Artykuły w czasopismach na temat „Organic reaction methodology”
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Chinchilla, Rafael, i Carmen Nájera. "The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry†". Chemical Reviews 107, nr 3 (marzec 2007): 874–922. http://dx.doi.org/10.1021/cr050992x.
Pełny tekst źródłaSharma, Sulekha. "Electro-organic Reactions: Direct and Indirect Electrolysis". Oriental Journal Of Chemistry 40, nr 2 (30.04.2024): 321–32. http://dx.doi.org/10.13005/ojc/400202.
Pełny tekst źródłaNoor, Rida, Ameer Fawad Zahoor, Muhammad Irfan, Syed Makhdoom Hussain, Sajjad Ahmad, Ali Irfan, Katarzyna Kotwica-Mojzych i Mariusz Mojzych. "Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications". Molecules 27, nr 17 (2.09.2022): 5654. http://dx.doi.org/10.3390/molecules27175654.
Pełny tekst źródłaLei, Ming, Qingtong Zhang, Douyong Min i 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, nr 2 (1.04.2020): 280–86. http://dx.doi.org/10.1166/jbmb.2020.1949.
Pełny tekst źródłaJimenez, David Esteban Quintero, Lucas Lima Zanin, Luan Farinelli Diniz, Javier Ellena i André Luiz Meleiro Porto. "Green Synthetic Methodology of (E)-2-cyano-3-aryl Selective Knoevenagel Adducts Under Microwave Irradiation". Current Microwave Chemistry 6, nr 1 (24.10.2019): 54–60. http://dx.doi.org/10.2174/2213335606666190906123431.
Pełny tekst źródłaLei, Jie, Jia Xu, Dian-Yong Tang, Jing-Wei Shao, Hong-yu Li, Zhong-Zhu Chen i Zhi-Gang Xu. "A concise and unexpected one-pot methodology for the synthesis of pyrazinone-fused pyridones". Organic Chemistry Frontiers 7, nr 18 (2020): 2657–63. http://dx.doi.org/10.1039/d0qo00590h.
Pełny tekst źródłaHakkou, H., D. Carrié, L. Paquin i J. P. Bazureau. "Ionic liquid-phase organic synthesis (IoLiPOS) methodology applied to cross aldol reaction". Russian Journal of Organic Chemistry 47, nr 3 (marzec 2011): 371–73. http://dx.doi.org/10.1134/s1070428011030079.
Pełny tekst źródłaReddy, K. Sateesh, Bandi Siva, S. Divya Reddy, N. Reddy Naresh, T. V. Pratap, B. Venkateswara Rao, Yi-An Hong i in. "In Situ FTIR Spectroscopic Monitoring of the Formation of the Arene Diazonium Salts and Its Applications to the Heck–Matsuda Reaction". Molecules 25, nr 9 (8.05.2020): 2199. http://dx.doi.org/10.3390/molecules25092199.
Pełny tekst źródłaRadhika, Sankaran, Mohan Neetha, Thaipparambil Aneeja i Gopinathan Anilkumar. "Microwave-assisted Amination Reactions: An Overview". Current Organic Chemistry 24, nr 19 (1.12.2020): 2235–55. http://dx.doi.org/10.2174/1385272824999200914111246.
Pełny tekst źródłaRoy, Snigdha. "Prins-Friedel-Crafts Cyclization: Synthesis of Diversely Functionalized Six- Membered Oxacycles". Current Organic Chemistry 25, nr 5 (15.03.2021): 635–51. http://dx.doi.org/10.2174/1385272825666210114105020.
Pełny tekst źródłaSukhorukov, Alexey Yu. "Interrupted Nef and Meyer Reactions: A Growing Point for Diversity-Oriented Synthesis Based on Nitro Compounds". Molecules 28, nr 2 (10.01.2023): 686. http://dx.doi.org/10.3390/molecules28020686.
Pełny tekst źródłaCrespo, Lívia T. C., Mônica R. Senra, Pierre M. Esteves i 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, nr 8 (18.06.2019): 627–32. http://dx.doi.org/10.2174/1570178615666180803152951.
Pełny tekst źródłaCimarelli, Cristina, Samuele Bordi, Pamela Piermattei, Maura Pellei, Fabio Del Bello i Enrico Marcantoni. "An Efficient Lewis Acid Catalyzed Povarov Reaction for the One-Pot Stereocontrolled Synthesis of Polyfunctionalized Tetrahydroquinolines". Synthesis 49, nr 24 (7.09.2017): 5387–95. http://dx.doi.org/10.1055/s-0036-1589104.
Pełny tekst źródłaRoesner, Stefan, i Varinder K. Aggarwal. "Enantioselective synthesis of (R)-tolterodine using lithiation/borylation–protodeboronation methodology". Canadian Journal of Chemistry 90, nr 11 (listopad 2012): 965–74. http://dx.doi.org/10.1139/v2012-069.
Pełny tekst źródłaLiu, Li, Yue Li, Tiao Huang, Dulin Kong i 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 (7.09.2021): 2321–28. http://dx.doi.org/10.3762/bjoc.17.150.
Pełny tekst źródłaCao, Liwei, Mikhail Kabeshov, Steven V. Ley i Alexei A. Lapkin. "In silico rationalisation of selectivity and reactivity in Pd-catalysed C–H activation reactions". Beilstein Journal of Organic Chemistry 16 (25.06.2020): 1465–75. http://dx.doi.org/10.3762/bjoc.16.122.
Pełny tekst źródłaHopkins, Megan, Zachary Brandeburg, Andrew Hanson i Angus Lamar. "Visible-Light, Iodine-Promoted Formation of N-Sulfonyl Imines and N-Alkylsulfonamides from Aldehydes and Hypervalent Iodine Reagents". Molecules 23, nr 8 (24.07.2018): 1838. http://dx.doi.org/10.3390/molecules23081838.
Pełny tekst źródłada Silva, Caren D. G., Ramesh Katla, Beatriz F. dos Santos, José M. C. Tavares Junior, Tábata B. Albuquerque, Vicente L. Kupfer, Andrelson W. Rinaldi i 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, nr 21 (21.08.2019): 4014–22. http://dx.doi.org/10.1055/s-0037-1611913.
Pełny tekst źródłaRossi, Laura I., i 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, nr 3 (6.02.2012): 819–26. http://dx.doi.org/10.1351/pac-con-11-07-13.
Pełny tekst źródłaHavránková, Eva, Jozef Csöllei i 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, nr 19 (5.10.2019): 3586. http://dx.doi.org/10.3390/molecules24193586.
Pełny tekst źródłaYusof, Nurul Atikah Amin, Nursyamsyila Mat Hadzir, Siti Efliza Ashari, Nor Suhaila Mohamad Hanapi i Rossuriati Dol Hamid. "Optimization of Enzymatic Synthesis of Betulinic Acid Amide in Organic Solvent by Response Surface Methodology (RSM)". Indonesian Journal of Chemistry 19, nr 4 (13.08.2019): 849. http://dx.doi.org/10.22146/ijc.34903.
Pełny tekst źródłaLeyva, Elisa, Denisse de Loera, Claudia G. Espinosa-González i Saúl Noriega. "Physicochemical Properties and Photochemical Reactions in Organic Crystals". Current Organic Chemistry 23, nr 3 (9.05.2019): 215–55. http://dx.doi.org/10.2174/1385272822666190313152105.
Pełny tekst źródłaCozzi, Pier Giorgio, Alessandro Mignogna i Luca Zoli. "Catalytic enantioselective Reformatsky reactions". Pure and Applied Chemistry 80, nr 5 (1.01.2008): 891–901. http://dx.doi.org/10.1351/pac200880050891.
Pełny tekst źródłaEscalante, Froylán, Alejandra Carranza-Hernández, Adelina García-Zamora i Efrén Aguilar-Garnica. "Optimization of Lignin-Based Biocatalyst Production from Pine Sawdust and Wheat Straw". Molecules 23, nr 8 (27.07.2018): 1877. http://dx.doi.org/10.3390/molecules23081877.
Pełny tekst źródłaYoshida, Jun-ichi, Heejin Kim, Hyune-Jea Lee, Daiki Torii i Yongju Jeon. "Integrated Synthesis Using Isothiocyanate-Substituted Aryllithiums by Flow Chemistry". Synlett 31, nr 19 (21.08.2020): 1899–902. http://dx.doi.org/10.1055/s-0040-1707251.
Pełny tekst źródłaRuini, Chiara, Erika Ferrari, Caterina Durante, Giulia Lanciotti, Paolo Neri, Anna Maria Ferrari i 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, nr 9 (3.05.2024): 2132. http://dx.doi.org/10.3390/molecules29092132.
Pełny tekst źródłaKanwal, Iram, Aqsa Mujahid, Nasir Rasool, Komal Rizwan, Ayesha Malik, Gulraiz Ahmad, Syed Adnan Ali Shah, Umer Rashid i 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, nr 4 (20.04.2020): 443. http://dx.doi.org/10.3390/catal10040443.
Pełny tekst źródłaYaseen, Muhammad, Zahid Farooq, Mian H. R. Mahmood, Sheikh Asrar Ahmad, Shahbaz Nazir, Khalid Mahmood Anjum i Syed Ali Raza Naqvi. "Synthesis of Novel Symmetric Porphyrin Schiff Base Dimers by Solid–Liquid Reaction Methodology". Journal of Heterocyclic Chemistry 56, nr 5 (2.04.2019): 1520–29. http://dx.doi.org/10.1002/jhet.3526.
Pełny tekst źródłaMondal, Dipayan, Pankaj Lal Kalar, Shivam Kori, Shovanlal Gayen i Kalpataru Das. "Recent Developments on Synthesis of Indole Derivatives Through Green Approaches and Their Pharmaceutical Applications". Current Organic Chemistry 24, nr 22 (18.12.2020): 2665–93. http://dx.doi.org/10.2174/1385272824999201111203812.
Pełny tekst źródłaYoda, Hidemi, Tetsuya Sengoku, Yuichiro Nagai i Toshiyasu Inuzuka. "New Synthetic Methodology Toward Azaspiro-γ-Lactones by Oxidative C–H Spirocyclization". Synlett 30, nr 02 (17.12.2018): 199–202. http://dx.doi.org/10.1055/s-0037-1611941.
Pełny tekst źródłaHakkou, H., D. Carrie, L. Paquin i J. P. Bazureau. "ChemInform Abstract: Ionic Liquid-Phase Organic Synthesis (IoLiPOS) Methodology Applied to Cross Aldol Reaction." ChemInform 42, nr 34 (28.07.2011): no. http://dx.doi.org/10.1002/chin.201134024.
Pełny tekst źródłaHarrington, David A. "Theory of electrochemical impedance of surface reactions: second-harmonic and large-amplitude response". Canadian Journal of Chemistry 75, nr 11 (1.11.1997): 1508–17. http://dx.doi.org/10.1139/v97-181.
Pełny tekst źródłaNacher-Luis, Anna, i Isidro M. Pastor. "1-(3,4-Dimethoxyphenyl)-3-(4-methoxyphenyl)-3-(1H-1,2,4-triazol-1-yl)propan-1-one". Molbank 2024, nr 1 (12.03.2024): M1791. http://dx.doi.org/10.3390/m1791.
Pełny tekst źródłaChen, Lianfen, Chaoyi Zhao, Weixian Mo, Chunsheng Li i Xiaoming Lin. "X-H Bond Insertion Promoted by Heterogeneous Dirhodium Metal–Organic Cage with Alkynes as Safe Carbene Precursors". Molecules 28, nr 2 (6.01.2023): 608. http://dx.doi.org/10.3390/molecules28020608.
Pełny tekst źródłaKreisberg, Jennifer D., Philip Magnus i Shirin Shinde. "Pummerer reaction methodology for the synthesis of 5-thiophenyl substituted oxazoles". Tetrahedron Letters 43, nr 41 (październik 2002): 7393–96. http://dx.doi.org/10.1016/s0040-4039(02)01704-5.
Pełny tekst źródłaBoddapati, S. N. Murthy, Ramana Tamminana, Ravi Kumar Gollapudi, Sharmila Nurbasha, Mohamed E. Assal, Osamah Alduhaish, Mohammed Rafiq H. Siddiqui, Hari Babu Bollikolla i Syed Farooq Adil. "Copper-Promoted One-Pot Approach: Synthesis of Benzimidazoles". Molecules 25, nr 8 (14.04.2020): 1788. http://dx.doi.org/10.3390/molecules25081788.
Pełny tekst źródłaBuskes, Melissa J., i Maria-Jesus Blanco. "Impact of Cross-Coupling Reactions in Drug Discovery and Development". Molecules 25, nr 15 (31.07.2020): 3493. http://dx.doi.org/10.3390/molecules25153493.
Pełny tekst źródłaCordes, Martin, i Markus Kalesse. "Very Recent Advances in Vinylogous Mukaiyama Aldol Reactions and Their Applications to Synthesis". Molecules 24, nr 17 (22.08.2019): 3040. http://dx.doi.org/10.3390/molecules24173040.
Pełny tekst źródłaZhang, Xin Ran, Wei Guang Li i Peng Fei Ren. "Natural Organic Matter Removal by UV/ Chlorine Process: Modeling and Optimization". Advanced Materials Research 807-809 (wrzesień 2013): 466–71. http://dx.doi.org/10.4028/www.scientific.net/amr.807-809.466.
Pełny tekst źródłaITO, Hisanaka, Yuji HANZAWA i Takeo TAGUCHI. "Development of New Synthetic Methodology Based on Zirconium-Mediated Carbon-Carbon Bond Forming Reaction." Journal of Synthetic Organic Chemistry, Japan 52, nr 3 (1994): 217–25. http://dx.doi.org/10.5059/yukigoseikyokaishi.52.217.
Pełny tekst źródłaDas, Subrata, Rupak Banik, Brajesh Kumar, Subhadip Roy, Noorussabah, Khursheed Amhad i Pradip K. Sukul. "A Green Approach for Organic Transformations Using Microwave Reactor". Current Organic Synthesis 16, nr 5 (17.10.2019): 730–64. http://dx.doi.org/10.2174/1570179416666190412160048.
Pełny tekst źródłaDevarajan, Nainamalai, i 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, nr 15 (2018): 2322–31. http://dx.doi.org/10.1039/c8qo00519b.
Pełny tekst źródłaChen, Ting, Song Chen, Shaomin Fu, Song Qin i Bo Liu. "Carbon–Oxygen Homocoupling of 2-Naphthols through Electrochemical Oxidative Dearomatization". Synlett 30, nr 08 (11.04.2019): 903–9. http://dx.doi.org/10.1055/s-0037-1611777.
Pełny tekst źródłaKumar, Rakesh, Leonard I. Wiebe i 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, nr 9 (1.09.1994): 2005–10. http://dx.doi.org/10.1139/v94-256.
Pełny tekst źródłaRomero-Ortega, Moisés, Ignacio Medina-Mercado, Ivann Zaragoza-Galicia i Horacio Olivo. "2-Trifluoromethyl-1,3-diazabutadienes as Useful Intermediates for the Construction of 2-Trifluoromethylpyrimidine Derivatives". Synthesis 50, nr 20 (16.07.2018): 4133–39. http://dx.doi.org/10.1055/s-0037-1610444.
Pełny tekst źródłaBannwart, Linda M., Pascal S. Rieder i Marcel Mayor. "2-(3-Cyanopropyldimethylsilyl)ethyl as a Polar Sulfur Protecting Group". Synthesis 51, nr 22 (3.09.2019): 4153–64. http://dx.doi.org/10.1055/s-0039-1690184.
Pełny tekst źródłaPandarus, Valerica, Geneviève Gingras, François Béland, Rosaria Ciriminna i Mario Pagliaro. "Clean and fast cross-coupling of aryl halides in one-pot". Beilstein Journal of Organic Chemistry 10 (22.04.2014): 897–901. http://dx.doi.org/10.3762/bjoc.10.87.
Pełny tekst źródłaLiu, Geng-Xin, Xiao-Ting Jie, Ge-Jun Niu, Li-Sheng Yang, Xing-Lin Li, Jian Luo i 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 (27.03.2024): 661–71. http://dx.doi.org/10.3762/bjoc.20.59.
Pełny tekst źródłaPatel, Chetananda, Amit Kumar, Pooja Patil i Abha Sharma. "Efficient Synthesis of Medicinally Important Benzylidene-indolin-2-one Derivatives Catalyzed by Biodegradable Amino Sugar “Meglumine”". Letters in Organic Chemistry 16, nr 7 (30.05.2019): 600–605. http://dx.doi.org/10.2174/1570178615666181030095728.
Pełny tekst źródłaArigela, Rajesh K., Sudhir K. Sharma, Brijesh Kumar i Bijoy Kundu. "Microwave-assisted three-component domino reaction: Synthesis of indolodiazepinotriazoles". Beilstein Journal of Organic Chemistry 9 (19.02.2013): 401–5. http://dx.doi.org/10.3762/bjoc.9.41.
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