Статті в журналах з теми "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, and YU-FEN ZHAO. "A THEORETICAL STUDY ON THE MECHANISM OF 2:1 1, 3 DIPOLAR CYCLOADDITION REACTIONS." Journal of Theoretical and Computational Chemistry 06, no. 04 (December 2007): 861–67. http://dx.doi.org/10.1142/s0219633607003489.
Повний текст джерелаGrygorenko, Oleksandr O., Viktoriia S. Moskvina, Oleksandr V. Hryshchuk, and Andriy V. Tymtsunik. "Cycloadditions of Alkenylboronic Derivatives." Synthesis 52, no. 19 (June 24, 2020): 2761–80. http://dx.doi.org/10.1055/s-0040-1707159.
Повний текст джерелаSalem, Mohammed A., Moustafa A. Gouda, and Ghada G. El-Bana. "Chemistry of 2-(Piperazin-1-yl) Quinoline-3-Carbaldehydes." Mini-Reviews in Organic Chemistry 19, no. 4 (June 2022): 480–95. http://dx.doi.org/10.2174/1570193x18666211001124510.
Повний текст джерелаCaraculacu, Adrian A., Elena Scorţanu, and Georgeta Caraculacu. "New Parabanate Products by 1, 3-Dipolar Cycloaddition Reaction (‘Criss-Cross’ Cycloaddition)." High Performance Polymers 11, no. 4 (December 1999): 477–82. http://dx.doi.org/10.1088/0954-0083/11/4/311.
Повний текст джерелаOgurtsov, Vladimir A., and 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, no. 20 (October 14, 2022): 6887. http://dx.doi.org/10.3390/molecules27206887.
Повний текст джерелаWinne, Johan, Jan Hullaert, Bram Denoo, Mien Christiaens, and Brenda Callebaut. "Heterocycles as Moderators of Allyl Cation Cycloaddition Reactivity." Synlett 28, no. 18 (July 27, 2017): 2345–52. http://dx.doi.org/10.1055/s-0036-1588511.
Повний текст джерелаMohtat, Bita, Seyyed Amir Siadati, and 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, no. 3 (May 12, 2019): 213–21. http://dx.doi.org/10.1177/1468678319845863.
Повний текст джерелаEl-Sayed, Wael A., and 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, no. 1 (January 1, 2010): 57–66. http://dx.doi.org/10.1515/znb-2010-0110.
Повний текст джерелаHunnur, Raveendra K., Prashant R. Latthe, and 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, no. 9 (September 2005): 592–94. http://dx.doi.org/10.3184/030823405774308907.
Повний текст джерелаMawhinney, Robert C., Heidi M. Muchall, and Gilles H. Peslherbe. "A computational study of the 1,3-dipolar cycloaddition reaction mechanism for nitrilimines." Canadian Journal of Chemistry 83, no. 9 (September 1, 2005): 1615–25. http://dx.doi.org/10.1139/v05-179.
Повний текст джерелаDeng, Yongming, Qing-Qing Cheng, and Michael Doyle. "Asymmetric [3+3] Cycloaddition for Heterocycle Synthesis." Synlett 28, no. 14 (July 5, 2017): 1695–706. http://dx.doi.org/10.1055/s-0036-1588453.
Повний текст джерелаSantos, Hugo, Amy Distiller, Asha M. D'Souza, Quentin Arnoux, Jonathan M. White, Adam G. Meyer, and John H. Ryan. "1,3-Dipolar cycloaddition reactions of phthalic anhydrides with an azomethine ylide." Organic Chemistry Frontiers 2, no. 6 (2015): 705–12. http://dx.doi.org/10.1039/c5qo00062a.
Повний текст джерелаBoudriga, Sarra, Saoussen Haddad, Moheddine Askri, Armand Soldera, Michael Knorr, Carsten Strohmann, and 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, no. 20 (2019): 11082–91. http://dx.doi.org/10.1039/c8ra09884k.
Повний текст джерелаWanapun, D., K. A. Van Gorp, N. J. Mosey, M. A. Kerr, and T. K. Woo. "The mechanism of 1,3-dipolar cycloaddition reactions of cyclopropanes and nitrones A theoretical study." Canadian Journal of Chemistry 83, no. 10 (October 1, 2005): 1752–67. http://dx.doi.org/10.1139/v05-182.
Повний текст джерелаBelguedj, Roumaissa, Sofiane Bouacida, Hocine Merazig, Ali Belfaitah, and 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, no. 8 (August 1, 2015): 555–61. http://dx.doi.org/10.1515/znb-2015-0016.
Повний текст джерелаNewton, Rebecca, and G. Paul Savage. "Regioselective 1,3-Dipolar Cycloaddition Reactions of 4-Methylene-2-oxazolidinones with Benzonitrile Oxide." Australian Journal of Chemistry 61, no. 6 (2008): 432. http://dx.doi.org/10.1071/ch08111.
Повний текст джерелаPetrov, A. O., Georgiy V. Malkov, Sergei V. Karpov, A. V. Shastin, and A. V. Bakeshko. "Kinetic Study of the Polyaddition of Azide-Alkyne AB2 Monomers in Nonisotermic Conditions." Key Engineering Materials 816 (August 2019): 151–56. http://dx.doi.org/10.4028/www.scientific.net/kem.816.151.
Повний текст джерелаJulino, Markus, Philip R. Lowe, and 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, no. 2 (February 2000): 74–75. http://dx.doi.org/10.3184/030823400103166418.
Повний текст джерелаZhu, Shaohua, Yan Zhang, Peipei Li, Wenzhu Bi, Xiaolan Chen, and Yufen Zhao. "Synthesis of novel phosphorylated chrysin derivatives by 1, 3-dipolar cycloaddition reaction." Phosphorus, Sulfur, and Silicon and the Related Elements 192, no. 1 (October 18, 2016): 1–8. http://dx.doi.org/10.1080/10426507.2016.1223076.
Повний текст джерелаKhoroshunova, Yulia V., Denis A. Morozov, Andrey I. Taratayko, Polina D. Gladkikh, Yuri I. Glazachev, and Igor A. Kirilyuk. "Synthesis of 1-azaspiro[4.4]nonan-1-oxyls via intramolecular 1,3-dipolar cycloaddition." Beilstein Journal of Organic Chemistry 15 (August 27, 2019): 2036–42. http://dx.doi.org/10.3762/bjoc.15.200.
Повний текст джерелаLukevics, E., P. Arsenyan, I. Shestakova, O. Zharkova, I. Kanepe, R. Mezapuke, and O. Pudova. "Cytotoxic Activity of Silyl- and Germyl-Substituted 4,4-Dioxo-3a,6a-Dihydrothieno[2,3−d]isoxazolines-2." Metal-Based Drugs 7, no. 2 (January 1, 2000): 63–66. http://dx.doi.org/10.1155/mbd.2000.63.
Повний текст джерелаSvete, Jurij, Uroš Grošelj, Franc Požgan, and Bogdan Štefane. "Copper-Catalyzed Azomethine Imine–Alkyne Cycloadditions (CuAIAC)." Synthesis 50, no. 23 (October 5, 2018): 4501–24. http://dx.doi.org/10.1055/s-0037-1610284.
Повний текст джерелаZhang, Xiaofeng, Kenny Pham, Shuai Liu, Marc Legris, Alex Muthengi, Jerry P. Jasinski, and 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 (October 18, 2016): 2204–10. http://dx.doi.org/10.3762/bjoc.12.211.
Повний текст джерелаKalluraya, Balakrishna, Kaushik B R, and 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, no. 1 (July 5, 2020): 17–25. http://dx.doi.org/10.21467/jmm.7.1.17-25.
Повний текст джерелаGanushevich, Yulia, Almaz Zagidullin, Svetlana Kondrashova, Shamil Latypov, Vasili Miluykov, Peter Lönnecke, and Evamarie Hey-Hawkins. "Asymmetric 1,3-dipolar cycloaddition reaction of chiral 1-alkyl-1,2-diphospholes with diphenyldiazomethane." RSC Advances 10, no. 64 (2020): 39060–66. http://dx.doi.org/10.1039/d0ra08080b.
Повний текст джерелаBoitsov, Vitali M., Alexander V. Stepakov, Siqi Wang, Alexander S. Filatov, Stanislav V. Lozovskiy, Stanislav V. Shmakov, Olesya V. Khoroshilova, Anna G. Larina, and 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, no. 12 (January 18, 2021): 2114–32. http://dx.doi.org/10.1055/a-1360-9716.
Повний текст джерелаMishriky, Nawal, Adel S. Girgis, and 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, no. 1 (January 2000): 2–3. http://dx.doi.org/10.3184/030823400103165527.
Повний текст джерелаDumitrescu, Denisa, Sergiu Shova, Constantin Draghici, Marcel Mirel Popa, and Florea Dumitrascu. "Synthesis of 1-(2-Fluorophenyl)pyrazoles by 1,3-Dipolar Cycloaddition of the Corresponding Sydnones." Molecules 26, no. 12 (June 17, 2021): 3693. http://dx.doi.org/10.3390/molecules26123693.
Повний текст джерелаWang, Yongchao, Yu Chen, Shengli Duan, Yiyang Cao, Wenjin Sun, Mei Zhang, Delin Zhao, Donghua Hu та Jianwei Dong. "Diastereoselective Three-Component 1,3-Dipolar Cycloaddition to Access Functionalized β-Tetrahydrocarboline- and Tetrahydroisoquinoline-Fused Spirooxindoles". Molecules 29, № 8 (15 квітня 2024): 1790. http://dx.doi.org/10.3390/molecules29081790.
Повний текст джерелаKotha, Sambasivarao, Milind Meshram, and Nageswara Panguluri. "Advanced Approaches to Post-Assembly Modification of Peptides by Transition-Metal-Catalyzed Reactions." Synthesis 51, no. 09 (March 25, 2019): 1913–22. http://dx.doi.org/10.1055/s-0037-1612418.
Повний текст джерелаTao, Hongwen, Yinan Yuan, Jian Chen, Xianyong Yu, and Pinggui Yi. "Synthesis of Cholestan -3-One Derivatives Possessing a C-2 Spiro-Oxindole Substituent." Journal of Chemical Research 42, no. 1 (January 2018): 15–19. http://dx.doi.org/10.3184/174751918x15161933697781.
Повний текст джерелаPAVLOV, V. A., A. I. KURDYUKOV, V. V. PLEMENKOV, R. R. KHALIULLIN, and V. V. MOSKVA. "ChemInform Abstract: Dipolar (1 + 3)Cycloaddition Reaction of a Phosphorylnitrile Oxide with Cyclopropenes." ChemInform 26, no. 1 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199501059.
Повний текст джерелаKidou, Chihiro, Haruki Mizoguchi, Tatsuo Nehira та 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, № 15 (30 липня 2019): 1835–39. http://dx.doi.org/10.1055/s-0039-1690133.
Повний текст джерелаBelguedj, Roumaissa, Sofiane Bouacida, Hocine Merazig, Ali Belfaitah, Aissa Chibani, and Abdelmalek Bouraiou. "Synthesis and crystal structures of three novel benzimidazole/benzoindolizine hybrids." Zeitschrift für Naturforschung B 71, no. 3 (March 1, 2016): 231–39. http://dx.doi.org/10.1515/znb-2015-0164.
Повний текст джерелаSammor, Mervat S., Mustafa M. El-Abadelah, Ahmad Q. Hussein, Firas F. Awwadi, Salim S. Sabri, and Wolfgang Voelter. "A study on the reaction of 3-alkyl(aryl)imidazo[1,5-a]pyridines with ninhydrin." Zeitschrift für Naturforschung B 73, no. 6 (June 27, 2018): 413–21. http://dx.doi.org/10.1515/znb-2018-0039.
Повний текст джерелаShen, Yechen, and 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, no. 7 (July 1, 2021): 4110–15. http://dx.doi.org/10.1166/jnn.2021.19184.
Повний текст джерелаMatsumoto, Kiyoshi, Hirokazu Iida, Takane Uchida, Yoshimi Yabe, Akikazu Kakehi, and J. William Lown. "1,3-Dipolar cycloaddition reactions of monocyclic aziridines with dimethyl 1-cyclobutene-1,2-dicarboxylate." Canadian Journal of Chemistry 72, no. 10 (October 1, 1994): 2108–17. http://dx.doi.org/10.1139/v94-268.
Повний текст джерелаAdembri, Giorgio, M. Laura Paoli, and 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, no. 3 (March 2003): 126–27. http://dx.doi.org/10.3184/030823403103173453.
Повний текст джерелаHowell, Sarah J., Neil Spencer, and Douglas Philp. "Recognition-mediated regiocontrol of a dipolar cycloaddition reaction." Tetrahedron 57, no. 23 (June 2001): 4945–54. http://dx.doi.org/10.1016/s0040-4020(01)00402-1.
Повний текст джерелаAlmansour, Abdulrahman I., Natarajan Arumugam, Raju Suresh Kumar, Dhaifallah M. Al-thamili, Govindasami Periyasami, Karuppiah Ponmurugan, Naif Abdullah Al-Dhabi, Karthikeyan Perumal, and 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, no. 10 (May 22, 2019): 1962. http://dx.doi.org/10.3390/molecules24101962.
Повний текст джерелаRyan, John H., Nadia Spiccia, Leon S. M. Wong, and 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, no. 12 (2007): 898. http://dx.doi.org/10.1071/ch07282.
Повний текст джерелаNguyen, Duy Trinh, Nguyen Phu Thuong Nhan, Tran Thien Hien, Nguyen Dai Hai, Dai Viet N. Vo, and 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 (August 2018): 187–91. http://dx.doi.org/10.4028/www.scientific.net/ssp.279.187.
Повний текст джерелаÇelebi, N., O. Çetiner, A. Güleç, and L. Türker. "1,3-Dipolar Cycloaddition Reactions of Some 1-Aryl-Pyridinium-3-Olates." Bulletin des Sociétés Chimiques Belges 102, no. 7 (September 1, 2010): 467–77. http://dx.doi.org/10.1002/bscb.19931020706.
Повний текст джерелаÇelebi, N., and L. Türker. "1,3-Dipolar cycloaddition reactions of some 3-aryl-phthalazinium-1-olates." Bulletin des Sociétés Chimiques Belges 102, no. 10 (September 1, 2010): 625–30. http://dx.doi.org/10.1002/bscb.19931021001.
Повний текст джерелаCaballero, Ruben, Pilar de la Cruz, and Fernando Langa. "(Invited) Tether-Directed Regioselective Synthesis of Bispyrazolinofullerenes." ECS Meeting Abstracts MA2023-01, no. 12 (August 28, 2023): 1263. http://dx.doi.org/10.1149/ma2023-01121263mtgabs.
Повний текст джерелаBlanco-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, and Eduardo González-Zamora. "Synthesis of New bis 1- and 5-Substituted 1H-Tetrazoles via Huisgen-Type 1,3-Dipolar Cycloadditions." Proceedings 9, no. 1 (April 1, 2019): 32. http://dx.doi.org/10.3390/ecsoc-22-05780.
Повний текст джерелаCheng, Bin, Bian Bao, Bing Zu, Xiaoguang Duan, Shengguo Duan, Yun Li, and 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, no. 85 (2017): 54087–90. http://dx.doi.org/10.1039/c7ra12117b.
Повний текст джерелаGoulioukina, Nataliya S., Nikolay N. Makukhin, Egor D. Shinkarev, Yuri K. Grishin, Vitaly A. Roznyatovsky та 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, № 42 (2016): 10000–10010. http://dx.doi.org/10.1039/c6ob01780k.
Повний текст джерелаAntol, Ivana, Zoran Glasovac, and Davor Margetić. "Mechanistic DFT Study of 1,3-Dipolar Cycloadditions of Azides with Guanidine." Molecules 28, no. 5 (March 3, 2023): 2342. http://dx.doi.org/10.3390/molecules28052342.
Повний текст джерелаRen, Demin, Xiaolian Hu, Yulin Huang, and 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, no. 9 (September 2018): 453–55. http://dx.doi.org/10.3184/174751918x15349264445767.
Повний текст джерела