Статті в журналах з теми "Aromatic condensation"
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Witzig, Reto M., and Christof Sparr. "Synthesis of Enantioenriched Tetra-ortho-3,3′-substituted Biaryls by Small-Molecule-Catalyzed Noncanonical Polyketide Cyclizations." Synlett 31, no. 01 (October 22, 2019): 13–20. http://dx.doi.org/10.1055/s-0039-1690215.
Повний текст джерелаMoth‐Poulsen, Kasper, Theis Reenberg, Thomas Bjørnholm, and Jørn B. Christensen. "Microwave Assisted Condensation of Aromatic Methyl Groups with Aromatic Aldehydes." Synthetic Communications 34, no. 12 (December 31, 2004): 2215–21. http://dx.doi.org/10.1081/scc-120038503.
Повний текст джерелаMiller, J. Houston. "Aromatic excimers: evidence for polynuclear aromatic hydrocarbon condensation in flames." Proceedings of the Combustion Institute 30, no. 1 (January 2005): 1381–88. http://dx.doi.org/10.1016/j.proci.2004.08.192.
Повний текст джерелаKundu, Kshama, and Sandip Nayak. "Camphor-10-sulfonic acid catalyzed condensation of 2-naphthol with aromatic/aliphatic aldehydes to 14-aryl/alkyl-14H-dibenzo[a,j]xanthenes." Journal of the Serbian Chemical Society 79, no. 9 (2014): 1051–58. http://dx.doi.org/10.2298/jsc130805021k.
Повний текст джерелаHe, Yan-Hong, Gang-Qiang Wang, Ke-Ling Xu, and Zhi Guan. "An Efficient Procedure for the Synthesis of Polysubstituted Pyrroles in an Ionic Liquid." Zeitschrift für Naturforschung B 66, no. 2 (February 1, 2011): 191–96. http://dx.doi.org/10.1515/znb-2011-0212.
Повний текст джерелаPelageev, D. N., and V. Ph Anufriev. "Condensation of hydroxy naphthazarins with aromatic aldehydes." Russian Chemical Bulletin 57, no. 11 (November 2008): 2335–39. http://dx.doi.org/10.1007/s11172-008-0332-0.
Повний текст джерелаParomov, Artyom E., Sergey V. Sysolyatin, and Irina A. Shchurova. "Condensation of 4-Tert-butyl-2,6-dimethylbenzenesulfonamide with Glyoxal and Reaction Features: A New Process for Symmetric and Asymmetric Aromatic Sulfones." Molecules 27, no. 22 (November 12, 2022): 7793. http://dx.doi.org/10.3390/molecules27227793.
Повний текст джерелаFairhurst, Magnus, Muhammad Zeeshan, Bengt Haug, and Annette Bayer. "Aldol Condensations on a 3-Alkylidene-2,5-diketopiperazine: Synthesis of Two Marine Natural Products." Synlett 29, no. 10 (January 30, 2018): 1303–6. http://dx.doi.org/10.1055/s-0036-1591755.
Повний текст джерелаBadiger, Krishnappa B., and Kantharaju Kamanna. "Knoevenagel condensation reaction catalysed by agro-waste extract as a greener solvent catalyst." Organic Communications 14, no. 1 (March 26, 2021): 81–91. http://dx.doi.org/10.25135/acg.oc.99.21.01.1948.
Повний текст джерелаChang, Guan Jun, Lin Zhang, and Run Xiong Lin. "Synthesis of Poly(Aryl Sulfone Benzimidazole) Sulfone." Advanced Materials Research 284-286 (July 2011): 1867–70. http://dx.doi.org/10.4028/www.scientific.net/amr.284-286.1867.
Повний текст джерелаPopov-Pergal, Katarina, and Miroslav Pergal. "Base Catalyzed Condensation of Thiobarbituric Acid with Some Aromatic Aldehydes." Collection of Czechoslovak Chemical Communications 57, no. 5 (1992): 1153–55. http://dx.doi.org/10.1135/cccc19921153.
Повний текст джерелаDatta, Arup. "Bismuth (III) Triflate: A Mild, Efficient Promoter for the Synthesis of Trisubstituted Alkenes through Knoevenagel Condensation." Oriental Journal Of Chemistry 36, no. 05 (October 25, 2020): 843–49. http://dx.doi.org/10.13005/ojc/360507.
Повний текст джерелаGavilan Marin, Lisseth, Salma Bejaoui, Gregory Gate, Michael Haggmark, Nathan Svadlenak, Mattanjah de Vries, Ella Sciamma-O’Brien, and Farid Salama. "Low-temperature condensation of carbonaceous dust grains from PAHs." Proceedings of the International Astronomical Union 15, S350 (April 2019): 465–67. http://dx.doi.org/10.1017/s174392131900646x.
Повний текст джерелаAbdel-Latif, Nehad A. "Synthesis and Antidepressant Activity of Some New Coumarin Derivatives." Scientia Pharmaceutica 73, no. 4 (December 30, 2005): 193–216. http://dx.doi.org/10.3797/scipharm.aut-05-15.
Повний текст джерелаMedien, H. A. A. "Kinetic Studies of Condensation of Aromatic Aldehydes with Meldrum’s Acid." Zeitschrift für Naturforschung B 57, no. 11 (November 1, 2002): 1320–26. http://dx.doi.org/10.1515/znb-2002-1119.
Повний текст джерелаGreen, James R., Babajide I. Alo, Marek Majewski та Victor Snieckus. "γ-Silylated α,β-unsaturated amides — Preparation by [1,5]-sigmatropic rearrangement and use as masked dienolate equivalents in carbonyl condensations". Canadian Journal of Chemistry 87, № 6 (червень 2009): 745–59. http://dx.doi.org/10.1139/v09-054.
Повний текст джерелаLi, Ming, Yadong Zhang, Shitao Yu, Congxia Xie, Dong Liu, Shiwei Liu, Ruiyang Zhao, and Bing Bian. "Preparation and characterization of petroleum-based mesophase pitch by thermal condensation with in-process hydrogenation." RSC Advances 8, no. 53 (2018): 30230–38. http://dx.doi.org/10.1039/c8ra04679d.
Повний текст джерелаLan, Wu, and Jeremy S. Luterbacher. "Preventing Lignin Condensation to Facilitate Aromatic Monomer Production." CHIMIA International Journal for Chemistry 73, no. 7 (August 21, 2019): 591–98. http://dx.doi.org/10.2533/chimia.2019.591.
Повний текст джерелаSelvaraj, S., A. Dhanabalan, S. Perumal, and N. Arumugam. "CONDENSATION OF SOME AROMATIC ALDEHYDES WITH DIMETHYL SULFONE." Phosphorus and Sulfur and the Related Elements 39, no. 3-4 (October 1988): 217–20. http://dx.doi.org/10.1080/03086648808072878.
Повний текст джерелаNakamura, Asumaru. "Application of aromatic condensation polymers for membrane materials." Kobunshi 35, no. 12 (1986): 1078–81. http://dx.doi.org/10.1295/kobunshi.35.1078.
Повний текст джерелаWiedemeier, Daniel B., Samuel Abiven, William C. Hockaday, Marco Keiluweit, Markus Kleber, Caroline A. Masiello, Anna V. McBeath, et al. "Aromaticity and degree of aromatic condensation of char." Organic Geochemistry 78 (January 2015): 135–43. http://dx.doi.org/10.1016/j.orggeochem.2014.10.002.
Повний текст джерелаMcNulty, James, Jennifer A. Steere, and Sonja Wolf. "The ultrasound promoted Knoevenagel condensation of aromatic aldehydes." Tetrahedron Letters 39, no. 44 (October 1998): 8013–16. http://dx.doi.org/10.1016/s0040-4039(98)01789-4.
Повний текст джерелаKomorek, Joanna. "Internal Structure of Vitrinite and Sporinite in the View of Micro-FTIR Spectroscopy Using the Example of Coal from the Seam 405 of the Upper-Silesian Coal Basin (USCB)." Archives of Mining Sciences 61, no. 4 (December 1, 2016): 729–48. http://dx.doi.org/10.1515/amsc-2016-0050.
Повний текст джерелаIbrahim, Mohamed N., and Salah E. A. Sharif. "Synthesis, Characterization and Use of Schiff Bases as Fluorimetric Analytical Reagents." E-Journal of Chemistry 4, no. 4 (2007): 531–35. http://dx.doi.org/10.1155/2007/191805.
Повний текст джерелаSun, Yawei, Qiuyan Wang, Shuying Zhang, Hao Li, Jinli Zhang, Daqing Li, and Wei Li. "Synthesis of aromatic-doped polycaprolactone with tunable degradation behavior." Polymer Chemistry 9, no. 28 (2018): 3931–43. http://dx.doi.org/10.1039/c8py00374b.
Повний текст джерелаLei, Min, Lei Ma, and Lihong Hu. "VB1–Al2O3-catalyzed one-pot condensation of aromatic ketone, aromatic aldehyde, and amide." Tetrahedron Letters 51, no. 36 (September 2010): 4746–49. http://dx.doi.org/10.1016/j.tetlet.2010.07.008.
Повний текст джерелаIbrahim, Mohamed N., and Salaheddin A. I. Sharif. "Synthesis, Characterization and Use of Schiff Bases as Fluorimetric Analytical Reagents (Part II)." E-Journal of Chemistry 8, no. 1 (2011): 180–84. http://dx.doi.org/10.1155/2011/821616.
Повний текст джерелаNguyen, T. B., L. Ermolenko, and A. Al-Mourabit. "Redox condensation of o-halonitrobenzene with 1,2,3,4-tetrahydroisoquinoline: involvement of an unexpected auto-catalyzed redox cascade." Chemical Communications 52, no. 27 (2016): 4914–17. http://dx.doi.org/10.1039/c6cc01436d.
Повний текст джерелаDubey, Rahul, Vinay K. Singh, Laxmi Kant Sharma, Abhishek Upadhyay, Narendra Kumar, and Rana Krishna Pal Singh. "A convenient electro-catalyzed multicomponent synthesis of 4H-thiopyran derivatives." New Journal of Chemistry 41, no. 16 (2017): 7836–39. http://dx.doi.org/10.1039/c7nj01211j.
Повний текст джерелаBaum, James Clayton, Jimat Bolhassan, Richard Francis Langler, Paul Joseph Pujol, and Raj Kumar Raheja. "Sulfonyl esters. 2. CS cleavage in some substitution reactions of nitrobenzenesulfonates." Canadian Journal of Chemistry 68, no. 8 (August 1, 1990): 1450–55. http://dx.doi.org/10.1139/v90-222.
Повний текст джерелаRaunio, J., J. Mannoja, T. Nguyen, N. Ahmad, N. M. Kemppainen, R. G. Franzén, M. Kandhavelu, and N. R. Candeias. "Base catalysed N-functionalisation of boroxazolidones." RSC Advances 7, no. 33 (2017): 20620–27. http://dx.doi.org/10.1039/c7ra03266h.
Повний текст джерелаCoen, Serge, Laurence Martinet-Reboul, and Alain Périchaud. "Synthesis of Polyfunctional Aromatic Imines with Zwitterionic Character." Journal of Chemical Research 23, no. 10 (October 1999): 592–93. http://dx.doi.org/10.1177/174751989902301003.
Повний текст джерелаIranpoor, N., B. Zeynizadeh, and A. Aghapour. "Aldol Condensation of Cycloalkanones with Aromatic Aldehydes Catalysed with TiCl3(SO3CF3)." Journal of Chemical Research 23, no. 9 (September 1999): 554–55. http://dx.doi.org/10.1177/174751989902300918.
Повний текст джерелаYi, Fengping, Yanqing Peng, Gonghua Song, and Jizong Li. "Solid Phase Synthesis of Aminochalcones." Journal of Chemical Research 2005, no. 5 (May 2005): 311–12. http://dx.doi.org/10.3184/0308234054323931.
Повний текст джерелаEndud, Salasiah Binti, and Nadirah Zawani Binti Mohd Nesfu. "Bimetallic Basic Catalyst Comprising Niobium and Cesium Supported on MCM-48 for the Claisen-Schmidt Condensation." Advanced Materials Research 545 (July 2012): 379–84. http://dx.doi.org/10.4028/www.scientific.net/amr.545.379.
Повний текст джерелаSachar, Anand, Poonam Gupta, Shallu Gupta, and R. L. Sharma. "A novel approach towards the synthesis of tricyclic systems based on pyridine, pyran, thiopyran, azepine, oxepin, thiepin, and pyrimidine rings under different solvent conditions." Canadian Journal of Chemistry 88, no. 5 (May 2010): 478–84. http://dx.doi.org/10.1139/v10-015.
Повний текст джерелаRubinov, D. B., T. A. Zheldakova, R. A. Zheldakova, I. L. Rubinova, A. V. Baranovski, and F. A. Lakhvich. "Condensation of 2-acylcyclohexane-1,3-diones with aromatic aldehydes." Russian Journal of General Chemistry 82, no. 1 (January 2012): 122–30. http://dx.doi.org/10.1134/s1070363212010203.
Повний текст джерелаKozlov, N. G., and A. B. Tereshko. "Condensation of 5-quinolylamine with aromatic aldehydes and dimedone." Russian Journal of Organic Chemistry 53, no. 5 (May 2017): 686–90. http://dx.doi.org/10.1134/s1070428017050074.
Повний текст джерелаRusanov, Aleksandr L., D. Yu Likhatchev, and K. Müllen. "Proton-conducting electrolyte membranes based on aromatic condensation polymers." Russian Chemical Reviews 71, no. 9 (September 30, 2002): 761–74. http://dx.doi.org/10.1070/rc2002v071n09abeh000740.
Повний текст джерелаMcBeath, Anna V., and Ronald J. Smernik. "Variation in the degree of aromatic condensation of chars." Organic Geochemistry 40, no. 12 (December 2009): 1161–68. http://dx.doi.org/10.1016/j.orggeochem.2009.09.006.
Повний текст джерелаLetunov, V. I., and N. P. Soldatova. "Co-condensation of 2-aminopyridine, aromatic aldehydes, and ketones." Chemistry of Heterocyclic Compounds 23, no. 8 (August 1987): 861–64. http://dx.doi.org/10.1007/bf00473459.
Повний текст джерелаGordon, Neil J., and Slayton A. Evans. "Diastereoselective condensation of oxazaphosphites with aliphatic and aromatic aldehydes." Journal of Organic Chemistry 58, no. 20 (September 1993): 5293–94. http://dx.doi.org/10.1021/jo00072a002.
Повний текст джерелаRakhimov, A. I., and I. E. Kryukov. "ChemInform Abstract: Condensation of 1,3,6-Trimethyluracil with Aromatic Aldehydes." ChemInform 32, no. 4 (January 23, 2001): no. http://dx.doi.org/10.1002/chin.200104076.
Повний текст джерелаDumbre, Deepa, Mohammad Hassan Amin, Qing Loh, Vasant R. Choudahry, P. R. Selvakannan, and Suresh K. Bhargava. "Nanocrystalline FeOClx grafted MCM-41 as active mesoporous catalyst for the solvent-free multi-condensation reaction." RSC Advances 6, no. 73 (2016): 69334–42. http://dx.doi.org/10.1039/c6ra14736d.
Повний текст джерелаCui, Wenlong, Chenze Zhao, Qingqing Zhu, and Cheli Wang. "Characterization of Sulfides in Atmospheric Residue Fractions Using Selective Oxidation Followed by Fourier Transform Ion Cyclotron Resonance Mass Spectrometry." Energies 15, no. 24 (December 10, 2022): 9361. http://dx.doi.org/10.3390/en15249361.
Повний текст джерелаYadav, J. S., B. V. Subba Reddy, K. Premalatha, and K. Shiva Shankar. "Bismuth(III)-catalyzed rapid and highly efficient synthesis of 2-aryl-1-arylmethyl-1H-benzimidazoles in water." Canadian Journal of Chemistry 86, no. 2 (February 1, 2008): 124–28. http://dx.doi.org/10.1139/v07-140.
Повний текст джерелаBandgar, Babasaheb P., Balaji L. Korbad, Sachin A. Patil, Sunita B. Bandgar, Hemant V. Chavan, and Baliram S. Hote. "Uncatalyzed Knoevenagel Condensation in PEG-600 at Room Temperature." Australian Journal of Chemistry 61, no. 9 (2008): 700. http://dx.doi.org/10.1071/ch08106.
Повний текст джерелаLi, Ming, Dong Liu, Bin Lou, Yadong Zhang, Shitao Yu, and Jnuwei Ding. "Hydroalkylation modification of naphthene-based aromatic-rich fraction and its influences on mesophase development." RSC Advances 8, no. 7 (2018): 3750–59. http://dx.doi.org/10.1039/c7ra12619k.
Повний текст джерелаDiksha, Devi, and Kumar Naresh. "RECENT DEVELOPMENTS IN KNOEVENAGEL CONDENSATION REACTION: A REVIEW." Journal of Advanced Scientific Research 13, no. 05 (June 30, 2022): 17–25. http://dx.doi.org/10.55218/jasr.202213502.
Повний текст джерелаSurya Prakash Rao, H., and A. Parthiban. "One-pot pseudo three-component reaction of nitroketene-N,S-acetals and aldehydes for synthesis of highly functionalized hexa-substituted 1,4-dihydropyridines." Org. Biomol. Chem. 12, no. 32 (2014): 6223–38. http://dx.doi.org/10.1039/c4ob00628c.
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