Academic literature on the topic 'Microwave-assisted click reaction'

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

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Microwave-assisted click reaction.'

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.

Journal articles on the topic "Microwave-assisted click reaction"

1

Munteanu, Maricica, SooWhan Choi, and Helmut Ritter. "Cyclodextrin Methacrylate via Microwave-Assisted Click Reaction." Macromolecules 41, no. 24 (December 23, 2008): 9619–23. http://dx.doi.org/10.1021/ma8018975.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Yamamura, Hatsuo, Kana Isshiki, Yusuke Fujita, Hisato Kato, Takashi Katsu, Kazufumi Masuda, Kayo Osawa, and Atsushi Miyagawa. "Gramicidin S-inspired antimicrobial cyclodextrin to disrupt gram-negative and gram-positive bacterial membranes." MedChemComm 10, no. 8 (2019): 1432–37. http://dx.doi.org/10.1039/c9md00229d.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Halwale, Amool, and B. Yadagiri. "Microwave Assisted Synthesis of Benzoxazole-Triazole Hybrid Derivatives as Antimicrobial Agents." Asian Journal of Chemistry 34, no. 4 (2022): 1015–20. http://dx.doi.org/10.14233/ajchem.2022.23546.

Full text
Abstract:
A series of new 1,3-benzoxazole based 1,2,3-triazoles compounds were synthesized using click reaction under conventional and microwave irradiation methods. The microwave irradiation method gave higher yields, shorter reaction time as compared to conventional method using green solvents, eco-friendly reaction conditions. All the targeted compounds were characterized by IR, 1H, 13C NMR and mass spectral analysis. Furthermore, the titled compounds were screened for their in vitro antimicrobial activity against bacterial strains such as Staphylococcus aureus, Bacillus subtilis, Klebsiella pneumoniae and Escherichia coli as well as fungi such as Aspergillus niger, Aspergillus flavus and Fusarium oxysporum. Most of the compounds displayed good to excellent antimicrobial activity in comparison to standard drugs.
APA, Harvard, Vancouver, ISO, and other styles
4

Dharavath, Ravinder, Nalaparaju Nagaraju, M. Ram Reddy, D. Ashok, M. Sarasija, M. Vijjulatha, Vani T, K. Jyothi, and G. Prashanthi. "Microwave-assisted synthesis, biological evaluation and molecular docking studies of new coumarin-based 1,2,3-triazoles." RSC Advances 10, no. 20 (2020): 11615–23. http://dx.doi.org/10.1039/d0ra01052a.

Full text
Abstract:
Coumarin-based 1,4-disubstituted 1,2,3-triazole derivatives were synthesized using a highly efficient, eco-friendly protocol via a copper(i)-catalyzed click reaction between various substituted arylazides and terminal alkynes.
APA, Harvard, Vancouver, ISO, and other styles
5

Chavez-Acevedo, Lizbeth, and Luis D. Miranda. "Synthesis of novel tryptamine-based macrocycles using an Ugi 4-CR/microwave assisted click-cycloaddition reaction protocol." Organic & Biomolecular Chemistry 13, no. 15 (2015): 4408–12. http://dx.doi.org/10.1039/c5ob00067j.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Rijkers, Dirk T. S., G. Wilma van Esse, Remco Merkx, Arwin J. Brouwer, Hans J. F. Jacobs, Roland J. Pieters, and Rob M. J. Liskamp. "Efficient microwave-assisted synthesis of multivalent dendrimeric peptides using cycloaddition reaction (click) chemistry." Chemical Communications, no. 36 (2005): 4581. http://dx.doi.org/10.1039/b507975f.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Cintas, 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.

Full text
Abstract:
The Huisgen 1,3-dipolar cycloaddition of azides and acetylenes catalyzed by Cu(I) salts, leading to 1,2,3-triazoles, is one of the most versatile "click reactions". We have developed a series of optimized protocols and new applications of this reaction starting from several substrates, comparing heterogeneous vs homogeneous catalysis, conventional heating vs microwave irradiation or simultaneous microwave/ultrasound irradiation. Both non-conventional techniques strongly promoted the cycloaddition (bromide → azide → triazole), that could be conveniently performed in a one-pot procedure. This was feasible even with such bulky molecules as functionalized β-cyclodextrins (β-CD), starting from 61-O-tosyl-β-CD or from heptakis[6-O-(tert-butyldimethylsilyl)]-21-O-propargyl-β-CD. "Greener" heterogeneous catalysis with charcoal-supported Cu(II) or Cu(I) (prepared under ultrasound) was advantageously employed.
APA, Harvard, Vancouver, ISO, and other styles
8

Garska, Bernd, Monir Tabatabai, and Helmut Ritter. "Calix[4]arene-click-cyclodextrin and supramolecular structures with watersoluble NIPAAM-copolymers bearing adamantyl units: “Rings on ring on chain”." Beilstein Journal of Organic Chemistry 6 (August 5, 2010): 784–88. http://dx.doi.org/10.3762/bjoc.6.83.

Full text
Abstract:
We describe the calixarene-cyclodextrin-coupling via click reaction starting from 5,11,17,23-tetra-tert-butyl-25,27-dipropargylether-26,28-hydroxy-calix[4]arene (calix[4]arene-dipropargylether) (2) onto 6I-azido-6I-deoxycyclomaltoheptaose (3) under microwave assisted conditions. The coupling was proven by MALDI-TOF mass spectrometry, 1H NMR and IR-spectroscopy. The pH dependent supramolecular complex formation with poly(NIPAAM) bearing attached adamantyl units was investigated by dynamic light scattering (DLS) and turbidity measurements.
APA, Harvard, Vancouver, ISO, and other styles
9

Yan, Lesan, Jianxun Ding, Ruogu Qi, Lixin Yang, Xiuli Hu, Yubin Huang, and Xiabin Jing. "Versatile synthesis of functional biodegradable polymers by ring-opening polymerization and microwave-assisted click reaction." Journal of Controlled Release 152 (November 2011): e249-e250. http://dx.doi.org/10.1016/j.jconrel.2011.09.042.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Librando, Ivy L., Abdallah G. Mahmoud, Sónia A. C. Carabineiro, M. Fátima C. Guedes da Silva, Carlos F. G. C. Geraldes, and Armando J. L. Pombeiro. "Synthesis of a Novel Series of Cu(I) Complexes Bearing Alkylated 1,3,5-Triaza-7-phosphaadamantane as Homogeneous and Carbon-Supported Catalysts for the Synthesis of 1- and 2-Substituted-1,2,3-triazoles." Nanomaterials 11, no. 10 (October 13, 2021): 2702. http://dx.doi.org/10.3390/nano11102702.

Full text
Abstract:
The N-alkylation of 1,3,5-triaza-7-phosphaadamantane (PTA) with ortho-, meta- and para-substituted nitrobenzyl bromide under mild conditions afforded three hydrophilic PTA ammonium salts, which were used to obtain a new set of seven water-soluble copper(I) complexes. The new compounds were fully characterized and their catalytic activity was investigated for the low power microwave assisted one-pot azide–alkyne cycloaddition reaction in homogeneous aqueous medium to obtain disubstituted 1,2,3-triazoles. The most active catalysts were immobilized on activated carbon (AC), multi-walled carbon nanotubes (CNT), as well as surface functionalized AC and CNT, with the most efficient support being the CNT treated with nitric acid and NaOH. In the presence of the immobilized catalyst, several 1,4-disubstituted-1,2,3-triazoles were obtained from the reaction of terminal alkynes, organic halides and sodium azide in moderate yields up to 80%. Furthermore, the catalyzed reaction of terminal alkynes, formaldehyde and sodium azide afforded 2-hydroxymethyl-2H-1,2,3-triazoles in high yields up to 99%. The immobilized catalyst can be recovered and recycled through simple workup steps and reused up to five consecutive cycles without a marked loss in activity. The described catalytic systems proceed with a broad substrate scope, under microwave irradiation in aqueous medium and according to “click rules”.
APA, Harvard, Vancouver, ISO, and other styles

Dissertations / Theses on the topic "Microwave-assisted click reaction"

1

D'Ercole, Annunziata. "Development and scale-up of synthetic strategies for exotic macrocyclisation to increase druggability of peptides as active pharmaceutical ingredients of industrial interest." Doctoral thesis, 2022. http://hdl.handle.net/2158/1264636.

Full text
Abstract:
In the framework of the PhD project of industrial interest, I have been involved in the development and optimization of synthetic procedures to obtain peptides of pharmaceutical interest, both on the laboratory scale and for the industrial production, in the context of the University-Industry Joint Laboratory PeptFarm of the University of Florence. This research develops through two parallel lines. The former is related to the development of a multigram, scalable cGMP-compliant MW-SP synthetic approach for the manufacture of the cyclic peptide Active Pharmaceutical Ingredient Eptifibatide acetate. Additionally, an alternative, patentable synthetic approach has been developed to overcome patent restrictions. On the other hand, the development of an efficient synthetic strategy for the preparation of a library of stapled peptides of pre-clinical interest derived from relaxin hormone was performed, aiming to investigate their biological role. Moreover, the feasibility of an oral administration of serelaxin gastroprotected formulations were investigated. According to the industrial perspective on research needs and opportunities in manufacturing, automation of as many steps as possible within an industrial production frame is pivotal to guarantee safety requirements. Solid-phase strategies are considered methods of election for medium-length peptide syntheses not only at the research scale but for large-scale production, as well. The possibility to use microwave-assisted technology on the large scale recently introduced, prompted us to evaluate the possibility to conveniently set-up a safe and fully cGMP-compliant pilot process to produce Eptifibatide acetate Active Pharmaceutical Ingredients (API), a generic hexapeptide, characterized by a single disulfide bridge. We investigated strategies based on the use of the microwave-assisted solid-phase peptide synthesis (MW-SPPS), by the use of a DIC/Oxyma Pure coupling protocol at 90 °C. This fully automated technology, previously accessible only at R&D level, has been recently made available also for the large-scale manufacturing of peptide APIs, taking constantly into account 6 the cost-effectiveness and dangerousness of each procedure. Accordingly, we developed an optimized process at the laboratory scale (1-5 mmol), which was subsequently successfully scaled-up to 70 mmol, obtaining all the information required by regulatory agencies to validate the process and qualify the pilot-scale plant. The process consists of 5 steps: 1) automated microwave-assisted solid phase synthesis of Eptifibatide linear precursor; 2) cleavage from the resin with concomitant amino acid side-chains deprotection; 3) disulfide-bond formation in solution; 4) purification by flash column chromatography; 5) ion-exchange solid phase extraction. Since the direct scale-up of a kg-scale, cGMP compliant peptide API production procedure is a challenge that requires an accurate understanding of each involved step, we preliminary performed a quality management risk assessment, which enabled a smooth and effective achievement of a successful final result. Moreover, in our optimization process, a reduction in time, solvents and waste have been obtained, ensuring compliance with the quality specifications, according to regulatory agencies requirements (FDA and EMA). Satisfactory results were obtained in terms of Eptifibatide acetate HPLC purity (99.6%) and Yield (22.1%). Additionally, the investigation of an alternative on-resin cyclization strategy for therapeutic peptide industrial production of Eptifibatide acetate has been carried out in parallel with the aim to develop a robust and economically competitive production process avoiding intermediate steps of isolation to preserve the recovery guaranteeing a GMPs quality product, to overcome patent restrictions. A scalable, fully automated approach performed entirely in the same reactor has been developed. We explored and compared four solid-phase disulfide formation approaches (A, B, C, D) between the C-terminal Cys and the N-terminal 3- Mercaptopropionic acid (MPA). These mainly differ one from each other for the final cyclization step, obtained by direct formation of an S-S disulfide bridge (strategies A-B) or via side-chain-to-tail amide bond formation (strategies C-D). Strategy D resulted the best one, thanks to the concomitant reduction of the Stert- butylthio (StBu) Cys protecting group (PG) and disulfide formation with the MPA reducing agent, enjoying the advantage of using an already qualified starting material. This strategy (D) represents an inventive (non-obvious) 7 strategy, (since we were the first to propose MPA to deprotect StBu on cysteine), which proposes for the first time to perform all the processes including disulfide bond formation in a single reactor (novelty), scalable on multigram-scale by Liberty Pro synthesizer (Industrial applicability). Therefore, according to the three patentability criteria required for a new production process: Novelty; inventive and industrial applicability, the present PhD work identifies a new patentable production process.1 In line with the synthesis of conformationally constraint relaxin derivatives, the present work describes the development of an innovative, efficient and reproducible MW-assisted Copper-Catalyzed Azide-Alkyne Cycloaddition (SP MW-CuAAC) performed on solid phase to prepare side-chain-to-side-chain clicked H1-relaxin single B-chain analogues, overcoming the several synthetic drawbacks (aggregation tendency and poor solubility) which hamper relaxins syntheses. All the relevant parameters, that are, resin (PEG-PS vs PS), solvent mixtures (H2O:t-BuOH:DCM 1:1:1, DMSO:DMF 1:2), catalytic system (CuBr vs CuSO4), microwave energy and reaction time were optimized using a systematic approach.2 Two generations of H1-relaxin single B-chain stapled analogues were obtained. First-generation (VR and VIR) and second-generation H1-relaxin single B-chain peptides (VII and VIIR; VIII and VIIIR; IX and IXR) were characterized by different lengths and different positions and orientations of the triazolyl ring, and were designed with the aim to stabilize the α-helix conformation and to expose the binding cassette motif. The α-helicity induced by the side-chain to side-chain stapling obtained was demonstrated by the circular dichroism (CD) performed both in phosphate buffer and in SDS micelle, thanks to the collaboration with Prof. A. Carotenuto (University of Naples Federico II). Moreover, in the frame of the collaboration with Prof. D. Bani (University of Florence) and Prof. A. Hossein (Institute of Neuroscience and Mental Health, University of Melbourne, Australia), H1-relaxin analogues were biologically tested, to verify binding to cells expressing the receptor RXFP1 and activity 8 through cAMP signaling pathway in HEK-293T cells stably expressing the RXFP1 receptor. Moreover, since the major challenge in the development of peptide drugs is to improve their oral bioavailability, we investigated the relative bio-potency of the intact serelaxin molecule (the recombinant form of human H2-relaxin) and the purified porcine one, in comparison with their proteolytic fragments, obtained after treatment with Simulated Intestinal Digestion Fluid (SIF). Signalling events downstream receptor activation in THP-1 human monocytic cells was measured.
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Microwave-assisted click reaction"

1

Rijkers, Dirk T. S., G. Wilma van Esse, Remco Merkx, Arwin J. Brouwer, Hans J. F. Jacobs, Roland J. Pieters, and Rob M. J. Liskamp. "Microwave-Assisted Synthesis of Multivalent Dendrimeric Peptides using Cycloaddition Reaction (‘Click’) Chemistry." In Understanding Biology Using Peptides, 152–53. New York, NY: Springer New York, 2006. http://dx.doi.org/10.1007/978-0-387-26575-9_60.

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!

To the bibliography