Artículos de revistas sobre el tema "N - Aryl Y - Lactam"
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Tsang, Wing Y., Naveed Ahmed, Karl Hemming y Michael I. Page. "Competitive endo- and exo-cyclic CN fission in the hydrolysis of N-aroyl β-lactams". Canadian Journal of Chemistry 83, n.º 9 (1 de septiembre de 2005): 1432–39. http://dx.doi.org/10.1139/v05-153.
Texto completoBarba, Victor, Cecilia Hernández, Susana Rojas-Lima, Norberto Farfán y Rosa Santillan. "Preparation of N-aryl-substituted spiro-β-lactams via Staudinger cycloaddition". Canadian Journal of Chemistry 77, n.º 12 (5 de diciembre de 1999): 2025–32. http://dx.doi.org/10.1139/v99-212.
Texto completoMöhrle, H. y M. Jeandrée. "Chinazolinderivate durch Cyclodehydrierung von N-(2-substituierten Aryl)-Piperidinen / Quinazoline Derivatives by Cyclodehydrogenation of N-(2-Substituted Aryl)-Piperidines". Zeitschrift für Naturforschung B 54, n.º 12 (1 de diciembre de 1999): 1577–88. http://dx.doi.org/10.1515/znb-1999-1217.
Texto completoFang, Zeguo, Lin Xie, Liang Wang, Qian Zhang y Dong Li. "Silver-catalyzed cascade cyclization and functionalization of N-aryl-4-pentenamides: an efficient route to γ-lactam-substituted quinone derivatives". RSC Advances 12, n.º 41 (2022): 26776–80. http://dx.doi.org/10.1039/d2ra05283k.
Texto completoSaliu, Francesco, Marco Orlandi y Maurizio Bruschi. "N-Aryl Lactams by Regioselective Ozonation of N-Aryl Cyclic Amines". ISRN Organic Chemistry 2012 (15 de octubre de 2012): 1–5. http://dx.doi.org/10.5402/2012/281642.
Texto completoHaldar, Pranab y Jayanta K. Ray. "CAN mediated decarboxylative hydroxylation/alkoxylation of N-aryl-γ-lactam-carboxylic acids at room temperature: an easy access to N-aryl-α-hydroxy/alkoxy-γ-lactams". Tetrahedron Letters 49, n.º 22 (mayo de 2008): 3659–62. http://dx.doi.org/10.1016/j.tetlet.2008.03.147.
Texto completoYurino, Taiga, Takeshi Ohkuma, Hamdiye Ece y Yuji Tange. "Silyl Cyanopalladate-Catalyzed Friedel–Crafts-Type Cyclization Affording 3-Aryloxindole Derivatives". Synlett 32, n.º 09 (26 de enero de 2021): 935–39. http://dx.doi.org/10.1055/a-1373-7017.
Texto completoPatra, Prasanta, Gandhi K. Kar, Aparna Sarkar, Jayanta K. Ray, Tista Dasgupta, Mahua Ghosh y Sugata Bhattacharya. "N-Aryl Modification in γ-Lactam: Design and Synthesis of Novel Monocyclic γ-Lactam Derivatives as Inhibitor for Bacterial Propagation". Synthetic Communications 42, n.º 20 (21 de junio de 2012): 3031–41. http://dx.doi.org/10.1080/00397911.2011.574807.
Texto completoDorbec, Matthieu, Jean-Claude Florent, Claude Monneret, Marie-Noëlle Rager y Emmanuel Bertounesque. "1-Aryltetralin privileged structure-based libraries: parallel synthesis of N-aryl and N-biaryl γ-lactam lignans". Tetrahedron 62, n.º 50 (diciembre de 2006): 11766–81. http://dx.doi.org/10.1016/j.tet.2006.09.026.
Texto completoPatra, Prasanta, Gandhi K. Kar, Aparna Sarkar, Jayanta K. Ray, Tista Dasgupta, Mahua Ghosh y Sugata Bhattacharya. "ChemInform Abstract: N-Aryl Modification in γ-Lactam: Design and Synthesis of Novel Monocyclic γ-Lactam Derivatives as Inhibitor for Bacterial Propagation." ChemInform 44, n.º 1 (1 de enero de 2013): no. http://dx.doi.org/10.1002/chin.201301160.
Texto completoBrowning, R. Greg, Vivek Badarinarayana, Hossen Mahmud y Carl J. Lovely. "Palladium-catalyzed aryl-amidation. Synthesis of non-racemic N-aryl lactams". Tetrahedron 60, n.º 2 (enero de 2004): 359–65. http://dx.doi.org/10.1016/j.tet.2003.11.008.
Texto completoZhang, Bo, Peng Feng, Li-Hui Sun, Yuxin Cui, Song Ye y Ning Jiao. "N-Heterocyclic Carbene-Catalyzed Homoenolate Additions with N-Aryl Ketimines as Electrophiles: Efficient Synthesis of Spirocyclic γ-Lactam Oxindoles". Chemistry - A European Journal 18, n.º 30 (26 de junio de 2012): 9198–203. http://dx.doi.org/10.1002/chem.201201375.
Texto completode Oliveira, Arnaldo G., Martí F. Wang, Rafaela C. Carmona, Danilo M. Lustosa, Sergei A. Gorbatov y Carlos R. D. Correia. "Enantioselective synthesis of β-aryl-γ-lactam derivatives via Heck–Matsuda desymmetrization of N-protected 2,5-dihydro-1H-pyrroles". Beilstein Journal of Organic Chemistry 20 (29 de abril de 2024): 940–49. http://dx.doi.org/10.3762/bjoc.20.84.
Texto completoJha, Amitabh, Ting-Yi Chou, Zainab ALJaroudi, Bobby D. Ellis y T. Stanley Cameron. "Aza-Diels–Alder reaction between N-aryl-1-oxo-1H-isoindolium ions and tert-enamides: Steric effects on reaction outcome". Beilstein Journal of Organic Chemistry 10 (14 de abril de 2014): 848–57. http://dx.doi.org/10.3762/bjoc.10.81.
Texto completoXi, Ning, Stephen Arvedson, Shawn Eisenberg, Nianhe Han, Michael Handley, Liang Huang, Qi Huang et al. "N-Aryl-γ-lactams as integrin αvβ3 antagonists". Bioorganic & Medicinal Chemistry Letters 14, n.º 11 (junio de 2004): 2905–9. http://dx.doi.org/10.1016/j.bmcl.2004.03.033.
Texto completoRay, Jayanta y Gopa Barman. "NaIO4-Mediated Decarboxylative Oxidation of γ-Lactam Carboxylic Acids: A Simple Approach towards N-Aryl Maleimide Derivatives". Synlett 2009, n.º 20 (18 de noviembre de 2009): 3333–35. http://dx.doi.org/10.1055/s-0029-1218379.
Texto completoZhang, Bo, Peng Feng, Li-Hui Sun, Yuxin Cui, Song Ye y Ning Jiao. "ChemInform Abstract: N-Heterocyclic Carbene-Catalyzed Homoenolate Additions with N-Aryl Ketimines as Electrophiles: Efficient Synthesis of Spirocyclic γ-Lactam Oxindoles." ChemInform 43, n.º 52 (18 de diciembre de 2012): no. http://dx.doi.org/10.1002/chin.201252095.
Texto completoDurán, Rocío, César Barrales-Martínez, Fabián Santana-Romo, Diego F. Rodríguez, Flavia C. Zacconi y Barbara Herrera. "Substitution Effects in Aryl Halides and Amides into the Reaction Mechanism of Ullmann-Type Coupling Reactions". Molecules 29, n.º 8 (13 de abril de 2024): 1770. http://dx.doi.org/10.3390/molecules29081770.
Texto completoW. Joachim Demnitz, F., Esther Aebischer, Edmond Bacher, Thomas H. Keller, Miriam Kurzmeyer, Marta L. Ortiz, Esteban Pombo-Villar y Hans-Peter Weber. "Synthesis of N-Arylrolipram Derivatives - Potent and Selective Phosphodiesterase-IV Inhibitors - by Copper Catalyzed Lactam-Aryl Halide Coupling". HETEROCYCLES 48, n.º 11 (1998): 2225. http://dx.doi.org/10.3987/com-98-8322.
Texto completoKirillov, N. F., E. A. Nikiforova, D. V. Baibarodskikh, T. A. Zakharova y L. S. Govorushkin. "Synthesis of New Bis(spiro-β-lactams) via Interaction of Methyl 1-Bromocycloalcanecarboxylates with Zinc and N,N′-Bis(arylmethylidene)benzidines". Journal of Chemistry 2019 (3 de febrero de 2019): 1–7. http://dx.doi.org/10.1155/2019/7496512.
Texto completoMore, Devidas A., Ganesh H. Shinde, Aslam C. Shaikh y M. Muthukrishnan. "Oxone promoted dehydrogenative Povarov cyclization of N-aryl glycine derivatives: an approach towards quinoline fused lactones and lactams". RSC Advances 9, n.º 52 (2019): 30277–91. http://dx.doi.org/10.1039/c9ra06212b.
Texto completoBarman, Gopa y Jayanta K. Ray. "A novel access to bisformylated pyrroles via decarboxylation of N-aryl-γ-lactam-carboxylic acids under Vilsmeier reaction conditions". Tetrahedron Letters 51, n.º 2 (enero de 2010): 297–300. http://dx.doi.org/10.1016/j.tetlet.2009.11.005.
Texto completoBarman, Gopa. "A facile synthesis of diformylated pyrroles by dehydroxylation of N-aryl-5-hydroxy-γ-lactam derivatives under Vilsmeier reaction conditions". Chemistry of Heterocyclic Compounds 51, n.º 10 (octubre de 2015): 869–71. http://dx.doi.org/10.1007/s10593-015-1789-z.
Texto completoAebischer, Esther, Edmond Bacher, F. W. Joachim Demnitz, Thomas H. Keller, Miriam Kurzmeyer, Marta L. Ortiz, Esteban Pombo-Villar y Hans-Peter Weber. "ChemInform Abstract: Synthesis of N-Arylrolipram Derivatives - Potent and Selective Phosphodiesterase-IV Inhibitors - by Copper-Catalyzed Lactam-Aryl Halide Coupling." ChemInform 30, n.º 9 (17 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199909132.
Texto completoKoleoso, Olusesan K., Mark R. J. Elsegood, Simon J. Teat y Marc C. Kimber. "Photoredox Approach to N-Acyl-N′-aryl-N,N′-aminals Using Enamides and Their Conversion to γ-Lactams". Organic Letters 20, n.º 4 (26 de enero de 2018): 1003–6. http://dx.doi.org/10.1021/acs.orglett.7b03946.
Texto completoWang, Eng-Chi, Keng-Shiang Huang, Gwo-Woei Lin, Jia-Ruei Lin y Ming-Kun Hsu. "A New Route toN-Aryl 2-Alkenamides,N-AllylN-Aryl 2-Alkenamides, andN-Aryl α,β-Unsaturated γ-Lactams fromN-Aryl 3-(Phenylsulfonyl)propanamides". Journal of the Chinese Chemical Society 48, n.º 1 (febrero de 2001): 83–90. http://dx.doi.org/10.1002/jccs.200100016.
Texto completoBentabed-Ababsa, Ghenia, Ekhlass Nassar, Ziad Fajloun, Florence Mongin, Rim Amara, Madani Hedidi, Joseph Khoury et al. "Synthesis of N-Aryl and N-Heteroaryl γ-, δ-, and ε-Lactams Using Deprotometalation–Iodination and N-Arylation, and Properties Thereof". Synthesis 28, n.º 19 (19 de julio de 2017): 4500–4516. http://dx.doi.org/10.1055/s-0036-1590798.
Texto completoLong, Timothy E., Edward Turos, Monika I. Konaklieva, Allison L. Blum, Amal Amry, Ejae A. Baker, Lita S. Suwandi et al. "Effect of Aryl Ring Fluorination on the Antibacterial Properties of C4 Aryl-Substituted N-Methylthio β-Lactams". Bioorganic & Medicinal Chemistry 11, n.º 8 (abril de 2003): 1859–63. http://dx.doi.org/10.1016/s0968-0896(03)00037-3.
Texto completoKolkenbrock, Stephan, Katja Parschat, Bernd Beermann, Hans-Jürgen Hinz y Susanne Fetzner. "N-Acetylanthranilate Amidase from Arthrobacter nitroguajacolicus Rü61a, an α/β-Hydrolase-Fold Protein Active towards Aryl-Acylamides and -Esters, and Properties of Its Cysteine-Deficient Variant". Journal of Bacteriology 188, n.º 24 (13 de octubre de 2006): 8430–40. http://dx.doi.org/10.1128/jb.01085-06.
Texto completoChaturvedi, Devdutt, Amit Chaturvedi, Nisha Mishra y Virendra Mishra. "Efficient, One-Pot, BF3·OEt2-Mediated Synthesis of Substituted N-Aryl Lactams". Synlett 23, n.º 18 (18 de octubre de 2012): 2627–30. http://dx.doi.org/10.1055/s-0032-1317326.
Texto completoHaldar, Pranab, Joyram Guin y Jayanta K. Ray. "Sodium borohydride–iodine mediated reduction of γ-lactam carboxylic acids followed by DDQ mediated oxidative aromatisation: a facile entry to N-aryl-formylpyrroles". Tetrahedron Letters 46, n.º 7 (febrero de 2005): 1071–74. http://dx.doi.org/10.1016/j.tetlet.2004.12.107.
Texto completoFilatov, Vadim E., Dmitrii A. Iuzabchuk, Viktor A. Tafeenko, Yuri K. Grishin, Vitaly A. Roznyatovsky, Dmitrii A. Lukianov, Yulia A. Fedotova et al. "Dispirooxindole-β-Lactams: Synthesis via Staudinger Ketene-Imine Cycloaddition and Biological Evaluation". International Journal of Molecular Sciences 23, n.º 12 (15 de junio de 2022): 6666. http://dx.doi.org/10.3390/ijms23126666.
Texto completoChaturvedi, Devdutt, Amit K. Chaturvedi, Nisha Mishra y Virendra Mishra. "An efficient and novel approach for the synthesis of substituted N-aryl lactams". Organic & Biomolecular Chemistry 10, n.º 46 (2012): 9148. http://dx.doi.org/10.1039/c2ob26230d.
Texto completoBarba, Victor, Cecilia Hernandez, Susana Rojas-Lima, Norberto Farfan y Rosa Santillan. "ChemInform Abstract: Preparation of N-Aryl-Substituted Spiro-β-lactams via Staudinger Cycloaddition." ChemInform 31, n.º 23 (8 de junio de 2010): no. http://dx.doi.org/10.1002/chin.200023109.
Texto completoHe, Zhi-Tao, Ya-Bing Wei, Hong-Jie Yu, Cai-Yun Sun, Chen-Guo Feng, Ping Tian y Guo-Qiang Lin. "Rhodium/diene-catalyzed asymmetric arylation of N-Boc-protected α,β-unsaturated δ-lactam with arylboronic acids: enantioselective synthesis of 4-aryl-2-piperidinones". Tetrahedron 68, n.º 45 (noviembre de 2012): 9186–91. http://dx.doi.org/10.1016/j.tet.2012.09.001.
Texto completoLavoie, Christopher M., Preston M. MacQueen y Mark Stradiotto. "Nickel-Catalyzed N-Arylation of Primary Amides and Lactams with Activated (Hetero)aryl Electrophiles". Chemistry - A European Journal 22, n.º 52 (16 de noviembre de 2016): 18752–55. http://dx.doi.org/10.1002/chem.201605095.
Texto completoChaturvedi, Devdutt, Amit K. Chaturvedi, Nisha Mishra y Virendra Mishra. "ChemInform Abstract: Efficient, One-Pot, BF3·OEt2-Mediated Synthesis of Substituted N-Aryl Lactams." ChemInform 44, n.º 13 (18 de marzo de 2013): no. http://dx.doi.org/10.1002/chin.201313088.
Texto completoHu, Yinqiao, Xiaolan Fu, Badru-Deen Barry, Xihe Bi y Dewen Dong. "Regiospecific β-lactam ring-opening/recyclization reactions of N-aryl-3-spirocyclic-β-lactams catalyzed by a Lewis–Brønsted acids combined superacid catalyst system: a new entry to 3-spirocyclicquinolin-4(1H)-ones". Chem. Commun. 48, n.º 5 (2012): 690–92. http://dx.doi.org/10.1039/c1cc15881c.
Texto completoPatra, Prasanta y Gandhi K. Kar. "Studies on the Suzuki reaction on methyl 1-(2-bromoaryl)-5-oxo-3-aryl/heteroaryl-pyrrolidin-2-carboxylate derivatives: synthesis of N-aryl modified monocyclic γ-lactam derivatives in search for newer antibacterial agents". Tetrahedron Letters 55, n.º 2 (enero de 2014): 326–28. http://dx.doi.org/10.1016/j.tetlet.2013.11.009.
Texto completoChaturvedi, Devdutt, Amit K. Chaturvedi, Nisha Mishra y Virendra Mishra. "ChemInform Abstract: An Efficient and Novel Approach for the Synthesis of Substituted N-Aryl Lactams." ChemInform 44, n.º 19 (18 de abril de 2013): no. http://dx.doi.org/10.1002/chin.201319192.
Texto completoHe, Zhi-Tao, Ya-Bing Wei, Hong-Jie Yu, Cai-Yun Sun, Chen-Guo Feng, Ping Tian y Guo-Qiang Lin. "ChemInform Abstract: Rhodium/Diene-Catalyzed Asymmetric Arylation of N-Boc-Protected α,β-Unsaturated δ-Lactam with Arylboronic Acids: Enantioselective Synthesis of 4-Aryl-2-piperidinones." ChemInform 44, n.º 11 (8 de marzo de 2013): no. http://dx.doi.org/10.1002/chin.201311149.
Texto completoWang, Shi-Meng, Chen Li, Jing Leng, Syed Nasir Abbas Bukhari y Hua-Li Qin. "Rhodium(iii)-catalyzed Oxidative Coupling of N-Methoxybenzamides and Ethenesulfonyl fluoride: a C–H Bond Activation Strategy for the Preparation of 2-Aryl ethenesulfonyl fluorides and Sulfonyl fluoride Substituted γ-Lactams". Organic Chemistry Frontiers 5, n.º 9 (2018): 1411–15. http://dx.doi.org/10.1039/c7qo01128h.
Texto completoPatra, Prasanta y Gandhi K. Kar. "ChemInform Abstract: Studies on the Suzuki Reaction on Methyl 1-(2-Bromoaryl)-5-oxo-3-aryl/heteroaryl-pyrrolidin-2-carboxylate Derivatives: Synthesis of N-Aryl Modified Monocyclic γ-Lactam Derivatives in Search for Newer Antibacterial Agents." ChemInform 45, n.º 25 (5 de junio de 2014): no. http://dx.doi.org/10.1002/chin.201425115.
Texto completoHaldar, Pranab, Gopa Barman y Jayanta K. Ray. "Sodium borohydride–iodine mediated reduction of γ-lactam carboxylic acids followed by DDQ mediated oxidative aromatisation: a simple approach towards N-aryl-formylpyrroles and 1,3-diaryl-formylpyrroles". Tetrahedron 63, n.º 14 (abril de 2007): 3049–56. http://dx.doi.org/10.1016/j.tet.2007.01.058.
Texto completoHaldar, Pranab y Jayanta K. Ray. "Chemoselective reduction of a lactam carbonyl group in the presence of a gem-dicarboxylate by sodium borohydride and iodine: a facile entry to N-aryl trisubstituted pyrroles". Tetrahedron Letters 44, n.º 45 (noviembre de 2003): 8229–31. http://dx.doi.org/10.1016/j.tetlet.2003.09.085.
Texto completoHu, Yinqiao, Xiaolan Fu, Badru-Deen Barry, Xihe Bi y Dewen Dong. "ChemInform Abstract: Regiospecific β-Lactam Ring-Opening/Recyclization Reactions of N-Aryl-3-spirocyclic-β-lactams Catalyzed by a Lewis-Broensted Acids Combined Superacid Catalyst System: A New Entry to 3-Spirocyclicquinolin-4(1H)-ones." ChemInform 43, n.º 20 (23 de abril de 2012): no. http://dx.doi.org/10.1002/chin.201220149.
Texto completoD'hooghe, Matthias, Stijn Dekeukeleire y Norbert De Kimpe. "Reactivity of N-(ω-haloalkyl)-β-lactams with regard to lithium aluminium hydride: novel synthesis of 1-(1-aryl-3-hydroxypropyl)aziridines and 3-aryl-3-(N-propylamino)propan-1-ols". Organic & Biomolecular Chemistry 6, n.º 7 (2008): 1190. http://dx.doi.org/10.1039/b719686e.
Texto completoErbay, Tuğçe G., Daniel P. Dempe, Bhaskar Godugu, Peng Liu y Kay M. Brummond. "Thiol Reactivity of N-Aryl α-Methylene-γ-lactams: A Reactive Group for Targeted Covalent Inhibitor Design". Journal of Organic Chemistry 86, n.º 17 (11 de agosto de 2021): 11926–36. http://dx.doi.org/10.1021/acs.joc.1c01335.
Texto completoWei, Cui, Jie‐Feng Zhu, Jin‐Qi Zhang, Qi Deng y Dong‐Liang Mo. "Synthesis of Spirofluorenyl‐ β ‐Lactams through Cycloaddition and Ring Contraction from N ‐Aryl Fluorenone Nitrones and Methylenecyclopropanes". Advanced Synthesis & Catalysis 361, n.º 17 (16 de julio de 2019): 3965–73. http://dx.doi.org/10.1002/adsc.201900523.
Texto completoMakhmudov, R. R., E. A. Nikiforova, D. P. Zverev, L. A. Balyukina y A. Р. Skachkov. "Synthesis and antinociceptive activity of 2,2’-(1,4-phenylene)bis[3-aryl-2-azaspiro[3.5]nonan-1-ones]". Proceedings of Universities. Applied Chemistry and Biotechnology 13, n.º 4 (26 de diciembre de 2023): 476–82. http://dx.doi.org/10.21285/2227-2925-2023-13-4-476-482.
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