. V. Aksenova. "ChemInform Abstract: Novel Three-Component Reaction of Perimidines with 1,3,5-Triazines and Carbonyl Compounds in Polyphosphoric Acid. An Efficient Method for peri-Anellation of a Carbocyclic and Pyridine Ring." ChemInform 43, no. 50 (November 29, 2012): no. http://dx.doi.org/10.1002/chin.201250165.
Повний текст джерелаGirisha, Marisiddaiah, Belakavadi K. Sagar, Hemmige S. Yathirajan, Ravindranath S. Rathore, Manpreet Kaur, Jerry P. Jasinski, and Christopher Glidewell. "Eight Schiff bases derived from various salicylaldehydes: phenol–imine and keto–amine forms, conformational disorder, and supramolecular assembly in one and two dimensions." Acta Crystallographica Section C Structural Chemistry 74, no. 10 (September 7, 2018): 1094–104. http://dx.doi.org/10.1107/s2053229618012287.
Повний текст джерелаDragutan, V., I. Dragutan, and A. T. Balaban. "Metathesis Catalysed by the Platinum Group Metals." Platinum Metals Review 44, no. 4 (October 1, 2000): 168–72. http://dx.doi.org/10.1595/003214000x444168172.
Повний текст джерелаBolton, R., and M. H. Sosabowski. "ChemInform Abstract: Polycyclic Compounds Comprising a Pyridine and Two or More Carbocyclic Rings." ChemInform 30, no. 44 (June 13, 2010): no. http://dx.doi.org/10.1002/chin.199944322.
Повний текст джерелаOkumura, Mikiko, and David Sarlah. "Arenophile-Mediated Photochemical Dearomatization of Nonactivated Arenes." CHIMIA International Journal for Chemistry 74, no. 7 (August 12, 2020): 577–83. http://dx.doi.org/10.2533/chimia.2020.577.
Повний текст джерелаZhaocui, Xudong, Hanqiao, Xinyi, Guoxu, and Leiling. "Five New Meroterpenoids from the Fruiting Bodies of the Basidiomycete Clitocybe clavipes with Cytotoxic Activity." Molecules 24, no. 22 (November 6, 2019): 4015. http://dx.doi.org/10.3390/molecules24224015.
Повний текст джерелаMasdeu, Carme, Maria Fuertes, Endika Martin-Encinas, Asier Selas, Gloria Rubiales, Francisco Palacios, and Concepcion Alonso. "Fused 1,5-Naphthyridines: Synthetic Tools and Applications." Molecules 25, no. 15 (July 31, 2020): 3508. http://dx.doi.org/10.3390/molecules25153508.
Повний текст джерелаOrtuño, Rosa M. "Carbocycle-Based Organogelators: Influence of Chirality and Structural Features on Their Supramolecular Arrangements and Properties." Gels 7, no. 2 (May 1, 2021): 54. http://dx.doi.org/10.3390/gels7020054.
Повний текст джерелаYuan, Chengye, and Chaozhong Li. "STUDIES ON ORGANOPHOSPHORUS COMPOUNDS 90. STEREOSELECTIVE SYNTHESIS OF FUSED CARBOCYCLIC AND ISOXAZOLINE RINGS VIA INTRAMOLECULAR SILYL NITRONATE-OLEFIN CYCLOADDITIONS." Phosphorus, Sulfur, and Silicon and the Related Elements 103, no. 1-4 (June 1995): 133–35. http://dx.doi.org/10.1080/10426509508027372.
Повний текст джерелаSchaper, Wiebke, Ilona Lange, Dagmar Henschel, Oliver Moers, Armand Blaschette, and Peter G. Jones. "Polysulfonylamine, CXL [1]. N-Cycloalkyldimesylamine C„H2n-1/N(SO2CH3)2: Synthesen (n = 3 -6 ), Festkörper-Molekülstrukturen (n = 4 -6 ) Und Rolle Schwacher Wasserstoffbrücken C-H···O In Den Kristallstrukturen." Zeitschrift für Naturforschung B 56, no. 8 (August 1, 2001): 765–77. http://dx.doi.org/10.1515/znb-2001-0810.
Повний текст джерелаYuan, Chengye, та Chaozhong Li. "Studies on organophosphorus compounds 80. Stereoselective synthesis of fused carbocyclic and isoxazoline rings via intramolecular cycloaddition of nitrile oxides derived from α-nitroalkenes". Tetrahedron Letters 34, № 37 (вересень 1993): 5959–62. http://dx.doi.org/10.1016/s0040-4039(00)73826-3.
Повний текст джерелаYUAN, C., та C. LI. "ChemInform Abstract: Studies on Organo-Phosphorus Compounds. Part 80. Stereoselective Synthesis of Fused Carbocyclic and Isoxazoline Rings via Intramolecular Cycloaddition of Nitrile Oxides Derived from α-Nitroalkenes." ChemInform 25, № 4 (19 серпня 2010): no. http://dx.doi.org/10.1002/chin.199404207.
Повний текст джерелаSingha, Tushar, Ganesh Arjun Kadam, and Durga Prasad Hari. "Photocatalyzed redox-neutral decarboxylative Dowd-Beckwith radical-polar crossover reaction: an efficient approach to functionalized medium-sized carbocyclic compounds." Chemical Science, 2023. http://dx.doi.org/10.1039/d3sc01908j.
Повний текст джерелаPal, Shantanu, Girish Chandra, Samir Kumar Mondal, and Birkishore Mahto. "Current Strategies on the Enantioselective Synthesis of Modified Nucleosides." Synlett, November 16, 2023. http://dx.doi.org/10.1055/a-2212-8502.
Повний текст джерелаFikatas, Antonios, Peter Vervaeke, Eef Meyen, Nuria Llor, Sergi Ordeix, Ine Boonen, Magda Bletsa, et al. "A Novel Series of Indole Alkaloid Derivatives Inhibit Dengue and Zika Virus Infection by Interference with the Viral Replication Complex." Antimicrobial Agents and Chemotherapy 65, no. 8 (July 16, 2021). http://dx.doi.org/10.1128/aac.02349-20.
Повний текст джерелаJansa, Petr, Ivana Císařová, and Eliška Matoušová. "Oxidative Cleavage and Ring Reconstruction in the Synthesis of Amaryllidaceae Alkaloid Analogues." European Journal of Organic Chemistry, November 29, 2023. http://dx.doi.org/10.1002/ejoc.202301021.
Повний текст джерелаBao, Ming, and Michael P. Doyle. "Asymmetric [3+n]‐cycloaddition reactions of donor‐acceptor cyclopropanes." ChemCatChem, October 17, 2023. http://dx.doi.org/10.1002/cctc.202301090.
Повний текст джерелаZhao, Dong-Lin, Lu-Jia Yang, Ting Shi, Chao-Yi Wang, Chang-Lun Shao, and Chang-Yun Wang. "Potent Phytotoxic Harziane Diterpenes from a Soft Coral-Derived Strain of the Fungus Trichoderma harzianum XS-20090075." Scientific Reports 9, no. 1 (September 16, 2019). http://dx.doi.org/10.1038/s41598-019-49778-7.
Повний текст джерелаJankowiak, Aleksandra, Piotr Kaszynski, William R. Tilford, Kiminori Ohta, Adam Januszko, Takashi Nagamine, and Yasuyuki Endo. "Ring-alkyl connecting group effect on mesogenic properties of p-carborane derivatives and their hydrocarbon analogues." Beilstein Journal of Organic Chemistry 5 (December 30, 2009). http://dx.doi.org/10.3762/bjoc.5.83.
Повний текст джерелаTakahashi, Hidetoshi, Kazuhiro Yoshida, and Akira Yanagisawa. "ChemInform Abstract: Synthesis of Carbocyclic Aromatic Compounds Using Ruthenium-Catalyzed Ring-Closing Enyne Metathesis." ChemInform 40, no. 39 (September 29, 2009). http://dx.doi.org/10.1002/chin.200939041.
Повний текст джерелаBabar, Kashaf, Ameer Fawad Zahoor, Sajjad Ahmad, and Rabia Akhtar. "Recent synthetic strategies toward the synthesis of spirocyclic compounds comprising six-membered carbocyclic/heterocyclic ring systems." Molecular Diversity, July 21, 2020. http://dx.doi.org/10.1007/s11030-020-10126-x.
Повний текст джерелаSinnwell, Michael A., Ryan H. Groeneman, Benjamin J. Ingenthron, Changan Li, and Leonard R. MacGillivray. "Supramolecular construction of a cyclobutane ring system with four different substituents in the solid state." Communications Chemistry 4, no. 1 (May 10, 2021). http://dx.doi.org/10.1038/s42004-021-00493-3.
Повний текст джерелаKumar, K. Shiva, Kishan Gugulothu, Sabbasani Rajasekhara Reddy, and Katta Venkateswarlu. "A Critical Review on Recent Advances in Base-Assisted Smiles Rearrangement." Current Organic Chemistry 26 (May 9, 2022). http://dx.doi.org/10.2174/1385272826666220509143140.
Повний текст джерелаChawla, Pooja A., Parul Grover, Lovekesh Mehta, Anjleena Malhotra, Garima Kapoor, Kandasamy Nagarajan, Parvin Kumar, and Viney Chawla. "Exploring the multitarget potential of iridoids: Advances and Applications." Current Topics in Medicinal Chemistry 23 (December 22, 2022). http://dx.doi.org/10.2174/1568026623666221222142217.
Повний текст джерелаEjaz, Syeda Abida, Aftab Farid, Seema Zargar, Pervaiz Ali Channar, Mubashir Aziz, Tanveer A. Wani, Hafiz Muhammad Attaullah, et al. "Computational and theoretical chemistry of newly synthesized and characterized 2,2’-(5,5’-(1,4-phenylene)bis(1H-tetrazole-5,1-diyl))bis-N-acetamides." BMC Chemistry 17, no. 1 (August 14, 2023). http://dx.doi.org/10.1186/s13065-023-01011-3.
Повний текст джерелаLiu, Min, Nuo Yan, Haowen Tian, Bo Li, and Dongbing Zhao. "Ring Expansion toward Disila‐carbocycles via Highly Selective C−Si/C−Si Bond Cross‐Exchange." Angewandte Chemie, February 22, 2024. http://dx.doi.org/10.1002/ange.202319187.
Повний текст джерелаLiu, Min, Nuo Yan, Haowen Tian, Bo Li, and Dongbing Zhao. "Ring Expansion toward Disila‐carbocycles via Highly Selective C−Si/C−Si Bond Cross‐Exchange." Angewandte Chemie International Edition, February 22, 2024. http://dx.doi.org/10.1002/anie.202319187.
Повний текст джерелаMiguélez, Rubén, Pablo Barrio, and José M. González. "Recent Advances in the Catalytic Synthesis of the Cyclopentene Core." Chemical Record, October 11, 2023. http://dx.doi.org/10.1002/tcr.202300254.
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