Relevant bibliographies by topics / Microwave-assisted organic synthesis (MAOS)

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Microwave-assisted organic synthesis (MAOS)'

Author: Grafiati
Published: 3 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Microwave-assisted organic synthesis (MAOS)"

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Abid, Mohammed, Béla Török, and Xudong Huang. "Microwave-Assisted Tandem Processes for the Synthesis of N-Heterocycles." Australian Journal of Chemistry 62, no. 3 (2009): 208. http://dx.doi.org/10.1071/ch08474.

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Over the years, microwave-assisted organic synthesis (MAOS) became a commonly applied mainstream tool for the synthesis of heterocyclic compounds. The broad range of emerging applications in this field is mainly due to the significant contribution of MAOS to the development of ecofriendly processes. Various transformations have been developed for the synthesis of N-heterocycles under microwave conditions, including fast and selective processes. Tandem reactions involving greener reaction media, solvent-free conditions, and solid-phase synthesis are of exceptional interest in this area. In most
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Abid, Mohammed, Béla Török, and Xudong Huang. "Corrigendum to: Microwave-Assisted Tandem Processes for the Synthesis of N-Heterocycles." Australian Journal of Chemistry 62, no. 4 (2009): 392. http://dx.doi.org/10.1071/ch08474_co.

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Over the years, microwave-assisted organic synthesis (MAOS) became a commonly applied mainstream tool for the synthesis of heterocyclic compounds. The broad range of emerging applications in this field is mainly due to the significant contribution of MAOS to the development of ecofriendly processes. Various transformations have been developed for the synthesis of N-heterocycles under microwave conditions, including fast and selective processes. Tandem reactions involving greener reaction media, solvent-free conditions, and solid-phase synthesis are of exceptional interest in this area. In most
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Rodríguez, A. M., P. Prieto, A. de la Hoz, A. Díaz-Ortiz, and J. I. García. "The issue of ‘molecular radiators’ in microwave-assisted reactions. Computational calculations on ring closing metathesis (RCM)." Org. Biomol. Chem. 12, no. 15 (2014): 2436–45. http://dx.doi.org/10.1039/c3ob42536c.

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Elgemeie, Galal H., and Doaa M. Masoud. "Recent trends in microwave assisted synthesis of fluorescent dyes." Pigment & Resin Technology 45, no. 6 (2016): 381–407. http://dx.doi.org/10.1108/prt-04-2015-0036.

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Purpose This paper aims to focus on the most popular technique nowadays, the use of microwave irradiation in organic synthesis; in a few years, most chemists will use microwave energy to heat chemical reactions on a laboratory scale. Also, many scientists use microwave technology in the industry. They have turned to microwave synthesis as a frontline methodology for their projects. Microwave and microwave-assisted organic synthesis (MAOS) has emerged as a new “lead” in organic synthesis. Design/methodology/approach Using microwave radiation for synthesis and design of fluorescent dyes is of gr
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Budiana, S., B. Andreana, D. U. C. Rahayu, D. A. Nurani, Y. K. Krisnandi, and E. Budianto. "Synthesis of imidazoline-palmitic derivative using MAOS (microwave assisted organic synthesis) method." IOP Conference Series: Materials Science and Engineering 763 (April 29, 2020): 012006. http://dx.doi.org/10.1088/1757-899x/763/1/012006.

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Somani, R. R., G. J. Sanap, and P. K. Chaskar. "USE OF FACTORIAL DESIGN IN OPTIMIZATION OF MICROWAVE ASSISTED ORGANIC SYNTHESIS OF SOME AZOLES." INDIAN DRUGS 55, no. 10 (2018): 24–33. http://dx.doi.org/10.53879/id.55.10.11401.

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In the era of environment friendly chemistry, Microwave Assisted Organic Synthesis (MAOS) has proved to be an effective tool to achieve maximum yield in minimum time without compromising on quality. The present work focuses on synthesis of some bioactive heterocyclic azoles using MAOS. However, the synthetic reactions are optimized using a known technique of factorial designing. Here, 32 factorial design approach is used to achieve the set targets of yields and purity. The outcome has been very promising and opens up new avenues for organic chemists who face challenges in optimizing organic re
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Franco, Daiana Portella, Lucas Caruso, Nathalia Fonseca Nadur, Thiago Moreira Pereira, Renata Barbosa Lacerda, and Arthur Eugen Kümmerle. "Recent Advances in Microwave-Assisted Synthesis and Functionalization of 1,2,3- and 1,2,4-triazoles." Current Organic Chemistry 25, no. 23 (2021): 2815–39. http://dx.doi.org/10.2174/1385272825666211011111408.

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Triazoles are five-membered aromatic heterocyclics, which exhibit two isosteric forms (1,2,3-triazoles and 1,2,4-triazoles), as well as multiple applications in medicinal, agricultural, supramolecular, and materials sciences. Famous examples of triazoles include drugs, such as fluconazole, ribavirin, cefatrizine, and tazobactam, as well as herbicides, such as cafenstrole and metosulam. This review aims to present the recent major examples of the application of microwave-assisted organic synthesis (MAOS) to the syntheses and endfunctionalizations of 1,4- and 1,5-disubstituted 1,2,3-triazoles, 1
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García Velázquez, Daniel, Rafael Luque, and Ángel Gutiérrez Ravelo. "Microwave-Assisted Synthesis and Properties of Novel Hexaazatrinaphthylene Dendritic Scaffolds." Molecules 25, no. 21 (2020): 5038. http://dx.doi.org/10.3390/molecules25215038.

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A novel family of water-soluble π-conjugated hexaazatrinaphthylenes-based dendritic architectures constructed by hexaketocyclohexane and 1,2,4,5-benzenetetramine units is developed in a microwave-assisted organic synthesis (MAOS) approach. The structures and purity of these compounds are verified by 1H and 13C-NMR, MALDI-TOF MS, UV-vis, elemental analysis, DSC, AFM, STM and cyclic voltammetry.
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Handayani, Sri, Cornelia Budimarwanti, and Winarto Haryadi. "Microwave-Assisted Organic Reactions: Eco-friendly Synthesis of Dibenzylidenecyclohexanone Derivatives via Crossed Aldol Condensation." Indonesian Journal of Chemistry 17, no. 2 (2017): 336. http://dx.doi.org/10.22146/ijc.25460.

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The synthesis of dibenzylidenecyclohexanone derivatives via environmentally friendly Microwave Assisted Organic Synthesis (MAOS) crossed aldol condensation had been carried out. The condensation reaction to synthesize the dibenzylidenecyclohexanone 8b was performed by reacting benzaldehyde 4 and cyclohexanone 2 (mole ratio of 2:1) with NaOH as catalyst for 2 min under microwave irradiation. The benzaldehyde derivatives used in this study were 4-methoxybenzaldehyde and 3,4-dimethoxybenzaldehyde and gave of (2E,6E)-bis(4-methoxy benzylidene)cyclohexanone 8a and (2E,6E)-bis(3,4-dimethoxybenzylide
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Prieto, P., A. de la Hoz, A. Díaz-Ortiz, and A. M. Rodríguez. "Understanding MAOS through computational chemistry." Chemical Society Reviews 46, no. 2 (2017): 431–51. http://dx.doi.org/10.1039/c6cs00393a.

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Dissertations / Theses on the topic "Microwave-assisted organic synthesis (MAOS)"

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Öhrngren, Per. "Tertiary Alcohol- or β-Hydroxy γ-Lactam-Based HIV-1 Protease Inhibitors : Microwave Applications in Batch and Continuous Flow Organic Synthesis". Doctoral thesis, Uppsala universitet, Avdelningen för organisk farmaceutisk kemi, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-160190.

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Since the outbreak of the HIV/AIDS pandemic in the 1980s, the disease has cost the lives of over 30 million people, and a further 33 million are currently living with the HIV infection. With the appropriate treatment, HIV/AIDS can today be regarded as a chronic but manageable disease. However, treatment is not available globally and UNAIDS still estimates that there are currently 5000 AIDS-related deaths worldwide per day. HIV protease inhibitors (PIs) constitute one of the fundaments of HIV treatment, and are commonly used in so-called highly active antiretroviral therapy (HAART), together wi
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Desai, Bimbisar. "Microwave assisted organic synthesis." Thesis, University of Surrey, 2002. http://epubs.surrey.ac.uk/842821/.

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The area of chemical research and synthesis increasingly recognises the need for improved technologies and methods, which involves chemical processes with less energy consumption, time savings, reduction and/or minimisation of waste, simple processes and an overall clean production. Microwave heating has been exploited in a variety of disciplines for many useful applications and organic synthesis is an area, which has benefited significantly over the past decade. The present study investigates organic reactions accelerated under microwave irradiations. In particular, the study involves use of
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Kajiwara, Yuichi. "Microwave-Assisted Synthesis of Organic-Inorganic Hybrids." 京都大学 (Kyoto University), 2011. http://hdl.handle.net/2433/142241.

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Zawahreh, Yousef 'Issa. "A novel microwave synthesis of calcium hydroxyapatite : optimisation and investigation of a microwave assisted reaction route." Thesis, Queen Mary, University of London, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.251711.

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Liao, Xiangjun 1970. "Dielectric properties and their application in microwave-assisted organic chemical reactions." Thesis, McGill University, 2002. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=38220.

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This study was designed to develop some predictive models for the dielectric properties of the chemicals and chemical reactions and make use of dielectric properties and microwave irradiation in the chemical reactions. Specifically, the dielectric properties of the following systems were investigated at microwave frequencies of 2450 and 915 MHz: (1) C1--C5 alcohols, (2) glucose aqueous solutions, (3) lysine aqueous solutions, (4) mimicked esterification reaction model systems of parahydroxybenzoic acid with methanol, 1-propanol and 1-butanol in the presence of para-toluene sulfonic acid as a c
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Lineberry, Aaron M. "Microwave-Assisted Synthesis of Small Ring Thia-Aza Mixed-Donor Ligands." University of Akron / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=akron1310944928.

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Grabicka, Bogna E. "Microwave-Assisted Synthesis of Ordered Mesoporous Organosilicas with Surface and Bridging Groups." Kent State University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=kent1290459085.

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Dai, Jianming. "Microwave-assisted extraction and synthesis studies and the scale-up study with the aid of FDTD simulation." Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=100342.

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The research undertaken in this thesis includes microwave-assisted extraction (MAE), synthesis, and the investigation of the scale-up of the microwave-assisted processes with the numerical aid.<br>The main goal of this research is to study the various problems associated with the scale-up of the microwave-assisted extraction and synthesis processes. Laboratory studies were carried out to investigate the microwave-assisted extraction of known components from peppermint leaves and American ginseng. Various factors that influence the extraction processes were studied. Microwave-assisted extractio
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Shanks, David. "Design, Synthesis and Evaluation of Catalytic Chalcogenide Antioxidants." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-6164.

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Fiorini, Valentina. "Sintesi di leganti ciclopentadienonici e piridilimidazolici per complessi metallici. Metodo classico e microonde a confronto." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2013. http://amslaurea.unibo.it/6015/.

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In questo elaborato è stata messa a punto una procedura sintetica, semplice e veloce che sfrutta la tecnica microonde per la sintesi di tetraarilciclopentadienoni variamente sostituiti mediante una condensazione bis-aldolica tra 1,3 difenilacetone con dichetoni aromatici variamente sostituiti. Questa nuova tecnica consente di ottenere tetraarilciclopentadienoni con rese da basse a buone in 25 minuti a 70°C. La stessa procedura sintetica è stata valutata per ottenere leganti piridilimidazolici, usando come fonte di azoto NH4OAc. Basse rese e la formazione di svariati sottoprodotti ha diretto lo
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Books on the topic "Microwave-assisted organic synthesis (MAOS)"

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Tierney, Jason P., and Pelle Lidstrm, eds. Microwave Assisted Organic Synthesis. Blackwell Publishing Ltd., 2005. http://dx.doi.org/10.1002/9781444305548.

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Tierney, Jason, Pelle Lidström, and Pelle Lidström. Microwave Assisted Organic Synthesis. Wiley & Sons, Incorporated, John, 2009.

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Microwave-assisted Organic Synthesis. Elsevier, 2005. http://dx.doi.org/10.1016/s1460-1567(05)x8001-1.

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(Editor), Jason P. Tierney, and Pelle Lidstrom (Editor), eds. Microwave Assisted Organic Synthesis. Blackwell, 2005.

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Ameta, Suresh C., Rakshit Ameta, Pinki B. Punjabi, and Chetna Ameta. Microwave-Assisted Organic Synthesis. Taylor & Francis Group, 2021.

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Tierney, Jason, and Pelle Lidström. Microwave Assisted Organic Synthesis. Wiley & Sons, Limited, John, 2009.

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Kappe, C. Oliver, and Erik van der Eycken. Microwave-Assisted Synthesis of Heterocycles. Springer, 2014.

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Bogdal, D. Microwave-Assisted Organic Synthesis: One Hundred Reaction Procedures. Elsevier Science & Technology Books, 2005.

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Bogdal, D. Microwave-Assisted Organic Synthesis: One Hundred Reaction Procedures. Elsevier Science & Technology Books, 2006.

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Microwave-assisted organic synthesis: A green chemical approach. Apple Academic Press Inc., 2015.

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Book chapters on the topic "Microwave-assisted organic synthesis (MAOS)"

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Alcázar, Jesus, and Juan de M. Muñoz. "Microwave-Assisted Continuous Flow Organic Synthesis (MACOS)." In Microwaves in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527651313.ch25.

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Bougrin, Khalid, and Rachid Benhida. "Microwave-Assisted Cycloaddition Reactions." In Microwaves in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527651313.ch17.

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Luque, Rafael, Alina Mariana Balu, and Duncan J. Macquarrie. "Microwave-Assisted Heterogeneously Catalyzed Processes." In Microwaves in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527651313.ch18.

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Appukkuttan, Prasad, and Erik Van der Eycken. "Microwave-Assisted Natural Product Chemistry." In Microwave Methods in Organic Synthesis. Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/128_051.

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Stolle, Achim, Peter Scholz, and Bernd Ondruschka. "Gaseous Reactants in Microwave-Assisted Synthesis." In Microwaves in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527651313.ch11.

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Corsaro, Antonino, Venerando Pistarà, Maria Assunta Chiacchio, and Giovanni Romeo. "A Journey into Recent Microwave-Assisted Carbohydrate Chemistry." In Microwaves in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527651313.ch21.

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Ondruschka, Bernd, Werner Bonrath, and Didier Stuerga. "Development and Design of Reactors in Microwave-Assisted Chemistry." In Microwaves in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527651313.ch2.

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Kruithof, Art, Eelco Ruijter, and Romano V. A. Orru. "Microwave-Assisted Multicomponent Reactions in the Synthesis of Heterocycles." In Microwaves in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527651313.ch24.

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Appukkuttan, Prasad, Vaibhav P. Mehta, and Erik Van der Eycken. "Recent Advances in Microwave-Assisted Solid-Phase Synthesis of Heterocycles." In Solid-Phase Organic Synthesis. John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118141649.ch8.

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Sharma, Nandini, Upendra K. Sharma, and Erik V. Van der Eycken. "Microwave-Assisted Organic Synthesis: Overview of Recent Applications." In Green Techniques for Organic Synthesis and Medicinal Chemistry. John Wiley & Sons, Ltd, 2018. http://dx.doi.org/10.1002/9781119288152.ch17.

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Conference papers on the topic "Microwave-assisted organic synthesis (MAOS)"

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Mangalagiu, Violeta, Dorina Amariucai-Mantu, Dumitrela Diaconu, Vasilichia Antoci, and Ionel Mangalagiu. "MICROWAVE AND ULTRASOUND ASSISTED SYNTHESIS AS ECOLOGICALLY FRIENDLY METHODS IN NITROGEN HETEROCYCLIC CHEMISTRY." In SGEM International Multidisciplinary Scientific GeoConference. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024v/6.2/s23.04.

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On the last few years, microwave and ultrasound irradiation has become a successful tool in modern medicinal and organic chemistry especially (but not only) because in many cases synthesis became ecologically friendly. As part of our ongoing efforts in the field of nitrogen heterocyclic derivatives, we present herein some core results obtained by our group in the field of N-alkylation and 3+2 cycloadditions reactions applied in the nitrogen heterocycles series, by using microwave and ultrasound irradiation. Comparative with conventional thermal heating, undeniable advantages of using microwave
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Lestari, I. I., D. U. C. Rahayu, D. A. Nurani, Y. K. Krisnandi, and E. Budianto. "Ethylenediamine-derived imidazoline synthesis using MAOS (Microwave Assisted Organic Synthesis) method." In PROCEEDINGS OF THE 4TH INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES (ISCPMS2018). AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5132493.

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Mujahiduzzakka, M., D. U. C. Rahayu, D. A. Nurani, and Y. K. Krisnandi. "Synthesis of oleic imidazoline derivative using MAOS (microwave assisted organic synthesis) method as corrosion inhibitor towards carbon steel." In PROCEEDINGS OF THE 5TH INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES (ISCPMS2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0008006.

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Andra, M. I., D. U. C. Rahayu, I. Abdullah, and Y. Krisnandi. "Ester-imidazoline: Modification of imidazoline using MAOS (microwave assisted organic synthesis) method as corrosion inhibitor towards carbon steel." In PROCEEDINGS OF THE 5TH INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES (ISCPMS2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0008002.

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Yuniastuti, A., D. U. C. Rahayu, D. A. Nurani, Y. K. Krisnandi, and E. Budianto. "Synthesis of imidazoline-linoleic derivative using MAOS (Microwave Assisted Organic Synthesis) method and its activity as corrosion inhibitor towards carbon steel." In PROCEEDINGS OF THE 4TH INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES (ISCPMS2018). AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5132494.

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Jordis, Ulrich, Klaus Gerdes, C. Kappe, and Jennifer Kremsner. "Development of Multi-Gram Scale Microwave Assisted Organic Synthesis (MAOS): Suzuki Coupling towards 2,4-Dimethyl-8-[2'-(2H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-5,8-dihydro-6H-pyrido[2,3-d]pyrimidin-7-one (Tasosartan)." In The 9th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01637.

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Seijas, Julio A., M. Pilar Vázquez-Tato, and Jose Crecente-Campo. "Microwave Assisted Synthesis of Coumarocoumarins." In The 16th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01111.

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Pizzo, Chiara, Peter Wipf, and Graciela Mahler. "Microwave assisted synthesis of biologically relevant selenosemicarbazones." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0067-1.

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Seijas, Julio, M. Vázquez-Tato, and José Crecente-Campo. "Microwave-assisted synthesis of 3-arylcoumarins." In The 12th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01259.

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Srivastava, Shweta, and Vandana Srivastava. "Microwave-Assisted Synthesis of Phthalein Dyes." In The 13th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00151.

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