Статті в журналах з теми "Organic reaction methodology"
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Chinchilla, Rafael, and Carmen Nájera. "The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry†." Chemical Reviews 107, no. 3 (March 2007): 874–922. http://dx.doi.org/10.1021/cr050992x.
Повний текст джерелаSharma, Sulekha. "Electro-organic Reactions: Direct and Indirect Electrolysis." Oriental Journal Of Chemistry 40, no. 2 (April 30, 2024): 321–32. http://dx.doi.org/10.13005/ojc/400202.
Повний текст джерелаNoor, Rida, Ameer Fawad Zahoor, Muhammad Irfan, Syed Makhdoom Hussain, Sajjad Ahmad, Ali Irfan, Katarzyna Kotwica-Mojzych, and Mariusz Mojzych. "Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications." Molecules 27, no. 17 (September 2, 2022): 5654. http://dx.doi.org/10.3390/molecules27175654.
Повний текст джерелаLei, Ming, Qingtong Zhang, Douyong Min, and Shuangfei Wang. "The Treatment of Absorbable Organic Halogens and Organic Compounds in Simulated Bleaching Effluents Through the Response Surface Methodology Optimized Fenton System." Journal of Biobased Materials and Bioenergy 14, no. 2 (April 1, 2020): 280–86. http://dx.doi.org/10.1166/jbmb.2020.1949.
Повний текст джерелаJimenez, David Esteban Quintero, Lucas Lima Zanin, Luan Farinelli Diniz, Javier Ellena, and André Luiz Meleiro Porto. "Green Synthetic Methodology of (E)-2-cyano-3-aryl Selective Knoevenagel Adducts Under Microwave Irradiation." Current Microwave Chemistry 6, no. 1 (October 24, 2019): 54–60. http://dx.doi.org/10.2174/2213335606666190906123431.
Повний текст джерелаLei, Jie, Jia Xu, Dian-Yong Tang, Jing-Wei Shao, Hong-yu Li, Zhong-Zhu Chen, and Zhi-Gang Xu. "A concise and unexpected one-pot methodology for the synthesis of pyrazinone-fused pyridones." Organic Chemistry Frontiers 7, no. 18 (2020): 2657–63. http://dx.doi.org/10.1039/d0qo00590h.
Повний текст джерелаHakkou, H., D. Carrié, L. Paquin, and J. P. Bazureau. "Ionic liquid-phase organic synthesis (IoLiPOS) methodology applied to cross aldol reaction." Russian Journal of Organic Chemistry 47, no. 3 (March 2011): 371–73. http://dx.doi.org/10.1134/s1070428011030079.
Повний текст джерелаReddy, K. Sateesh, Bandi Siva, S. Divya Reddy, N. Reddy Naresh, T. V. Pratap, B. Venkateswara Rao, Yi-An Hong, et al. "In Situ FTIR Spectroscopic Monitoring of the Formation of the Arene Diazonium Salts and Its Applications to the Heck–Matsuda Reaction." Molecules 25, no. 9 (May 8, 2020): 2199. http://dx.doi.org/10.3390/molecules25092199.
Повний текст джерелаRadhika, Sankaran, Mohan Neetha, Thaipparambil Aneeja, and Gopinathan Anilkumar. "Microwave-assisted Amination Reactions: An Overview." Current Organic Chemistry 24, no. 19 (December 1, 2020): 2235–55. http://dx.doi.org/10.2174/1385272824999200914111246.
Повний текст джерелаRoy, Snigdha. "Prins-Friedel-Crafts Cyclization: Synthesis of Diversely Functionalized Six- Membered Oxacycles." Current Organic Chemistry 25, no. 5 (March 15, 2021): 635–51. http://dx.doi.org/10.2174/1385272825666210114105020.
Повний текст джерелаSukhorukov, Alexey Yu. "Interrupted Nef and Meyer Reactions: A Growing Point for Diversity-Oriented Synthesis Based on Nitro Compounds." Molecules 28, no. 2 (January 10, 2023): 686. http://dx.doi.org/10.3390/molecules28020686.
Повний текст джерелаCrespo, Lívia T. C., Mônica R. Senra, Pierre M. Esteves та Marcio C. S. de Mattos. "Tribromoisocyanuric Acid as a Green Cohalogenating Reagent: An Efficient Transformation of Alkynes into α,α-Dibromoketones and Vicinal Dibromoalkenes". Letters in Organic Chemistry 16, № 8 (18 червня 2019): 627–32. http://dx.doi.org/10.2174/1570178615666180803152951.
Повний текст джерелаCimarelli, Cristina, Samuele Bordi, Pamela Piermattei, Maura Pellei, Fabio Del Bello, and Enrico Marcantoni. "An Efficient Lewis Acid Catalyzed Povarov Reaction for the One-Pot Stereocontrolled Synthesis of Polyfunctionalized Tetrahydroquinolines." Synthesis 49, no. 24 (September 7, 2017): 5387–95. http://dx.doi.org/10.1055/s-0036-1589104.
Повний текст джерелаRoesner, Stefan, and Varinder K. Aggarwal. "Enantioselective synthesis of (R)-tolterodine using lithiation/borylation–protodeboronation methodology." Canadian Journal of Chemistry 90, no. 11 (November 2012): 965–74. http://dx.doi.org/10.1139/v2012-069.
Повний текст джерелаLiu, Li, Yue Li, Tiao Huang, Dulin Kong, and Mingshu Wu. "A novel methodology for the efficient synthesis of 3-monohalooxindoles by acidolysis of 3-phosphate-substituted oxindoles with haloid acids." Beilstein Journal of Organic Chemistry 17 (September 7, 2021): 2321–28. http://dx.doi.org/10.3762/bjoc.17.150.
Повний текст джерелаCao, Liwei, Mikhail Kabeshov, Steven V. Ley, and Alexei A. Lapkin. "In silico rationalisation of selectivity and reactivity in Pd-catalysed C–H activation reactions." Beilstein Journal of Organic Chemistry 16 (June 25, 2020): 1465–75. http://dx.doi.org/10.3762/bjoc.16.122.
Повний текст джерелаHopkins, Megan, Zachary Brandeburg, Andrew Hanson, and Angus Lamar. "Visible-Light, Iodine-Promoted Formation of N-Sulfonyl Imines and N-Alkylsulfonamides from Aldehydes and Hypervalent Iodine Reagents." Molecules 23, no. 8 (July 24, 2018): 1838. http://dx.doi.org/10.3390/molecules23081838.
Повний текст джерелаda Silva, Caren D. G., Ramesh Katla, Beatriz F. dos Santos, José M. C. Tavares Junior, Tábata B. Albuquerque, Vicente L. Kupfer, Andrelson W. Rinaldi, and Nelson L. C. Domingues. "Cobalt Used as a Novel and Reusable Catalyst: A New and One-Pot Synthesis of Isatin-Derived N,S-Acetals Using Substituted Isatins and Thiols." Synthesis 51, no. 21 (August 21, 2019): 4014–22. http://dx.doi.org/10.1055/s-0037-1611913.
Повний текст джерелаRossi, Laura I., and Manuel I. Velasco. "Alternatives to free molecular halogens as chemoselective reactants: Catalysis of organic reactions with reusable complexes of halogen metal salts." Pure and Applied Chemistry 84, no. 3 (February 6, 2012): 819–26. http://dx.doi.org/10.1351/pac-con-11-07-13.
Повний текст джерелаHavránková, Eva, Jozef Csöllei, and Pavel Pazdera. "New Approach for the One-Pot Synthesis of 1,3,5-Triazine Derivatives: Application of Cu(I) Supported on a Weakly Acidic Cation-Exchanger Resin in a Comparative Study." Molecules 24, no. 19 (October 5, 2019): 3586. http://dx.doi.org/10.3390/molecules24193586.
Повний текст джерелаYusof, Nurul Atikah Amin, Nursyamsyila Mat Hadzir, Siti Efliza Ashari, Nor Suhaila Mohamad Hanapi, and Rossuriati Dol Hamid. "Optimization of Enzymatic Synthesis of Betulinic Acid Amide in Organic Solvent by Response Surface Methodology (RSM)." Indonesian Journal of Chemistry 19, no. 4 (August 13, 2019): 849. http://dx.doi.org/10.22146/ijc.34903.
Повний текст джерелаLeyva, Elisa, Denisse de Loera, Claudia G. Espinosa-González, and Saúl Noriega. "Physicochemical Properties and Photochemical Reactions in Organic Crystals." Current Organic Chemistry 23, no. 3 (May 9, 2019): 215–55. http://dx.doi.org/10.2174/1385272822666190313152105.
Повний текст джерелаCozzi, Pier Giorgio, Alessandro Mignogna, and Luca Zoli. "Catalytic enantioselective Reformatsky reactions." Pure and Applied Chemistry 80, no. 5 (January 1, 2008): 891–901. http://dx.doi.org/10.1351/pac200880050891.
Повний текст джерелаEscalante, Froylán, Alejandra Carranza-Hernández, Adelina García-Zamora, and Efrén Aguilar-Garnica. "Optimization of Lignin-Based Biocatalyst Production from Pine Sawdust and Wheat Straw." Molecules 23, no. 8 (July 27, 2018): 1877. http://dx.doi.org/10.3390/molecules23081877.
Повний текст джерелаYoshida, Jun-ichi, Heejin Kim, Hyune-Jea Lee, Daiki Torii, and Yongju Jeon. "Integrated Synthesis Using Isothiocyanate-Substituted Aryllithiums by Flow Chemistry." Synlett 31, no. 19 (August 21, 2020): 1899–902. http://dx.doi.org/10.1055/s-0040-1707251.
Повний текст джерелаRuini, Chiara, Erika Ferrari, Caterina Durante, Giulia Lanciotti, Paolo Neri, Anna Maria Ferrari, and Roberto Rosa. "Integrated Approach of Life Cycle Assessment and Experimental Design in the Study of A Model Organic Reaction: New Perspectives in Renewable Vanillin-Derived Chemicals." Molecules 29, no. 9 (May 3, 2024): 2132. http://dx.doi.org/10.3390/molecules29092132.
Повний текст джерелаKanwal, Iram, Aqsa Mujahid, Nasir Rasool, Komal Rizwan, Ayesha Malik, Gulraiz Ahmad, Syed Adnan Ali Shah, Umer Rashid, and Nadiah Mad Nasir. "Palladium and Copper Catalyzed Sonogashira cross Coupling an Excellent Methodology for C-C Bond Formation over 17 Years: A Review." Catalysts 10, no. 4 (April 20, 2020): 443. http://dx.doi.org/10.3390/catal10040443.
Повний текст джерелаYaseen, Muhammad, Zahid Farooq, Mian H. R. Mahmood, Sheikh Asrar Ahmad, Shahbaz Nazir, Khalid Mahmood Anjum, and Syed Ali Raza Naqvi. "Synthesis of Novel Symmetric Porphyrin Schiff Base Dimers by Solid–Liquid Reaction Methodology." Journal of Heterocyclic Chemistry 56, no. 5 (April 2, 2019): 1520–29. http://dx.doi.org/10.1002/jhet.3526.
Повний текст джерелаMondal, Dipayan, Pankaj Lal Kalar, Shivam Kori, Shovanlal Gayen, and Kalpataru Das. "Recent Developments on Synthesis of Indole Derivatives Through Green Approaches and Their Pharmaceutical Applications." Current Organic Chemistry 24, no. 22 (December 18, 2020): 2665–93. http://dx.doi.org/10.2174/1385272824999201111203812.
Повний текст джерелаYoda, Hidemi, Tetsuya Sengoku, Yuichiro Nagai та Toshiyasu Inuzuka. "New Synthetic Methodology Toward Azaspiro-γ-Lactones by Oxidative C–H Spirocyclization". Synlett 30, № 02 (17 грудня 2018): 199–202. http://dx.doi.org/10.1055/s-0037-1611941.
Повний текст джерелаHakkou, H., D. Carrie, L. Paquin, and J. P. Bazureau. "ChemInform Abstract: Ionic Liquid-Phase Organic Synthesis (IoLiPOS) Methodology Applied to Cross Aldol Reaction." ChemInform 42, no. 34 (July 28, 2011): no. http://dx.doi.org/10.1002/chin.201134024.
Повний текст джерелаHarrington, David A. "Theory of electrochemical impedance of surface reactions: second-harmonic and large-amplitude response." Canadian Journal of Chemistry 75, no. 11 (November 1, 1997): 1508–17. http://dx.doi.org/10.1139/v97-181.
Повний текст джерелаNacher-Luis, Anna, and Isidro M. Pastor. "1-(3,4-Dimethoxyphenyl)-3-(4-methoxyphenyl)-3-(1H-1,2,4-triazol-1-yl)propan-1-one." Molbank 2024, no. 1 (March 12, 2024): M1791. http://dx.doi.org/10.3390/m1791.
Повний текст джерелаChen, Lianfen, Chaoyi Zhao, Weixian Mo, Chunsheng Li, and Xiaoming Lin. "X-H Bond Insertion Promoted by Heterogeneous Dirhodium Metal–Organic Cage with Alkynes as Safe Carbene Precursors." Molecules 28, no. 2 (January 6, 2023): 608. http://dx.doi.org/10.3390/molecules28020608.
Повний текст джерелаKreisberg, Jennifer D., Philip Magnus, and Shirin Shinde. "Pummerer reaction methodology for the synthesis of 5-thiophenyl substituted oxazoles." Tetrahedron Letters 43, no. 41 (October 2002): 7393–96. http://dx.doi.org/10.1016/s0040-4039(02)01704-5.
Повний текст джерелаBoddapati, S. N. Murthy, Ramana Tamminana, Ravi Kumar Gollapudi, Sharmila Nurbasha, Mohamed E. Assal, Osamah Alduhaish, Mohammed Rafiq H. Siddiqui, Hari Babu Bollikolla, and Syed Farooq Adil. "Copper-Promoted One-Pot Approach: Synthesis of Benzimidazoles." Molecules 25, no. 8 (April 14, 2020): 1788. http://dx.doi.org/10.3390/molecules25081788.
Повний текст джерелаBuskes, Melissa J., and Maria-Jesus Blanco. "Impact of Cross-Coupling Reactions in Drug Discovery and Development." Molecules 25, no. 15 (July 31, 2020): 3493. http://dx.doi.org/10.3390/molecules25153493.
Повний текст джерелаCordes, Martin, and Markus Kalesse. "Very Recent Advances in Vinylogous Mukaiyama Aldol Reactions and Their Applications to Synthesis." Molecules 24, no. 17 (August 22, 2019): 3040. http://dx.doi.org/10.3390/molecules24173040.
Повний текст джерелаZhang, Xin Ran, Wei Guang Li, and Peng Fei Ren. "Natural Organic Matter Removal by UV/ Chlorine Process: Modeling and Optimization." Advanced Materials Research 807-809 (September 2013): 466–71. http://dx.doi.org/10.4028/www.scientific.net/amr.807-809.466.
Повний текст джерелаITO, Hisanaka, Yuji HANZAWA, and Takeo TAGUCHI. "Development of New Synthetic Methodology Based on Zirconium-Mediated Carbon-Carbon Bond Forming Reaction." Journal of Synthetic Organic Chemistry, Japan 52, no. 3 (1994): 217–25. http://dx.doi.org/10.5059/yukigoseikyokaishi.52.217.
Повний текст джерелаDas, Subrata, Rupak Banik, Brajesh Kumar, Subhadip Roy, Noorussabah, Khursheed Amhad, and Pradip K. Sukul. "A Green Approach for Organic Transformations Using Microwave Reactor." Current Organic Synthesis 16, no. 5 (October 17, 2019): 730–64. http://dx.doi.org/10.2174/1570179416666190412160048.
Повний текст джерелаDevarajan, Nainamalai, and Palaniswamy Suresh. "Copper-catalyzed oxidative coupling of arylboronic acids with aryl carboxylic acids: Cu3(BTC)2 MOF as a sustainable catalyst to access aryl esters." Organic Chemistry Frontiers 5, no. 15 (2018): 2322–31. http://dx.doi.org/10.1039/c8qo00519b.
Повний текст джерелаChen, Ting, Song Chen, Shaomin Fu, Song Qin, and Bo Liu. "Carbon–Oxygen Homocoupling of 2-Naphthols through Electrochemical Oxidative Dearomatization." Synlett 30, no. 08 (April 11, 2019): 903–9. http://dx.doi.org/10.1055/s-0037-1611777.
Повний текст джерелаKumar, Rakesh, Leonard I. Wiebe, and Edward E. Knaus. "A mild and efficient methodology for the synthesis of 5-halogeno uracil nucleosides that occurs via a 5-halogeno-6-azido-5,6-dihydro intermediate." Canadian Journal of Chemistry 72, no. 9 (September 1, 1994): 2005–10. http://dx.doi.org/10.1139/v94-256.
Повний текст джерелаRomero-Ortega, Moisés, Ignacio Medina-Mercado, Ivann Zaragoza-Galicia, and Horacio Olivo. "2-Trifluoromethyl-1,3-diazabutadienes as Useful Intermediates for the Construction of 2-Trifluoromethylpyrimidine Derivatives." Synthesis 50, no. 20 (July 16, 2018): 4133–39. http://dx.doi.org/10.1055/s-0037-1610444.
Повний текст джерелаBannwart, Linda M., Pascal S. Rieder, and Marcel Mayor. "2-(3-Cyanopropyldimethylsilyl)ethyl as a Polar Sulfur Protecting Group." Synthesis 51, no. 22 (September 3, 2019): 4153–64. http://dx.doi.org/10.1055/s-0039-1690184.
Повний текст джерелаPandarus, Valerica, Geneviève Gingras, François Béland, Rosaria Ciriminna, and Mario Pagliaro. "Clean and fast cross-coupling of aryl halides in one-pot." Beilstein Journal of Organic Chemistry 10 (April 22, 2014): 897–901. http://dx.doi.org/10.3762/bjoc.10.87.
Повний текст джерелаLiu, Geng-Xin, Xiao-Ting Jie, Ge-Jun Niu, Li-Sheng Yang, Xing-Lin Li, Jian Luo, and Wen-Hao Hu. "Palladium-catalyzed three-component radical-polar crossover carboamination of 1,3-dienes or allenes with diazo esters and amines." Beilstein Journal of Organic Chemistry 20 (March 27, 2024): 661–71. http://dx.doi.org/10.3762/bjoc.20.59.
Повний текст джерелаPatel, Chetananda, Amit Kumar, Pooja Patil, and Abha Sharma. "Efficient Synthesis of Medicinally Important Benzylidene-indolin-2-one Derivatives Catalyzed by Biodegradable Amino Sugar “Meglumine”." Letters in Organic Chemistry 16, no. 7 (May 30, 2019): 600–605. http://dx.doi.org/10.2174/1570178615666181030095728.
Повний текст джерелаArigela, Rajesh K., Sudhir K. Sharma, Brijesh Kumar, and Bijoy Kundu. "Microwave-assisted three-component domino reaction: Synthesis of indolodiazepinotriazoles." Beilstein Journal of Organic Chemistry 9 (February 19, 2013): 401–5. http://dx.doi.org/10.3762/bjoc.9.41.
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