Статті в журналах з теми "Greener synthesis"
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Mooney, Madison, Audithya Nyayachavadi, and Simon Rondeau-Gagné. "Eco-friendly semiconducting polymers: from greener synthesis to greener processability." Journal of Materials Chemistry C 8, no. 42 (2020): 14645–64. http://dx.doi.org/10.1039/d0tc04085a.
Повний текст джерелаKharissova, Oxana V., H. V. Rasika Dias, Boris I. Kharisov, Betsabee Olvera Pérez, and Victor M. Jiménez Pérez. "The greener synthesis of nanoparticles." Trends in Biotechnology 31, no. 4 (April 2013): 240–48. http://dx.doi.org/10.1016/j.tibtech.2013.01.003.
Повний текст джерелаLawrenson, Stefan, Michael North, Fanny Peigneguy, and Anne Routledge. "Greener solvents for solid-phase synthesis." Green Chemistry 19, no. 4 (2017): 952–62. http://dx.doi.org/10.1039/c6gc03147a.
Повний текст джерелаPolshettiwar, Vivek, and Rajender S. Varma. "Greener and expeditious synthesis of bioactive heterocycles using microwave irradiation." Pure and Applied Chemistry 80, no. 4 (January 1, 2008): 777–90. http://dx.doi.org/10.1351/pac200880040777.
Повний текст джерелаJicsinszky, László, and Giancarlo Cravotto. "Toward a Greener World—Cyclodextrin Derivatization by Mechanochemistry." Molecules 26, no. 17 (August 27, 2021): 5193. http://dx.doi.org/10.3390/molecules26175193.
Повний текст джерелаLawrenson, Stefan B. "Greener solvents for solid-phase organic synthesis." Pure and Applied Chemistry 90, no. 1 (January 26, 2018): 157–65. http://dx.doi.org/10.1515/pac-2017-0505.
Повний текст джерелаBhardwaj, Brahamdutt, Pritam Singh, Arun Kumar, Sandeep Kumar, and Vikas Budhwar. "Eco-Friendly Greener Synthesis of Nanoparticles." Advanced Pharmaceutical Bulletin 10, no. 4 (August 9, 2020): 566–76. http://dx.doi.org/10.34172/apb.2020.067.
Повний текст джерелаKharissova, Oxana V., Boris I. Kharisov, César Máximo Oliva González, Yolanda Peña Méndez, and Israel López. "Greener synthesis of chemical compounds and materials." Royal Society Open Science 6, no. 11 (November 2019): 191378. http://dx.doi.org/10.1098/rsos.191378.
Повний текст джерелаGangurde, S. A., K. S. Laddha, and S. V. Joshi. "A GREENER APPROACH TO SYNTHESIS OF DIACEREIN." INDIAN DRUGS 56, no. 04 (April 28, 2019): 7–12. http://dx.doi.org/10.53879/id.56.04.11784.
Повний текст джерелаIravani, Siavash, and Rajender S. Varma. "Greener synthesis of lignin nanoparticles and their applications." Green Chemistry 22, no. 3 (2020): 612–36. http://dx.doi.org/10.1039/c9gc02835h.
Повний текст джерелаAmrillah, Tahta, Che Azurahanim Che Abdullah, Angga Hermawan, Fitri Nur Indah Sari, and Vani Novita Alvani. "Towards Greener and More Sustainable Synthesis of MXenes: A Review." Nanomaterials 12, no. 23 (December 1, 2022): 4280. http://dx.doi.org/10.3390/nano12234280.
Повний текст джерелаMartin, Vincent, Peter H. G. Egelund, Henrik Johansson, Sebastian Thordal Le Quement, Felix Wojcik, and Daniel Sejer Pedersen. "Greening the synthesis of peptide therapeutics: an industrial perspective." RSC Advances 10, no. 69 (2020): 42457–92. http://dx.doi.org/10.1039/d0ra07204d.
Повний текст джерелаIngle, Vilas, Amarsinha Gorepatil, Pratapsinha Gorepatil, Mahadev Gaikwad, and Akshay Ghumare. "PYRROLIDINE: AN EFFICIENT CATALYST FOR THE SYNTHESIS OF 2-ARYL-2, 3- DIHYDROQUINOLIN-4(1H)-ONE DERIVATIVES IN AQUEOUS ETHANOL MEDIA." Journal of Advanced Scientific Research 13, no. 04 (April 30, 2022): 41–44. http://dx.doi.org/10.55218/jasr.202213407.
Повний текст джерелаNasrollahzadeh, Mahmoud, Mohaddeseh Sajjadi, Siavash Iravani, and Rajender S. Varma. "Trimetallic Nanoparticles: Greener Synthesis and Their Applications." Nanomaterials 10, no. 9 (September 9, 2020): 1784. http://dx.doi.org/10.3390/nano10091784.
Повний текст джерелаKovács, Rita, Alajos Grün, Sándor Garadnay, István Greiner, and György Keglevich. "“Greener” synthesis of bisphosphonic/dronic acid derivatives." Green Processing and Synthesis 3, no. 2 (April 1, 2014): 111–16. http://dx.doi.org/10.1515/gps-2013-0107.
Повний текст джерелаKumari, N., D. Varandani, and B. R. Mehta. "Greener Synthesis of CZTS: Structural, KPFM studies." Materials Today: Proceedings 5, no. 11 (2018): 23281–85. http://dx.doi.org/10.1016/j.matpr.2018.11.061.
Повний текст джерелаCheng, Shuiming, Shengdong Zhu, Yuanxin Wu, Rui Chen, Ziniu Yu, and Xinya Zhang. "A GREENER SYNTHESIS TECHNOLOGY FOR LOMEFLOXACIN HYDROCHLORIDE." Chemical Engineering Communications 196, no. 8 (March 24, 2009): 901–5. http://dx.doi.org/10.1080/00986440902743794.
Повний текст джерелаRibeiro, M. Gabriela T. C., and Adélio A. S. C. Machado. "Metal−Acetylacetonate Synthesis Experiments: Which Is Greener?" Journal of Chemical Education 88, no. 7 (July 2011): 947–53. http://dx.doi.org/10.1021/ed100174f.
Повний текст джерелаAvalos, Martín, Reyes Babiano, Pedro Cintas, José L. Jiménez, and Juan C. Palacios. "Greener Media in Chemical Synthesis and Processing." Angewandte Chemie International Edition 45, no. 24 (June 12, 2006): 3904–8. http://dx.doi.org/10.1002/anie.200504285.
Повний текст джерелаSatheesh, A., H. Usha, D. S. Priya, A. V. L. N. H. Hariharan, and M. V. V. Ramanjaneyulu. "Greener Protocol for the Synthesis of Carbamates." Journal of Scientific Research 15, no. 2 (May 1, 2023): 481–88. http://dx.doi.org/10.3329/jsr.v15i2.60649.
Повний текст джерелаGhosh, Suman Kr, and Rajagopal Nagarajan. "Deep eutectic solvent mediated synthesis of quinazolinones and dihydroquinazolinones: synthesis of natural products and drugs." RSC Advances 6, no. 33 (2016): 27378–87. http://dx.doi.org/10.1039/c6ra00855k.
Повний текст джерелаLane, Mary Kate Mitchell, and Julie B. Zimmerman. "Controlling metal oxide nanoparticle size and shape with supercritical fluid synthesis." Green Chemistry 21, no. 14 (2019): 3769–81. http://dx.doi.org/10.1039/c9gc01619h.
Повний текст джерелаSantoro, Stefano, Juliano B. Azeredo, Vanessa Nascimento, Luca Sancineto, Antonio L. Braga, and Claudio Santi. "“The green side of the moon: ecofriendly aspects of organoselenium chemistry”." RSC Adv. 4, no. 60 (2014): 31521–35. http://dx.doi.org/10.1039/c4ra04493b.
Повний текст джерелаFerrazzano, Lucia, Martina Catani, Alberto Cavazzini, Giulia Martelli, Dario Corbisiero, Paolo Cantelmi, Tommaso Fantoni, et al. "Sustainability in peptide chemistry: current synthesis and purification technologies and future challenges." Green Chemistry 24, no. 3 (2022): 975–1020. http://dx.doi.org/10.1039/d1gc04387k.
Повний текст джерелаLi, Hengzhao, Yuntong Zhang, Zihan Yan, Zemin Lai, Ruoyan Yang, Mengqi Peng, Yanhao Sun, and Jie An. "Methanol as the C1 source: redox coupling of nitrobenzenes and alcohols for the synthesis of benzimidazoles." Green Chemistry 24, no. 2 (2022): 748–53. http://dx.doi.org/10.1039/d1gc03907e.
Повний текст джерелаTan, Long, Yufeng Zhou, Fuqiang Ren, Daniele Benetti, Fan Yang, Haiguang Zhao, Federico Rosei, Mohamed Chaker, and Dongling Ma. "Ultrasmall PbS quantum dots: a facile and greener synthetic route and their high performance in luminescent solar concentrators." Journal of Materials Chemistry A 5, no. 21 (2017): 10250–60. http://dx.doi.org/10.1039/c7ta01372h.
Повний текст джерелаDadhania, Harsh N., Dipak K. Raval, and Abhishek N. Dadhania. "Magnetically retrievable magnetite (Fe3O4) immobilized ionic liquid: an efficient catalyst for the preparation of 1-carbamatoalkyl-2-naphthols." Catalysis Science & Technology 5, no. 10 (2015): 4806–12. http://dx.doi.org/10.1039/c5cy00849b.
Повний текст джерелаKhatami, Mehrdad, Hajar Alijani, Meysam Nejad, and Rajender Varma. "Core@shell Nanoparticles: Greener Synthesis Using Natural Plant Products." Applied Sciences 8, no. 3 (March 10, 2018): 411. http://dx.doi.org/10.3390/app8030411.
Повний текст джерелаBohra, Hassan, and Mingfeng Wang. "Direct C–H arylation: a “Greener” approach towards facile synthesis of organic semiconducting molecules and polymers." Journal of Materials Chemistry A 5, no. 23 (2017): 11550–71. http://dx.doi.org/10.1039/c7ta00617a.
Повний текст джерелаJamalipour Soufi, Ghazaleh, and Siavash Iravani. "Eco-friendly and sustainable synthesis of biocompatible nanomaterials for diagnostic imaging: current challenges and future perspectives." Green Chemistry 22, no. 9 (2020): 2662–87. http://dx.doi.org/10.1039/d0gc00734j.
Повний текст джерелаOmori, Alvaro Takeo, Camila de Souza de Oliveira, Kleber Tellini Andrade, and Marina Gonçalves Capeletto. "Sassafras oil, carrot bits and microwaves: green lessons learned from the formal total synthesis of (−)-talampanel." RSC Advances 5, no. 125 (2015): 103563–65. http://dx.doi.org/10.1039/c5ra19483k.
Повний текст джерелаFonte, Mélanie, Cátia Teixeira, and Paula Gomes. "Improved synthesis of antiplasmodial 4-aminoacridines and 4,9-diaminoacridines." RSC Advances 14, no. 9 (2024): 6253–61. http://dx.doi.org/10.1039/d4ra00091a.
Повний текст джерелаSingh, Shambhu Nath, Sarva Jayaprakash, K. Venkateshwara Reddy, Ali Nakhi, and Manojit Pal. "A metal catalyst-free and one-pot synthesis of (3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)methanol derivatives in water." RSC Advances 5, no. 103 (2015): 84889–93. http://dx.doi.org/10.1039/c5ra14478g.
Повний текст джерелаByrne, Fergal P., Jamie M. Z. Assemat, Amy E. Stanford, Thomas J. Farmer, James W. Comerford, and Alessandro Pellis. "Enzyme-catalyzed synthesis of malonate polyesters and their use as metal chelating materials." Green Chemistry 23, no. 14 (2021): 5043–48. http://dx.doi.org/10.1039/d1gc01783g.
Повний текст джерелаWang, Xiaoxue, Yujie Qian, Hanyu Gao, Connor W. Coley, Yiming Mo, Regina Barzilay, and Klavs F. Jensen. "Towards efficient discovery of green synthetic pathways with Monte Carlo tree search and reinforcement learning." Chemical Science 11, no. 40 (2020): 10959–72. http://dx.doi.org/10.1039/d0sc04184j.
Повний текст джерелаAdil, Syed Farooq, Mohamed E. Assal, Mujeeb Khan, Abdulrahman Al-Warthan, Mohammed Rafiq H. Siddiqui, and Luis M. Liz-Marzán. "Biogenic synthesis of metallic nanoparticles and prospects toward green chemistry." Dalton Transactions 44, no. 21 (2015): 9709–17. http://dx.doi.org/10.1039/c4dt03222e.
Повний текст джерелаGiaccherini, Andrea, Giuseppe Cucinotta, Stefano Martinuzzi, Enrico Berretti, Werner Oberhauser, Alessandro Lavacchi, Giovanni Orazio Lepore, et al. "Green and scalable synthesis of nanocrystalline kuramite." Beilstein Journal of Nanotechnology 10 (October 29, 2019): 2073–83. http://dx.doi.org/10.3762/bjnano.10.202.
Повний текст джерелаChauhan, Kalpana, Rahul Sharma, Rohini Dharela, Ghanshyam Singh Chauhan, and Rakesh Kumar Singhal. "Chitosan-thiomer stabilized silver nano-composites for antimicrobial and antioxidant applications." RSC Advances 6, no. 79 (2016): 75453–64. http://dx.doi.org/10.1039/c6ra13466a.
Повний текст джерелаNthunya, Lebea N., Monaheng L. Masheane, Soraya P. Malinga, Tobias G. Barnard, Edward N. Nxumalo, Bhekie B. Mamba, and Sabelo D. Mhlanga. "UV-assisted reduction of in situ electrospun antibacterial chitosan-based nanofibres for removal of bacteria from water." RSC Advances 6, no. 98 (2016): 95936–43. http://dx.doi.org/10.1039/c6ra19472a.
Повний текст джерелаYayayürük, Aslı Erdem, and Onur Yayayürük. "Applications of Green Chemistry Approaches in Environmental Analysis." Current Analytical Chemistry 15, no. 7 (October 15, 2019): 745–58. http://dx.doi.org/10.2174/1573411015666190314154632.
Повний текст джерелаAnsary, Abu A., Asad Syed, Abdallah M. Elgorban, Ali H. Bahkali, Rajender S. Varma, and Mohd Sajid Khan. "Neodymium Selenide Nanoparticles: Greener Synthesis and Structural Characterization." Biomimetics 7, no. 4 (October 3, 2022): 150. http://dx.doi.org/10.3390/biomimetics7040150.
Повний текст джерелаIngold, Mariana, Victoria de la Sovera, Rosina Dapueto, Paola Hernández, Williams Porcal, and Gloria V. López. "Greener Synthesis of Antiproliferative Furoxans via Multicomponent Reactions." Molecules 27, no. 6 (March 8, 2022): 1756. http://dx.doi.org/10.3390/molecules27061756.
Повний текст джерелаMason, Brian P., Kristin E. Price, Jeremy L. Steinbacher, Andrew R. Bogdan, and D. Tyler McQuade. "Greener Approaches to Organic Synthesis Using Microreactor Technology." Chemical Reviews 107, no. 6 (June 2007): 2300–2318. http://dx.doi.org/10.1021/cr050944c.
Повний текст джерелаAzizi, Najmedin, Sahar Dezfooli, and Mohammad Mahmoudi Hashemi. "Greener synthesis of spirooxindole in deep eutectic solvent." Journal of Molecular Liquids 194 (June 2014): 62–67. http://dx.doi.org/10.1016/j.molliq.2014.01.009.
Повний текст джерелаJohnson, Eric C., Pablo E. Guzmán, Leah A. Wingard, Jesse J. Sabatini, and Rose A. Pesce-Rodriguez. "A Convenient and “Greener” Synthesis of Methyl Nitroacetate." Organic Process Research & Development 21, no. 7 (June 15, 2017): 1088–90. http://dx.doi.org/10.1021/acs.oprd.7b00093.
Повний текст джерелаVarughese, Deepu John, Maghar S. Manhas, and Ajay K. Bose. "Microwave enhanced greener synthesis of indazoles via nitrenes." Tetrahedron Letters 47, no. 38 (September 2006): 6795–97. http://dx.doi.org/10.1016/j.tetlet.2006.07.062.
Повний текст джерелаAkelis, Liudvikas, Jolanta Rousseau, Robertas Juskenas, Jelena Dodonova, Cyril Rousseau, Stéphane Menuel, Dominique Prevost, Sigitas Tumkevičius, Eric Monflier, and Frédéric Hapiot. "Greener Paal-Knorr Pyrrole Synthesis by Mechanical Activation." European Journal of Organic Chemistry 2016, no. 1 (December 9, 2015): 31–35. http://dx.doi.org/10.1002/ejoc.201501223.
Повний текст джерелаMargetic, Davor. "Mechanochemical Organic Synthesis - Powerful Tool in Greener Chemistry." Universal Journal of Green Chemistry 1, no. 1 (May 15, 2023): 44–56. http://dx.doi.org/10.37256/ujgc.1120232176.
Повний текст джерелаChithiravel, Rengasamy, Kandasamy Rajaguru, Shanmugam Muthusubramanian, and Nattamai Bhuvanesh. "A direct green route towards the synthesis of 2-aroyl-3,5-diarylthiophenes from 1,5-diketones." RSC Advances 5, no. 105 (2015): 86414–20. http://dx.doi.org/10.1039/c5ra17829k.
Повний текст джерелаSundar, Sasikala, and Shakkthivel Piraman. "Greener saponin induced morphologically controlled various polymorphs of nanostructured iron oxide materials for biosensor applications." RSC Advances 5, no. 91 (2015): 74408–15. http://dx.doi.org/10.1039/c5ra15166j.
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