Artykuły w czasopismach na temat „Electrophilic nitrogens”
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Aeyad, Tahani, Jason Williams, Anthony Meijer i Iain Coldham. "Lithiation–Substitution of N-Boc-2-phenylazepane". Synlett 28, nr 20 (17.08.2017): 2765–68. http://dx.doi.org/10.1055/s-0036-1590857.
Pełny tekst źródłaLEVONEN, Anna-Liisa, Aimee LANDAR, Anup RAMACHANDRAN, Erin K. CEASER, Dale A. DICKINSON, Giuseppe ZANONI, Jason D. MORROW i Victor M. DARLEY-USMAR. "Cellular mechanisms of redox cell signalling: role of cysteine modification in controlling antioxidant defences in response to electrophilic lipid oxidation products". Biochemical Journal 378, nr 2 (1.03.2004): 373–82. http://dx.doi.org/10.1042/bj20031049.
Pełny tekst źródłaCeaser, E. K., D. R. Moellering, S. Shiva, A. Ramachandran, A. Landar, A. Venkartraman, J. Crawford i in. "Mechanisms of signal transduction mediated by oxidized lipids: the role of the electrophile-responsive proteome". Biochemical Society Transactions 32, nr 1 (1.02.2004): 151–55. http://dx.doi.org/10.1042/bst0320151.
Pełny tekst źródłaPalillero-Cisneros, Angel, Paola G. Gordillo-Guerra, Fernando García-Alvarez, Olivier Jackowski, Franck Ferreira, Fabrice Chemla, Joel L. Terán i Alejandro Perez-Luna. "α-(Aminomethyl)acrylates as acceptors in radical–polar crossover 1,4-additions of dialkylzincs: insights into enolate formation and trapping". Beilstein Journal of Organic Chemistry 19 (21.09.2023): 1443–51. http://dx.doi.org/10.3762/bjoc.19.103.
Pełny tekst źródłaCao, Chengyao, Jinyu Sheng i Chao Chen. "Cu-Catalyzed Cascade Annulation of Diaryliodonium Salts and Nitriles: Synthesis of Nitrogen-Containing Heterocycles". Synthesis 49, nr 23 (11.10.2017): 5081–92. http://dx.doi.org/10.1055/s-0036-1589515.
Pełny tekst źródłaSlivka, Mikhailo, i Mikhailo Onysko. "The Use of Electrophilic Cyclization for the Preparation of Condensed Heterocycles". Synthesis 53, nr 19 (19.05.2021): 3497–512. http://dx.doi.org/10.1055/s-0040-1706036.
Pełny tekst źródłaChandra, Swaroop, B. Suryaprasad, N. Ramanathan i K. Sundararajan. "Nitrogen as a pnicogen?: evidence for π-hole driven novel pnicogen bonding interactions in nitromethane–ammonia aggregates using matrix isolation infrared spectroscopy and ab initio computations". Physical Chemistry Chemical Physics 23, nr 10 (2021): 6286–97. http://dx.doi.org/10.1039/d0cp06273a.
Pełny tekst źródłaBhadra, Biswa Nath, Yong Su Baek, Cheol Ho Choi i Sung Hwa Jhung. "How neutral nitrogen-containing compounds are oxidized in oxidative-denitrogenation of liquid fuel with TiO2@carbon". Physical Chemistry Chemical Physics 23, nr 14 (2021): 8368–74. http://dx.doi.org/10.1039/d1cp00633a.
Pełny tekst źródłaAgeshina, Alexandra A., Gleb A. Chesnokov, Maxim A. Topchiy, Igor V. Alabugin, Mikhail S. Nechaev i Andrey F. Asachenko. "Making endo-cyclizations favorable again: a conceptually new synthetic approach to benzotriazoles via azide group directed lithiation/cyclization of 2-azidoaryl bromides". Organic & Biomolecular Chemistry 17, nr 18 (2019): 4523–34. http://dx.doi.org/10.1039/c9ob00615j.
Pełny tekst źródłaShen, Kun, i Qiu Wang. "Copper-catalyzed diamination of unactivated alkenes with hydroxylamines". Chemical Science 6, nr 7 (2015): 4279–83. http://dx.doi.org/10.1039/c5sc00897b.
Pełny tekst źródłaVaradwaj, Pradeep R., Arpita Varadwaj, Helder M. Marques i Koichi Yamashita. "The Nitrogen Bond, or the Nitrogen-Centered Pnictogen Bond: The Covalently Bound Nitrogen Atom in Molecular Entities and Crystals as a Pnictogen Bond Donor". Compounds 2, nr 1 (15.03.2022): 80–110. http://dx.doi.org/10.3390/compounds2010007.
Pełny tekst źródłaSimonneau, Antoine, Pierre Garcia, Jean-Philippe Goddard, Virginie Mouriès-Mansuy, Max Malacria i Louis Fensterbank. "Combination of gold catalysis and Selectfluor for the synthesis of fluorinated nitrogen heterocycles". Beilstein Journal of Organic Chemistry 7 (7.10.2011): 1379–86. http://dx.doi.org/10.3762/bjoc.7.162.
Pełny tekst źródłaMakarov, Anton S., Alexander A. Fadeev i Maxim G. Uchuskin. "Intramolecular iron-catalyzed transannulation of furans with O-acetyl oximes: synthesis of functionalized pyrroles". Organic Chemistry Frontiers 8, nr 23 (2021): 6553–60. http://dx.doi.org/10.1039/d1qo01281a.
Pełny tekst źródłaSenthil Kumar Raju, Archana Settu, Archana Thiyagarajan, Divya Rama, Praveen Sekar i Shridharshini Kumar. "Synthetic approaches of medicinally important Schiff bases: An updated Review". World Journal of Advanced Research and Reviews 16, nr 3 (30.12.2022): 838–52. http://dx.doi.org/10.30574/wjarr.2022.16.3.1394.
Pełny tekst źródłaSenthil Kumar Raju, Archana Settu, Archana Thiyagarajan, Divya Rama, Praveen Sekar i Shridharshini Kumar. "Biological applications of Schiff bases: An overview". GSC Biological and Pharmaceutical Sciences 21, nr 3 (30.12.2022): 203–15. http://dx.doi.org/10.30574/gscbps.2022.21.3.0484.
Pełny tekst źródłaPrieto, Alexis, Olivier Baudoin, Didier Bouyssi i Nuno Monteiro. "Electrophilic trifluoromethylation of carbonyl compounds and their nitrogen derivatives under copper catalysis". Chemical Communications 52, nr 5 (2016): 869–81. http://dx.doi.org/10.1039/c5cc05954b.
Pełny tekst źródłaLuan, Xinjun, i Jingxun Yu. "Hydroxylamines as One-Atom Nitrogen Sources for Metal-Catalyzed Cycloadditions". Synthesis 53, nr 08 (25.01.2021): 1423–33. http://dx.doi.org/10.1055/s-0040-1706017.
Pełny tekst źródłaJinan, Dilsha, Pinku Prasad Mondal, Anagha Veluthanath Nair i Basudev Sahoo. "O-Protected NH-free hydroxylamines: emerging electrophilic aminating reagents for organic synthesis". Chemical Communications 57, nr 99 (2021): 13495–505. http://dx.doi.org/10.1039/d1cc05282a.
Pełny tekst źródłaKang, Jun Yong, i Hai Huang. "Triflic Anhydride (Tf2O)-Activated Transformations of Amides, Sulfoxides and Phosphorus Oxides via Nucleophilic Trapping". Synthesis 54, nr 05 (27.10.2021): 1157–202. http://dx.doi.org/10.1055/a-1679-8205.
Pełny tekst źródłaAppiarius, Yannik, Tim Stauch, Enno Lork, Pascal Rusch, Nadja C. Bigall i Anne Staubitz. "From a 1,2-azaborinine to large BN-PAHs via electrophilic cyclization: synthesis, characterization and promising optical properties". Organic Chemistry Frontiers 8, nr 1 (2021): 10–17. http://dx.doi.org/10.1039/d0qo00723d.
Pełny tekst źródłaRen, Yun-Lai, Huantao Shang, Jianji Wang, Xinzhe Tian, Shuang Zhao, Qian Wang i Fuwei Li. "Nitrogen Dioxide-Catalyzed Electrophilic Iodination of Arenes". Advanced Synthesis & Catalysis 355, nr 17 (8.11.2013): 3437–42. http://dx.doi.org/10.1002/adsc.201300581.
Pełny tekst źródłaRamirez-Balderrama, Kathy, Erasmo Orrantia-Borunda i Norma Flores-Holguin. "Calculation of global and local reactivity descriptors of carbodiimides, a DFT study". Journal of Theoretical and Computational Chemistry 16, nr 03 (2.03.2017): 1750019. http://dx.doi.org/10.1142/s0219633617500195.
Pełny tekst źródłaZmijewski, J. W., A. Landar, N. Watanabe, D. A. Dickinson, N. Noguchi i V. M. Darley-Usmar. "Cell signalling by oxidized lipids and the role of reactive oxygen species in the endothelium". Biochemical Society Transactions 33, nr 6 (26.10.2005): 1385–89. http://dx.doi.org/10.1042/bst0331385.
Pełny tekst źródłaLi, Jiaquan, Hongqi Sun, Shaobin Wang, Yu Dong i Shaomin Liu. "Selective oxidation of alcohols by graphene-like carbon with electrophilic oxygen and integrated pyridinic nitrogen active sites". Nanoscale 13, nr 30 (2021): 12979–90. http://dx.doi.org/10.1039/d1nr03157k.
Pełny tekst źródłaLuo, Xuewei, Sheng Wang i Chanjuan Xi. "Cp2TiCl2-catalyzed highly regioselective hydroamination of styrenes with hydroxylamines". Organic Chemistry Frontiers 5, nr 7 (2018): 1184–87. http://dx.doi.org/10.1039/c7qo01068k.
Pełny tekst źródłaLi, Huimin, Lihao Liao i Xiaodan Zhao. "Organoselenium-Catalyzed Aza-Wacker Reactions: Efficient Access to Isoquinolinium Imides and an Isoquinoline N-Oxide". Synlett 30, nr 14 (28.06.2019): 1688–92. http://dx.doi.org/10.1055/s-0039-1690103.
Pełny tekst źródłaHarjivan, Shrika G., Pedro F. Pinheiro, Inês L. Martins, Ana L. Godinho, Riccardo Wanke, Pedro P. Santos, Sofia A. Pereira, Frederick A. Beland, M. Matilde Marques i Alexandra M. M. Antunes. "Quinoid derivatives of the nevirapine metabolites 2-hydroxy- and 3-hydroxy-nevirapine: activation pathway to amino acid adducts". Toxicology Research 4, nr 6 (2015): 1565–77. http://dx.doi.org/10.1039/c5tx00176e.
Pełny tekst źródłaComparini, Lucrezia Margherita, i Mauro Pineschi. "Recent Progresses in the Catalytic Stereoselective Dearomatization of Pyridines". Molecules 28, nr 17 (22.08.2023): 6186. http://dx.doi.org/10.3390/molecules28176186.
Pełny tekst źródłaFrontier, Alison J., Shukree Abdul-Rashed i Connor Holt. "Alkynyl Prins and Alkynyl Aza-Prins Annulations: Scope and Synthetic Applications". Synthesis 52, nr 14 (9.04.2020): 1991–2007. http://dx.doi.org/10.1055/s-0039-1690869.
Pełny tekst źródłaRakowski DuBois, M., L. D. Vasquez, R. F. Ciancanelli i B. C. Noll. "Electrophilic Substitution of Nitrogen Heterocycles by Molybdenum Sulfide Complexes". Organometallics 19, nr 18 (wrzesień 2000): 3507–15. http://dx.doi.org/10.1021/om000218u.
Pełny tekst źródłaRen, Yun-Lai, Huantao Shang, Jianji Wang, Xinzhe Tian, Shuang Zhao, Qian Wang i Fuwei Li. "ChemInform Abstract: Nitrogen Dioxide-Catalyzed Electrophilic Iodination of Arenes." ChemInform 45, nr 19 (23.04.2014): no. http://dx.doi.org/10.1002/chin.201419057.
Pełny tekst źródłaSarkar, Sounak, Mysore S. Pavan i T. N. Guru Row. "Experimental validation of ‘pnicogen bonding’ in nitrogen by charge density analysis". Physical Chemistry Chemical Physics 17, nr 4 (2015): 2330–34. http://dx.doi.org/10.1039/c4cp04690k.
Pełny tekst źródłaBédé, Lucie A., Mawa Koné, Guy R. M. Koné, Simplice C. S. Ouattara, Lamoussa Ouattara i El Hadji S. Bamba. "Tautomeric Equilibrium Modeling: Stability and Reactivity of Benzothiazole and Derivatives". International Journal of Chemistry 11, nr 1 (29.04.2019): 84. http://dx.doi.org/10.5539/ijc.v11n1p84.
Pełny tekst źródłaLu, Mengsi, Oliver Allemann, Jun Xu, Anthony Linden, Kim K. Baldridge i Jay S. Siegel. "Peraryl-X-onium ions of nitrogen and oxygen". Organic Chemistry Frontiers 6, nr 15 (2019): 2640–46. http://dx.doi.org/10.1039/c9qo00633h.
Pełny tekst źródłaMotornov, Vladimir, i Petr Beier. "NH-1,2,3-triazoles as versatile building blocks in denitrogenative transformations". RSC Advances 13, nr 49 (2023): 34646–51. http://dx.doi.org/10.1039/d3ra06045d.
Pełny tekst źródłaMurai, Toshiaki. "Thioamide dianions derived from N-arylmethyl thioamides: Generation and application as carbon nucleophiles adjacent to the nitrogen atom". Pure and Applied Chemistry 82, nr 3 (18.02.2010): 541–54. http://dx.doi.org/10.1351/pac-con-09-08-04.
Pełny tekst źródłaDas, Tamal Kanti, i Akkattu T. Biju. "Imines as acceptors and donors in N-heterocyclic carbene (NHC) organocatalysis". Chemical Communications 56, nr 61 (2020): 8537–52. http://dx.doi.org/10.1039/d0cc03290e.
Pełny tekst źródłaJoost, Maximilian, Wesley J. Transue i Christopher C. Cummins. "Diazomethane umpolung atop anthracene: an electrophilic methylene transfer reagent". Chemical Science 9, nr 6 (2018): 1540–43. http://dx.doi.org/10.1039/c7sc04506a.
Pełny tekst źródłaLi, Juan, Ning Wang, Wen-Tao Liu, Hong-Lin Ding, Yue An i Cheng-Wei Lü. "A revisit to the Gattermann reaction: interesting synthesis of nitrogen heterocyclic aromatic halides and their fluorescence properties". New J. Chem. 41, nr 20 (2017): 12225–30. http://dx.doi.org/10.1039/c7nj02672b.
Pełny tekst źródłaJarvo, Elizabeth, i Timothy Barker. "Developments in Transition-Metal-Catalyzed Reactions Using Electrophilic Nitrogen Sources". Synthesis 2011, nr 24 (27.10.2011): 3954–64. http://dx.doi.org/10.1055/s-0031-1289581.
Pełny tekst źródłaQiang, Peirong, Zuobang Sun, Bai Xue i Fan Zhang. "π-Extended Ladder-Type Conjugated Polymers via BN-Annulation". Organic Materials 03, nr 02 (kwiecień 2021): 221–27. http://dx.doi.org/10.1055/s-0041-1727181.
Pełny tekst źródłaChaudhari, Raju, i Sahebrao Rindhe. "Synthesis and antimicrobial activities of novel n-substituted 8-(1-alkyl/alkylsulphonyl/alkoxycarbonyl-benzimidazol-2-ylmethoxy)-5-chloroquinolines". Journal of the Serbian Chemical Society 76, nr 9 (2011): 1199–206. http://dx.doi.org/10.2298/jsc100817105c.
Pełny tekst źródłaRanjith, Jala, i Hyun-Joon Ha. "Synthetic Applications of Aziridinium Ions". Molecules 26, nr 6 (22.03.2021): 1774. http://dx.doi.org/10.3390/molecules26061774.
Pełny tekst źródłaMueller, Louis G., Allen Chao, Embarek AlWedi i Fraser F. Fleming. "One-step synthesis of imidazoles from Asmic (anisylsulfanylmethyl isocyanide)". Beilstein Journal of Organic Chemistry 17 (24.06.2021): 1499–502. http://dx.doi.org/10.3762/bjoc.17.106.
Pełny tekst źródłaReisenbauer, Julia C., Ori Green, Allegra Franchino, Patrick Finkelstein i Bill Morandi. "Late-stage diversification of indole skeletons through nitrogen atom insertion". Science 377, nr 6610 (2.09.2022): 1104–9. http://dx.doi.org/10.1126/science.add1383.
Pełny tekst źródłaBeaumier, Evan P., Brennan S. Billow, Amrendra K. Singh, Shannon M. Biros i Aaron L. Odom. "A complex with nitrogen single, double, and triple bonds to the same chromium atom: synthesis, structure, and reactivity". Chemical Science 7, nr 4 (2016): 2532–36. http://dx.doi.org/10.1039/c5sc04608d.
Pełny tekst źródłaSchiemenza, Günter Paulus, Simon Pörksen, Paulina M. Dominiak i Krzysztof Wozniak. "peri-Interactions in Naphthalenes, 6 [1]. On Hypercoordination of Phosphorus in 8-Dialkylamino-naphth-1-yl Phosphonium Salts". Zeitschrift für Naturforschung B 57, nr 1 (1.01.2002): 8–18. http://dx.doi.org/10.1515/znb-2002-0102.
Pełny tekst źródłaPabel, Jörg, Elmar Wadenstorfer i Klaus T. Wanner. "Asymmetric Synthesis of Pyrido[1,2-c]pyrimidinones". Zeitschrift für Naturforschung B 64, nr 6 (1.06.2009): 653–61. http://dx.doi.org/10.1515/znb-2009-0610.
Pełny tekst źródłaFujioka, Hiromichi, Yasuyuki Kita, Ozora Kubo, Kento Senami, Kazuhisa Okamoto i Takashi Okitsu. "Organic Chemistry Using Weakly Electrophilic Salts: The Reaction with Nitrogen Nucleophiles". HETEROCYCLES 79, nr 1 (2009): 1113. http://dx.doi.org/10.3987/com-08-s(d)69.
Pełny tekst źródłaChambers, Richard D., Alan M. Kenwright, Mandy Parsons, Graham Sandford i John S. Moilliet. "Elemental fluorine. Part 14.1 Electrophilic fluorination and nitrogen functionalisation of hydrocarbons". Journal of the Chemical Society, Perkin Transactions 1, nr 19 (3.09.2002): 2190–97. http://dx.doi.org/10.1039/b204776b.
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