Littérature scientifique sur le sujet « Greener synthesis »
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Articles de revues sur le sujet "Greener synthesis"
Mooney, Madison, Audithya Nyayachavadi et 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.
Texte intégralKharissova, Oxana V., H. V. Rasika Dias, Boris I. Kharisov, Betsabee Olvera Pérez et Victor M. Jiménez Pérez. « The greener synthesis of nanoparticles ». Trends in Biotechnology 31, no 4 (avril 2013) : 240–48. http://dx.doi.org/10.1016/j.tibtech.2013.01.003.
Texte intégralLawrenson, Stefan, Michael North, Fanny Peigneguy et Anne Routledge. « Greener solvents for solid-phase synthesis ». Green Chemistry 19, no 4 (2017) : 952–62. http://dx.doi.org/10.1039/c6gc03147a.
Texte intégralPolshettiwar, Vivek, et Rajender S. Varma. « Greener and expeditious synthesis of bioactive heterocycles using microwave irradiation ». Pure and Applied Chemistry 80, no 4 (1 janvier 2008) : 777–90. http://dx.doi.org/10.1351/pac200880040777.
Texte intégralJicsinszky, László, et Giancarlo Cravotto. « Toward a Greener World—Cyclodextrin Derivatization by Mechanochemistry ». Molecules 26, no 17 (27 août 2021) : 5193. http://dx.doi.org/10.3390/molecules26175193.
Texte intégralLawrenson, Stefan B. « Greener solvents for solid-phase organic synthesis ». Pure and Applied Chemistry 90, no 1 (26 janvier 2018) : 157–65. http://dx.doi.org/10.1515/pac-2017-0505.
Texte intégralBhardwaj, Brahamdutt, Pritam Singh, Arun Kumar, Sandeep Kumar et Vikas Budhwar. « Eco-Friendly Greener Synthesis of Nanoparticles ». Advanced Pharmaceutical Bulletin 10, no 4 (9 août 2020) : 566–76. http://dx.doi.org/10.34172/apb.2020.067.
Texte intégralKharissova, Oxana V., Boris I. Kharisov, César Máximo Oliva González, Yolanda Peña Méndez et Israel López. « Greener synthesis of chemical compounds and materials ». Royal Society Open Science 6, no 11 (novembre 2019) : 191378. http://dx.doi.org/10.1098/rsos.191378.
Texte intégralGangurde, S. A., K. S. Laddha et S. V. Joshi. « A GREENER APPROACH TO SYNTHESIS OF DIACEREIN ». INDIAN DRUGS 56, no 04 (28 avril 2019) : 7–12. http://dx.doi.org/10.53879/id.56.04.11784.
Texte intégralIravani, Siavash, et 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.
Texte intégralThèses sur le sujet "Greener synthesis"
Howie, Rowena Anne. « Metal-organic frameworks : towards greener synthesis ». Thesis, University of Nottingham, 2017. http://eprints.nottingham.ac.uk/41707/.
Texte intégralNada, Majid Hameed. « Greener synthesis of nanocrystalline ZSM-5 ». Thesis, University of Iowa, 2016. https://ir.uiowa.edu/etd/3149.
Texte intégralHarsanyi, Antal. « Elemental fluorine for the greener synthesis of life-science building blocks ». Thesis, Durham University, 2016. http://etheses.dur.ac.uk/11705/.
Texte intégralLuitel, Govinda Prasad. « Greener synthesis of some new isoxazolidine and isoxazoline derivatives via 1,3-dipolar cycloaddition reactions and studies of biological activities of the cycloadducts ». Thesis, University of North Bengal, 2017. http://ir.nbu.ac.in/handle/123456789/2576.
Texte intégralNasr, Kifah. « Enzyme-catalyzed synthesis of polyesters by step-growth polymerization : a promising approach towards a greener synthetic pathway ». Electronic Thesis or Diss., Université de Lille (2018-2021), 2021. http://www.theses.fr/2021LILUR030.
Texte intégralEnzyme-catalyzed polymerization have been witnessing a growing attention in recent years as an eco-friendly substitute to metal-based catalysis. The objective of our work is to synthesize a series of polyesters via enzymatic catalysis based on different aliphatic and aromatic diols and diesters, where we focused on the influence of reaction parameters, monomer structures, and depicted the advantages and limitation of enzymatic catalysis in polymer synthesis. The enzyme used throughout our work was Novozym 435, a lipase from Candida antarctica, immobilized on an acrylic resin. In Chapter 1, we reviewed the different methods and approaches used in the literature to synthesize polymers via enzymatic catalysis. In Chapter 2, we performed the reaction between hexane-1,6-diol and diethyl adipate via a two-step polycondensation approach where we monitored the effect of certain parameters on the number average molecular weight (Mn). The influence of temperature, vacuum, and the amount of enzyme loading were determined using a central composite design. Other factors such as the reaction media, oligomerization time, and catalyst recyclability were also assessed. In Chapter 3 furan-based copolyesters were synthesized, where we showed that we can incorporate higher amounts of furan when using aliphatic diols with longer chains such as dodecane-1,12-diol. In Chapter 4, levoglucosan, an anhydrous 6-carbon ring structure and a pyrolysis product of carbohydrates such as starch and cellulose, was reacted against different chain length diesters in the presence of aliphatic diols and Novozym 435 as a catalyst. The polyesters produced were limited in their number average molecular weight (Mn) and the amount of levoglucosan that was successfully incorporated into the polymeric structure. Nevertheless, by increasing the chain length of the diester, we were able to produce a copolymer containing higher amounts of levoglucosan and a higher molecular weight
Rai, Neelam. « Greener synthesis and 1, 3-dipolar cycloaddition reactions of a amino nitrones and studies of biological activities of the cycloadducts ». Thesis, University of North Bengal, 2017. http://ir.nbu.ac.in/handle/123456789/2663.
Texte intégralMestres, Ricard Sola. « Greener approaches for chemical synthesis : ball mill and microwave assisted synthesis of fluoxetine and duloxetine and enantioselective catalysed addition of organometallic reagents to aldehydes ». Thesis, Manchester Metropolitan University, 2017. http://e-space.mmu.ac.uk/618791/.
Texte intégralSaba, Sumbal. « Synthesis of unsymmetrical diorganyl chalcogenides by using arylboronic acids or C (sp2)-H bond functionalization of arenes under greener conditions ». reponame:Repositório Institucional da UFSC, 2016. https://repositorio.ufsc.br/xmlui/handle/123456789/168202.
Texte intégralMade available in DSpace on 2016-09-20T05:02:32Z (GMT). No. of bitstreams: 1 341356.pdf: 20337282 bytes, checksum: 2c692523891aae34c8c39befe4a17c29 (MD5) Previous issue date: 2016
No presente trabalho desenvolveram-se procedimentos robustos, econômicos e sustentável para a síntese de dicalcogentos de organoíla não simétricos usando uma variedade de ácidos borônicos arílicos substituídos e arenos [O- ou N-] subtituídos. Na primeira parte, desenvolvemos um sistema catalítico oxidativo que combina iodo/DMSO para a síntese de uma grande variedade de dicalcogenetos de diorganoíla não simétricos (S, Se, Te), utilizando vários ácidos borônicos arílicos sob irradiação de micro-ondas. As reações foram realizadas pela mistura de ácidos boronicos com os dicalgenetos desejados, na presença de 10 mol% de iodo, um equiv. ácidos borônicos arílicos II, 0,5 equiv. de vários dicalcogenetos de diorganoíla I e 2 equiv. de DMSO (como oxidante). Os produtos calcogenados desejados III foram obtidos em rendimentos de bons a excelentes. Todas as reações foram realizadas sem a exclusão de ar e umidade a 100 °C durante 10 minutos sob irradiação de microondas. Vários substituintes com diferentes efeitos eletrônicos e estéricos foram tolerados nas condições ótimas de reação. A metodologia desenvolvida demonstrou ser robusta e pode ser facilmente efetuada na escala de 10 mmol, sem qualquer perda significativa de rendimento. A química aqui descrita representa um protocolo livre de solvente e de metal de transição para a preparação de calcogenetos de diorganoíla não simétricos. O escopo da presente metodologia de acoplamento foi estendido usando trifluoroboratos de potássio vinilícos IV como uma alternativa para os ácidos borônicos, utilizando os parâmetros da condição otimizada. A reação de ditelureto e disseleneto de dirganoíla I ocorreu sem problemas e proporcionou a formação dos produtos acoplados correspondentes em rendimentos isolados de 87% e 89%. Considerando a importância dos compostos organocalcogênio, na segunda etapa deste trabalho, desenvolveu-se um método regiosseletivo, rápido e ambientalmente seguro, catalisado por iodo para a síntese de calcogentos de organoíla. Essa metodologia ocorre pela formação de ligações C-Se / C-S via clivagem oxidativa de ligação C (sp2) -H utilizando arenos [O- ou N-] substituídos. Esse processo é realizado pela calcogenação direta de dicalcogenetos de organoíla I com vários arenos VI, catalisados por 20 mol% de iodo na presença de 3 equivalentes de DMSO (como oxidante). Essa metodologia regiosseletiva, sob irradiação de micro-ondas, permitiu obter os produtos desejados funcionalizados com um substituinte organocalcogenoíla, em 10 min, em bons rendimentos. Outras vantagens desse método são: condições livres de solvente e metal de transição; procedimento experimental sem a exclusão de ar e umidade. A reação também foi efetuada em escala de 10 mmol sem perda significativa de rendimento. Além disso, por este protocolo, foi possível funcionalizar heteroarenos biologicamente importantes contendo S/Se, tais como: pirimidinas, piridinas e tiazóis. A versatilidade da metodologia desenvolvida permitiu ainda a utilização de tiofenol VIII e hidrazidas de sulfonila VIII como agentes sulfenilação e N,N-dimetilanilina IX alternativos, levando-se o produto tiolado X desejados em bom rendimentos, em um tempo de reação curto usando irradiação de micro-ondas.
Abstract : In the present work we developed robust, economical and greener procedures for the synthesis of unsymmetrical diorganyl chalcogenides by using various substituted arylboronic acids and [O or N]- containing arenes. In the first part, we developed Iodine/DMSO catalyzed oxidative system for the synthesis of a variety of unsymmetrical diorganyl chalcogenides (S, Se, Te) using various arylboronic acids under microwave irradiations. The desired chalcogenated products III were obtained in good to excellent yields in the presence of 10 mol% of iodine, one equiv. of arylboronic acids II, half equiv. of various diorganyl dichalcogenides I and 2 equiv. of DMSO (as an oxidant). All the reactions were performed without the exclusion of air and moisture at 100 0C for 10 min under microwave irradiation. Various substituents with different electronic and steric effects tolerated in the optimized reaction conditions. The developed methodology was shown to be robust and could easily be scaled-up without any significant loss of yield. The chemistry described herein represents a transition metal and solvent free method for the preparation of unsymmetrical diorganyl chalcogenides. We were also successful in scaling up the reaction in up to 10 mmol. The scope of this coupling methodology was extended by using potassium vinyltrifluoroborate IV as an alternative to boronic acid in these tellurylation and selenylation reactions by applying the optimal reaction parameters. The reaction of ditelluride and diselenide I proceeded smoothly and afforded the corresponding coupled products V in 87% and 89% isolated yield. Considering the importance of diorganyl chalcogenides, we developed a regioselective, rapid and greener iodine-catalyzed method for the synthesis of diorganyl chalcogenides through oxidative C Se/C S formation via direct C(sp2)-H bond cleavage using [O or N]-containing arenes. In this work, we reported the synthesis of unsymmetrical diorganyl chalcogenides VII via direct chalcogenation reactions between dichalcogenides I and various arenes VI catalyzed by 20 mol% of iodine in the presence of 3 equiv. of DMSO (as an oxidant). This regioselective methodology allowed us to obtain desired chalcogenated product in good to excellent yields under transition metal and solvent-free conditions, without the exclusion of air and moisture, applying microwave irradiations for 10 min. The reaction was also scaled-up to 10 mmol. Additionally, by this protocol, we were able to access biologically important Se/S containing heteroarenes, such as, pyrimidines, pyridines, thiazole. The versatility of the developed methodology was observed by using thiophenol VIII and sulfonyl hydrazides VIII as another sulfenylating agents and N,N-dimethylaniline IX, affording the desired sulfonated product X in very good yield, in a short reaction time using MW irradiation.
Dhakal, Ram Chandra. « New Approaches To Heterocycle Synthesis : A Greener Route To Structurally Complex Protonated Azomethine Imines, And Their Use In 1,3-Dipolar Cycloadditions ». ScholarWorks @ UVM, 2017. http://scholarworks.uvm.edu/graddis/777.
Texte intégralSharma, Prawin Kumar. « Greener approach to the synthesis of some novel class of isoxazolidine and isoxazoline derivatives using N-methyl and N-phenyl-a-chloro nitrones ». Thesis, University of North Bengal, 2016. http://ir.nbu.ac.in/handle/123456789/1884.
Texte intégralLivres sur le sujet "Greener synthesis"
Nag, Ahindra. Greener Synthesis of Organic Compounds, Drugs and Natural Products. Boca Raton : CRC Press, 2022. http://dx.doi.org/10.1201/9781003089162.
Texte intégralWuts, Peter G. M., dir. Greene's Protective Groups in Organic Synthesis. Hoboken, New Jersey : John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118905074.
Texte intégralPatti, Angela. Green Approaches To Asymmetric Catalytic Synthesis. Dordrecht : Angela Patti, 2011.
Trouver le texte intégralKoichi, Mikami, dir. Green reaction media in organic synthesis. Oxford : Blackwell Pub., 2005.
Trouver le texte intégralMittal, Vikas. Renewable polymers : Synthesis, processing, and technology. Hoboken, N.J : John Wiley & Sons, 2012.
Trouver le texte intégral1962-, Anastas Paul T., Bartlett Laurence et Williamson Tracy C. 1963-, dir. Green chemical syntheses and processes. Washington, D.C : American Chemical Society, 2000.
Trouver le texte intégralRoberto, Ballini, dir. Eco-friendly synthesis of fine chemicals. Cambridge, UK : RSC Pub., 2009.
Trouver le texte intégralMicro- and nanostructured polymer systems : From synthesis to applications. Toronto : Apple Academic Press, 2015.
Trouver le texte intégralZhang, Wei, et Berkeley W. Cue. Green techniques for organic synthesis and medicinal chemistry. Chichester, West Sussex : John Wiley & Sons, 2012.
Trouver le texte intégralInstilling religion in Greek and Turkish Nationalism : A "sacred synthesis". New York : Palgrave Macmillan, 2013.
Trouver le texte intégralChapitres de livres sur le sujet "Greener synthesis"
Studzińska, Renata, Renata Kołodziejska et Daria Kupczyk. « Greener Synthesis of Potential Drugs ». Dans Greener Synthesis of Organic Compounds, Drugs and Natural Products, 195–227. Boca Raton : CRC Press, 2022. http://dx.doi.org/10.1201/9781003089162-12.
Texte intégralKołodziejska, Renata, Renata Studzińska, Hanna Pawluk et Alina Woźniak. « Greener Synthesis of Natural Products ». Dans Greener Synthesis of Organic Compounds, Drugs and Natural Products, 241–87. Boca Raton : CRC Press, 2022. http://dx.doi.org/10.1201/9781003089162-14.
Texte intégralOldenhuis, Nathan J., Aaron M. Whittaker et Vy M. Dong. « Greener Methods for Amide Bond Synthesis ». Dans Methods in Pharmacology and Toxicology, 35–96. New York, NY : Springer New York, 2021. http://dx.doi.org/10.1007/978-1-0716-1579-9_2.
Texte intégralMatsubara, Hiroshi, Takuji Kawamoto et Ilhyong Ryu. « CHAPTER 11. Challenges of Using Fluorous Solvents for Greener Organic Synthesis ». Dans Sustainable Organic Synthesis, 313–38. Cambridge : Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781839164842-00313.
Texte intégralPatil, Aniruddha B., et Bhalchandra M. Bhanage. « Sonochemistry : A Greener Protocol for Nanoparticles Synthesis ». Dans Handbook of Nanoparticles, 143–66. Cham : Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-15338-4_4.
Texte intégralPatil, Aniruddha B., et Bhalchandra M. Bhanage. « Sonochemistry : A Greener Protocol for Nanoparticles Synthesis ». Dans Handbook of Nanoparticles, 1–20. Cham : Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-13188-7_4-1.
Texte intégralMiller, Roland M., Francis J. Osonga et Omowunmi A. Sadik. « Synthesis and Biological Applications of Greener Nanoparticles ». Dans Interfaces Between Nanomaterials and Microbes, 247–68. First edition. | Boca Raton : CRC Press, Taylor & Francis Group, 2021. | “A science publishers book.” : CRC Press, 2021. http://dx.doi.org/10.1201/9780429321269-11.
Texte intégralAcosta-Guzmán, Paola, et Diego Gamba-Sánchez. « Greener Methods for Halogenation of Aromatic Compounds ». Dans Greener Synthesis of Organic Compounds, Drugs and Natural Products, 41–56. Boca Raton : CRC Press, 2022. http://dx.doi.org/10.1201/9781003089162-3.
Texte intégralEksiler, Kubra, Yoshito Andou et Tessei Kawano. « Chapter 11. Fabrication of Biodegradable Cellulose Composite Through a Greener Reaction Process ». Dans Cellulose Nanoparticles : Synthesis and Manufacturing, 236–57. Cambridge : Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781788019545-00236.
Texte intégralVillaseñor-Basulto, Déborah L., Mary-Magdalene Pedavoah et Eric R. Bandala. « Plant Materials for the Synthesis of Nanomaterials : Greener Sources ». Dans Handbook of Ecomaterials, 1–18. Cham : Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-48281-1_88-1.
Texte intégralActes de conférences sur le sujet "Greener synthesis"
Monteiro, J. L., A. F. Torre, M. P. Paixão et A. G. Corrêa. « Asymmetric synthesis of pyranocumarins under greener conditions ». Dans 15th Brazilian Meeting on Organic Synthesis. São Paulo : Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013101414540.
Texte intégralde la Torre, Beatriz G., Ashish Kumar, Yahya Jad, Jonathan M. Collins, Simona Serban, Othman Almusaim et Fernando Albericio. « Solid-phase peptide synthesis : the Greener, the Better ». Dans 35th European Peptide Symposium. Prompt Scientific Publishing, 2018. http://dx.doi.org/10.17952/35eps.2018.099.
Texte intégralFeu, Karla S., Anna M. Deobald, Arlene G. Corrêa et Marcio W. Paixão. « Tandem Organocatalytic Functionalization and Fisher Indole Synthesis : A Greener Approach for the Synthesis of Indoles ». Dans 14th Brazilian Meeting on Organic Synthesis. São Paulo : Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0342-1.
Texte intégralKumari, Sonam, Renu Sharma et Ruchi Bharti. « ZnO nanoparticles : A promosing greener catalytic approach for synthesis of bioactive heterocycles ». Dans INTERNATIONAL CONFERENCE ON HUMANS AND TECHNOLOGY : A HOLISTIC AND SYMBIOTIC APPROACH TO SUSTAINABLE DEVELOPMENT : ICHT 2022. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0114413.
Texte intégralGupta, Girish Kumar, Vinod Kumar et Vipin Saini. « Greener synthesis and DNA photocleavage activity of 1, 5-Diaryl-3-trifluoromethylpyrazole derivatives ». Dans The 21st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland : MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04827.
Texte intégralOnyenkeadi, Victor, Suela Kellici et Basu Saha. « Greener Synthesis of 1,2-Butylene Carbonate from CO2 Using Graphene-Inorganic Nanocomposite Catalysis ». Dans 10TH International Conference on Sustainable Energy and Environmental Protection. University of Maribor Press, 2017. http://dx.doi.org/10.18690/978-961-286-052-3.15.
Texte intégralArya, Kapil, Diwan Rawat et Pooja Gusain. « Greener One Pot Synthesis of 2-Amino-4-arylquinoline-3-carbonitriles in Neat Water Under Microwaves ». Dans The 16th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland : MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01061.
Texte intégralAgarwal, Shikha, Dinesh Kr Agarwal, Priyanka Kalal et Divyani Gandhi. « A comparative study : Greener vs conventional synthesis of 4H-pyrimido[2,1-b]benzothiazoles via Biginelli reaction ». Dans 2ND INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC 2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5032807.
Texte intégral« Greener Synthesis of Chitosan/Acrylic Acid (AA) Hydrogel and Its Application as Drying Agent for Organic Solvents and Crude Oil Fractions ». Dans June 29-30, 2017 London (UK). DiRPUB, 2017. http://dx.doi.org/10.15242/dirpub.c0617017.
Texte intégralVieira, Lucas Campos Curcino, et Arlene G. Corrêa. « Green synthesis of chalcone derivatives via Suzuki coupling ». Dans 14th Brazilian Meeting on Organic Synthesis. São Paulo : Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0238-1.
Texte intégralRapports d'organisations sur le sujet "Greener synthesis"
Saffron, Christopher, et John W. Frost. Large Scale Green Synthesis of 1,2,4-Butanetriol. Fort Belvoir, VA : Defense Technical Information Center, mars 2007. http://dx.doi.org/10.21236/ada466203.
Texte intégralFrost, John W. Green Synthesis of D-1,2,4 - Butantetroil from D-Glucose. Fort Belvoir, VA : Defense Technical Information Center, janvier 2008. http://dx.doi.org/10.21236/ada593490.
Texte intégralFrost, John W. Green Synthesis of D-1,2,4-Butanetriol from D-Glucose. Fort Belvoir, VA : Defense Technical Information Center, décembre 2009. http://dx.doi.org/10.21236/ada548856.
Texte intégralFrost, John W. Green Synthesis of D-1,2,4-Butanetriol from D-Glucose. Fort Belvoir, VA : Defense Technical Information Center, janvier 2009. http://dx.doi.org/10.21236/ada548871.
Texte intégralFrost, John W. Green Synthesis of Phloroglucinol : Exploiting Pseudomonas fluorescens and Scale-Up. Fort Belvoir, VA : Defense Technical Information Center, janvier 2008. http://dx.doi.org/10.21236/ada593488.
Texte intégralFrost, John W. Green Synthesis of Phloroglucinol : Exploiting Pseudomonas fluorescens and Scale-Up. Fort Belvoir, VA : Defense Technical Information Center, janvier 2010. http://dx.doi.org/10.21236/ada548823.
Texte intégralFrost, John W. Green Synthesis of Phloroglucinol : Exploiting Pseudomonas fluorescens and Scale-Up. Fort Belvoir, VA : Defense Technical Information Center, janvier 2009. http://dx.doi.org/10.21236/ada548824.
Texte intégralFrost, John W. Green Synthesis of Phloroglucinol : Exploiting Pseudomonas fluorescens and Scale-Up. Fort Belvoir, VA : Defense Technical Information Center, octobre 2009. http://dx.doi.org/10.21236/ada548825.
Texte intégralPindwal, Aradhana. Lanthanide alkyl and silyl compounds : Synthesis, reactivity and catalysts for green. Office of Scientific and Technical Information (OSTI), janvier 2016. http://dx.doi.org/10.2172/1342556.
Texte intégralRahmathullah, Azmathullah. Green synthesis of Solanum xanthocarpum mediated selenium nanoparticles and its biomedical applications. Peeref, novembre 2022. http://dx.doi.org/10.54985/peeref.2211p7161250.
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