Journal articles on the topic 'Cycloaddition Huisgen'
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Watt, Jacinta A., Carlie T. Gannon, Karen J. Loft, Zoran Dinev, and Spencer J. Williams. "'Click' Preparation of Carbohydrate 1-Benzotriazoles, 1,4-Disubstituted, and 1,4,5-Trisubstituted Triazoles and their Utility as Glycosyl Donors." Australian Journal of Chemistry 61, no. 11 (2008): 837. http://dx.doi.org/10.1071/ch08364.
Full textDanese, Martina, Marta Bon, GiovanniMaria Piccini, and Daniele Passerone. "The reaction mechanism of the azide–alkyne Huisgen cycloaddition." Physical Chemistry Chemical Physics 21, no. 35 (2019): 19281–87. http://dx.doi.org/10.1039/c9cp02386k.
Full textDemarteau, Jérémy, Julien De Winter, Christophe Detrembleur, and Antoine Debuigne. "Ethylene/vinyl acetate-based macrocycles via organometallic-mediated radical polymerization and CuAAC ‘click’ reaction." Polymer Chemistry 9, no. 3 (2018): 273–78. http://dx.doi.org/10.1039/c7py01891f.
Full textJoshi, S. M., V. Gómez-Vallejo, V. Salinas, and J. Llop. "Synthesis of 13N-labelled polysubstituted triazoles via Huisgen cycloaddition." RSC Advances 6, no. 111 (2016): 109633–38. http://dx.doi.org/10.1039/c6ra24670b.
Full textPatil, Jayavant D., Supriya A. Patil, and Dattaprasad M. Pore. "A polymer supported ascorbate functionalized task specific ionic liquid: an efficient reusable catalyst for 1,3-dipolar cycloaddition." RSC Advances 5, no. 27 (2015): 21396–404. http://dx.doi.org/10.1039/c4ra16481d.
Full textChen, Yun, Wei-Qiang Zhang, Bin-Xun Yu, et al. "A robust and recyclable polyurea-encapsulated copper(i) chloride for one-pot ring-opening/Huisgen cycloaddition/CO2 capture in water." Green Chemistry 18, no. 23 (2016): 6357–66. http://dx.doi.org/10.1039/c6gc01956k.
Full textSingh, Dileep Kumar, та Mahendra Nath. "Synthesis and photophysical properties of β-triazole bridged porphyrin–coumarin dyads". RSC Advances 5, № 83 (2015): 68209–17. http://dx.doi.org/10.1039/c5ra13955d.
Full textAmini, Mojtaba, Hadi Naslhajian, S. Morteza F. Farnia, Hee Kyoung Kang, Sanjeev Gautam, and Keun Hwa Chae. "Polyoxomolybdate-stabilized Cu2O nanoparticles as an efficient catalyst for the azide–alkyne cycloaddition." New Journal of Chemistry 40, no. 6 (2016): 5313–17. http://dx.doi.org/10.1039/c6nj00868b.
Full textCollot, Mayeul, Christian Wilms, and Jean-Maurice Mallet. "Functionalizable red emitting calcium sensor bearing a 1,4-triazole chelating moiety." RSC Advances 5, no. 9 (2015): 6993–7000. http://dx.doi.org/10.1039/c4ra12858c.
Full textMa, Mingyang, and Younghwan Kwon. "Reactive cycloalkane plasticizers covalently linked to energetic polyurethane binders via facile control of an in situ Cu-free azide–alkyne 1,3-dipolar cycloaddition reaction." Polymer Chemistry 9, no. 45 (2018): 5452–61. http://dx.doi.org/10.1039/c8py00969d.
Full textWei, Gaofei, Weijing Luan, Shuai Wang, et al. "A library of 1,2,3-triazole-substituted oleanolic acid derivatives as anticancer agents: design, synthesis, and biological evaluation." Organic & Biomolecular Chemistry 13, no. 5 (2015): 1507–14. http://dx.doi.org/10.1039/c4ob01605j.
Full textMitrofanov, Alexander, Stéphane Brandès, Frédéric Herbst, Séverinne Rigolet, Alla Bessmertnykh-Lemeune, and Irina Beletskaya. "Immobilization of copper complexes with (1,10-phenanthrolinyl)phosphonates on titania supports for sustainable catalysis." Journal of Materials Chemistry A 5, no. 24 (2017): 12216–35. http://dx.doi.org/10.1039/c7ta01195d.
Full textWang, Tengjiao, André J. van der Vlies, Hiroshi Uyama, and Urara Hasegawa. "Nitric oxide-releasing polymeric furoxan conjugates." Polymer Chemistry 6, no. 44 (2015): 7737–48. http://dx.doi.org/10.1039/c5py01335f.
Full textBarlow, T. M. A., M. Jida, K. Guillemyn, D. Tourwé, V. Caveliers, and S. Ballet. "Efficient one-pot synthesis of amino-benzotriazolodiazocinone scaffolds via catalyst-free tandem Ugi–Huisgen reactions." Organic & Biomolecular Chemistry 14, no. 20 (2016): 4669–77. http://dx.doi.org/10.1039/c6ob00438e.
Full textBlanco-Carapia, Roberto E., Julio C. Flores-Reyes, Yizrell Medina-Martínez, et al. "Synthesis of New bis 1- and 5-Substituted 1H-Tetrazoles via Huisgen-Type 1,3-Dipolar Cycloadditions." Proceedings 9, no. 1 (2019): 32. http://dx.doi.org/10.3390/ecsoc-22-05780.
Full textChandrasekaran, S., V. Sudhir, and R. Baig. "Huisgen [2+3]-Cycloaddition Route to Triazolopyrazinones." Synfacts 2008, no. 7 (2008): 0687. http://dx.doi.org/10.1055/s-2008-1078476.
Full textKawamichi, Takehide, Yasuhide Inokuma, Masaki Kawano, and Makoto Fujita. "Regioselecitive Huisgen Cycloaddition within Porous Coordination Networks." Angewandte Chemie 122, no. 13 (2010): 2425–27. http://dx.doi.org/10.1002/ange.201000018.
Full textKawamichi, Takehide, Yasuhide Inokuma, Masaki Kawano, and Makoto Fujita. "Regioselecitive Huisgen Cycloaddition within Porous Coordination Networks." Angewandte Chemie International Edition 49, no. 13 (2010): 2375–77. http://dx.doi.org/10.1002/anie.201000018.
Full textPedersen, Daniel Sejer, and Andrew David Abell. "ChemInform Abstract: Huisgen Cycloaddition in Peptidomimetic Chemistry." ChemInform 43, no. 22 (2012): no. http://dx.doi.org/10.1002/chin.201222213.
Full textJochyms, Quentin, Pierre Guillot, Emmanuel Mignard, and Jean-Marc Vincent. "A fluorosurfactant and photoreducible CuII-tren click catalyst: surfactant and catalytic properties at liquid/liquid interfaces." Dalton Transactions 44, no. 45 (2015): 19700–19707. http://dx.doi.org/10.1039/c5dt02039e.
Full textBentounsi, Yousra, Konstantinos Seintis, Dorine Ameline, et al. "Chemistry on the electrodes: post-functionalization and stability enhancement of anchored dyes on mesoporous metal oxide photoelectrochemical cells with copper-free Huisgen cycloaddition reaction." Journal of Materials Chemistry A 8, no. 25 (2020): 12633–40. http://dx.doi.org/10.1039/d0ta04982d.
Full textAlexandrino, Evandro M., Philipp Buchold, Manfred Wagner, et al. "A molecular “screw-clamp”: accelerating click reactions in miniemulsions." Chem. Commun. 50, no. 72 (2014): 10495–98. http://dx.doi.org/10.1039/c4cc04119d.
Full textLiu, Ze Xi, Bin Bin Chen, Meng Li Liu, Hong Yan Zou, and Cheng Zhi Huang. "Cu(i)-Doped carbon quantum dots with zigzag edge structures for highly efficient catalysis of azide–alkyne cycloadditions." Green Chemistry 19, no. 6 (2017): 1494–98. http://dx.doi.org/10.1039/c6gc03288e.
Full textBarlow, T. M. A., M. Jida, D. Tourwé, and S. Ballet. "Efficient synthesis of conformationally constrained, amino-triazoloazepinone-containing di- and tripeptides via a one-pot Ugi–Huisgen tandem reaction." Org. Biomol. Chem. 12, no. 36 (2014): 6986–89. http://dx.doi.org/10.1039/c4ob01381f.
Full textGhodsinia, Sara S. E., Batool Akhlaghinia, and Roya Jahanshahi. "Direct access to stabilized CuI using cuttlebone as a natural-reducing support for efficient CuAAC click reactions in water." RSC Advances 6, no. 68 (2016): 63613–23. http://dx.doi.org/10.1039/c6ra13314b.
Full textJayaramulu, Kolleboyina, Venkata M. Suresh, and Tapas Kumar Maji. "Stabilization of Cu2O nanoparticles on a 2D metal–organic framework for catalytic Huisgen 1,3-dipolar cycloaddition reaction." Dalton Transactions 44, no. 1 (2015): 83–86. http://dx.doi.org/10.1039/c4dt02661f.
Full textGöbel, Dominik, Marius Friedrich, Enno Lork, and Boris J. Nachtsheim. "Clickable azide-functionalized bromoarylaldehydes – synthesis and photophysical characterization." Beilstein Journal of Organic Chemistry 16 (July 14, 2020): 1683–92. http://dx.doi.org/10.3762/bjoc.16.139.
Full textMontagnat, Oliver D., Guillaume Lessene та Andrew B. Hughes. "Synthesis of Azide-alkyne Fragments for 'Click' Chemical Applications. Formation of Chiral 1,4-Disubstituted-(β-alkyl)-γ-1,2,3-triazole Scaffolds from Orthogonally Protected Chiral β-Alkyl-trialkylsilyl-γ-pentynyl Azides and Chiral β-Alkyl-γ-pentynyl-alcohols". Australian Journal of Chemistry 63, № 11 (2010): 1541. http://dx.doi.org/10.1071/ch10306.
Full textColliat-Dangus, Guillaume, Mona M. Obadia, Yakov S. Vygodskii, Anatoli Serghei, Alexander S. Shaplov, and Eric Drockenmuller. "Unconventional poly(ionic liquid)s combining motionless main chain 1,2,3-triazolium cations and high ionic conductivity." Polymer Chemistry 6, no. 23 (2015): 4299–308. http://dx.doi.org/10.1039/c5py00526d.
Full textMosbach, K., L. Ye, H. Zhang, T. Piacham, M. Drew, and M. Patek. "MIP for Regioselective Huisgen 1,3-Dipolar Cycloaddition Reaction." Synfacts 2006, no. 7 (2006): 0742. http://dx.doi.org/10.1055/s-2006-941904.
Full textPehere, Ashok D., та Andrew D. Abell. "New β-Strand Templates Constrained by Huisgen Cycloaddition". Organic Letters 14, № 5 (2012): 1330–33. http://dx.doi.org/10.1021/ol3002199.
Full textBreugst, Martin, and Hans‐Ulrich Reißig. "Die Huisgen‐Reaktion: Meilensteine der 1,3‐dipolaren Cycloaddition." Angewandte Chemie 132, no. 30 (2020): 12389–404. http://dx.doi.org/10.1002/ange.202003115.
Full textHladíková, Veronika, Jiří Váňa, and Jiří Hanusek. "[3 + 2]-Cycloaddition reaction of sydnones with alkynes." Beilstein Journal of Organic Chemistry 14 (June 5, 2018): 1317–48. http://dx.doi.org/10.3762/bjoc.14.113.
Full textSiadati, Seyyed Amir. "Beyond the Alternatives that Switch the Mechanism of the 1,3-Dipolar CyCloadditions from Concerted to Stepwise or Vice Versa: A Literature Review." Progress in Reaction Kinetics and Mechanism 41, no. 4 (2016): 331–44. http://dx.doi.org/10.3184/146867816x14719552202168.
Full textSarkate, Aniket P., Kshipra S. Karnik, Pravin S. Wakte, Ajinkya P. Sarkate, Ashwini V. Izankar, and Devanand B. Shinde. "Copper-catalyzed Convenient Synthesis and SAR Studies of Substituted-1,2,3-triazole as Antimicrobial Agents." Letters in Drug Design & Discovery 16, no. 1 (2018): 3–10. http://dx.doi.org/10.2174/1570180815666180326153322.
Full textMamgain, Ritu. "Cu(I) Catalyzed Coumarin-1,2,3-Triazole Hybrids: Click Chemistry." Asian Journal of Chemistry 31, no. 11 (2019): 2543–47. http://dx.doi.org/10.14233/ajchem.2019.22183.
Full textCormier, Morgan, Eric Fouquet, and Philippe Hermange. "Expedient synthesis of a symmetric cycloheptyne-Co2(CO)6 complex for orthogonal Huisgen cycloadditions." Organic Chemistry Frontiers 6, no. 8 (2019): 1114–17. http://dx.doi.org/10.1039/c9qo00086k.
Full textWoo, Hyunje, Hyuntae Kang, Aram Kim, et al. "Azide-Alkyne Huisgen [3+2] Cycloaddition Using CuO Nanoparticles." Molecules 17, no. 11 (2012): 13235–52. http://dx.doi.org/10.3390/molecules171113235.
Full textYousuf, Syed Khalid, Debaraj Mukherjee, Baldev Singh, Sudip Maity, and Subhash Chandra Taneja. "Cu–Mn bimetallic catalyst for Huisgen [3+2]-cycloaddition." Green Chemistry 12, no. 9 (2010): 1568. http://dx.doi.org/10.1039/c005088a.
Full textBreugst, Martin, and Hans‐Ulrich Reissig. "The Huisgen Reaction: Milestones of the 1,3‐Dipolar Cycloaddition." Angewandte Chemie International Edition 59, no. 30 (2020): 12293–307. http://dx.doi.org/10.1002/anie.202003115.
Full textFu, H., F. Wang, Y. Jiang, and Y. Zhao. "Cu-Catalyzed Huisgen Cycloaddition of Sulfonyl Azides ‘on Water∏." Synfacts 2008, no. 11 (2008): 1151. http://dx.doi.org/10.1055/s-0028-1083484.
Full textWu, Yong-Ming, Juan Deng, Xiang Fang, and Qing-Yun Chen. "Regioselective synthesis of fluoroalkylated [1,2,3]-triazoles by Huisgen cycloaddition." Journal of Fluorine Chemistry 125, no. 10 (2004): 1415–23. http://dx.doi.org/10.1016/j.jfluchem.2004.02.016.
Full textZuraev, A. V., A. V. Lishai, Yu V. Grigoriev, and O. A. Ivashkevich. "SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF SOME 1,4- AND 1,4,5-SUBSTITUTED-1H-1,2,3TRIAZOLES IN RELATION TO THE STAPHYLOCOCCUS AUREUS STRAIN." Doklady of the National Academy of Sciences of Belarus 62, no. 3 (2018): 293–97. http://dx.doi.org/10.29235/1561-8323-2018-62-3-293-297.
Full textLabrunie, Antoine, Teddy Lebailly, Amir Hossein Habibi, et al. "CuAAC-Based Assembly and Characterization of a New Molecular Dyad for Single Material Organic Solar Cell." Metals 9, no. 6 (2019): 618. http://dx.doi.org/10.3390/met9060618.
Full textSemioshkin, Andrey A., Sergey N. Osipov, Julia N. Grebenyuk, et al. "An Effective Approach to 1,2,3-Triazole-Containing 12-Vertex closo-Dodecaborates." Collection of Czechoslovak Chemical Communications 72, no. 12 (2007): 1717–24. http://dx.doi.org/10.1135/cccc20071717.
Full textHarmrolfs, Kirsten, Lena Mancuso, Binia Drung, Florenz Sasse, and Andreas Kirschning. "Preparation of new alkyne-modified ansamitocins by mutasynthesis." Beilstein Journal of Organic Chemistry 10 (March 3, 2014): 535–43. http://dx.doi.org/10.3762/bjoc.10.49.
Full textArigela, Rajesh K., Sudhir K. Sharma, Brijesh Kumar, and Bijoy Kundu. "Microwave-assisted three-component domino reaction: Synthesis of indolodiazepinotriazoles." Beilstein Journal of Organic Chemistry 9 (February 19, 2013): 401–5. http://dx.doi.org/10.3762/bjoc.9.41.
Full textIehl, Julien, Michel Holler, Jean-François Nierengarten та ін. "Photo-induced Energy Transfer in a Th-Symmetrical Hexakis-adduct of C60 Substituted with π-Conjugated Oligomers". Australian Journal of Chemistry 64, № 2 (2011): 153. http://dx.doi.org/10.1071/ch10319.
Full textOh, Chang, Kiseong Kim, and Soyung Kim. "Cyclopropane Intermediates from Insertion Reactions of Platinum–Carbenes: A Route to Heterospiranes." Synlett 29, no. 03 (2017): 354–58. http://dx.doi.org/10.1055/s-0036-1591489.
Full textCintas, Pedro, Katia Martina, Bruna Robaldo, Davide Garella, Luisa Boffa, and Giancarlo Cravotto. "Improved Protocols for Microwave-Assisted Cu(I)-Catalyzed Huisgen 1,3-Dipolar Cycloadditions." Collection of Czechoslovak Chemical Communications 72, no. 8 (2007): 1014–24. http://dx.doi.org/10.1135/cccc20071014.
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