Literatura académica sobre el tema "Greener synthesis"
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Artículos de revistas sobre el tema "Greener synthesis"
Mooney, Madison, Audithya Nyayachavadi y Simon Rondeau-Gagné. "Eco-friendly semiconducting polymers: from greener synthesis to greener processability". Journal of Materials Chemistry C 8, n.º 42 (2020): 14645–64. http://dx.doi.org/10.1039/d0tc04085a.
Texto completoKharissova, Oxana V., H. V. Rasika Dias, Boris I. Kharisov, Betsabee Olvera Pérez y Victor M. Jiménez Pérez. "The greener synthesis of nanoparticles". Trends in Biotechnology 31, n.º 4 (abril de 2013): 240–48. http://dx.doi.org/10.1016/j.tibtech.2013.01.003.
Texto completoLawrenson, Stefan, Michael North, Fanny Peigneguy y Anne Routledge. "Greener solvents for solid-phase synthesis". Green Chemistry 19, n.º 4 (2017): 952–62. http://dx.doi.org/10.1039/c6gc03147a.
Texto completoPolshettiwar, Vivek y Rajender S. Varma. "Greener and expeditious synthesis of bioactive heterocycles using microwave irradiation". Pure and Applied Chemistry 80, n.º 4 (1 de enero de 2008): 777–90. http://dx.doi.org/10.1351/pac200880040777.
Texto completoJicsinszky, László y Giancarlo Cravotto. "Toward a Greener World—Cyclodextrin Derivatization by Mechanochemistry". Molecules 26, n.º 17 (27 de agosto de 2021): 5193. http://dx.doi.org/10.3390/molecules26175193.
Texto completoLawrenson, Stefan B. "Greener solvents for solid-phase organic synthesis". Pure and Applied Chemistry 90, n.º 1 (26 de enero de 2018): 157–65. http://dx.doi.org/10.1515/pac-2017-0505.
Texto completoBhardwaj, Brahamdutt, Pritam Singh, Arun Kumar, Sandeep Kumar y Vikas Budhwar. "Eco-Friendly Greener Synthesis of Nanoparticles". Advanced Pharmaceutical Bulletin 10, n.º 4 (9 de agosto de 2020): 566–76. http://dx.doi.org/10.34172/apb.2020.067.
Texto completoKharissova, Oxana V., Boris I. Kharisov, César Máximo Oliva González, Yolanda Peña Méndez y Israel López. "Greener synthesis of chemical compounds and materials". Royal Society Open Science 6, n.º 11 (noviembre de 2019): 191378. http://dx.doi.org/10.1098/rsos.191378.
Texto completoGangurde, S. A., K. S. Laddha y S. V. Joshi. "A GREENER APPROACH TO SYNTHESIS OF DIACEREIN". INDIAN DRUGS 56, n.º 04 (28 de abril de 2019): 7–12. http://dx.doi.org/10.53879/id.56.04.11784.
Texto completoIravani, Siavash y Rajender S. Varma. "Greener synthesis of lignin nanoparticles and their applications". Green Chemistry 22, n.º 3 (2020): 612–36. http://dx.doi.org/10.1039/c9gc02835h.
Texto completoTesis sobre el tema "Greener synthesis"
Howie, Rowena Anne. "Metal-organic frameworks : towards greener synthesis". Thesis, University of Nottingham, 2017. http://eprints.nottingham.ac.uk/41707/.
Texto completoNada, Majid Hameed. "Greener synthesis of nanocrystalline ZSM-5". Thesis, University of Iowa, 2016. https://ir.uiowa.edu/etd/3149.
Texto completoHarsanyi, Antal. "Elemental fluorine for the greener synthesis of life-science building blocks". Thesis, Durham University, 2016. http://etheses.dur.ac.uk/11705/.
Texto completoLuitel, 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.
Texto completoNasr, 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.
Texto completoEnzyme-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.
Texto completoMestres, 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/.
Texto completoSaba, 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.
Texto completoMade 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.
Texto completoSharma, 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.
Texto completoLibros sobre el tema "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.
Texto completoWuts, Peter G. M., ed. Greene's Protective Groups in Organic Synthesis. Hoboken, New Jersey: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118905074.
Texto completoPatti, Angela. Green Approaches To Asymmetric Catalytic Synthesis. Dordrecht: Angela Patti, 2011.
Buscar texto completoKoichi, Mikami, ed. Green reaction media in organic synthesis. Oxford: Blackwell Pub., 2005.
Buscar texto completoMittal, Vikas. Renewable polymers: Synthesis, processing, and technology. Hoboken, N.J: John Wiley & Sons, 2012.
Buscar texto completo1962-, Anastas Paul T., Bartlett Laurence y Williamson Tracy C. 1963-, eds. Green chemical syntheses and processes. Washington, D.C: American Chemical Society, 2000.
Buscar texto completoRoberto, Ballini, ed. Eco-friendly synthesis of fine chemicals. Cambridge, UK: RSC Pub., 2009.
Buscar texto completoMicro- and nanostructured polymer systems: From synthesis to applications. Toronto: Apple Academic Press, 2015.
Buscar texto completoZhang, Wei y Berkeley W. Cue. Green techniques for organic synthesis and medicinal chemistry. Chichester, West Sussex: John Wiley & Sons, 2012.
Buscar texto completoInstilling religion in Greek and Turkish Nationalism: A "sacred synthesis". New York: Palgrave Macmillan, 2013.
Buscar texto completoCapítulos de libros sobre el tema "Greener synthesis"
Studzińska, Renata, Renata Kołodziejska y Daria Kupczyk. "Greener Synthesis of Potential Drugs". En Greener Synthesis of Organic Compounds, Drugs and Natural Products, 195–227. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003089162-12.
Texto completoKołodziejska, Renata, Renata Studzińska, Hanna Pawluk y Alina Woźniak. "Greener Synthesis of Natural Products". En Greener Synthesis of Organic Compounds, Drugs and Natural Products, 241–87. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003089162-14.
Texto completoOldenhuis, Nathan J., Aaron M. Whittaker y Vy M. Dong. "Greener Methods for Amide Bond Synthesis". En 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.
Texto completoMatsubara, Hiroshi, Takuji Kawamoto y Ilhyong Ryu. "CHAPTER 11. Challenges of Using Fluorous Solvents for Greener Organic Synthesis". En Sustainable Organic Synthesis, 313–38. Cambridge: Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781839164842-00313.
Texto completoPatil, Aniruddha B. y Bhalchandra M. Bhanage. "Sonochemistry: A Greener Protocol for Nanoparticles Synthesis". En Handbook of Nanoparticles, 143–66. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-15338-4_4.
Texto completoPatil, Aniruddha B. y Bhalchandra M. Bhanage. "Sonochemistry: A Greener Protocol for Nanoparticles Synthesis". En Handbook of Nanoparticles, 1–20. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-13188-7_4-1.
Texto completoMiller, Roland M., Francis J. Osonga y Omowunmi A. Sadik. "Synthesis and Biological Applications of Greener Nanoparticles". En 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.
Texto completoAcosta-Guzmán, Paola y Diego Gamba-Sánchez. "Greener Methods for Halogenation of Aromatic Compounds". En Greener Synthesis of Organic Compounds, Drugs and Natural Products, 41–56. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003089162-3.
Texto completoEksiler, Kubra, Yoshito Andou y Tessei Kawano. "Chapter 11. Fabrication of Biodegradable Cellulose Composite Through a Greener Reaction Process". En Cellulose Nanoparticles : Synthesis and Manufacturing, 236–57. Cambridge: Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781788019545-00236.
Texto completoVillaseñor-Basulto, Déborah L., Mary-Magdalene Pedavoah y Eric R. Bandala. "Plant Materials for the Synthesis of Nanomaterials: Greener Sources". En Handbook of Ecomaterials, 1–18. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-48281-1_88-1.
Texto completoActas de conferencias sobre el tema "Greener synthesis"
Monteiro, J. L., A. F. Torre, M. P. Paixão y A. G. Corrêa. "Asymmetric synthesis of pyranocumarins under greener conditions". En 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013101414540.
Texto completode la Torre, Beatriz G., Ashish Kumar, Yahya Jad, Jonathan M. Collins, Simona Serban, Othman Almusaim y Fernando Albericio. "Solid-phase peptide synthesis: the Greener, the Better". En 35th European Peptide Symposium. Prompt Scientific Publishing, 2018. http://dx.doi.org/10.17952/35eps.2018.099.
Texto completoFeu, Karla S., Anna M. Deobald, Arlene G. Corrêa y Marcio W. Paixão. "Tandem Organocatalytic Functionalization and Fisher Indole Synthesis: A Greener Approach for the Synthesis of Indoles". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0342-1.
Texto completoKumari, Sonam, Renu Sharma y Ruchi Bharti. "ZnO nanoparticles: A promosing greener catalytic approach for synthesis of bioactive heterocycles". En 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.
Texto completoGupta, Girish Kumar, Vinod Kumar y Vipin Saini. "Greener synthesis and DNA photocleavage activity of 1, 5-Diaryl-3-trifluoromethylpyrazole derivatives". En The 21st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04827.
Texto completoOnyenkeadi, Victor, Suela Kellici y Basu Saha. "Greener Synthesis of 1,2-Butylene Carbonate from CO2 Using Graphene-Inorganic Nanocomposite Catalysis". En 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.
Texto completoArya, Kapil, Diwan Rawat y Pooja Gusain. "Greener One Pot Synthesis of 2-Amino-4-arylquinoline-3-carbonitriles in Neat Water Under Microwaves". En The 16th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01061.
Texto completoAgarwal, Shikha, Dinesh Kr Agarwal, Priyanka Kalal y Divyani Gandhi. "A comparative study: Greener vs conventional synthesis of 4H-pyrimido[2,1-b]benzothiazoles via Biginelli reaction". En 2ND INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC 2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5032807.
Texto completo"Greener Synthesis of Chitosan/Acrylic Acid (AA) Hydrogel and Its Application as Drying Agent for Organic Solvents and Crude Oil Fractions". En June 29-30, 2017 London (UK). DiRPUB, 2017. http://dx.doi.org/10.15242/dirpub.c0617017.
Texto completoVieira, Lucas Campos Curcino y Arlene G. Corrêa. "Green synthesis of chalcone derivatives via Suzuki coupling". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0238-1.
Texto completoInformes sobre el tema "Greener synthesis"
Saffron, Christopher y John W. Frost. Large Scale Green Synthesis of 1,2,4-Butanetriol. Fort Belvoir, VA: Defense Technical Information Center, marzo de 2007. http://dx.doi.org/10.21236/ada466203.
Texto completoFrost, John W. Green Synthesis of D-1,2,4 - Butantetroil from D-Glucose. Fort Belvoir, VA: Defense Technical Information Center, enero de 2008. http://dx.doi.org/10.21236/ada593490.
Texto completoFrost, John W. Green Synthesis of D-1,2,4-Butanetriol from D-Glucose. Fort Belvoir, VA: Defense Technical Information Center, diciembre de 2009. http://dx.doi.org/10.21236/ada548856.
Texto completoFrost, John W. Green Synthesis of D-1,2,4-Butanetriol from D-Glucose. Fort Belvoir, VA: Defense Technical Information Center, enero de 2009. http://dx.doi.org/10.21236/ada548871.
Texto completoFrost, John W. Green Synthesis of Phloroglucinol: Exploiting Pseudomonas fluorescens and Scale-Up. Fort Belvoir, VA: Defense Technical Information Center, enero de 2008. http://dx.doi.org/10.21236/ada593488.
Texto completoFrost, John W. Green Synthesis of Phloroglucinol: Exploiting Pseudomonas fluorescens and Scale-Up. Fort Belvoir, VA: Defense Technical Information Center, enero de 2010. http://dx.doi.org/10.21236/ada548823.
Texto completoFrost, John W. Green Synthesis of Phloroglucinol: Exploiting Pseudomonas fluorescens and Scale-Up. Fort Belvoir, VA: Defense Technical Information Center, enero de 2009. http://dx.doi.org/10.21236/ada548824.
Texto completoFrost, John W. Green Synthesis of Phloroglucinol: Exploiting Pseudomonas fluorescens and Scale-Up. Fort Belvoir, VA: Defense Technical Information Center, octubre de 2009. http://dx.doi.org/10.21236/ada548825.
Texto completoPindwal, Aradhana. Lanthanide alkyl and silyl compounds: Synthesis, reactivity and catalysts for green. Office of Scientific and Technical Information (OSTI), enero de 2016. http://dx.doi.org/10.2172/1342556.
Texto completoRahmathullah, Azmathullah. Green synthesis of Solanum xanthocarpum mediated selenium nanoparticles and its biomedical applications. Peeref, noviembre de 2022. http://dx.doi.org/10.54985/peeref.2211p7161250.
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