Relevant bibliographies by topics / Copper-catalyzed 3+2 cycloaddition

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Copper-catalyzed 3+2 cycloaddition'

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Published: 24 April 2022

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Journal articles on the topic "Copper-catalyzed 3+2 cycloaddition"

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Cheng, C. H., H. T. Chang, and T. Jayanth. "Copper-Catalyzed Diastereoselective [3+2] Cycloaddition." Synfacts 2007, no. 7 (July 2007): 0720. http://dx.doi.org/10.1055/s-2007-968623.

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Siva Prasanna Sanka, R. V., Balaji K., Yves Leterrier, Shyam Pandey, Monika Srivastava, Anurag Srivastava, Wolfgang H. Binder, Sravendra Rana, and Véronique Michaud. "Nitrogen-doped graphene stabilized copper nanoparticles for Huisgen [3+2] cycloaddition “click” chemistry." Chemical Communications 55, no. 44 (2019): 6249–52. http://dx.doi.org/10.1039/c9cc02057h.

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Schienebeck, Casi M., Xiaoxun Li, Xing-zhong Shu, and Weiping Tang. "3-Acyloxy-1,4-enyne: A new five-carbon synthon for rhodium-catalyzed [5 + 2] cycloadditions." Pure and Applied Chemistry 86, no. 3 (March 20, 2014): 409–17. http://dx.doi.org/10.1515/pac-2014-5042.

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Abstract Seven-membered rings are ubiquitous in natural products and pharmaceutical agents, and their syntheses continue to stimulate the development of novel synthetic methods. The [5 + 2] cycloaddition is one of the most efficient ways to access seven-membered rings since the two-carbon components (alkenes, alkynes, or allenes) are readily available. Prior to our study, however, there was only one type of transition-metal-catalyzed [5 + 2] cycloaddition: the reaction between vinylcyclopropanes and alkenes, alkynes, or allenes. We recently developed a new type of transition-metal-catalyzed [5 + 2] cycloaddition, where the five-carbon building block is 3-acyloxy-1,4-enyne (ACE). Our recent progress on Rh-catalyzed intra- and intermolecular [5 + 2] cycloadditions of ACEs and alkynes is summarized in this article. Using chiral propargylic esters, bicyclic products were prepared in high optical purity by the intramolecular [5 + 2] cycloadditions. Monocyclic seven-membered rings were synthesized by intermolecular [5 + 2] cycloaddition of ACEs and alkynes. Kinetic studies indicated that the rate of this intermolecular cycloaddition was significantly accelerated when the acetate was replaced by dimethylaminobenzoate. DFT calculations suggested that novel metallacycles were generated by a Rh-promoted oxidative cycloaddition of 1,4-enynes accompanied by a 1,2-acyloxy migration of propargylic esters.
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Xie, Ying, Yulong Li, Xun Chen, Yingle Liu, and Wei Zhang. "Copper/amine-catalyzed formal regioselective [3 + 2] cycloaddition of an α,β-unsaturated O-acetyl oxime with enals." Organic Chemistry Frontiers 5, no. 10 (2018): 1698–701. http://dx.doi.org/10.1039/c8qo00204e.

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Xie, Zhiyu, Fei Li, Liangfeng Niu, Hongbing Li, Jincai Zheng, Ruijing Han, Zhiyu Ju, Shanshan Li, and Dandan Li. "CuBr/NHPI co-catalyzed aerobic oxidative [3 + 2] cycloaddition-aromatization to access 5,6-dihydro-pyrrolo[2,1-a]isoquinolines." Organic & Biomolecular Chemistry 18, no. 35 (2020): 6889–98. http://dx.doi.org/10.1039/d0ob01403f.

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Wang, Qian, Timothy R. Chan, Robert Hilgraf, Valery V. Fokin, K. Barry Sharpless, and M. G. Finn. "Bioconjugation by Copper(I)-Catalyzed Azide-Alkyne [3 + 2] Cycloaddition." Journal of the American Chemical Society 125, no. 11 (March 2003): 3192–93. http://dx.doi.org/10.1021/ja021381e.

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Yuan, Yang, Zhan-Jiang Zheng, Fei Ye, Jun-Han Ma, Zheng Xu, Xing-Feng Bai, Li Li, and Li-Wen Xu. "Highly efficient desymmetrization of cyclopropenes to azabicyclo[3.1.0]hexanes with five continuous stereogenic centers by copper-catalyzed [3 + 2] cycloadditions." Organic Chemistry Frontiers 5, no. 18 (2018): 2759–64. http://dx.doi.org/10.1039/c8qo00761f.

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An unprecedented copper-catalyzed desymmetrization/cycloaddition reaction of 1,1-disubstituted cyclopropenes provides an efficient access to azabicyclo[3.1.0]hexanes bearing five continuous carbon-stereogenic centers.
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Xu, Bing, Zhan-Ming Zhang, Bing Liu, Shan Xu, Lu-Jia Zhou, and Junliang Zhang. "Copper(i)-catalyzed asymmetric exo-selective [3+2] cycloaddition of azomethine ylides with β-trifluoromethyl β,β-disubstituted enones." Chemical Communications 53, no. 58 (2017): 8152–55. http://dx.doi.org/10.1039/c7cc03015k.

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A copper-catalyzed asymmetricexo-selective dipolar cycloaddition of β-trifluoromethyl β,β-disubstituted enones with azomethine ylides was developed, which provides an efficient access to valuable pyrrolidines bearing a trifluoromethylated all-carbon quaternary stereocenter.
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Link, A. James, and David A. Tirrell. "Cell Surface Labeling ofEscherichia colivia Copper(I)-Catalyzed [3+2] Cycloaddition." Journal of the American Chemical Society 125, no. 37 (September 2003): 11164–65. http://dx.doi.org/10.1021/ja036765z.

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Román-Maldonado, Eloisa, Horacio Reyes, Miguel A. Sanchez-Carmona, Nelly González-Rivas, and Erick Cuevas-Yañez. "1-(2-Chlorobenzyloxy)-3-[1,2,3]triazol-1-yl-propan-2-ol Derivatives: Synthesis, Characterization, and DFT-Based Descriptors Analysis." Journal of Chemistry 2017 (2017): 1–9. http://dx.doi.org/10.1155/2017/4783608.

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A novel series of 1-(2-chlorobenzyloxy)-3-[1,2,3]triazol-1-yl-propan-2-ol derivatives was designed and synthesized using copper catalyzed alkyne-azide cycloaddition in the key step. Theoretical investigation of molecular and electronic properties by means of global and local reactivity indexes of the synthetized compounds was carried out, using DFT (Density Functional Theory) at PBEPBE/6-31++G⁎⁎level.
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Dissertations / Theses on the topic "Copper-catalyzed 3+2 cycloaddition"

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Zhang, Li. "Ruthenium-catalyzed azide-alkyne cycloaddition, and cyclometallation of 2-vinylpyridine with MCl[subscript 2](PPh[subscript 3])[subscript 3] and MHCl(PPh[subscript 3])[subscript 3] (M=Ru, Os) /." View abstract or full-text, 2008. http://library.ust.hk/cgi/db/thesis.pl?CHEM%202008%20ZHANG.

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Decuypère, Elodie. "Etude de réactions de cycloaddition [3+2] impliquant des composés mésoioniques et des dipolarophiles." Thesis, Université Paris-Saclay (ComUE), 2016. http://www.theses.fr/2016SACLS395.

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Le premier objectif de ce travail a consisté à développer la réaction CuSAC (découverte au laboratoire) pour la synthèse régiosélective de pyrazoles poly-substitués, dans un contexte de méthodologie de synthèse. Il existe de nombreux composés biologiquement actifs contenant le motif pyrazole et peu de méthodes régiosélectives décrites pour les synthétiser. Développer une nouvelle réaction pour obtenir des pyrazoles poly-substitués de façon contrôlée était donc très intéressant pour des applications synthétiques.Le deuxième objectif a été d’appliquer cette réaction à la bioconjugaison et notamment au développement de sondes profluorescentes Des coumarines-sydnones subissant un effet d’extinction de fluorescence par le phénomène PeT ont été développées. Suite au couplage avec un alcyne, le pyrazole formé n’éteint plus lafluorescence de la coumarine. Ce type de sondes est très intéressant pour le marquage de biomolécules, car il n’y a aucun parasitage de fluorescence et donc ne nécessite aucun lavage.Le troisième objectif de la thèse a été d’explorer la réactivité des composés mésoioniques pour un alcyne, sous une catalyse au cuivre, dans le but de découvrir de nouvelles réactions click. Un criblage de 24 composés dans 9 conditions de catalyses différentes, faisant plus de 200 réactions réalisées, a été effectué. Deux réactions ont été révélées, dont une très prometteuse. Celle-ci permet dans la même opération de lier deux partenaires tout en libérant un fragment d’un des deux partenaires. Cette réaction a été étudiée dans le but de développer un outil de théranostique où être utilisée pour la mise au point de nouveaux espaceurs clivables
The first aim of this work was the development of a new regioselective synthetic access to poly-substituted pyrazoles via the CuSAC reaction, previously discovered in the laboratory. The development of new reactions leading to poly-substituted pyrazoles with a full control of regioselectivity is highly interesting for synthetic applications.The second aim of this work was the application of this reaction for the labeling of complex biomolecules. To broaden the scope of the CuSAC, fluorogenic coumarin-sydnones which undergo fluorescence extinction via PeT have been designed and synthetized. Following the coupling reaction, the newly formed pyrazole core allows huge enhancement of the fluorescence signal.This kind of probes is highly interesting in the specific labelling of biomolecules avoiding washing steps.The last project of this thesis have been focused on the discovery of new [3+2] cycloaddition reaction implying a mesoionic compound and a terminal alkyne under copper catalysis. 24 mesoionic dipoles were screened for their ability to react with a terminal alkyne in 9 different catalytic conditions, yielding to more than 200 reactions screened. Two hits were identified, one of them holding great promise. This hit allows an efficient “click and release” reaction which should find tremendous applications, especially in the fields of theranostic and cleavable linker development
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HU, JIEYU. "COPPER(I) CATALYZED EXO-SELECTIVE [CN+C+CC] 1,3-DIPOLAR CYCLOADDITIONS and STUDIES TOWARDS THE TOTAL SYNTHESIS OF KAITOCEPHALIN." Case Western Reserve University School of Graduate Studies / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=case1269965489.

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Yoshinaga, Yukako. "New Design of Bipyridine Ligands for Copper-Catalyzed Asymmetric Molecular Transformations." Kyoto University, 2020. http://hdl.handle.net/2433/253507.

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Li, Jihui. "Copper-Catalyzed Domino C-N Bond Formation for Synthesis of N-Containing Compounds (Benzimidazoles, Imidazoles, and Guanidines) - Approach toward Total Synthesis of Natural Product Raputindoles." Thesis, Paris 11, 2013. http://www.theses.fr/2013PA112130.

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Cette thèse est constituée de trois parties : 1) Le contexte bibliographique, 2) le développement de réactions domino cupro-catalysées et 3) une approche vers la synthèse totale des raputindoles.La première partie introduit d’abord le concept de réactions domino ainsi que leurs applications, puis les réactions catalysées par du cuivre permettant de former des liaisons C-N sont passées en revue en incluant les couplages de Ullmann, Goldberg et de Chan-Lam, les séquences d’activation oxydante de liaisons C-H/formation de liaison C-N, l’insertion de nitrènes et l’hydroamination de liaisons C-C multiples. En se basant sur ces réactions élémentaires permettant de former une liaison C-N unique, les développements récents de réactions domino sont ensuite détaillés.La deuxième partie peut être subdivisée en 3 sections : 1) la synthèse de benzimidazoles, 2) la synthèse d’imidazoles and 3) la synthèse de guanidines. Un rappel des méthodes existantes pour la synthèse de ces motifs est proposé dans chaque section. Notre travail, basé sur la formation de liaisons C-N multiples selon une séquence cupro-catalysée domino, est ensuite détaillé. Celui-ci nous a permis d’aboutir au développement de voies d’accès aux benzimidazoles, en utilisant une réaction séquentielle catalysée par du cuivre en présence d’oxygène à partir d’acides boroniques et d’amidines, à la synthèse d’imidazoles par une réaction de di-amination d’alcynes vrai par des amidines et à l’obtention de guanidines et de 2-aminobenzimidines par une réaction à 3 composant. Ces réactions domino montrent une bonne efficacité et permettent d’assembler des hétérocycles à partir de précurseurs aisément accessibles.La dernière partie est consacrée à la synthèse des raputindoles. La structure, les activités et les réactions clé pour la construction de ces alcaloïdes sont discuté d’abord, nous amenant à proposer une rétrosynthèse pour accéder à ces molécules. Les réactions qui ont retenues notre attention pour construire ces molécules sont une annelation [3+2] irido-catalysée d’acides o-formylarylboronique et de 1,3-diènes, la synthèse de Leimgruber-Batcho pour obtenir des indoles et une séquence d’alkylboration-protodéboration. A partir de cela 3 stratégies ont été évaluées, montrant que l’accès à ce type de composé naturel est envisageable en combinant ces étapes
This thesis consists in three parts: bibliographic background, copper-catalyzed reactions for synthesis of N-containing compounds, approach to the synthesis of raputindoles.The first part introduces the domino reactions and their applications, then, copper-mediated reactions for construction of C-N bond formation are reviewed including Ullmann, Goldberg and Chan-Lam coupling, oxidative C-H activation/C-N formation, insertion of nitrenes and carbenoids, and hydroamination of multi-C-C bonds. This can be used as guides to design domino reaction. Following these copper-mediated single C-N bond formation reactions, recent developments of copper-catalyzed domino reactions for synthesis of heterocycles are described.The second part can be divided into three sections: 1) synthesis of benzimidazoles, 2) synthesis of imidazoles and 3) synthesis of guanidines. Each section summarizes the existing methods used for their synthesis. Following it, our synthetic work involving copper-catalyzed C-N bond formation domino reactions is discussed in detail. Our objectives include the synthesis of benzimidazoles through copper-catalyzed sequential reaction of benzamidines and boronic acids, synthesis of imidazoles via copper-catalyzed domino reaction of benzamidines and acetylenes, and synthesis of guanidines and 2-aminobenzimidazoles by Cu-catalyzed three-component reaction of cyanamides, boronic acids and amines. These copper-catalyzed domino reactions show high efficiencies from readily available and simple starting materials.The last part is about the total synthesis of raputindoles. The structure and bioactivities of raputindoles and key reactions for the total synthesis of raputindoles are introduced first, the synthetic strategies are then proposed on basis of relative synthetic methods. The key reactions we use for the synthesis of raputindoles are iridium catalyzed [3+2] annulation of o-formylarylboronic acids and 1,3-dienes, Leimgruber-Batcho indole synthesis, transition-metal catalyzed SN2 substitution and alkylborylation-protondeborylation. According to the three strategies we proposed, lots of relative reactions were investigated. The results show that it is possible to synthesize the raputindole molecules based on the iridium catalyzed [3+2] annulation of 2-formylarylboronic acids and 1,3-dienes
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Tsai, Yen-Ching, and 蔡燕青. "Gold and Copper Catalyzed [3+2] Cycloaddition Reactions." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/68325797617962500922.

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Chen, Jie Yang, and 陳杰陽. "Copper catalyzed [2+2]-cycloadditions of terminal alkynes with hydroxylamines & Copper catalyzed [3+2]-cycloadditions of allene ethers with hydroxylamines." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/50702253744015724183.

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碩士
國立清華大學
化學系
103
In first chapter describes the copper-catalyzed [2+2]-cycloaddition of hydroxylamines with terminal alkynes in oxygen atmosphere to form corresponding β-lactams derivatives. β-lactam functionality commonly found in many natural products as well as biologically active molecules. The utility of this [2+2]-cycloaddition is manifested by wide scope of hydroxylamines and terminal alkynes. The second chapter describes one-pot copper-catalyzed [3+2]-cycloaddition of hydroxylamine with allene ether in oxygen atmosphere to form isoxazolidine derivatives. The use hydroxylamines provides a more convenient method to access isoxazolidine derivatives through insitu generated nitrone.
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Jones, Regan Andrew. "The asymmetric total synthesis of (+)-geniposide via phosphine-catalyzed [3+2] cycloaddition." Thesis, 2009. http://hdl.handle.net/2152/ETD-UT-2009-05-16.

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The iridoids are a large family of monoterpenoid natural products that possess a wide range of biological activities. A great deal of research has already been done in the field of iridoid total synthesis, but limitations still remain. Specifically, few syntheses of iridoid β-glycosides have been reported. This work describes the 14 step asymmetric total synthesis of the iridoid β-glycoside (+)-geniposide utilizing a phosphine-catalyzed [3+2] cycloaddition as the key step. Other noteworthy steps in the synthesis include a palladium-catalyzed kinetic resolution and a previously unutilized method for iridoid glycosidation. In addition to describing the synthesis of (+)-geniposide, this dissertation will also review 1) phosphine-catalyzed cycloaddition reactions and 2) previous enantioselective total syntheses of iridoid glycosides.
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Prince, Ashleigh Lauren. "Homogeneous and Heterogeneous Approaches to 1,2,4-Triazine-Accelerated Copper-Catalyzed Azide-Alkyne Cycloadditions." 2011. http://trace.tennessee.edu/utk_graddiss/1117.

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Over the last decade, the domain of click chemistry has grown exponentially and has significantly impacted the fields of organic synthesis, medicinal chemistry, molecular biology, and materials science. The ideal model of a click reaction has become the copper-catalyzed azide-alkyne cycloaddition (CuAAC). Inherent limitations of CuAAC, including high temperatures, long reaction times, and difficult purifications, have been minimized by the development of nitrogen-based ligands. Herein, we present a novel application of 1,2,4-triazines by investigating their use as accelerants for CuAAC. A diverse library of 1,2,4-triazines were synthesized in order to examine the molecular determinants of their catalytic activity. These ligands were found to be potent accelerants, at catalytic concentrations, in the presence of both copper(I) and copper(II) salts. Remarkably, these catalyzed reactions proceeded at room temperature, generating high isolated yields, in both polar and nonpolar solvents. 5,6-Diphenyl-3-(pyridin-2-yl)1,2,4-triazine was the most active ligand studied, producing an 89% yield in a model click reaction within one hour. Additional experiments with an array of azides and alkynes yielded similar results, defining a broad substrate scope for 1,2,4-triazines as catalysts for click chemistry. Heterogeneous 1,2,4-triazines were designed using different solid supports and different sites of attachment with respect to the 1,2,4-triazine ligand. The primary advantages offered by these immobilized catalysts are the prevention of metal contamination in 1,2,3-triazole products and the recyclability of the catalyst. Results indicated that 1,2,4-triazine-functionalized silica was a more effective accelerant of CuAAC, whereas polystyrene-supported 1,2,4-triazines displayed modest activity. In coordination with copper(II), 1,2,4-triazines appended onto silica generated isolated yields greater than 90% after four consecutive reaction cycles with minimal copper leaching. Further research will utilize both homogeneous and heterogeneous 1,2,4-triazine-accelerated CuAAC in the derivatization of solid supports for energy-related chemical processes and in the synthesis of novel enzyme inhibitors.
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Wei, Chu-Hung, and 韋竹鴻. "Cobalt-Catalyzed Asymmetric Reductive Coupling and [3+2] Reductive Cycloaddition of Alkynes with Enones." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/69369055786383257131.

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博士
國立清華大學
化學系
99
In the thesis, a CoI2/(R)-BINAP, Zn, ZnI2 and H2O system efficiently catalyzed the intermolecular asymmetric reductive coupling of alkynes (1a-1g) with cyclic enones (2a-2d) at room temperature for 24 hour to afford highly enantioselective β-substituted cyclic enones. The reaction proceeds with highly regio- and stereoselectivity. In addition, by identify the absolute configuration of products 2.3a and 2.3f, a possible mechanism that involves the formation of cobaltacyclopentene intermediate from alkyne and cyclic enone is proposed. In addition, two different catalyzing system: CoBr2/dppe, Mn, ZnCl2, CH3CN and CoI2/BINAP, Zn, ZnI2, 1,4-dioxane, efficiently catalyzed the intermolecular reductive [3+2] cycloaddition of alkynes (1a-1l) with cyclic enones (2a-2e) at 40oC for 24 hour to afford highly stereoselective bicyclo[2.2.1]hept-2-en-1-ol and bicyclo[3.2.1]oct-6-en-1-ol derivatives respectively. This reaction also expanded a new reaction type of alkynes and enones in transition metal catalyzed reaction. We utilized the isotope experiment to further understand the mechanism. . Finally, we developed a new system: CoI2/(R,R′,S,S′)-Duanphos, Zn, ZnI2, 1,4-dioxane, efficiently catalyzed the intermolecular asymmetric reductive [3+2] cycloaddition of alkynes (1a-1i) with cyclic enones (2a-2e) at room temperature for 24 hour to afford highly enantio- and stereoselective bicyclo[2.2.1]hept-2-en-1-ol and bicyclo[3.2.1]oct-6- en-1-ol derivatives. In addition, by identify the absolute configuration of products 3.3a, a possible mechanism that involves the formation of cobaltacyclopentene intermediate from alkyne and cyclic enone is proposed. We discussed the result depend on alkyne and enones by asymmetric reductive coupling and asymmetric reductive [3+2] cycloaddition experiment, and further investigate the interdependent between these two reactions
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Book chapters on the topic "Copper-catalyzed 3+2 cycloaddition"

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Qiu, Zaozao. "Nickel-Catalyzed [2+2+2] Cycloaddition of 1,2-o-Carboryne with Alkynes." In Late Transition Metal-Carboryne Complexes, 71–83. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-24361-5_5.

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Ricardo, Carolynne L., and Tomislav Pintauer. "Highly Efficient Organic and Macromolecular Synthesis Using Sequential Copper Catalyzed Azide-Alkyne [3+2] Cycloaddition and ATRA/ATRP." In ACS Symposium Series, 73–98. Washington, DC: American Chemical Society, 2012. http://dx.doi.org/10.1021/bk-2012-1100.ch006.

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Ohta, Yusuke. "Construction of 2-(Aminomethyl)indoles Through Copper-Catalyzed Domino Three-Component Coupling and Cyclization." In Copper-Catalyzed Multi-Component Reactions, 9–45. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-15473-7_2.

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Brandsma, L., H. D. Verkruijsse, and S. F. Vasilevsky. "Copper(l)-Halide-Catalyzed Substitution of sp 2-HaIogen by Alkoxide." In Application of Transition Metal Catalysts in Organic Synthesis, 85–105. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-60328-0_6.

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Malleron, J. L., J. C. Fiaud, and J. Y. Legros. "Carbonylative [2+2] Cycloaddition." In Handbook of Palladium-Catalyzed Organic Reactions, 272–73. Elsevier, 1997. http://dx.doi.org/10.1016/b978-012466615-3/50073-2.

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Sarkar, T. K. "Palladium(0)-Catalyzed [3+2] Cycloaddition." In Compounds of Groups 15 (As, Sb, Bi) and Silicon Compounds, 1. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-004-01007.

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Jiang, G. J., Y. Wang, and Z. X. Yu. "Palladium-Catalyzed Asymmetric [3 + 2] Trimethylenemethane Cycloaddition Reactions." In Stereoselective Pericyclic Reactions, Cross Coupling, and C—H and C—X Activation, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-203-00029.

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Jiang, G. J., Y. Wang, and Z. X. Yu. "Phosphine-Catalyzed [3 + 2]-Cycloaddition Reactions of Allenoates with Dienophiles." In Stereoselective Pericyclic Reactions, Cross Coupling, and C—H and C—X Activation, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-203-00023.

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Jiang, G. J., Y. Wang, and Z. X. Yu. "Cycloaddition Reactions Catalyzed by Planar-Chiral 2-Phospha[3]ferrocenophanes." In Stereoselective Pericyclic Reactions, Cross Coupling, and C—H and C—X Activation, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-203-00027.

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Sarma, Diganta, Jasmin Sultana, Roktopol Hazarika, and Bidyutjyoti Dutta. "Basic Ionic Liquid Catalyzed Cycloaddition Reactions for the Synthesis of 1, 2, 3-Triazoles." In Advances in Organic Synthesis, 379–417. BENTHAM SCIENCE PUBLISHERS, 2021. http://dx.doi.org/10.2174/9789814998482121150008.

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Conference papers on the topic "Copper-catalyzed 3+2 cycloaddition"

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Ramasami, Ponnadurai, Hanusha Bhakhoa, and Lydia Rhyman. "Copper(I) Catalyzed [3+2] Cycloaddition Reaction with Mechanistic Disparity: A DFT Study." In The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-e017.

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