Статті в журналах з теми "Aryl Y"
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Wang, Xi-Cun, Fang Wang, Zheng-Jun Quan, Man-Gang Wang, and Zheng Li. "An efficient and clean synthesis of 1-aroyl-3-aryl-4-substituted imidazole-2-thiones in water." Journal of Chemical Research 2005, no. 11 (November 2005): 689–90. http://dx.doi.org/10.3184/030823405774909423.
Повний текст джерелаSteparuk, Elena V., Dmitrii L. Obydennov, and Vyacheslav Y. Sosnovskikh. "Synthesis of 5-Aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones." Molbank 2023, no. 2 (June 10, 2023): M1668. http://dx.doi.org/10.3390/m1668.
Повний текст джерелаYing, Jun, Zhengjie Le, Zhi-Peng Bao, and Xiao-Feng Wu. "Palladium-catalyzed double carbonylation of propargyl amines and aryl halides to access 1-aroyl-3-aryl-1,5-dihydro-2H-pyrrol-2-ones." Organic Chemistry Frontiers 7, no. 8 (2020): 1006–10. http://dx.doi.org/10.1039/d0qo00007h.
Повний текст джерелаPassananti, Monica, Flavio Cermola, Marina DellaGreca, Maria Rosaria Iesce, Lucio Previtera, Rosalia Sferruzza, and Fabio Temussi. "Photochemical Behaviour of Carbamates Structurally Related to Herbicides in Aqueous Media: Nucleophilic Solvent Trapping versus Radical Reactions." International Journal of Photoenergy 2014 (2014): 1–6. http://dx.doi.org/10.1155/2014/864361.
Повний текст джерелаJugelt, W. "Über Aryl-aroyl-diazomethane." Zeitschrift für Chemie 5, no. 12 (September 2, 2010): 455–56. http://dx.doi.org/10.1002/zfch.19650051206.
Повний текст джерелаMkrtchyan, Satenik, Michał Jakubczyk, Suneel Lanka, Michael Pittelkow, and Viktor O. Iaroshenko. "Cu-Catalyzed Arylation of Bromo-Difluoro-Acetamides by Aryl Boronic Acids, Aryl Trialkoxysilanes and Dimethyl-Aryl-Sulfonium Salts: New Entries to Aromatic Amides." Molecules 26, no. 10 (May 16, 2021): 2957. http://dx.doi.org/10.3390/molecules26102957.
Повний текст джерелаBhaskar Reddy, Dandu, Biradavolu Seenaiah, Adivireddi Padmaja, and Pallela Venkata Ramana Reddy. "Synthesis of Some New Bis[1-(2-aroyl-3-aryl)cyclopropylcarbonyl]benzenes and Pyridines under Phase Transfer Catalysis (PTC) Method." Collection of Czechoslovak Chemical Communications 58, no. 6 (1993): 1437–44. http://dx.doi.org/10.1135/cccc19931437.
Повний текст джерелаRasheed, O. K., I. R. Hardcastle, J. Raftery, and P. Quayle. "Aryne generation vs. Truce-Smiles and fries rearrangements during the Kobayashi fragmentation reaction: a new bi-aryl synthesis." Organic & Biomolecular Chemistry 13, no. 29 (2015): 8048–52. http://dx.doi.org/10.1039/c5ob01239b.
Повний текст джерелаGlaum, Marcus, Wolfgang Kläaui, Brian W. Skelton та Allan H. White. "Synthesis, X-Ray Crystal Structure and Reactivity of [(tmeda)(p-tolyl)Pd(μ2-I)AgL], an Unusual Silver Iodide Complex; Reversible CO Insertion into the Pd-C Bond of [Pd(PPh3)(p-tolyl)L] (L - = [(C5H5)Co{P(OR)2O}3] - , R = Me, Pri)". Australian Journal of Chemistry 50, № 11 (1997): 1047. http://dx.doi.org/10.1071/c97074.
Повний текст джерелаQuesnel, Jeffrey S., Alexander Fabrikant, and Bruce A. Arndtsen. "A flexible approach to Pd-catalyzed carbonylations via aroyl dimethylaminopyridinium salts." Chemical Science 7, no. 1 (2016): 295–300. http://dx.doi.org/10.1039/c5sc02949j.
Повний текст джерелаSoni, Love Kumar, Tamanna Narsinghani, and Rica Jain. "Synthesis and Antibacterial Screening of Some 1-Aroyl-3-aryl Thiourea Derivatives." ISRN Medicinal Chemistry 2014 (January 29, 2014): 1–6. http://dx.doi.org/10.1155/2014/393102.
Повний текст джерелаSingh, Surjeet, Pratik Yadav, Satya Narayan Sahu, Ismail Althagafi, Abhinav Kumar, Brijesh Kumar, Vishnu Ji Ram, and Ramendra Pratap. "Synthesis of 1-amino-2-aroyl/acetylnaphthalenes through a base mediated one pot inter and intramolecular C–C bond formation strategy." Org. Biomol. Chem. 12, no. 26 (2014): 4730–37. http://dx.doi.org/10.1039/c4ob00432a.
Повний текст джерелаSathishkannan, Gopal, V. John Tamilarasan, and Kannupal Srinivasan. "Nucleophilic ring-opening reactions of trans-2-aroyl-3-aryl-cyclopropane-1,1-dicarboxylates with hydrazines." Organic & Biomolecular Chemistry 15, no. 6 (2017): 1400–1406. http://dx.doi.org/10.1039/c6ob02552h.
Повний текст джерелаZhang, Tianyou, Jingyi Qiao, He Song, Feng Xu, Xiaochong Liu, Chunzhao Xu, Junjie Ma, Hao Liu, Zhizhong Sun, and Wenyi Chu. "Cu(OAc)2-Mediated benzimidazole-directed C–H cyanation using 2-(4-methylpiperazin-1-yl)acetonitrile as the cyano source." New Journal of Chemistry 43, no. 23 (2019): 9084–89. http://dx.doi.org/10.1039/c9nj00776h.
Повний текст джерелаKoch, Vanessa, and Stefan Bräse. "Pd-mediated cross-coupling of C-17 lithiated androst-16-en-3-ol – access to functionalized arylated steroid derivatives." Organic & Biomolecular Chemistry 15, no. 1 (2017): 92–95. http://dx.doi.org/10.1039/c6ob02496c.
Повний текст джерелаLinnemannstöns, Marvin, Jan Schwabedissen, Beate Neumann, Hans‐Georg Stammler, Raphael J. F. Berger, and Norbert W. Mitzel. "Aryl–Aryl Interactions in (Aryl‐Perhalogenated) 1,2‐Diaryldisilanes." Chemistry – A European Journal 26, no. 10 (January 30, 2020): 2169–73. http://dx.doi.org/10.1002/chem.201905727.
Повний текст джерелаYing, Jun, Zhengjie Le, and Xiao-Feng Wu. "Palladium-catalyzed double-carbonylative cyclization of propargyl alcohols and aryl triflates to expedite construction of 4-aroyl-furan-2(5H)-ones." Organic Chemistry Frontiers 7, no. 18 (2020): 2757–60. http://dx.doi.org/10.1039/d0qo00874e.
Повний текст джерелаWang, Lizhong, Zhenjie Su, Siran Qian, Weijian Ye, and Cunde Wang. "Efficient Preparation of 2,3-Disubstituted Cyclopropane-1-Carbonitriles via Selective Decarboxylation of 1-Cyanocyclopropane-1-Carboxylates." Journal of Chemical Research 41, no. 11 (November 2017): 636–40. http://dx.doi.org/10.3184/174751917x15094552081161.
Повний текст джерелаHigashino, Takeo, Masumi Takemoto, Akira Miyashita, and Eisaku Hayashi. "Aryl Migration of Heteroaromatics Having Aroyl Group." HETEROCYCLES 23, no. 1 (1985): 209. http://dx.doi.org/10.3987/r-1985-01-0209.
Повний текст джерелаCzarnecka, Anna, Emilia Kowalska, Agnieszka Bodzioch, Joanna Skalik, Marek Koprowski, Krzysztof Owsianik, and Piotr Bałczewski. "A selective removal of the secondary hydroxy group from ortho-dithioacetal-substituted diarylmethanols." Beilstein Journal of Organic Chemistry 14 (May 29, 2018): 1229–37. http://dx.doi.org/10.3762/bjoc.14.105.
Повний текст джерелаShemyakina, Olesya, Olga Volostnykh, Anton Stepanov, Igor Ushakov, and Tatyana Borodina. "Synthesis of Functionalized 5-Amino-3(2H)-furanones via Base-Catalyzed Ring-Cleavage/Recyclization of 4-Cyano-3(2H)-furanones in the Presence of Water." Synthesis 50, no. 24 (August 15, 2018): 4905–14. http://dx.doi.org/10.1055/s-0037-1609916.
Повний текст джерелаTanari, Yulinda, Darda Efendi, Roedhy Poerwanto, Didy Sopandie, and Ketty Suketi. "Aplikasi Kalsium dan NAA untuk Mengendalikan Getah Kuning Buah Manggis (Garcinia mangostana L.)." Jurnal Hortikultura Indonesia 9, no. 1 (April 2, 2018): 10–18. http://dx.doi.org/10.29244/jhi.9.1.10-18.
Повний текст джерелаKramer, Søren. "Homogeneous Gold-Catalyzed Aryl–Aryl Coupling Reactions." Synthesis 52, no. 14 (April 2, 2020): 2017–30. http://dx.doi.org/10.1055/s-0039-1690882.
Повний текст джерелаNagaki, Aiichiro, and Yosuke Ashikari. "Homogeneous Catalyzed Aryl–Aryl Cross-Couplings in Flow." Synthesis 53, no. 11 (January 18, 2021): 1879–88. http://dx.doi.org/10.1055/a-1360-7798.
Повний текст джерелаKim, Yeojin, Kwang Ho Song, and Sunwoo Lee. "Synthesis of S-aryl thioesters via palladium-catalyzed thiocarbonylation of aryl iodides and aryl sulfonyl hydrazides." Organic Chemistry Frontiers 7, no. 19 (2020): 2938–43. http://dx.doi.org/10.1039/d0qo00748j.
Повний текст джерелаKaminský, Jakub, Hana Dvořáková, Jan Štursa, and Jitka Moravcová. "Problems with a conformation assignment of aryl-substituted resorc[4]arenes." Collection of Czechoslovak Chemical Communications 76, no. 10 (2011): 1199–222. http://dx.doi.org/10.1135/cccc2010104.
Повний текст джерелаUtri, Gerhard, Karl-Eberhard Schwarzhans, and Günter M. Allmaier. "Ferrocenyl-aryl-plumbane / Ferrocenyl-aryl-plumbanes." Zeitschrift für Naturforschung B 45, no. 6 (June 1, 1990): 755–62. http://dx.doi.org/10.1515/znb-1990-0606.
Повний текст джерелаSapountzis, Ioannis, Wenwei Lin, Christiane C. Kofink, Christina Despotopoulou, and Paul Knochel. "Eisenkatalysierte Aryl-Aryl-Kreuzkupplungen mit Kupferreagentien." Angewandte Chemie 117, no. 11 (March 4, 2005): 1682–85. http://dx.doi.org/10.1002/ange.200462013.
Повний текст джерелаWencel-Delord, Joanna, Corinna Nimphius, Frederic W. Patureau, and Frank Glorius. "[RhIIICp*]-katalysierte dehydrierende Aryl-Aryl-Bindungsknüpfung." Angewandte Chemie 124, no. 9 (January 27, 2012): 2290–94. http://dx.doi.org/10.1002/ange.201107842.
Повний текст джерелаSingh, Sonia, Mohammad H. Mosslemin, and Alireza Hassanabadi. "Synthesis of 5-Aryl-1,3-Dimethyl-7-Selenoxopyrimidino[4,5-d]Pyrimidine-2,4(1H,3H)-Dione." Journal of Chemical Research 42, no. 5 (May 1, 2018): 264–66. http://dx.doi.org/10.3184/174751918x15265512038216.
Повний текст джерелаCheng, Jiang, Rui Yang, Xiaopeng Wu, Song Sun та Jin-Tao Yu. "Rhodium-Catalyzed Annulation of 2-Arylimidazoles and α-Aroyl Sulfoxonium Ylides toward 5-Arylimidazo[2,1-a]isoquinolines". Synthesis 50, № 17 (28 червня 2018): 3487–92. http://dx.doi.org/10.1055/s-0037-1610124.
Повний текст джерелаRibas, Xavi, Raül Xifra, and Xavier Fontrodona. "Bis-Phenoxo-CuII2 Complexes: Formal Aromatic Hydroxylation via Aryl-CuIII Intermediate Species." Molecules 25, no. 20 (October 9, 2020): 4595. http://dx.doi.org/10.3390/molecules25204595.
Повний текст джерелаLiu, Mingyang, Zhanrong Zhang, Huizhen Liu, Tianbin Wu, and Buxing Han. "Dehydroxyalkylative halogenation of C(aryl)–C bonds of aryl alcohols." Chemical Communications 56, no. 52 (2020): 7120–23. http://dx.doi.org/10.1039/d0cc02306j.
Повний текст джерелаYahav-Levi, Anette, Israel Goldberg, and Arkadi Vigalok. "Aryl-Halide versus Aryl−Aryl Reductive Elimination in Pt(IV)−Phosphine Complexes." Journal of the American Chemical Society 128, no. 27 (July 2006): 8710–11. http://dx.doi.org/10.1021/ja062166r.
Повний текст джерелаGhosh, Manoj Kumar, and Nilendri Rout. "Aryl‐Aryl Cross‐Coupling with Hypervalent Iodine Reagents: Aryl Group Transfer Reactions." ChemistrySelect 5, no. 43 (November 18, 2020): 13644–55. http://dx.doi.org/10.1002/slct.202003396.
Повний текст джерелаSoleiman-Beigi, M., and Z. Arzehgar. "A Novel Method for the Direct Synthesis of Symmetrical and Unsymmetrical Sulfides and Disulfides from Aryl Halides and Ethyl Potassium Xanthogenate." Synlett 29, no. 07 (January 31, 2018): 986–92. http://dx.doi.org/10.1055/s-0037-1609081.
Повний текст джерелаPorwal, Digvijay, and Martin Oestreich. "B(C6F5)3-Catalyzed Reduction of Sulfoxides and Sulfones to Sulfides with Hydrosilanes." Synthesis 49, no. 20 (July 5, 2017): 4698–702. http://dx.doi.org/10.1055/s-0036-1588476.
Повний текст джерелаCui, Mingyu, Dingkai Wang, Yanjun Li, Wei Zhao, Chong Liang, Xutang Liu, Shuiyuan Fu, Luyao Wang, and Xianyong Wei. "Preparation of magnetic silica supported Brønsted acidic ionic liquids for the depolymerization of lignin to aromatic monomers." New Journal of Chemistry 46, no. 9 (2022): 4167–78. http://dx.doi.org/10.1039/d1nj04777a.
Повний текст джерелаLeng, Yuting, Yangjie Wu, Shanshan Zhang, Chuang Liu, Xiaojun Wu, Wen Li, He Li, and Shiwei Wang. "Synthesis of 1,3,4-Oxadiazoles by Iodine-Mediated Oxidative Cyclization of Methyl Ketones with 4-Phenylsemicarbazide." Synlett 33, no. 03 (November 25, 2021): 269–72. http://dx.doi.org/10.1055/a-1707-0965.
Повний текст джерелаIshida, H., and H. Nakajima. "Preparation of aryl alcohols from aryl halides." Zeolites 15, no. 4 (May 1995): 383. http://dx.doi.org/10.1016/0144-2449(95)99140-i.
Повний текст джерелаCastelani, Priscila, Silas Luque, and João V. Comasseto. "Dilithium aryl cyanocuprates from butyl aryl tellurides." Tetrahedron Letters 45, no. 23 (May 2004): 4473–75. http://dx.doi.org/10.1016/j.tetlet.2004.04.062.
Повний текст джерелаWencel-Delord, Joanna, Corinna Nimphius, Frederic W. Patureau, and Frank Glorius. "[RhIIICp*]-Catalyzed Dehydrogenative ArylAryl Bond Formation." Angewandte Chemie International Edition 51, no. 9 (January 27, 2012): 2247–51. http://dx.doi.org/10.1002/anie.201107842.
Повний текст джерелаChotana, Ghayoor A., Jose R. Montero Bastidas, Susanne L. Miller, Milton R. Smith, and Robert E. Maleczka. "One-Pot Iridium Catalyzed C–H Borylation/Sonogashira Cross-Coupling: Access to Borylated Aryl Alkynes." Molecules 25, no. 7 (April 10, 2020): 1754. http://dx.doi.org/10.3390/molecules25071754.
Повний текст джерелаHimmelstrup, Jonas, Mikkel B. Buendia, Xing-Wen Sun, and Søren Kramer. "Enantioselective aryl–aryl coupling facilitated by chiral binuclear gold complexes." Chemical Communications 55, no. 86 (2019): 12988–91. http://dx.doi.org/10.1039/c9cc07175j.
Повний текст джерелаChen, Xue, Yuan Liang, Wen-Wen Wang, Chengping Miao, Xue-Qiang Chu, Weidong Rao, Hao Xu, Xiaocong Zhou, and Zhi-Liang Shen. "Palladium-Catalyzed Esterification of Aryl Fluorosulfates with Aryl Formates." Molecules 29, no. 9 (April 26, 2024): 1991. http://dx.doi.org/10.3390/molecules29091991.
Повний текст джерелаWu, Xiao-Feng. "Palladium-catalyzed carbonylative transformation of aryl chlorides and aryl tosylates." RSC Advances 6, no. 87 (2016): 83831–37. http://dx.doi.org/10.1039/c6ra18388c.
Повний текст джерелаAgrawal, Toolika, and Silas P. Cook. "Iron-Catalyzed Coupling of Aryl Sulfamates and Aryl/Vinyl Tosylates with Aryl Grignards." Organic Letters 16, no. 19 (September 17, 2014): 5080–83. http://dx.doi.org/10.1021/ol5024344.
Повний текст джерелаGodt, Adelheid, Ömer Ünsal, and Mark Roos. "Synthesis of 3,5-Disubstituted 4-Hydroxybenzoates by Aryl−Aryl and Alkynyl−Aryl Coupling." Journal of Organic Chemistry 65, no. 9 (May 2000): 2837–42. http://dx.doi.org/10.1021/jo991907m.
Повний текст джерелаWu, Xiongyu, Jenny K. Ekegren, and Mats Larhed. "Microwave-Promoted Aminocarbonylation of Aryl Iodides, Aryl Bromides, and Aryl Chlorides in Water." Organometallics 25, no. 6 (March 2006): 1434–39. http://dx.doi.org/10.1021/om051044p.
Повний текст джерелаBasu, Souradeep, Alexander H. Sandtorv, and David R. Stuart. "Imide arylation with aryl(TMP)iodonium tosylates." Beilstein Journal of Organic Chemistry 14 (May 11, 2018): 1034–38. http://dx.doi.org/10.3762/bjoc.14.90.
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