Статті в журналах з теми "Construction of Heterocyclic and Carbocyclic Rings"
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Cardoso, Ana L., and Maria I. L. Soares. "1,3-Dipolar Cycloadditions Involving Allenes: Synthesis of Five-Membered Rings." Current Organic Chemistry 23, no. 27 (January 15, 2020): 3064–134. http://dx.doi.org/10.2174/1385272823666191203122959.
Повний текст джерелаGrillo, Alessandro, and Bruno Mattia Bizzarri. "Catalytic Enantioselective Diels Alder Reaction: Application in the Synthesis of Antiviral Agents." Catalysts 12, no. 2 (January 25, 2022): 150. http://dx.doi.org/10.3390/catal12020150.
Повний текст джерелаBognár, Balázs, Györgyi Úr, Cecília Sár, Olga H. Hankovszky, Kálmán Hideg, and Tamás Kálai. "Synthesis and Application of Stable Nitroxide Free Radicals Fused with Carbocycles and Heterocycles." Current Organic Chemistry 23, no. 4 (May 22, 2019): 480–501. http://dx.doi.org/10.2174/1385272823666190318163321.
Повний текст джерелаTrost, Barry M., Zhongxing Huang, and Ganesh M. Murhade. "Catalytic palladium-oxyallyl cycloaddition." Science 362, no. 6414 (November 1, 2018): 564–68. http://dx.doi.org/10.1126/science.aau4821.
Повний текст джерелаCha, J. K., and J. Oh. "[4 + 3] Cycloaddition Reactions of Cyclic Oxyallyls in Natural Product Synthesis." Current Organic Chemistry 2, no. 3 (May 1998): 217–32. http://dx.doi.org/10.2174/1385272802666220128192145.
Повний текст джерелаChen, Feng-Zheng, Qing-Xiang Xiang, Yuan-Qin Zhang та Jun-Ru Xiong. "(1β,2α,3α,7α,11α,13β)-1,3,7,11-Tetraacetoxy-2,13-bis(benzyloxy)-21-methyl-19,21-secohetisan-19-al hemihydrate". Acta Crystallographica Section E Structure Reports Online 65, № 6 (29 травня 2009): o1432. http://dx.doi.org/10.1107/s1600536809018315.
Повний текст джерелаBoyd, Derek R., Narain D. Sharma, Ludmila V. Modyanova, Jonathan G. Carroll, John F. Malone, Christopher CR Allen, John TG Hamilton, David T. Gibson, Rebecca E. Parales, and Howard Dalton. "Dioxygenase-catalyzed cis-dihydroxylation of pyridine-ring systems." Canadian Journal of Chemistry 80, no. 6 (June 1, 2002): 589–600. http://dx.doi.org/10.1139/v02-062.
Повний текст джерелаTaticchi, Aldo, Lucio Minuti, Daniela Lanari, Assunta Marrocchi, Ilaria Tesei, and Eszter Gacs-Baitz. "Synthesis of helical [2.2]paracyclophanes containing carbocyclic and heterocyclic five-membered rings." Tetrahedron 60, no. 51 (December 2004): 11759–64. http://dx.doi.org/10.1016/j.tet.2004.09.114.
Повний текст джерелаLiu, Yuxiao, Yu Liu, Charles S. Shanahan, Xichen Xu, and Michael P. Doyle. "A survey of enoldiazo nucleophilicity in selective C–C bond forming reactions for the synthesis of natural product-like frameworks." Org. Biomol. Chem. 12, no. 28 (2014): 5227–34. http://dx.doi.org/10.1039/c4ob00709c.
Повний текст джерелаYadav, Deepak, and Rajeev S. Menon. "Recent developments in the chemistry of allenyl sulfones." Organic & Biomolecular Chemistry 18, no. 3 (2020): 365–78. http://dx.doi.org/10.1039/c9ob01912j.
Повний текст джерелаHirst, Gavin C., Paul N. Howard, and Larry E. Overman. "Stereocontrolled construction of carbocyclic rings by sequential cationic cyclization-pinacol rearrangements." Journal of the American Chemical Society 111, no. 4 (February 1989): 1514–15. http://dx.doi.org/10.1021/ja00186a065.
Повний текст джерелаBiswas, Swapan Kumar. "Recent development of Silver-catalyzed Oxo- and Aza cyclization." International Journal of Experimental Research and Review 26 (December 30, 2021): 90–98. http://dx.doi.org/10.52756/ijerr.2021.v26.007.
Повний текст джерелаXuan, Jun, Liang-Qiu Lu, Jia-Rong Chen, and Wen-Jing Xiao. "Visible-Light-Driven Photoredox Catalysis in the Construction of Carbocyclic and Heterocyclic Ring Systems." European Journal of Organic Chemistry 2013, no. 30 (July 9, 2013): 6755–70. http://dx.doi.org/10.1002/ejoc.201300596.
Повний текст джерелаde Andrade, Vitor, and Marcio de Mattos. "N-Halo Reagents: Modern Synthetic Approaches for Heterocyclic Synthesis." Synthesis 51, no. 09 (March 27, 2019): 1841–70. http://dx.doi.org/10.1055/s-0037-1611746.
Повний текст джерелаMichaut, Antoine, and Jean Rodriguez. "Selective Construction of Carbocyclic Eight-Membered Rings by Ring-Closing Metathesis of Acyclic Precursors." Angewandte Chemie International Edition 45, no. 35 (September 4, 2006): 5740–50. http://dx.doi.org/10.1002/anie.200600787.
Повний текст джерелаAshfeld, Brandon L., and Zachary D. Tucker. "(4+1)-Cycloadditions Exploiting the Biphilicity of Oxyphosphonium Enolates and RhII/PdII-Stabilized Metallocarbenes for the Construction of Five-Membered Frameworks." Synlett 32, no. 12 (January 26, 2021): 1157–68. http://dx.doi.org/10.1055/s-0040-1706009.
Повний текст джерелаLoska, Rafał, and Mieczysław Mąkosza. "Introduction of Carbon Substituents into Nitroarenes via Nucleophilic Substitution of Hydrogen: New Developments." Synthesis 52, no. 21 (June 18, 2020): 3095–110. http://dx.doi.org/10.1055/s-0040-1707149.
Повний текст джерелаXuan, Jun, Liang-Qiu Lu, Jia-Rong Chen, and Wen-Jing Xiao. "ChemInform Abstract: Visible-Light-Driven Photoredox Catalysis in the Construction of Carbocyclic and Heterocyclic Ring Systems." ChemInform 45, no. 1 (December 12, 2013): no. http://dx.doi.org/10.1002/chin.201401252.
Повний текст джерелаMaji, Pradip Kumar. "Synthesis of Pyrimidine-Annulated Five-Membered Heterocycles: An Overview." Current Organic Chemistry 23, no. 20 (December 24, 2019): 2204–69. http://dx.doi.org/10.2174/1385272823666191019111627.
Повний текст джерелаSoares, Maria I. L., Ana L. Cardoso, and Teresa M. V. D. Pinho e Melo. "Diels–Alder Cycloaddition Reactions in Sustainable Media." Molecules 27, no. 4 (February 15, 2022): 1304. http://dx.doi.org/10.3390/molecules27041304.
Повний текст джерелаOjima, Iwao. "New cyclization reactions in organic syntheses." Pure and Applied Chemistry 74, no. 1 (January 1, 2002): 159–66. http://dx.doi.org/10.1351/pac200274010159.
Повний текст джерелаJandl, Christian, and Alexander Pöthig. "Dimerization of a mixed-carbene PdII dibromide complex by elemental iodine." Acta Crystallographica Section C Structural Chemistry 73, no. 12 (November 24, 2017): 1131–36. http://dx.doi.org/10.1107/s2053229617016412.
Повний текст джерелаPellissier, Hélène. "The Use of Domino Reactions for the Synthesis of Chiral Rings." Synthesis 52, no. 24 (July 22, 2020): 3837–54. http://dx.doi.org/10.1055/s-0040-1707905.
Повний текст джерелаKitamura, Masato, Kengo Miyata, Tomoaki Seki, Namdev Vatmurge, and Shinji Tanaka. "CpRu-catalyzed asymmetric dehydrative allylation." Pure and Applied Chemistry 85, no. 6 (April 15, 2013): 1121–32. http://dx.doi.org/10.1351/pac-con-12-10-02.
Повний текст джерелаZard, Samir Z. "The xanthate route to six-membered carbocycles." Journal of Chemical Research 46, no. 2 (March 2022): 174751982210881. http://dx.doi.org/10.1177/17475198221088194.
Повний текст джерелаLin, Wei-Yu, Karthick Govindan, Tamilselvan Duraisamy, Alageswaran Jayaram, and Gopal Chandru Senadi. "Copper-Catalyzed Oxidative Cyclization of 2-Aminobenzamide Derivatives: Efficient Syntheses of Quinazolinones and Indazolones." Synthesis 54, no. 04 (October 12, 2021): 1115–24. http://dx.doi.org/10.1055/a-1667-3977.
Повний текст джерелаHua, Ruimao. "Isoquinolone Syntheses by Annulation Protocols." Catalysts 11, no. 5 (May 11, 2021): 620. http://dx.doi.org/10.3390/catal11050620.
Повний текст джерелаSbei, Najoua, Anna V. Listratova, Alexander A. Titov, and Leonid G. Voskressensky. "Recent Advances in Electrochemistry for the Synthesis of N-Heterocycles." Synthesis 51, no. 12 (May 7, 2019): 2455–73. http://dx.doi.org/10.1055/s-0037-1611797.
Повний текст джерелаIto, Hideto, Tomoya Harada, Hirohisa Ohmiya, and Masaya Sawamura. "Intramolecular hydroamination of alkynic sulfonamides catalyzed by a gold–triethynylphosphine complex: Construction of azepine frameworks by 7-exo-dig cyclization." Beilstein Journal of Organic Chemistry 7 (July 8, 2011): 951–59. http://dx.doi.org/10.3762/bjoc.7.106.
Повний текст джерелаKawada, Hatsuo, Mitsuhiro Iwamoto, Masayuki Utsugi, Masayuki Miyano, and Masahisa Nakada. "Synthetic Studies on the Taxane Skeleton: Construction of Eight-Membered Carbocyclic Rings by the IntramolecularB-Alkyl Suzuki−Miyaura Cross-Coupling Reaction." Organic Letters 6, no. 24 (November 2004): 4491–94. http://dx.doi.org/10.1021/ol0481939.
Повний текст джерелаLi, Yang, Yan-peng Li, Jun He, Ding Liu, Qi-zhi Zhang, Kang Li, Xing Zheng, Guo-Tao Tang, Yu Guo, and Yunmei Liu. "The Relationship between Pharmacological Properties and Structure- Activity of Chrysin Derivatives." Mini-Reviews in Medicinal Chemistry 19, no. 7 (March 28, 2019): 555–68. http://dx.doi.org/10.2174/1389557518666180424094821.
Повний текст джерелаFaheem, Mohd, Anjani K. Tiwari, and Vinay K. Singh. "A Review on Modern Synthetic Route for the Construction of 1, 3-Diazanaphthalene Moiety." Current Organic Chemistry 24, no. 10 (August 11, 2020): 1108–38. http://dx.doi.org/10.2174/1385272824999200528124440.
Повний текст джерелаLelyukh, M. I. "Biological activity of heterocyclic systems based on functionally substituted 1,3,4-thia(oxa)diazoles (a review)." Farmatsevtychnyi zhurnal, no. 6 (December 21, 2019): 43–53. http://dx.doi.org/10.32352/10.32352/0367-3057.6.19.05.
Повний текст джерелаDuc, Dau Xuan. "Recent Progress in the Synthesis of Benzo[b]thiophene." Current Organic Chemistry 24, no. 19 (December 1, 2020): 2256–71. http://dx.doi.org/10.2174/1385272824999200820151545.
Повний текст джерелаDai, Xiaoyu, Yuanen Ma, Linzhou Zhang, Zhiming Xu, Xuewen Sun, and Suoqi Zhao. "Optimization of Molecular Composition Distribution of Slurry Oil by Supercritical Fluid Extraction to Improve the Structure and Performance of Mesophase Pitch." Energies 15, no. 19 (September 25, 2022): 7041. http://dx.doi.org/10.3390/en15197041.
Повний текст джерелаDuc, Dau Xuan. "Recent Achievement in the Synthesis of Benzo[b]furans." Current Organic Synthesis 17, no. 7 (October 28, 2020): 498–517. http://dx.doi.org/10.2174/1570179417666200625212639.
Повний текст джерелаSedenkova, Kseniya N., Olga V. Ryzhikova, Svetlana A. Stepanova, Alexei D. Averin, Sergei V. Kositov, Yuri K. Grishin, Igor P. Gloriozov, and Elena B. Averina. "Bis(oxiranes) Containing Cyclooctane Core: Synthesis and Reactivity towards NaN3." Molecules 27, no. 20 (October 14, 2022): 6889. http://dx.doi.org/10.3390/molecules27206889.
Повний текст джерелаBarange, Deepak Kumar, Venkateswara Rao Batchu, Dhillirao Gorja, Vijaya Raghavan Pattabiraman, Lakshmi Kumar Tatini, J. Moses Babu, and Manojit Pal. "Regioselective construction of six-membered fused heterocyclic rings via Pd/C-mediated C–C coupling followed by iodocyclization strategy: a new entry to 2H-1,2-benzothiazine-1,1-dioxides." Tetrahedron 63, no. 8 (February 2007): 1775–89. http://dx.doi.org/10.1016/j.tet.2006.12.040.
Повний текст джерелаBlanco, Maria C., Alirio Palma, Justo Cobo, and Christopher Glidewell. "Nine closely related tetrahydro-1,4-epoxy-1-benzazepines carrying pendant heterocyclic substituents: hydrogen-bonded supramolecular assembly in zero, one and two dimensions." Acta Crystallographica Section C Crystal Structure Communications 68, no. 3 (February 24, 2012): o131—o140. http://dx.doi.org/10.1107/s010827011200707x.
Повний текст джерелаHuang, Qiu-Ying, Yang Zhao, and Xiang-Ru Meng. "Syntheses, structures and characterization of isomorphous CoII and NiII coordination polymers based on 2-[(1H-imidazol-1-yl)methyl]-6-methyl-1H-benzimidazole and benzene-1,4-dicarboxylate." Acta Crystallographica Section C Structural Chemistry 73, no. 8 (July 31, 2017): 645–51. http://dx.doi.org/10.1107/s2053229617010877.
Повний текст джерелаAbomelha, Hanna. "Synthesis of novel dyes based on thiophene analogues with antibacterial activity for dyeing polyester fabrics." Pigment & Resin Technology 48, no. 4 (July 1, 2019): 337–47. http://dx.doi.org/10.1108/prt-02-2018-0012.
Повний текст джерелаZhang, Cai, Demao Chen, Jie-Ping Wan, and Yunyun Liu. "Recent Advances in Electrochemical Cascade Cyclization Reactions." Synthesis, February 20, 2023. http://dx.doi.org/10.1055/a-2039-1728.
Повний текст джерелаHuo, Hengrui, and Yuefa Gong. "Construction of heterocyclic rings from cyclopropenes." Organic & Biomolecular Chemistry, 2022. http://dx.doi.org/10.1039/d1ob02450g.
Повний текст джерелаAjavakom, Vachiraporn, Potchanee Pandokrak, Sofia S. Salim, Gamal A. I. Moustafa, Richard K. Bellingham, Joseph T. Hill-Cousins, Anawat Ajavakom, and Richard Brown. "Formation of seven-membered rings by RCM of vinyl bromides." Synlett, May 6, 2022. http://dx.doi.org/10.1055/a-1845-4195.
Повний текст джерелаHIRST, G. C., P. N. HOWARD, and L. E. OVERMAN. "ChemInform Abstract: Stereocontrolled Construction of Carbocyclic Rings by Sequential Cationic Cyclization-Pinacol Rearrangements." ChemInform 20, no. 23 (June 6, 1989). http://dx.doi.org/10.1002/chin.198923107.
Повний текст джерелаZhang, Xuntong, Chenpeng Gao, and James P. Morken. "Enantioselective Construction of Carbocyclic and Heterocyclic Tertiary Boronic Esters by Conjunctive Cross-Coupling Reaction." Journal of the American Chemical Society, July 24, 2023. http://dx.doi.org/10.1021/jacs.3c05815.
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 джерелаCastagnolo, Daniele, Fei Zhao, Domiziana Masci, and Elena Tomarelli. "Biocatalytic and Chemo-Enzymatic Approaches for the Synthesis of Heterocycles." Synthesis, July 28, 2020. http://dx.doi.org/10.1055/s-0040-1707210.
Повний текст джерелаHou, Meifeng, Jiajun Li, Fucai Rao, Zuliang Chen, and Yingjing Wei. "Diastereoselective Synthesis of Tetrahydrobenzo[b]azocines by Lu(OTf)3 Catalyzed [4 + 4] Cycloaddition of Donor–Acceptor Cyclobutanes with Anthranils." Chemical Communications, 2022. http://dx.doi.org/10.1039/d2cc00829g.
Повний текст джерелаFlores, Daniel M., Michael L. Neville, and Valerie A. Schmidt. "Intermolecular 2+2 imine-olefin photocycloadditions enabled by Cu(I)-alkene MLCT." Nature Communications 13, no. 1 (May 19, 2022). http://dx.doi.org/10.1038/s41467-022-30393-6.
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