Log in

Relevant bibliographies by topics / Azide-alkyne cycloaddition / Journal articles

To see the other types of publications on this topic, follow the link: Azide-alkyne cycloaddition.

Journal articles on the topic 'Azide-alkyne cycloaddition'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Azide-alkyne cycloaddition.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Cormier, 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 text

Abstract:

A cycloheptyne dicobalt-carbonyl complex with a terminal alkyne was synthesized by a short procedure, and was able to react selectively in Strain Promoted Alkyne Azide Cycloaddition (SPAAC) or Copper Catalysed Alkyne Azide Cycloaddition (CuAAC) depending on the conditions.

APA, Harvard, Vancouver, ISO, and other styles

2

Chen, Ping-Fan, Kung-Kai Kuo, Jaya Kishore Vandavasi, Siva Senthil Kumar Boominathan, Chung-Yu Chen, and Jeh-Jeng Wang. "Metal-free cycloaddition to synthesize naphtho[2,3-d][1,2,3]triazole-4,9-diones." Organic & Biomolecular Chemistry 13, no. 35 (2015): 9261–66. http://dx.doi.org/10.1039/c5ob01322d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Ohata, Jun, Farrukh Vohidov, and Zachary T. Ball. "Convenient analysis of protein modification by chemical blotting with fluorogenic “click” reagents." Molecular BioSystems 11, no. 11 (2015): 2846–49. http://dx.doi.org/10.1039/c5mb00510h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Kore, Nitin, and Pavel Pazdera. "New Stable Cu(I) Catalyst Supported on Weakly Acidic Polyacrylate Resin for “Click” Chemistry: Synthesis of 1,2,3-Triazole and Novel Synthesis of 1,2,3-Triazol-5-amine." Current Organic Synthesis 15, no. 4 (June 12, 2018): 552–65. http://dx.doi.org/10.2174/1570179415666180110152642.

Full text

Abstract:

Aim and Objective: The aim of our work is to demonstrate catalytic application of our previously reported simple Cu(I) ion supported on weakly acidic polyacrylate resin for Azide-Alkyne cycloaddition (CuAAC), Azide-Nitrile cycloaddition and in synthesis of 1-azido-4-methoxybenzene. Material and Method: To investigate the catalytic ability of title Cu(I) catalyst we performed the reaction of different aryl azide with a broader spectrum of different terminal alkyne and nitrile compounds. Results: The title supported Cu(I) catalyzes cycloaddition reactions of aryl azide with aliphatic, aromatic, and heterocyclic terminal alkynes and corresponding 1,4-disubstituted 1,2,3-triazoles were obtained almost in the quantitative yields. The cycloaddition reactions of aryl azide with nitriles consisting α-hydrogen on carbon attached to cyano group under catalytic action of the title supported Cu(I) ended up with the formation of 1,4- disubstituted 1,2,3-triazol-5-amines in quantitative yields. The title catalyst found to be active for nucleophilic substitution of aide group (-N3) to 4-Iodoanisole. Conclusion: It was found that both studied Azide-Alkyne cycloaddition and Azide-Nitrile cycloaddition syntheses are regioselective and quantitative in yield. The title catalyst used is economical, easily preparable, separable, and recyclable. Therefore, the studied syntheses may be regarded as environmentally clean and green processes.

APA, Harvard, Vancouver, ISO, and other styles

5

Fürniss, Daniel, Timo Mack, Frank Hahn, Sidonie B. L. Vollrath, Katarzyna Koroniak, Ute Schepers, and Stefan Bräse. "Peptoids and polyamines going sweet: Modular synthesis of glycosylated peptoids and polyamines using click chemistry." Beilstein Journal of Organic Chemistry 9 (January 10, 2013): 56–63. http://dx.doi.org/10.3762/bjoc.9.7.

Full text

Abstract:

Sugar moieties are present in a wide range of bioactive molecules. Thus, having versatile and fast methods for the decoration of biomimetic molecules with sugars is of fundamental importance. The glycosylation of peptoids and polyamines as examples of such biomimetic molecules is reported here. The method uses Cu-catalyzed azide alkyne cycloaddition to promote the reaction of azidosugars with either polyamines or peptoids. In addition, functionalized nucleic acids were attached to polyamines via the same route. Based on a modular solid-phase synthesis of peralkynylated peptoids with up to six alkyne groups, the latter were modified with azidosugar building blocks by using copper-catalyzed azide alkyne cycloadditions. In addition, the up-scaling of some particular azide-modified sugars is described.

APA, Harvard, Vancouver, ISO, and other styles

6

Meldal, Morten, and Christian Wenzel Tornøe. "Cu-Catalyzed Azide−Alkyne Cycloaddition." Chemical Reviews 108, no. 8 (August 2008): 2952–3015. http://dx.doi.org/10.1021/cr0783479.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Hema, Kuntrapakam, and Kana M. Sureshan. "Topochemical Azide–Alkyne Cycloaddition Reaction." Accounts of Chemical Research 52, no. 11 (October 10, 2019): 3149–63. http://dx.doi.org/10.1021/acs.accounts.9b00398.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Stone, M. Rhia L., Muriel Masi, Wanida Phetsang, Jean-Marie Pagès, Matthew A. Cooper, and Mark A. T. Blaskovich. "Fluoroquinolone-derived fluorescent probes for studies of bacterial penetration and efflux." MedChemComm 10, no. 6 (2019): 901–6. http://dx.doi.org/10.1039/c9md00124g.

Full text

Abstract:

Fluorescent probes derived from the fluoroquinolone antibiotic ciprofloxacin were synthesised using a Cu(i)-catalysed azide–alkyne cycloaddition (CuAAC) to link a ciprofloxacin azide derivative with alkyne-substituted green and blue fluorophores.

APA, Harvard, Vancouver, ISO, and other styles

9

Nierengarten, Jean-François. "Copper-catalyzed alkyne-azide cycloaddition for the functionalization of fullerene building blocks." Pure and Applied Chemistry 84, no. 4 (December 14, 2011): 1027–37. http://dx.doi.org/10.1351/pac-con-11-08-21.

Full text

Abstract:

In this paper, we report our ongoing progress in the preparation of fullerene-azide or fullerene-alkyne building blocks, allowing their further chemical transformation under the copper-catalyzed alkyne-azide cycloaddition (CuAAC) reaction conditions.

APA, Harvard, Vancouver, ISO, and other styles

10

Wendler, Felix, Tobias Rudolph, Helmar Görls, Nils Jasinski, Vanessa Trouillet, Christopher Barner-Kowollik, and Felix H. Schacher. "Maleimide-functionalized poly(2-ethyl-2-oxazoline): synthesis and reactivity." Polymer Chemistry 7, no. 13 (2016): 2419–26. http://dx.doi.org/10.1039/c6py00033a.

Full text

Abstract:

Poly(2-ethyl-2-oxazoline)s end-functionalized with a maleimide moiety were prepared from azide-terminated PEtOx_x-N₃viacopper-catalyzed azide–alkyne cycloaddition (CuAAC) with an alkyne-bearing maleimide (MI).

APA, Harvard, Vancouver, ISO, and other styles

11

Yan, Yan-Mei, Hao-Yang Li, Min Zhang, Rong-Xin Wang, Chen-Guang Zhou, Zhen-Xing Ren, and Ming-Wu Ding. "One-Pot Synthesis of [1,2,3]Triazolo[1,5-a]quinoxalin-4(5H)-ones by a Metal-Free Sequential Ugi-4CR/Alkyne–Azide Cycloaddition Reaction." Synlett 31, no. 01 (November 25, 2019): 73–76. http://dx.doi.org/10.1055/s-0037-1610737.

Full text

Abstract:

A convenient and one-pot approach to prepare [1,2,3]triazolo[1,5-a]quinoxalin-4(5H)-ones by a metal-free sequential Ugi-4CR/alkyne–azide cycloaddition reaction has been developed. The reaction of 2-azidobenzenamines, aldehydes, propiolic acids, and isocyanides produced the Ugi adducts, which were transformed to the [1,2,3]triazolo[1,5-a]quinoxalin-4(5H)-ones in moderate to good yields via alkyne–azide cycloaddition reaction.

APA, Harvard, Vancouver, ISO, and other styles

12

Colliat-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 text

Abstract:

We report the synthesis of poly(1,2,3-triazolium ionic liquid)s by the polyaddition of α-azide-ω-alkyne monomers with short n-hexyl and diethylene glycol spacers by both copper(I)-catalyzed and thermal Huisgen azide–alkyne 1,3-dipolar cycloaddition.

APA, Harvard, Vancouver, ISO, and other styles

13

Fong, Darryl, Grace M. Andrews, and Alex Adronov. "Functionalization of polyfluorene-wrapped carbon nanotubes via copper-mediated azide–alkyne cycloaddition." Polymer Chemistry 9, no. 21 (2018): 2873–79. http://dx.doi.org/10.1039/c8py00377g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Sibbersen, Christian, Lennart Lykke, Niels Gregersen, Karl Anker Jørgensen, and Mogens Johannsen. "A cleavable azide resin for direct click chemistry mediated enrichment of alkyne-labeled proteins." Chem. Commun. 50, no. 81 (2014): 12098–100. http://dx.doi.org/10.1039/c4cc05246c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Anancharoenwong, Ekasit, Jean Francois Pilard, Irène Campistron, Albert Laguerre, Frédéric Gohier, and Sophie Bistac. " Preparation of New Polyols Based on Cis-1,4-Polyisoprene by Using 1,3-Dipolar Cycloaddition." Advanced Materials Research 844 (November 2013): 381–84. http://dx.doi.org/10.4028/www.scientific.net/amr.844.381.

Full text

Abstract:

This research focuses on synthesis and modification of polyol precursors derived from cis-1,4-polyisoprene (PI). These new polyol precursors can be converted to high value-added polyurethane (PU). The epoxidized hydroxytelechelic PI (EHTPI) prepared by chemical modification from PI was used as starting material for polyol synthesis. 1,3-Dipolar cycloaddition between a terminal alkyne and an azide has rapidly become the most popular click reaction. We applied this reaction to couple azide-functionalized PI and alkyne-functionalized sugar for preparing polyols. For azide functionalization, 1-methyl epoxidized cyclohexane was used as a model molecule, and various conditions for epoxide ring opening of 1-methyl epoxidized cyclohexane and EHTPI were investigated. The cycloaddition of alkyne and azide was carried out in the presence of sodium ascorbate and copper sulfate. The polyol precursors obtained might be used to prepare biodegradable polyol PU.

APA, Harvard, Vancouver, ISO, and other styles

16

Göbel, 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 text

Abstract:

Herein, we present a facile synthesis of three azide-functionalized fluorophores and their covalent attachment as triazoles in Huisgen-type cycloadditions with model alkynes. Besides two ortho- and para-bromo-substituted benzaldehydes, the azide functionalization of a fluorene-based structure will be presented. The copper(I)-catalyzed azide–alkyne cycloaddition (CuAAC) of the so-synthesized azide-functionalized bromocarbaldehydes with terminal alkynes, exhibiting different degrees of steric demand, was performed in high efficiency. Finally, we investigated the photophysical properties of the azide-functionalized arenes and their covalently linked triazole derivatives to gain deeper insight towards the effect of these covalent linkers on the emission behavior.

APA, Harvard, Vancouver, ISO, and other styles

17

Vanhaecht, Stef, Jeroen Jacobs, Luc Van Meervelt, and Tatjana N. Parac-Vogt. "A versatile and highly efficient post-functionalization method for grafting organic molecules onto Anderson-type polyoxometalates." Dalton Transactions 44, no. 44 (2015): 19059–62. http://dx.doi.org/10.1039/c5dt03559g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Svete, 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.

Full text

Abstract:

Although the first example of copper-catalyzed azomethine imine–alkyne cycloaddition (CuAIAC) was published only a year after the seminal papers of Meldal and Sharpless on Cu-catalyzed azide–alkyne cycloaddition (CuAAC), the CuAIAC reaction has remained overlooked by the synthetic community for almost a decade. Since 2010, however, CuAIAC reaction started to emerge as a promising supplement to the well-known CuAAC reaction. The present review surveys primarily the literature on CuAIAC reaction since 2003. Beside this, azomethine imine–alkyne cycloadditions catalyzed by other metals, selected examples of metal-free reactions, and related [3+3] and [3+4] cycloadditions of azomethine imines are presented. All these experimental data indicate the viability of CuAIAC in organic synthesis and the applicability in ‘click’ chemistry.1 Introduction2 Reactions with Acyclic Azomethine Imines3 Reactions with C,N-Cyclic Azomethine Imines4 Reactions with N,N-Cyclic Azomethine Imines5 Reactions with C,N,N-Cyclic Azomethine Imines6 The Mechanism of the CuAIAC Reaction7 Conclusions and Outlook

APA, Harvard, Vancouver, ISO, and other styles

19

Ma, 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 text

Abstract:

The kinetic performance of a spacer-controlled Huisgen azide–alkyne cycloaddition reaction for alkyne-bearing reactive cycloalkane plasticizers is explored in combination with the computational protocol.

APA, Harvard, Vancouver, ISO, and other styles

20

Taher, Abu, Debkumar Nandi, Rafique Ul Islam, Meenakshi Choudhary, and Kaushik Mallick. "Microwave assisted azide–alkyne cycloaddition reaction using polymer supported Cu(i) as a catalytic species: a solventless approach." RSC Advances 5, no. 59 (2015): 47275–83. http://dx.doi.org/10.1039/c5ra04490a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Cai, Xuekang, Dan Wang, Yasi Gao, Long Yi, Xing Yang, and Zhen Xi. "Tetra-fluorinated aromatic azide for highly efficient bioconjugation in living cells." RSC Advances 9, no. 1 (2019): 23–26. http://dx.doi.org/10.1039/c8ra09303b.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Haldón, Estela, M. Carmen Nicasio, and Pedro J. Pérez. "Copper-catalysed azide–alkyne cycloadditions (CuAAC): an update." Organic & Biomolecular Chemistry 13, no. 37 (2015): 9528–50. http://dx.doi.org/10.1039/c5ob01457c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Moon, Jeongbin, In-Seong Jo, Jeong Hoon Yoon, Yeongha Kim, Joon Suk Oh, David J. Pine, and Gi-Ra Yi. "DNA functionalization of colloidal particles via physisorption of azide-functionalized diblock copolymers." Soft Matter 15, no. 35 (2019): 6930–33. http://dx.doi.org/10.1039/c9sm01243e.

Full text

Abstract:

DNA-coated colloids are prepared simply by physical adsorption of azide-functionalized amphiphilic diblock copolymers onto hydrophobic inorganic particles, followed by strain-promoted azide–alkyne cycloaddition (SPAAC) reaction.

APA, Harvard, Vancouver, ISO, and other styles

24

Engel, Annikka, Eike Dornsiepen, and Stefanie Dehnen. "Click reactions and intramolecular condensation reactions on azido-adamantyl-functionalized tin sulfide clusters." Inorganic Chemistry Frontiers 6, no. 8 (2019): 1973–76. http://dx.doi.org/10.1039/c9qi00424f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Amgarten, Beatrice, Rakesh Rajan, Nuria Martínez-Sáez, Bruno L. Oliveira, Inês S. Albuquerque, Roger A. Brooks, David G. Reid, Melinda J. Duer, and Gonçalo J. L. Bernardes. "Collagen labelling with an azide-proline chemical reporter in live cells." Chemical Communications 51, no. 25 (2015): 5250–52. http://dx.doi.org/10.1039/c4cc07974d.

Full text

Abstract:

Biosynthetic incorporation of an azide-proline chemical reporter into collagen allows selective imaging in live foetal ovine osteoblasts using a strain-promoted [3+2] azide–alkyne cycloaddition reaction.

APA, Harvard, Vancouver, ISO, and other styles

26

Lis, Christian, and Thorsten Berg. "Synthesis of TRIPCO: A New Cyclooctyne for iSPAAC." Synlett 30, no. 08 (April 10, 2019): 939–42. http://dx.doi.org/10.1055/s-0037-1611481.

Full text

Abstract:

Strain-promoted azide–alkyne cycloadditions (SPAAC) are widely used for labeling azide-functionalized biomolecules in living cells but create mixtures of isomeric triazoles. We recently expanded the scope of SPAAC to the isomer-free generation of large functional molecules in living cells by designing the symmetrical pyrrolocyclooctynes PYRROC and SYPCO, which do not form isomers in SPAAC. Here, we present the synthesis and kinetic characterization of the cyclooctyne TRIPCO as a new reagent for isomer-free SPAAC (iSPAAC). TRIPCO was found to react faster than PYRROC and SYPCO in the [3+2] cycloaddition with benzyl azide.

APA, Harvard, Vancouver, ISO, and other styles

27

Surya Prakash Rao, H., and Guravaiah Chakibanda. "Raney Ni catalyzed azide-alkyne cycloaddition reaction." RSC Adv. 4, no. 86 (2014): 46040–48. http://dx.doi.org/10.1039/c4ra07057g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Lauer, Milena Helmer, Charlotte Vranken, Jochem Deen, Wout Frederickx, Willem Vanderlinden, Nathaniel Wand, Volker Leen, Marcelo H. Gehlen, Johan Hofkens, and Robert K. Neely. "Methyltransferase-directed covalent coupling of fluorophores to DNA." Chemical Science 8, no. 5 (2017): 3804–11. http://dx.doi.org/10.1039/c6sc04229e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Pérez, Juana M., Rafael Cano, and Diego J. Ramón. "Multicomponent azide–alkyne cycloaddition catalyzed by impregnated bimetallic nickel and copper on magnetite." RSC Adv. 4, no. 46 (2014): 23943–51. http://dx.doi.org/10.1039/c4ra03149k.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Saikia, Bhaskar Jyoti, and Swapan Kumar Dolui. "Preparation and characterization of an azide–alkyne cycloaddition based self-healing system via a semiencapsulation method." RSC Advances 5, no. 112 (2015): 92480–89. http://dx.doi.org/10.1039/c5ra17666b.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Liu, Xueping, Ying Wu, Minghui Zhang, and Ke Zhang. "Efficient polymer dimerization method based on self-accelerating click reaction." RSC Advances 10, no. 12 (2020): 6794–800. http://dx.doi.org/10.1039/c9ra09919k.

Full text

Abstract:

A convenient and efficient method was developed to prepare topological polymers with a symmetric molecular structure by dimerizing azide terminated polymers based on the self-accelerating double strain-promoted azide–alkyne cycloaddition reaction.

APA, Harvard, Vancouver, ISO, and other styles

32

Zhai, Wenlei, Louise Male, and John S. Fossey. "Glucose selective bis-boronic acid click-fluor." Chemical Communications 53, no. 14 (2017): 2218–21. http://dx.doi.org/10.1039/c6cc08534b.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Guo, Yuan-Yang, Bo Zhang, Luying Wang, Shenlong Huang, Shilei Wang, Yanbo You, Gongming Zhu, Anlian Zhu, Mingwei Geng, and Lingjun Li. "An efficient and easily-accessible ligand for Cu(i)-catalyzed azide–alkyne cycloaddition bioconjugation." Chemical Communications 56, no. 92 (2020): 14401–3. http://dx.doi.org/10.1039/d0cc06348g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

El Malah, Tamer, Randa E. Abdel Mageid, Hanem M. Awad, and Hany F. Nour. "Copper(i)-catalysed azide–alkyne cycloaddition and antiproliferative activity of mono- and bis-1,2,3-triazole derivatives." New Journal of Chemistry 44, no. 42 (2020): 18256–63. http://dx.doi.org/10.1039/d0nj04308g.

Full text

Abstract:

A series of mono- and bis-1,2,3-triazole derivatives were prepared via the copper(i)-catalysed azide–alkyne cycloaddition between substituted aromatic derivatives, comprising one or two terminal alkyne groups and a selection of aromatic azides.

APA, Harvard, Vancouver, ISO, and other styles

35

Chauhan, Rohit Singh, Dhvani Oza, Seema Yadav, Chandrakanta Dash, Alexandra M. Z. Slawin, and Neelam Shivran. "Copper complexes of arylselenolate-based ligands: synthesis and catalytic activity in azide–alkyne cycloaddition reactions." New Journal of Chemistry 43, no. 5 (2019): 2381–88. http://dx.doi.org/10.1039/c8nj04602f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Lim, Minkyung, Heejin Lee, Minseok Kang, Woncheol Yoo, and Hakjune Rhee. "Azide–alkyne cycloaddition reactions in water via recyclable heterogeneous Cu catalysts: reverse phase silica gel and thermoresponsive hydrogels." RSC Advances 8, no. 11 (2018): 6152–59. http://dx.doi.org/10.1039/c8ra00306h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Weterings, Jimmy, Cristianne J. F. Rijcken, Harald Veldhuis, Tommi Meulemans, Darya Hadavi, Matt Timmers, Maarten Honing, Hans Ippel, and Rob M. J. Liskamp. "TMTHSI, a superior 7-membered ring alkyne containing reagent for strain-promoted azide–alkyne cycloaddition reactions." Chemical Science 11, no. 33 (2020): 9011–16. http://dx.doi.org/10.1039/d0sc03477k.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Sun, Jiarui, Xiangsheng Cheng, John Kamanda Mansaray, Weihong Fei, Jieping Wan, and Weijun Yao. "A copper-catalyzed three component reaction of aryl acetylene, sulfonyl azide and enaminone to form iminolactone via 6π electrocyclization." Chemical Communications 54, no. 99 (2018): 13953–56. http://dx.doi.org/10.1039/c8cc06868b.

Full text

Abstract:

We developed a copper-catalyzed three component reaction of aryl acetylene, enaminone and sulfonyl azide to construct iminolactone via copper-catalyzed alkyne–azide cycloaddition (CuAAC), Michael addition of metalated ketenimine followed by elimination and 6π electrocyclization.

APA, Harvard, Vancouver, ISO, and other styles

39

Zhai, Wenlei, Brette M. Chapin, Akina Yoshizawa, Hui-Chen Wang, Stephen A. Hodge, Tony D. James, Eric V. Anslyn, and John S. Fossey. "“Click-fluors”: triazole-linked saccharide sensors." Organic Chemistry Frontiers 3, no. 8 (2016): 918–28. http://dx.doi.org/10.1039/c6qo00171h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Rachel, N. M., and J. N. Pelletier. "One-pot peptide and protein conjugation: a combination of enzymatic transamidation and click chemistry." Chemical Communications 52, no. 12 (2016): 2541–44. http://dx.doi.org/10.1039/c5cc09163b.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Kakuta, T., T. Yamagishi, and T. Ogoshi. "Supramolecular chemistry of pillar[n]arenes functionalised by a copper(i)-catalysed alkyne–azide cycloaddition “click” reaction." Chemical Communications 53, no. 38 (2017): 5250–66. http://dx.doi.org/10.1039/c7cc01833a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Pathigoolla, Atchutarao, and Kana M. Sureshan. "The topochemical synthesis of triazole-linked homobasic DNA." Chemical Communications 52, no. 5 (2016): 886–88. http://dx.doi.org/10.1039/c5cc08834h.

Full text

Abstract:

Triazolyl-DNA (^TLDNA), DNA wherein phosphodiester units are replaced by triazole units, is of great interest. By adopting Topochemical Azide–Alkyne Cycloaddition (TAAC) reaction, we have synthesized homobasic ^TLDNA oligomers. 5′-ethynyl-3′-azido-2′,3′,5′-tri-deoxycytosine, which crystallized with proximal placement of azide and alkyne units of adjacent molecules, underwent TAAC reaction to ^TLDNA oligomers.

APA, Harvard, Vancouver, ISO, and other styles

43

Vernekar, Sanjeev Kumar V., Li Qiu, Jeana Zacharias, Robert J. Geraghty, and Zhengqiang Wang. "Synthesis and antiviral evaluation of 4′-(1,2,3-triazol-1-yl)thymidines." Med. Chem. Commun. 5, no. 5 (2014): 603–8. http://dx.doi.org/10.1039/c4md00039k.

Full text

Abstract:

The Cu(i)-catalyzed azide–alkyne cycloaddition (CuAAC) of 4′-azidothymidine (5) generated a series of 1,2,3-triazole analogues (9) with moderate anti-HIV activities, while a similar cycloaddition reaction catalyzed by Ru(ii) failed.

APA, Harvard, Vancouver, ISO, and other styles

44

Tian, He, Thomas P. Sakmar, and Thomas Huber. "A simple method for enhancing the bioorthogonality of cyclooctyne reagent." Chemical Communications 52, no. 31 (2016): 5451–54. http://dx.doi.org/10.1039/c6cc01321j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Husain, Ali A., and Kirpal S. Bisht. "Synthesis of a novel resorcin[4]arene–glucose conjugate and its catalysis of the CuAAC reaction for the synthesis of 1,4-disubstituted 1,2,3-triazoles in water." RSC Advances 9, no. 18 (2019): 10109–16. http://dx.doi.org/10.1039/c9ra00972h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Islam, Rafique Ul, Abu Taher, Meenakshi Choudhary, Michael J. Witcomb, and Kaushik Mallick. "A polymer supported Cu(i) catalyst for the ‘click reaction’ in aqueous media." Dalton Transactions 44, no. 3 (2015): 1341–49. http://dx.doi.org/10.1039/c4dt02962c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Baldassari, Lucas L., Eduardo A. Cechinatto, and Angélica V. Moro. "Triple copper catalysis for the synthesis of vinyl triazoles." Green Chemistry 21, no. 13 (2019): 3556–60. http://dx.doi.org/10.1039/c9gc01066a.

Full text

Abstract:

Herein, we report our studies on the synthesis of vinyl 1,2,3-triazoles through a one-pot sequence, enabled by the same copper catalyst, of three different reactions: hydroboration involving an alkyne, azidation for a vinyl boronate and azide–alkyne cycloaddition.

APA, Harvard, Vancouver, ISO, and other styles

48

Post, Elias A. J., Andrew J. Bissette, and Stephen P. Fletcher. "Self-reproducing micelles coupled to a secondary catalyst." Chemical Communications 54, no. 63 (2018): 8777–80. http://dx.doi.org/10.1039/c8cc02136h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Gu, Lingyue, Kévin Renault, Anthony Romieu, Jean-Alexandre Richard, and Rajavel Srinivasan. "Synthesis and spectral properties of 6′-triazolyl-dihydroxanthene-hemicyanine fused near-infrared dyes." New Journal of Chemistry 44, no. 28 (2020): 12208–15. http://dx.doi.org/10.1039/d0nj01724h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Liu, Xifeng, Ping Gong, Pengfei Song, Feng Xie, A. Lee Miller II, Shigao Chen, and Lichun Lu. "Fast functionalization of ultrasound microbubbles using strain promoted click chemistry." Biomaterials Science 6, no. 3 (2018): 623–32. http://dx.doi.org/10.1039/c8bm00004b.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!