Artykuły w czasopismach na temat „N - Aryl Y - Lactam”
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Tsang, Wing Y., Naveed Ahmed, Karl Hemming i Michael I. Page. "Competitive endo- and exo-cyclic CN fission in the hydrolysis of N-aroyl β-lactams". Canadian Journal of Chemistry 83, nr 9 (1.09.2005): 1432–39. http://dx.doi.org/10.1139/v05-153.
Pełny tekst źródłaBarba, Victor, Cecilia Hernández, Susana Rojas-Lima, Norberto Farfán i Rosa Santillan. "Preparation of N-aryl-substituted spiro-β-lactams via Staudinger cycloaddition". Canadian Journal of Chemistry 77, nr 12 (5.12.1999): 2025–32. http://dx.doi.org/10.1139/v99-212.
Pełny tekst źródłaMöhrle, H., i 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, nr 12 (1.12.1999): 1577–88. http://dx.doi.org/10.1515/znb-1999-1217.
Pełny tekst źródłaFang, Zeguo, Lin Xie, Liang Wang, Qian Zhang i 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, nr 41 (2022): 26776–80. http://dx.doi.org/10.1039/d2ra05283k.
Pełny tekst źródłaSaliu, Francesco, Marco Orlandi i Maurizio Bruschi. "N-Aryl Lactams by Regioselective Ozonation of N-Aryl Cyclic Amines". ISRN Organic Chemistry 2012 (15.10.2012): 1–5. http://dx.doi.org/10.5402/2012/281642.
Pełny tekst źródłaHaldar, Pranab, i 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, nr 22 (maj 2008): 3659–62. http://dx.doi.org/10.1016/j.tetlet.2008.03.147.
Pełny tekst źródłaYurino, Taiga, Takeshi Ohkuma, Hamdiye Ece i Yuji Tange. "Silyl Cyanopalladate-Catalyzed Friedel–Crafts-Type Cyclization Affording 3-Aryloxindole Derivatives". Synlett 32, nr 09 (26.01.2021): 935–39. http://dx.doi.org/10.1055/a-1373-7017.
Pełny tekst źródłaPatra, Prasanta, Gandhi K. Kar, Aparna Sarkar, Jayanta K. Ray, Tista Dasgupta, Mahua Ghosh i 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, nr 20 (21.06.2012): 3031–41. http://dx.doi.org/10.1080/00397911.2011.574807.
Pełny tekst źródłaDorbec, Matthieu, Jean-Claude Florent, Claude Monneret, Marie-Noëlle Rager i Emmanuel Bertounesque. "1-Aryltetralin privileged structure-based libraries: parallel synthesis of N-aryl and N-biaryl γ-lactam lignans". Tetrahedron 62, nr 50 (grudzień 2006): 11766–81. http://dx.doi.org/10.1016/j.tet.2006.09.026.
Pełny tekst źródłaPatra, Prasanta, Gandhi K. Kar, Aparna Sarkar, Jayanta K. Ray, Tista Dasgupta, Mahua Ghosh i 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, nr 1 (1.01.2013): no. http://dx.doi.org/10.1002/chin.201301160.
Pełny tekst źródłaBrowning, R. Greg, Vivek Badarinarayana, Hossen Mahmud i Carl J. Lovely. "Palladium-catalyzed aryl-amidation. Synthesis of non-racemic N-aryl lactams". Tetrahedron 60, nr 2 (styczeń 2004): 359–65. http://dx.doi.org/10.1016/j.tet.2003.11.008.
Pełny tekst źródłaZhang, Bo, Peng Feng, Li-Hui Sun, Yuxin Cui, Song Ye i 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, nr 30 (26.06.2012): 9198–203. http://dx.doi.org/10.1002/chem.201201375.
Pełny tekst źródłade Oliveira, Arnaldo G., Martí F. Wang, Rafaela C. Carmona, Danilo M. Lustosa, Sergei A. Gorbatov i 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 (29.04.2024): 940–49. http://dx.doi.org/10.3762/bjoc.20.84.
Pełny tekst źródłaJha, Amitabh, Ting-Yi Chou, Zainab ALJaroudi, Bobby D. Ellis i 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 (14.04.2014): 848–57. http://dx.doi.org/10.3762/bjoc.10.81.
Pełny tekst źródłaXi, Ning, Stephen Arvedson, Shawn Eisenberg, Nianhe Han, Michael Handley, Liang Huang, Qi Huang i in. "N-Aryl-γ-lactams as integrin αvβ3 antagonists". Bioorganic & Medicinal Chemistry Letters 14, nr 11 (czerwiec 2004): 2905–9. http://dx.doi.org/10.1016/j.bmcl.2004.03.033.
Pełny tekst źródłaRay, Jayanta, i Gopa Barman. "NaIO4-Mediated Decarboxylative Oxidation of γ-Lactam Carboxylic Acids: A Simple Approach towards N-Aryl Maleimide Derivatives". Synlett 2009, nr 20 (18.11.2009): 3333–35. http://dx.doi.org/10.1055/s-0029-1218379.
Pełny tekst źródłaZhang, Bo, Peng Feng, Li-Hui Sun, Yuxin Cui, Song Ye i 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, nr 52 (18.12.2012): no. http://dx.doi.org/10.1002/chin.201252095.
Pełny tekst źródłaDurán, Rocío, César Barrales-Martínez, Fabián Santana-Romo, Diego F. Rodríguez, Flavia C. Zacconi i Barbara Herrera. "Substitution Effects in Aryl Halides and Amides into the Reaction Mechanism of Ullmann-Type Coupling Reactions". Molecules 29, nr 8 (13.04.2024): 1770. http://dx.doi.org/10.3390/molecules29081770.
Pełny tekst źródłaW. Joachim Demnitz, F., Esther Aebischer, Edmond Bacher, Thomas H. Keller, Miriam Kurzmeyer, Marta L. Ortiz, Esteban Pombo-Villar i Hans-Peter Weber. "Synthesis of N-Arylrolipram Derivatives - Potent and Selective Phosphodiesterase-IV Inhibitors - by Copper Catalyzed Lactam-Aryl Halide Coupling". HETEROCYCLES 48, nr 11 (1998): 2225. http://dx.doi.org/10.3987/com-98-8322.
Pełny tekst źródłaKirillov, N. F., E. A. Nikiforova, D. V. Baibarodskikh, T. A. Zakharova i 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 (3.02.2019): 1–7. http://dx.doi.org/10.1155/2019/7496512.
Pełny tekst źródłaMore, Devidas A., Ganesh H. Shinde, Aslam C. Shaikh i M. Muthukrishnan. "Oxone promoted dehydrogenative Povarov cyclization of N-aryl glycine derivatives: an approach towards quinoline fused lactones and lactams". RSC Advances 9, nr 52 (2019): 30277–91. http://dx.doi.org/10.1039/c9ra06212b.
Pełny tekst źródłaBarman, Gopa, i 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, nr 2 (styczeń 2010): 297–300. http://dx.doi.org/10.1016/j.tetlet.2009.11.005.
Pełny tekst źródłaBarman, 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, nr 10 (październik 2015): 869–71. http://dx.doi.org/10.1007/s10593-015-1789-z.
Pełny tekst źródłaAebischer, Esther, Edmond Bacher, F. W. Joachim Demnitz, Thomas H. Keller, Miriam Kurzmeyer, Marta L. Ortiz, Esteban Pombo-Villar i 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, nr 9 (17.06.2010): no. http://dx.doi.org/10.1002/chin.199909132.
Pełny tekst źródłaKoleoso, Olusesan K., Mark R. J. Elsegood, Simon J. Teat i Marc C. Kimber. "Photoredox Approach to N-Acyl-N′-aryl-N,N′-aminals Using Enamides and Their Conversion to γ-Lactams". Organic Letters 20, nr 4 (26.01.2018): 1003–6. http://dx.doi.org/10.1021/acs.orglett.7b03946.
Pełny tekst źródłaWang, Eng-Chi, Keng-Shiang Huang, Gwo-Woei Lin, Jia-Ruei Lin i 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, nr 1 (luty 2001): 83–90. http://dx.doi.org/10.1002/jccs.200100016.
Pełny tekst źródłaBentabed-Ababsa, Ghenia, Ekhlass Nassar, Ziad Fajloun, Florence Mongin, Rim Amara, Madani Hedidi, Joseph Khoury i in. "Synthesis of N-Aryl and N-Heteroaryl γ-, δ-, and ε-Lactams Using Deprotometalation–Iodination and N-Arylation, and Properties Thereof". Synthesis 28, nr 19 (19.07.2017): 4500–4516. http://dx.doi.org/10.1055/s-0036-1590798.
Pełny tekst źródłaLong, Timothy E., Edward Turos, Monika I. Konaklieva, Allison L. Blum, Amal Amry, Ejae A. Baker, Lita S. Suwandi i in. "Effect of Aryl Ring Fluorination on the Antibacterial Properties of C4 Aryl-Substituted N-Methylthio β-Lactams". Bioorganic & Medicinal Chemistry 11, nr 8 (kwiecień 2003): 1859–63. http://dx.doi.org/10.1016/s0968-0896(03)00037-3.
Pełny tekst źródłaKolkenbrock, Stephan, Katja Parschat, Bernd Beermann, Hans-Jürgen Hinz i 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, nr 24 (13.10.2006): 8430–40. http://dx.doi.org/10.1128/jb.01085-06.
Pełny tekst źródłaChaturvedi, Devdutt, Amit Chaturvedi, Nisha Mishra i Virendra Mishra. "Efficient, One-Pot, BF3·OEt2-Mediated Synthesis of Substituted N-Aryl Lactams". Synlett 23, nr 18 (18.10.2012): 2627–30. http://dx.doi.org/10.1055/s-0032-1317326.
Pełny tekst źródłaHaldar, Pranab, Joyram Guin i 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, nr 7 (luty 2005): 1071–74. http://dx.doi.org/10.1016/j.tetlet.2004.12.107.
Pełny tekst źródłaFilatov, Vadim E., Dmitrii A. Iuzabchuk, Viktor A. Tafeenko, Yuri K. Grishin, Vitaly A. Roznyatovsky, Dmitrii A. Lukianov, Yulia A. Fedotova i in. "Dispirooxindole-β-Lactams: Synthesis via Staudinger Ketene-Imine Cycloaddition and Biological Evaluation". International Journal of Molecular Sciences 23, nr 12 (15.06.2022): 6666. http://dx.doi.org/10.3390/ijms23126666.
Pełny tekst źródłaChaturvedi, Devdutt, Amit K. Chaturvedi, Nisha Mishra i Virendra Mishra. "An efficient and novel approach for the synthesis of substituted N-aryl lactams". Organic & Biomolecular Chemistry 10, nr 46 (2012): 9148. http://dx.doi.org/10.1039/c2ob26230d.
Pełny tekst źródłaBarba, Victor, Cecilia Hernandez, Susana Rojas-Lima, Norberto Farfan i Rosa Santillan. "ChemInform Abstract: Preparation of N-Aryl-Substituted Spiro-β-lactams via Staudinger Cycloaddition." ChemInform 31, nr 23 (8.06.2010): no. http://dx.doi.org/10.1002/chin.200023109.
Pełny tekst źródłaHe, Zhi-Tao, Ya-Bing Wei, Hong-Jie Yu, Cai-Yun Sun, Chen-Guo Feng, Ping Tian i 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, nr 45 (listopad 2012): 9186–91. http://dx.doi.org/10.1016/j.tet.2012.09.001.
Pełny tekst źródłaLavoie, Christopher M., Preston M. MacQueen i Mark Stradiotto. "Nickel-Catalyzed N-Arylation of Primary Amides and Lactams with Activated (Hetero)aryl Electrophiles". Chemistry - A European Journal 22, nr 52 (16.11.2016): 18752–55. http://dx.doi.org/10.1002/chem.201605095.
Pełny tekst źródłaChaturvedi, Devdutt, Amit K. Chaturvedi, Nisha Mishra i Virendra Mishra. "ChemInform Abstract: Efficient, One-Pot, BF3·OEt2-Mediated Synthesis of Substituted N-Aryl Lactams." ChemInform 44, nr 13 (18.03.2013): no. http://dx.doi.org/10.1002/chin.201313088.
Pełny tekst źródłaHu, Yinqiao, Xiaolan Fu, Badru-Deen Barry, Xihe Bi i 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, nr 5 (2012): 690–92. http://dx.doi.org/10.1039/c1cc15881c.
Pełny tekst źródłaPatra, Prasanta, i 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, nr 2 (styczeń 2014): 326–28. http://dx.doi.org/10.1016/j.tetlet.2013.11.009.
Pełny tekst źródłaChaturvedi, Devdutt, Amit K. Chaturvedi, Nisha Mishra i Virendra Mishra. "ChemInform Abstract: An Efficient and Novel Approach for the Synthesis of Substituted N-Aryl Lactams." ChemInform 44, nr 19 (18.04.2013): no. http://dx.doi.org/10.1002/chin.201319192.
Pełny tekst źródłaHe, Zhi-Tao, Ya-Bing Wei, Hong-Jie Yu, Cai-Yun Sun, Chen-Guo Feng, Ping Tian i 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, nr 11 (8.03.2013): no. http://dx.doi.org/10.1002/chin.201311149.
Pełny tekst źródłaWang, Shi-Meng, Chen Li, Jing Leng, Syed Nasir Abbas Bukhari i 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, nr 9 (2018): 1411–15. http://dx.doi.org/10.1039/c7qo01128h.
Pełny tekst źródłaPatra, Prasanta, i 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, nr 25 (5.06.2014): no. http://dx.doi.org/10.1002/chin.201425115.
Pełny tekst źródłaHaldar, Pranab, Gopa Barman i 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, nr 14 (kwiecień 2007): 3049–56. http://dx.doi.org/10.1016/j.tet.2007.01.058.
Pełny tekst źródłaHaldar, Pranab, i 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, nr 45 (listopad 2003): 8229–31. http://dx.doi.org/10.1016/j.tetlet.2003.09.085.
Pełny tekst źródłaHu, Yinqiao, Xiaolan Fu, Badru-Deen Barry, Xihe Bi i 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, nr 20 (23.04.2012): no. http://dx.doi.org/10.1002/chin.201220149.
Pełny tekst źródłaD'hooghe, Matthias, Stijn Dekeukeleire i 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, nr 7 (2008): 1190. http://dx.doi.org/10.1039/b719686e.
Pełny tekst źródłaErbay, Tuğçe G., Daniel P. Dempe, Bhaskar Godugu, Peng Liu i 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, nr 17 (11.08.2021): 11926–36. http://dx.doi.org/10.1021/acs.joc.1c01335.
Pełny tekst źródłaWei, Cui, Jie‐Feng Zhu, Jin‐Qi Zhang, Qi Deng i Dong‐Liang Mo. "Synthesis of Spirofluorenyl‐ β ‐Lactams through Cycloaddition and Ring Contraction from N ‐Aryl Fluorenone Nitrones and Methylenecyclopropanes". Advanced Synthesis & Catalysis 361, nr 17 (16.07.2019): 3965–73. http://dx.doi.org/10.1002/adsc.201900523.
Pełny tekst źródłaMakhmudov, R. R., E. A. Nikiforova, D. P. Zverev, L. A. Balyukina i 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, nr 4 (26.12.2023): 476–82. http://dx.doi.org/10.21285/2227-2925-2023-13-4-476-482.
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