Artykuły w czasopismach na temat „1,3-dipolar cycloaddition reaction”
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WANG, JING-FANG, DONG-QING WEI, CHUN-FANG WANG, YONG YE, YI-XUE LI, YONG LUO, WEN-WU WANG, LUN-ZU LIU i YU-FEN ZHAO. "A THEORETICAL STUDY ON THE MECHANISM OF 2:1 1, 3 DIPOLAR CYCLOADDITION REACTIONS". Journal of Theoretical and Computational Chemistry 06, nr 04 (grudzień 2007): 861–67. http://dx.doi.org/10.1142/s0219633607003489.
Pełny tekst źródłaGrygorenko, Oleksandr O., Viktoriia S. Moskvina, Oleksandr V. Hryshchuk i Andriy V. Tymtsunik. "Cycloadditions of Alkenylboronic Derivatives". Synthesis 52, nr 19 (24.06.2020): 2761–80. http://dx.doi.org/10.1055/s-0040-1707159.
Pełny tekst źródłaSalem, Mohammed A., Moustafa A. Gouda i Ghada G. El-Bana. "Chemistry of 2-(Piperazin-1-yl) Quinoline-3-Carbaldehydes". Mini-Reviews in Organic Chemistry 19, nr 4 (czerwiec 2022): 480–95. http://dx.doi.org/10.2174/1570193x18666211001124510.
Pełny tekst źródłaCaraculacu, Adrian A., Elena Scorţanu i Georgeta Caraculacu. "New Parabanate Products by 1, 3-Dipolar Cycloaddition Reaction (‘Criss-Cross’ Cycloaddition)". High Performance Polymers 11, nr 4 (grudzień 1999): 477–82. http://dx.doi.org/10.1088/0954-0083/11/4/311.
Pełny tekst źródłaOgurtsov, Vladimir A., i Oleg A. Rakitin. "New Cycloadditon Reaction of 2-Chloroprop-2-enethioamides with Dialkyl Acetylenedicarboxylates: Synthesis of Dialkyl 2-[4,5-Bis(alkoxycarbonyl)-2-(aryl{alkyl}imino)-3(2H)-thienylidene]-1,3-dithiole-4,5-dicarboxylates". Molecules 27, nr 20 (14.10.2022): 6887. http://dx.doi.org/10.3390/molecules27206887.
Pełny tekst źródłaWinne, Johan, Jan Hullaert, Bram Denoo, Mien Christiaens i Brenda Callebaut. "Heterocycles as Moderators of Allyl Cation Cycloaddition Reactivity". Synlett 28, nr 18 (27.07.2017): 2345–52. http://dx.doi.org/10.1055/s-0036-1588511.
Pełny tekst źródłaMohtat, Bita, Seyyed Amir Siadati i Mohammad A. Khalilzadeh. "Understanding the mechanism of the 1,3-dipolar cycloaddition reaction between a thioformaldehyde S-oxide and cyclobutadiene: Competition between the stepwise and concerted routes". Progress in Reaction Kinetics and Mechanism 44, nr 3 (12.05.2019): 213–21. http://dx.doi.org/10.1177/1468678319845863.
Pełny tekst źródłaEl-Sayed, Wael A., i Adel A. H. Abdel-Rahman. "Copper-catalyzed Synthesis and Antimicrobial Activity of Disubstituted 1,2,3-Triazoles Starting from 1-Propargyluracils and Ethyl (4-Azido- 1,2,3-trihydroxybutyl)furan-3-carboxylate". Zeitschrift für Naturforschung B 65, nr 1 (1.01.2010): 57–66. http://dx.doi.org/10.1515/znb-2010-0110.
Pełny tekst źródłaHunnur, Raveendra K., Prashant R. Latthe i Bharati V. Badami. "1,3-Dipolar Cycloaddition Reactions in Heterocyclic Synthesis. Synthesis of [1-[4-(thiazolyl/imidazothiazolyl/triazolyl)phenyl]-1H-pyrazole-3,4-dicarboxylate esters from 3-(4-acetylphenyl)sydnone". Journal of Chemical Research 2005, nr 9 (wrzesień 2005): 592–94. http://dx.doi.org/10.3184/030823405774308907.
Pełny tekst źródłaMawhinney, Robert C., Heidi M. Muchall i Gilles H. Peslherbe. "A computational study of the 1,3-dipolar cycloaddition reaction mechanism for nitrilimines". Canadian Journal of Chemistry 83, nr 9 (1.09.2005): 1615–25. http://dx.doi.org/10.1139/v05-179.
Pełny tekst źródłaDeng, Yongming, Qing-Qing Cheng i Michael Doyle. "Asymmetric [3+3] Cycloaddition for Heterocycle Synthesis". Synlett 28, nr 14 (5.07.2017): 1695–706. http://dx.doi.org/10.1055/s-0036-1588453.
Pełny tekst źródłaSantos, Hugo, Amy Distiller, Asha M. D'Souza, Quentin Arnoux, Jonathan M. White, Adam G. Meyer i John H. Ryan. "1,3-Dipolar cycloaddition reactions of phthalic anhydrides with an azomethine ylide". Organic Chemistry Frontiers 2, nr 6 (2015): 705–12. http://dx.doi.org/10.1039/c5qo00062a.
Pełny tekst źródłaBoudriga, Sarra, Saoussen Haddad, Moheddine Askri, Armand Soldera, Michael Knorr, Carsten Strohmann i Christopher Golz. "Highly diastereoselective construction of novel dispiropyrrolo[2,1-a]isoquinoline derivativesviamulticomponent 1,3-dipolar cycloaddition of cyclic diketones-based tetrahydroisoquinoliniumN-ylides". RSC Advances 9, nr 20 (2019): 11082–91. http://dx.doi.org/10.1039/c8ra09884k.
Pełny tekst źródłaWanapun, D., K. A. Van Gorp, N. J. Mosey, M. A. Kerr i T. K. Woo. "The mechanism of 1,3-dipolar cycloaddition reactions of cyclopropanes and nitrones A theoretical study". Canadian Journal of Chemistry 83, nr 10 (1.10.2005): 1752–67. http://dx.doi.org/10.1139/v05-182.
Pełny tekst źródłaBelguedj, Roumaissa, Sofiane Bouacida, Hocine Merazig, Ali Belfaitah i Abdelmalek Bouraiou. "1-(2′-Benzimidazolylmethyl)-pyridinium ylide in the one-pot synthesis of indolizine and benzimidazo[1,2-a]pyridine derivatives". Zeitschrift für Naturforschung B 70, nr 8 (1.08.2015): 555–61. http://dx.doi.org/10.1515/znb-2015-0016.
Pełny tekst źródłaNewton, Rebecca, i G. Paul Savage. "Regioselective 1,3-Dipolar Cycloaddition Reactions of 4-Methylene-2-oxazolidinones with Benzonitrile Oxide". Australian Journal of Chemistry 61, nr 6 (2008): 432. http://dx.doi.org/10.1071/ch08111.
Pełny tekst źródłaPetrov, A. O., Georgiy V. Malkov, Sergei V. Karpov, A. V. Shastin i A. V. Bakeshko. "Kinetic Study of the Polyaddition of Azide-Alkyne AB2 Monomers in Nonisotermic Conditions". Key Engineering Materials 816 (sierpień 2019): 151–56. http://dx.doi.org/10.4028/www.scientific.net/kem.816.151.
Pełny tekst źródłaJulino, Markus, Philip R. Lowe i Malcolm F. G. Stevens. "Structural Studies on Bioactive Compounds. Part 31. Interaction of 9-azidoacridine and 1-morpholinocyclohexene: Formation, Decomposition and Rearrangement of the Intermediate 1,2,3-triazoline". Journal of Chemical Research 2000, nr 2 (luty 2000): 74–75. http://dx.doi.org/10.3184/030823400103166418.
Pełny tekst źródłaZhu, Shaohua, Yan Zhang, Peipei Li, Wenzhu Bi, Xiaolan Chen i Yufen Zhao. "Synthesis of novel phosphorylated chrysin derivatives by 1, 3-dipolar cycloaddition reaction". Phosphorus, Sulfur, and Silicon and the Related Elements 192, nr 1 (18.10.2016): 1–8. http://dx.doi.org/10.1080/10426507.2016.1223076.
Pełny tekst źródłaKhoroshunova, Yulia V., Denis A. Morozov, Andrey I. Taratayko, Polina D. Gladkikh, Yuri I. Glazachev i Igor A. Kirilyuk. "Synthesis of 1-azaspiro[4.4]nonan-1-oxyls via intramolecular 1,3-dipolar cycloaddition". Beilstein Journal of Organic Chemistry 15 (27.08.2019): 2036–42. http://dx.doi.org/10.3762/bjoc.15.200.
Pełny tekst źródłaLukevics, E., P. Arsenyan, I. Shestakova, O. Zharkova, I. Kanepe, R. Mezapuke i O. Pudova. "Cytotoxic Activity of Silyl- and Germyl-Substituted 4,4-Dioxo-3a,6a-Dihydrothieno[2,3−d]isoxazolines-2". Metal-Based Drugs 7, nr 2 (1.01.2000): 63–66. http://dx.doi.org/10.1155/mbd.2000.63.
Pełny tekst źródłaSvete, Jurij, Uroš Grošelj, Franc Požgan i Bogdan Štefane. "Copper-Catalyzed Azomethine Imine–Alkyne Cycloadditions (CuAIAC)". Synthesis 50, nr 23 (5.10.2018): 4501–24. http://dx.doi.org/10.1055/s-0037-1610284.
Pełny tekst źródłaZhang, Xiaofeng, Kenny Pham, Shuai Liu, Marc Legris, Alex Muthengi, Jerry P. Jasinski i Wei Zhang. "Stereoselective synthesis of fused tetrahydroquinazolines through one-pot double [3 + 2] dipolar cycloadditions followed by [5 + 1] annulation". Beilstein Journal of Organic Chemistry 12 (18.10.2016): 2204–10. http://dx.doi.org/10.3762/bjoc.12.211.
Pełny tekst źródłaKalluraya, Balakrishna, Kaushik B R i H. M. Somashekarappa. "Effect of Gamma- Irradiation on Structure, Morphology and Thermal Properties of Novel Polyamide Based Thermoset Obtained by Double Cycloaddition". Journal of Modern Materials 7, nr 1 (5.07.2020): 17–25. http://dx.doi.org/10.21467/jmm.7.1.17-25.
Pełny tekst źródłaGanushevich, Yulia, Almaz Zagidullin, Svetlana Kondrashova, Shamil Latypov, Vasili Miluykov, Peter Lönnecke i Evamarie Hey-Hawkins. "Asymmetric 1,3-dipolar cycloaddition reaction of chiral 1-alkyl-1,2-diphospholes with diphenyldiazomethane". RSC Advances 10, nr 64 (2020): 39060–66. http://dx.doi.org/10.1039/d0ra08080b.
Pełny tekst źródłaBoitsov, Vitali M., Alexander V. Stepakov, Siqi Wang, Alexander S. Filatov, Stanislav V. Lozovskiy, Stanislav V. Shmakov, Olesya V. Khoroshilova, Anna G. Larina i Stanislav I. Selivanov. "Construction of Spiro[3-azabicyclo[3.1.0]hexanes] via 1,3-Dipolar Cycloaddition of 1,2-Diphenylcyclopropenes to Ninhydrin-Derived Azomethine Ylides". Synthesis 53, nr 12 (18.01.2021): 2114–32. http://dx.doi.org/10.1055/a-1360-9716.
Pełny tekst źródłaMishriky, Nawal, Adel S. Girgis i Yehia A. Ibrahim. "Regioselective Synthesis of Spiro[Naphthalene-2(1H),3′-[3H]Pyrazol]-1-Ones Utilizing 1,3-Dipolar Cycloaddition of Nitrilimines". Journal of Chemical Research 2000, nr 1 (styczeń 2000): 2–3. http://dx.doi.org/10.3184/030823400103165527.
Pełny tekst źródłaDumitrescu, Denisa, Sergiu Shova, Constantin Draghici, Marcel Mirel Popa i Florea Dumitrascu. "Synthesis of 1-(2-Fluorophenyl)pyrazoles by 1,3-Dipolar Cycloaddition of the Corresponding Sydnones". Molecules 26, nr 12 (17.06.2021): 3693. http://dx.doi.org/10.3390/molecules26123693.
Pełny tekst źródłaWang, Yongchao, Yu Chen, Shengli Duan, Yiyang Cao, Wenjin Sun, Mei Zhang, Delin Zhao, Donghua Hu i Jianwei Dong. "Diastereoselective Three-Component 1,3-Dipolar Cycloaddition to Access Functionalized β-Tetrahydrocarboline- and Tetrahydroisoquinoline-Fused Spirooxindoles". Molecules 29, nr 8 (15.04.2024): 1790. http://dx.doi.org/10.3390/molecules29081790.
Pełny tekst źródłaKotha, Sambasivarao, Milind Meshram i Nageswara Panguluri. "Advanced Approaches to Post-Assembly Modification of Peptides by Transition-Metal-Catalyzed Reactions". Synthesis 51, nr 09 (25.03.2019): 1913–22. http://dx.doi.org/10.1055/s-0037-1612418.
Pełny tekst źródłaTao, Hongwen, Yinan Yuan, Jian Chen, Xianyong Yu i Pinggui Yi. "Synthesis of Cholestan -3-One Derivatives Possessing a C-2 Spiro-Oxindole Substituent". Journal of Chemical Research 42, nr 1 (styczeń 2018): 15–19. http://dx.doi.org/10.3184/174751918x15161933697781.
Pełny tekst źródłaPAVLOV, V. A., A. I. KURDYUKOV, V. V. PLEMENKOV, R. R. KHALIULLIN i V. V. MOSKVA. "ChemInform Abstract: Dipolar (1 + 3)Cycloaddition Reaction of a Phosphorylnitrile Oxide with Cyclopropenes." ChemInform 26, nr 1 (18.08.2010): no. http://dx.doi.org/10.1002/chin.199501059.
Pełny tekst źródłaKidou, Chihiro, Haruki Mizoguchi, Tatsuo Nehira i Akira Sakakura. "Enantioselective 1,3-Dipolar Cycloaddition Reaction of Nitrones with α-(Acyloxy)acroleins Catalyzed by Dipeptide-Derived Chiral Tri- or Diammonium Salts". Synlett 30, nr 15 (30.07.2019): 1835–39. http://dx.doi.org/10.1055/s-0039-1690133.
Pełny tekst źródłaBelguedj, Roumaissa, Sofiane Bouacida, Hocine Merazig, Ali Belfaitah, Aissa Chibani i Abdelmalek Bouraiou. "Synthesis and crystal structures of three novel benzimidazole/benzoindolizine hybrids". Zeitschrift für Naturforschung B 71, nr 3 (1.03.2016): 231–39. http://dx.doi.org/10.1515/znb-2015-0164.
Pełny tekst źródłaSammor, Mervat S., Mustafa M. El-Abadelah, Ahmad Q. Hussein, Firas F. Awwadi, Salim S. Sabri i Wolfgang Voelter. "A study on the reaction of 3-alkyl(aryl)imidazo[1,5-a]pyridines with ninhydrin". Zeitschrift für Naturforschung B 73, nr 6 (27.06.2018): 413–21. http://dx.doi.org/10.1515/znb-2018-0039.
Pełny tekst źródłaShen, Yechen, i Younghwan Kwon. "Synthesis and Characterization of Reactive Energetic Plasticizers for Poly(glycidyl azide-co-tetramethylene glycol)-Based Polyurethane Binders". Journal of Nanoscience and Nanotechnology 21, nr 7 (1.07.2021): 4110–15. http://dx.doi.org/10.1166/jnn.2021.19184.
Pełny tekst źródłaMatsumoto, Kiyoshi, Hirokazu Iida, Takane Uchida, Yoshimi Yabe, Akikazu Kakehi i J. William Lown. "1,3-Dipolar cycloaddition reactions of monocyclic aziridines with dimethyl 1-cyclobutene-1,2-dicarboxylate". Canadian Journal of Chemistry 72, nr 10 (1.10.1994): 2108–17. http://dx.doi.org/10.1139/v94-268.
Pełny tekst źródłaAdembri, Giorgio, M. Laura Paoli i Alessandro Sega. "Influence of the Solvent on the stereoselectivity of 1,3-Dipolar cycloaddition of Nitrile Oxides on Several 4-Substituted 2-Cyclopentenones". Journal of Chemical Research 2003, nr 3 (marzec 2003): 126–27. http://dx.doi.org/10.3184/030823403103173453.
Pełny tekst źródłaHowell, Sarah J., Neil Spencer i Douglas Philp. "Recognition-mediated regiocontrol of a dipolar cycloaddition reaction". Tetrahedron 57, nr 23 (czerwiec 2001): 4945–54. http://dx.doi.org/10.1016/s0040-4020(01)00402-1.
Pełny tekst źródłaAlmansour, Abdulrahman I., Natarajan Arumugam, Raju Suresh Kumar, Dhaifallah M. Al-thamili, Govindasami Periyasami, Karuppiah Ponmurugan, Naif Abdullah Al-Dhabi, Karthikeyan Perumal i Dhanaraj Premnath. "Domino Multicomponent Approach for the Synthesis of Functionalized Spiro-Indeno[1,2-b]quinoxaline Heterocyclic Hybrids and Their Antimicrobial Activity, Synergistic Effect and Molecular Docking Simulation". Molecules 24, nr 10 (22.05.2019): 1962. http://dx.doi.org/10.3390/molecules24101962.
Pełny tekst źródłaRyan, John H., Nadia Spiccia, Leon S. M. Wong i Andrew B. Holmes. "Synthesis of 5-Aryloxazolidines via 1,3-Dipolar Cycloaddition Reaction of a Non-Stabilized Azomethine Ylide with Aromatic Aldehydes". Australian Journal of Chemistry 60, nr 12 (2007): 898. http://dx.doi.org/10.1071/ch07282.
Pełny tekst źródłaNguyen, Duy Trinh, Nguyen Phu Thuong Nhan, Tran Thien Hien, Nguyen Dai Hai, Dai Viet N. Vo i Long Giang Bach. "A Simple Approach for Immobilization of Fe-Core/Au-Shell Magnetic Nanoparticles on Multi-Walled Carbon Nanotubes via Cu(I) Huisgen Cycloaddition: Preparation and Characterization". Solid State Phenomena 279 (sierpień 2018): 187–91. http://dx.doi.org/10.4028/www.scientific.net/ssp.279.187.
Pełny tekst źródłaÇelebi, N., O. Çetiner, A. Güleç i L. Türker. "1,3-Dipolar Cycloaddition Reactions of Some 1-Aryl-Pyridinium-3-Olates". Bulletin des Sociétés Chimiques Belges 102, nr 7 (1.09.2010): 467–77. http://dx.doi.org/10.1002/bscb.19931020706.
Pełny tekst źródłaÇelebi, N., i L. Türker. "1,3-Dipolar cycloaddition reactions of some 3-aryl-phthalazinium-1-olates". Bulletin des Sociétés Chimiques Belges 102, nr 10 (1.09.2010): 625–30. http://dx.doi.org/10.1002/bscb.19931021001.
Pełny tekst źródłaCaballero, Ruben, Pilar de la Cruz i Fernando Langa. "(Invited) Tether-Directed Regioselective Synthesis of Bispyrazolinofullerenes". ECS Meeting Abstracts MA2023-01, nr 12 (28.08.2023): 1263. http://dx.doi.org/10.1149/ma2023-01121263mtgabs.
Pełny tekst źródłaBlanco-Carapia, Roberto E., Julio C. Flores-Reyes, Yizrell Medina-Martínez, Perla Islas-Jácome, Diego Pérez-Martínez, Leticia Lomas-Romero, Ilich A. Ibarra, Alejandro Islas-Jácome i Eduardo González-Zamora. "Synthesis of New bis 1- and 5-Substituted 1H-Tetrazoles via Huisgen-Type 1,3-Dipolar Cycloadditions". Proceedings 9, nr 1 (1.04.2019): 32. http://dx.doi.org/10.3390/ecsoc-22-05780.
Pełny tekst źródłaCheng, Bin, Bian Bao, Bing Zu, Xiaoguang Duan, Shengguo Duan, Yun Li i Hongbin Zhai. "Synthesis of spiro-3H-indazoles via 1,3-dipolar cycloaddition of arynes with 6-diazocyclohex-2-en-1-one derivatives and fused-2H-indazoles by subsequent rearrangement". RSC Advances 7, nr 85 (2017): 54087–90. http://dx.doi.org/10.1039/c7ra12117b.
Pełny tekst źródłaGoulioukina, Nataliya S., Nikolay N. Makukhin, Egor D. Shinkarev, Yuri K. Grishin, Vitaly A. Roznyatovsky i Irina P. Beletskaya. "Base mediated 1,3-dipolar cycloaddition of α-substituted vinyl phosphonates with diazo compounds for synthesis of 3-pyrazolylphosphonates and 5-pyrazolcarboxylates". Organic & Biomolecular Chemistry 14, nr 42 (2016): 10000–10010. http://dx.doi.org/10.1039/c6ob01780k.
Pełny tekst źródłaAntol, Ivana, Zoran Glasovac i Davor Margetić. "Mechanistic DFT Study of 1,3-Dipolar Cycloadditions of Azides with Guanidine". Molecules 28, nr 5 (3.03.2023): 2342. http://dx.doi.org/10.3390/molecules28052342.
Pełny tekst źródłaRen, Demin, Xiaolian Hu, Yulin Huang i Xiaofang Li. "Synthesis of Dispiro[Indeno[1,2-b]Quinoxaline-11,3′-Pyrrolizine-2′,2″-[1,3] Thiazolo[3,2-a]Pyrimidine Via Cycloaddition Reactions". Journal of Chemical Research 42, nr 9 (wrzesień 2018): 453–55. http://dx.doi.org/10.3184/174751918x15349264445767.
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