Artykuły w czasopismach na temat „Imines”
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Svete, Jurij, Uroš Grošelj, Franc Požgan i Bogdan Štefane. "Copper-Catalyzed Azomethine Imine–Alkyne Cycloadditions (CuAIAC)". Synthesis 50, nr 23 (5.10.2018): 4501–24. http://dx.doi.org/10.1055/s-0037-1610284.
Pełny tekst źródłaWulff, William, Xin Zhang i Yijing Dai. "The Acceleration of the Rearrangement of α-Hydroxy Aldimines by Lewis or Brønsted Acids". Synlett 29, nr 15 (28.08.2018): 2015–18. http://dx.doi.org/10.1055/s-0037-1610262.
Pełny tekst źródłaGonciarz, Agnieszka, Robert Pich, Krzysztof Artur Bogdanowicz, Beata Jewloszewicz, Wojciech Przybył, Karolina Dysz, Agnieszka Dylong i in. "UV–Vis Absorption Properties of New Aromatic Imines and Their Compositions with Poly({4,8-bis[(2-Ethylhexyl)oxy]Benzo[1,2-b:4,5-b′]Dithiophene-2,6-diyl}{3-Fluoro-2-[(2-Ethylhexyl)Carbonyl]Thieno[3,4-b]Thiophenediyl})". Materials 12, nr 24 (13.12.2019): 4191. http://dx.doi.org/10.3390/ma12244191.
Pełny tekst źródłaMendes, Joseane A., Paulo R. R. Costa, Miguel Yus, Francisco Foubelo i Camilla D. Buarque. "N-tert-Butanesulfinyl imines in the asymmetric synthesis of nitrogen-containing heterocycles". Beilstein Journal of Organic Chemistry 17 (12.05.2021): 1096–140. http://dx.doi.org/10.3762/bjoc.17.86.
Pełny tekst źródłaGarrido-Castro, Alberto F., M. Carmen Maestro i José Alemán. "α-Functionalization of Imines via Visible Light Photoredox Catalysis". Catalysts 10, nr 5 (19.05.2020): 562. http://dx.doi.org/10.3390/catal10050562.
Pełny tekst źródłaNugent, Thomas C., Richard Vaughan Williams, Andrei Dragan, Alejandro Alvarado Méndez i Andrei V. Iosub. "An investigation of the observed, but counter-intuitive, stereoselectivity noted during chiral amine synthesis via N-chiral-ketimines". Beilstein Journal of Organic Chemistry 9 (15.10.2013): 2103–12. http://dx.doi.org/10.3762/bjoc.9.247.
Pełny tekst źródłaRawaa Daoud Sulaiman i Zaheda Ahmed Najim. "The Effect of Temperature and Thermodynamic Parameters on the Ionization Constants of Some Imines Derived from Vanillin with substituted aniline". Tikrit Journal of Pure Science 27, nr 4 (28.11.2022): 31–38. http://dx.doi.org/10.25130/tjps.v27i4.30.
Pełny tekst źródłaAn, Ran, Mengbi Guo, Yingbo Zang, Hang Xu, Zhuang Hou i Chun Guo. "Recent Advances in Synthesis of Benzazoles via Imines". Current Organic Chemistry 24, nr 17 (12.11.2020): 1897–942. http://dx.doi.org/10.2174/1385272824999200818180845.
Pełny tekst źródłaFreese, Tyll, Jan C. Namyslo, Martin Nieger i Andreas Schmidt. "Sulfur, mercury, and boron adducts of sydnone imine derived anionic N-heterocyclic carbenes". RSC Advances 9, nr 9 (2019): 4781–88. http://dx.doi.org/10.1039/c9ra00294d.
Pełny tekst źródłaZhang, Hanmo, E. Ben Hay, Stephen J. Geib i Dennis P. Curran. "Fates of imine intermediates in radical cyclizations of N-sulfonylindoles and ene-sulfonamides". Beilstein Journal of Organic Chemistry 11 (17.09.2015): 1649–55. http://dx.doi.org/10.3762/bjoc.11.181.
Pełny tekst źródłaMeng, Qingxi, Fen Wang i Ming Li. "Bisoxazoline–copper(I)-catalyzed aziridination of diazoacetate with imines — A DFT study". Canadian Journal of Chemistry 88, nr 10 (październik 2010): 981–90. http://dx.doi.org/10.1139/v10-099.
Pełny tekst źródłaBaig, Fayaz, Rajni Kant, Vivek K. Gupta i Madhushree Sarkar. "Effects of non covalent interactions in light emitting properties of bis-pyridyl-alkyl-di-imines". RSC Advances 5, nr 63 (2015): 51220–32. http://dx.doi.org/10.1039/c5ra09562j.
Pełny tekst źródłaBenz, Scott, i Andrew S. Murkin. "α-Ketol and α-iminol rearrangements in synthetic organic and biosynthetic reactions". Beilstein Journal of Organic Chemistry 17 (15.10.2021): 2570–84. http://dx.doi.org/10.3762/bjoc.17.172.
Pełny tekst źródłaZhao, Qun, Jin Zhang i Michal Szostak. "Ruthenium(0)-sequential catalysis for the synthesis of sterically hindered amines by C–H arylation/hydrosilylation". Chemical Communications 55, nr 61 (2019): 9003–6. http://dx.doi.org/10.1039/c9cc04072b.
Pełny tekst źródłaEdwards, Oliver E., Dusan Dvornik, Ralph J. Kolt i Barbara A. Blackwell. "Formation, reactions, and NMR spectra of 1,20-cycloatidanes". Canadian Journal of Chemistry 70, nr 5 (1.05.1992): 1397–405. http://dx.doi.org/10.1139/v92-178.
Pełny tekst źródłaLaha, Joydev K., K. S. Satyanarayana Tummalapalli i Krupal P. Jethava. "Implications of dynamic imine chemistry for the sustainable synthesis of nitrogen heterocycles via transimination followed by intramolecular cyclisation". Organic & Biomolecular Chemistry 14, nr 8 (2016): 2473–79. http://dx.doi.org/10.1039/c5ob02670a.
Pełny tekst źródłaBecica, Joseph, Andrew B. Jackson, William G. Dougherty, W. Scott Kassel i Nathan M. West. "Bis-tropolonate complexes of tungsten: scaffolds for selective side-on binding of nitriles, imines and ketones". Dalton Trans. 43, nr 23 (2014): 8738–48. http://dx.doi.org/10.1039/c4dt00734d.
Pełny tekst źródłaJuneja, Navkiran, Ethan Zahid, Daniel K. Unruh i Kristin M. Hutchins. "Solid-state behaviors of imines: colossal biaxial positive thermal expansion, motion capability, and phase transitions". CrystEngComm 23, nr 25 (2021): 4439–43. http://dx.doi.org/10.1039/d1ce00706h.
Pełny tekst źródłaLorenzini, Fabio, Paolo Marcazzan, Brian O. Patrick i Brian R. James. "Synthesis, characterization, and X-ray structures of three iridium(III)-hydrido-cyclometallated-imine complexes, including the first reported hydrido-(η1-imine)-Ir complex". Canadian Journal of Chemistry 86, nr 3 (1.03.2008): 253–60. http://dx.doi.org/10.1139/v07-153.
Pełny tekst źródłaMao, Kebin, Guoqin Fan, Yuanhong Liu, Shi Li, Xu You i Dan Liu. "Titanium-mediated reductive cross-coupling reactions of imines with terminal alkynes: An efficient route for the synthesis of stereodefined allylic amines". Beilstein Journal of Organic Chemistry 9 (27.03.2013): 621–27. http://dx.doi.org/10.3762/bjoc.9.69.
Pełny tekst źródłaA.S.P. Azzouz i D.B.AL-Bakzo. "Determination of Stability for imines derived from carbonyl compounds by conductivity measurements". Tikrit Journal of Pure Science 23, nr 3 (22.05.2018): 43–47. http://dx.doi.org/10.25130/tjps.v23i3.499.
Pełny tekst źródłaBanks, Surya R., J. Tanner Morningstar i Mark E. Welker. "Synthesis of Aminopropyltriethoxysilyl-Substituted Imines and Amides". Molbank 2021, nr 3 (18.07.2021): M1251. http://dx.doi.org/10.3390/m1251.
Pełny tekst źródłaBosica, Giovanna, Roderick Abdilla, Kaylie Demanuele i Josef Fiteni. "Facile imine synthesis under green conditions using Amberlyst® 15". PeerJ Organic Chemistry 4 (9.08.2022): e7. http://dx.doi.org/10.7717/peerj-ochem.7.
Pełny tekst źródłaWolfsberger, W. "N-(Halogendimethylsilyl)-1 -methylphospholanimine/N-(Halogenodimethylsilyl)-1 -methylphospholane Imines". Zeitschrift für Naturforschung B 55, nr 7 (1.07.2000): 557–60. http://dx.doi.org/10.1515/znb-2000-0701.
Pełny tekst źródłaZhang, Hongming, Jiahe Zhuang, Xiangrui Feng i Ben Ma. "Co0.6Ni0.4S2/rGO Photocatalyst for One-Pot Synthesis of Imines from Nitroaromatics and Aromatic Alcohols by Transfer Hydrogenation". Coatings 12, nr 12 (23.11.2022): 1799. http://dx.doi.org/10.3390/coatings12121799.
Pełny tekst źródłaSatyam, Killari, Battu Harish, Jagadeesh Babu Nanubolu i Surisetti Suresh. "N-Heterocyclic carbene (NHC)-catalyzed tandem imine umpolung–aza-Michael addition–oxidation of β-carboline cyclic imines". Chemical Communications 56, nr 18 (2020): 2803–6. http://dx.doi.org/10.1039/d0cc00321b.
Pełny tekst źródłaWang, Liming, Hao Wu, Ruxin Ding, Zhe Chen i Ying Jin. "Enantioselective Friedel-Crafts Reaction of Indoles with N-Tosylimines Employing Takemoto's Organocatalyst". Current Organic Chemistry 23, nr 15 (28.10.2019): 1688–94. http://dx.doi.org/10.2174/1385272823666190823115333.
Pełny tekst źródłaGamenara, Daniela, i Pablo Domínguez de María. "Enantioselective imine reduction catalyzed by imine reductases and artificial metalloenzymes". Org. Biomol. Chem. 12, nr 19 (2014): 2989–92. http://dx.doi.org/10.1039/c3ob42205d.
Pełny tekst źródłaKuznetsova, Juliana V., Varvara T. Tkachenko, Lada M. Petrovskaya, Maria E. Filkina, Dmitry E. Shybanov, Yuri K. Grishin, Vitaly A. Roznyatovsky i in. "[3+2]-Cycloaddition of Nitrile Imines to Parabanic Acid Derivatives—An Approach to Novel Spiroimidazolidinediones". International Journal of Molecular Sciences 25, nr 1 (19.12.2023): 18. http://dx.doi.org/10.3390/ijms25010018.
Pełny tekst źródłaGarcía-Hernández, Zureima, i François P. Gabbaï. "Synthesis and Properties of 2-(Dimesitylboryl)benzylideneamines". Zeitschrift für Naturforschung B 64, nr 11-12 (1.12.2009): 1381–86. http://dx.doi.org/10.1515/znb-2009-11-1219.
Pełny tekst źródłaAl-Shalaan, Abdulla M., Salim S. Al-Showiman i Ibrahim M. Al-Najjar. "Isomerization of imines in platinum-imine complexes". Inorganica Chimica Acta 121, nr 2 (listopad 1986): 127–29. http://dx.doi.org/10.1016/s0020-1693(00)84510-7.
Pełny tekst źródłaXu, Wengang, i Naohiko Yoshikai. "Cobalt-catalyzed directed C–H alkenylation of pivalophenone N–H imine with alkenyl phosphates". Beilstein Journal of Organic Chemistry 14 (28.03.2018): 709–15. http://dx.doi.org/10.3762/bjoc.14.60.
Pełny tekst źródłaFondo, Matilde, Julio Corredoira-Vázquez, Ana M. GarcíaDeibe i Jesús Sanmartín-Matalobos. "An Easy Approach to Obtain Alcohol-Amines by Reduction of Alcohol Functionalized Imines". Proceedings 9, nr 1 (14.03.2019): 2. http://dx.doi.org/10.3390/ecsoc-22-05697.
Pełny tekst źródłaLu, Gang, Peng Zhang, Dongqing Sun, Lei Wang, Kebin Zhou, Zhi-Xiang Wang i Guo-Cong Guo. "Gold catalyzed hydrogenations of small imines and nitriles: enhanced reactivity of Au surface toward H2via collaboration with a Lewis base". Chem. Sci. 5, nr 3 (2014): 1082–90. http://dx.doi.org/10.1039/c3sc52851k.
Pełny tekst źródłaGhashghaei, Ouldouz, Consiglia Annamaria Manna, Esther Vicente-García, Marc Revés i Rodolfo Lavilla. "Studies on the interaction of isocyanides with imines: reaction scope and mechanistic variations". Beilstein Journal of Organic Chemistry 10 (6.01.2014): 12–17. http://dx.doi.org/10.3762/bjoc.10.3.
Pełny tekst źródłaZarei, Maaroof. "One-step Synthesis of β-lactams Using Cyanuric Fluoride". Journal of Chemical Research 37, nr 1 (styczeń 2013): 25–27. http://dx.doi.org/10.3184/174751912x13545429290478.
Pełny tekst źródłaYamamoto, K., i Masayoshi Higuchi. "Dendritic polyphenylazomethines: Synthesis, structure, and metal-assembling function". Pure and Applied Chemistry 76, nr 7-8 (1.01.2004): 1399–408. http://dx.doi.org/10.1351/pac200476071399.
Pełny tekst źródłaWhittaker, Jacob, Suresh Moorthy, Jonathan Cremers, Jason R. Price, John C. McMurtrie i Jack K. Clegg. "Synthesis of Two 2,2′-Bipyridine Containing Macrocycles for the Preparation of Interlocked Architectures". Australian Journal of Chemistry 70, nr 5 (2017): 588. http://dx.doi.org/10.1071/ch16710.
Pełny tekst źródłaSadowski, Mikołaj, Jolanta Utnicka, Adrianna Wójtowicz i Karolina Kula. "The global and local Reactivity of C,N-diarylnitryle imines in [3+2] cycloaddition processes with trans-β-nitrostyrene according to Molecular Electron Density Theory: A computational study". Current Chemistry Letters 12, nr 2 (2023): 421–30. http://dx.doi.org/10.5267/j.ccl.2022.11.004.
Pełny tekst źródłaMwansa, Joseph M., Matthew J. Stirling i Michael I. Page. "Changing the kinetic order of enantiomer formation and distinguishing between iminium ion and imine as the reactive species in the asymmetric transfer hydrogenation of substituted imines using a cyclopentadienyl iridium (III) complex". Pure and Applied Chemistry 92, nr 1 (28.01.2020): 107–21. http://dx.doi.org/10.1515/pac-2019-0222.
Pełny tekst źródłaSong, Tao, Yanan Duan, Xiufang Chen i Yong Yang. "Switchable Access to Amines and Imines from Reductive Coupling of Nitroarenes with Alcohols Catalyzed by Biomass-Derived Cobalt Nanoparticles". Catalysts 9, nr 2 (29.01.2019): 116. http://dx.doi.org/10.3390/catal9020116.
Pełny tekst źródłaKandemir, Hakan, Ibrahim F. Sengul, Naresh Kumar i David StC Black. "Synthesis of Imine and Amine-Linked Macrocycles Containing Tris-Indoles". Australian Journal of Chemistry 70, nr 11 (2017): 1196. http://dx.doi.org/10.1071/ch17264.
Pełny tekst źródłaHonraedt, Aurélien, Lucía Méndez, Jean-Marc Campagne i Eric Leclerc. "A Three-Component Reaction for the One-Pot Preparation of β-Amino-α,α-Difluoroketones from Trimethyl(trifluoromethyl)silane (CF3TMS), Acylsilanes and Imines". Synthesis 49, nr 17 (13.06.2017): 4082–92. http://dx.doi.org/10.1055/s-0036-1588447.
Pełny tekst źródłaSeibel, Zara M., Jeffrey S. Bandar i Tristan H. Lambert. "Enantioenriched α-substituted glutamates/pyroglutamates via enantioselective cyclopropenimine-catalyzed Michael addition of amino ester imines". Beilstein Journal of Organic Chemistry 17 (17.08.2021): 2077–84. http://dx.doi.org/10.3762/bjoc.17.134.
Pełny tekst źródłaWang, Yunlong, Zongyang Li, Haiying Zhao i Zhenhua Zhang. "Rhodium-Catalyzed Double Isocyanide Insertion via a Vinylcarbodiimide Intermediate for the Synthesis of 2H-Pyrrol-2-imines". Synthesis 51, nr 17 (21.05.2019): 3250–58. http://dx.doi.org/10.1055/s-0037-1611830.
Pełny tekst źródłaUllah, Qasim, NAHID FATEMA, M. VIJJULATHA, Pathan Mohammad Arif, SALMAN AHMED KHAN, MOHAMMED ARIFUDDIN, Syed Kashif Ali i REHAB EBAID AZOOZ. "Green and Efficient Chemo-selective Synthesis of Chalcone Imines (α,β-Unsaturated imine) using Baker’s Yeast". Asian Journal of Chemistry 35, nr 11 (31.10.2023): 2809–14. http://dx.doi.org/10.14233/ajchem.2023.30302.
Pełny tekst źródłaLin, Qinghong, Djamal Djaidi, Roger Bishop, Donald C. Craig i Marcia L. Scudder. "Ritter Reactions. XIII Reactivity of Methyl Schiff Bases with Dimethyl Acetylenedicarboxylate and Mercaptoacetic Acid". Australian Journal of Chemistry 51, nr 9 (1998): 799. http://dx.doi.org/10.1071/c98025.
Pełny tekst źródłaRavula, Madhu, Siddaramagoud Bandalla, Vijaykumar Dosarapu, Mohan Kurra, Satyanarayana Mavurapu i Chandra Sekhar Vasam. "Selective Synthesis of Imines via Oxidative Coupling of Primary Amines and Oxidation of Secondary Amines by Peroxides and other Competent Oxidants: A Short Review". Oriental Journal Of Chemistry 40, nr 3 (27.06.2024): 611–29. http://dx.doi.org/10.13005/ojc/400301.
Pełny tekst źródłaFukumoto, Yoshiya, Masato Daijo i Naoto Chatani. "Rhenium(I)-catalyzed reaction of terminal alkynes with imines leading to allylamine derivatives". Pure and Applied Chemistry 86, nr 3 (20.03.2014): 283–89. http://dx.doi.org/10.1515/pac-2014-5003.
Pełny tekst źródłaConstantin, Catalin Paul, Andra Elena Bejan i Mariana Dana Damaceanu. "The Chromic Response to Environment of some Imine-Based Oligomers". Key Engineering Materials 826 (październik 2019): 91–101. http://dx.doi.org/10.4028/www.scientific.net/kem.826.91.
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