Статті в журналах з теми "Diazabutadienes"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Diazabutadienes".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Romero-Ortega, Moisés, Ignacio Medina-Mercado, Ivann Zaragoza-Galicia, and Horacio Olivo. "2-Trifluoromethyl-1,3-diazabutadienes as Useful Intermediates for the Construction of 2-Trifluoromethylpyrimidine Derivatives." Synthesis 50, no. 20 (July 16, 2018): 4133–39. http://dx.doi.org/10.1055/s-0037-1610444.
Повний текст джерелаRomero-Ortega, Moisés, Michelle Trujillo-Lagunas, Ignacio Medina-Mercado, Ivann Zaragoza-Galicia, and Horacio Olivo. "A Synthesis of 4-Chloro-2-(trichloromethyl)pyrimidines and Their Study in Nucleophilic Substitution." Synthesis 51, no. 02 (September 11, 2018): 530–37. http://dx.doi.org/10.1055/s-0037-1610270.
Повний текст джерелаSain, Bir, Satyendra P. Singh, and Jagir S. Sandhu. "Diazabutadienes in heterocyclic syntheses: reaction of 1,3-diazabutadienes with 2-oxazolin-5-ones." Tetrahedron Letters 32, no. 38 (September 1991): 5151–52. http://dx.doi.org/10.1016/s0040-4039(00)93452-x.
Повний текст джерелаSAIN, B., S. P. SINGH, and J. S. SANDHU. "ChemInform Abstract: Diazabutadienes in Heterocyclic Syntheses: Reaction of 1,3- Diazabutadienes with 2-Oxazolin-5-ones." ChemInform 23, no. 23 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199223188.
Повний текст джерелаAlvarez-Vald�s, Amparo, Mar�a Jos� Camaz�n, Jos� R. Masaguer, and Carmen Navarro-Ranninger. "Complexes of copper(II) with diazabutadienes." Transition Metal Chemistry 12, no. 1 (February 1987): 55–58. http://dx.doi.org/10.1007/bf01023133.
Повний текст джерелаBhadbhade, Mohan, Guy K. B. Clentsmith, and Leslie D. Field. "Sterically Hindered Diazabutadienes (DABs): Competing Reaction Pathways with MeLi." Organometallics 29, no. 23 (December 13, 2010): 6509–17. http://dx.doi.org/10.1021/om100850p.
Повний текст джерелаNandy Mazumdar, Sujit, Manoj Sharma, and Mohinder Pal Mahajan. "Diels-Alder cycloaddition reactions of 1,3-diazabutadienes with sulfene." Tetrahedron Letters 28, no. 23 (January 1987): 2641–42. http://dx.doi.org/10.1016/s0040-4039(00)96169-0.
Повний текст джерелаMazumdar, Sujit Nandy, Ibrahim Ibnusaud, and Mohinder Pal Mahajan. "Diels-alder cycloaddition reactions of 1,3-diazabutadienes with ketenes." Tetrahedron Letters 27, no. 48 (January 1986): 5875–76. http://dx.doi.org/10.1016/s0040-4039(00)85351-4.
Повний текст джерелаBubnov, Michael P., Vladimir K. Cherkasov, Irina A. Teplova, Nickolay O. Druzhkov, Ivan D. Grishin, Evgenii V. Baranov, Artem S. Bogomyakov, and Gleb A. Abakumov. "Novel dioxolene nickel complexes with sterically hindered diazabutadienes. Coupling of aza-ligands coordinated to nickel." Dalton Transactions 48, no. 28 (2019): 10516–25. http://dx.doi.org/10.1039/c9dt01309a.
Повний текст джерелаTrifonov, Alexander A., Boris G. Shestakov, Konstantin A. Lyssenko, Joulia Larionova, Georgy K. Fukin, and Anton V. Cherkasov. "Sterically Governed Redox Reactions. One-Electron Oxidation of Ytterbocenes by Diazabutadienes: Formation of Radical-Anionic Diazabutadiene vs Covalently Bonded Imino–Amido Ligand." Organometallics 30, no. 18 (September 26, 2011): 4882–89. http://dx.doi.org/10.1021/om200429h.
Повний текст джерелаMotz, Philip L., John P. Williams, John J. Alexander, Douglas M. Ho, John S. Ricci, and Wallace T. Miller. "Coupling of iminoacyl groups to diazabutadienes on manganese carbonyl complexes." Organometallics 8, no. 6 (June 1989): 1523–33. http://dx.doi.org/10.1021/om00108a025.
Повний текст джерелаMorrone, Stefania, Gayle Harrison, and Duncan W. Bruce. "Octahedral, liquid-crystalline complexes of 1,4-diazabutadienes with rhenium(I)." Advanced Materials 7, no. 7 (July 1995): 665–67. http://dx.doi.org/10.1002/adma.19950070715.
Повний текст джерелаDiel, Bruce N., Peter J. Deardorff та Catherine M. Zelenski. "Synthesis of new 2,3-perfluoroalkyl- and perfluoroaryl-1,4-diazabutadienes (α-diimines)". Tetrahedron Letters 40, № 49 (грудень 1999): 8523–27. http://dx.doi.org/10.1016/s0040-4039(99)01692-5.
Повний текст джерелаHe, Jing-Yu, Hong-Xing Xin, Hong Yan, Xiu-Qing Song, and Ru-Gang Zhong. "Convenient ultrasound-mediated synthesis of 1,4-diazabutadienes under solvent-free conditions." Ultrasonics Sonochemistry 18, no. 1 (January 2011): 466–69. http://dx.doi.org/10.1016/j.ultsonch.2010.08.002.
Повний текст джерелаDworczak, Renate, Walter M. F. Fabian, Claudia Reidlinger, Alice Rumpler, Jörg Schachner, and Klaus Zangger. "Nonlinear optical properties of diazabutadienes and -hexatrienes; experimental and computational aspects." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 58, no. 10 (August 2002): 2135–44. http://dx.doi.org/10.1016/s1386-1425(01)00678-3.
Повний текст джерелаPaparo, Albert, Stephen P. Best, K. Yuvaraj, and Cameron Jones. "Neutral, Anionic, and Paramagnetic 1,3,2-Diazaberyllacyles Derived from Reduced 1,4-Diazabutadienes." Organometallics 39, no. 23 (February 25, 2020): 4208–13. http://dx.doi.org/10.1021/acs.organomet.0c00017.
Повний текст джерелаAvalos, Martín, Reyes Babiano, Pedro Cintas, JoséL Jiménez, Juan C. Palacios, and Juan B. Sánchez. "A facile and expeditious entry to acyclic carbohydrate-derived 1,2-diazabutadienes." Tetrahedron: Asymmetry 6, no. 4 (April 1995): 945–56. http://dx.doi.org/10.1016/0957-4166(95)00104-w.
Повний текст джерелаRojas-Sáenz, Héctor, Galdina V. Suárez-Moreno, Iris Ramos-García, Angélica M. Duarte-Hernández, Edgar Mijangos, Adrián Peña-Hueso, Rosalinda Contreras, and Angelina Flores-Parra. "1,4-Dialkyl-1,4-diazabutadienes: their reactions with aluminum and indium halides." New J. Chem. 38, no. 1 (2014): 391–405. http://dx.doi.org/10.1039/c3nj01226c.
Повний текст джерелаKing, Arienne S., Liliya G. Nikolcheva, Christopher R. Graves, Anna Kaminski, Christopher M. Vogels, Robert HE Hudson, Robert J. Ireland, Stephen J. Duffy, and Stephen A. Westcott. "Synthesis and reactivity of palladium and platinum diimine complexes containing boronate esters." Canadian Journal of Chemistry 80, no. 9 (September 1, 2002): 1217–22. http://dx.doi.org/10.1139/v02-145.
Повний текст джерелаLuthardt, Peter, and Ernst-Ulrich Würthwein. "[2+2]- AND [4+2] cycloaddition reactions of 1,3-diazabutadienes with diphenylketene." Tetrahedron Letters 29, no. 8 (January 1988): 921–24. http://dx.doi.org/10.1016/s0040-4039(00)82482-x.
Повний текст джерелаHe, Jingyu, Hongxing Xin, Hong Yan, Xiuqing Song, and Rugang Zhong. "Synthesis of 1,4-Diazabutadienes (=N,N′-Ethane-1,2-diylidenebis[amines]) by Grinding." Helvetica Chimica Acta 94, no. 1 (January 2011): 159–62. http://dx.doi.org/10.1002/hlca.201000155.
Повний текст джерелаAlbert, I. D. L., S. Ramasesha, and P. K. Das. "Properties of some low-lying electronic states in polymethineimines and poly(2,3-diazabutadienes)." Physical Review B 43, no. 9 (March 15, 1991): 7013–19. http://dx.doi.org/10.1103/physrevb.43.7013.
Повний текст джерелаAVALOS, M., R. BABIANO, P. CINTAS, J. L. JIMENEZ, J. C. PALACIOS, and J. B. SANCHEZ. "ChemInform Abstract: A Facile and Expeditious Entry to Acyclic Carbohydrate-Derived 1,2- Diazabutadienes." ChemInform 26, no. 36 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199536242.
Повний текст джерелаRojas-Saenz, Hector, Galdina V. Suarez-Moreno, Iris Ramos-Garcia, Angelica M. Duarte-Hernandez, Edgar Mijangos, Adrian Pena-Hueso, Rosalinda Contreras, and Angelina Flores-Parra. "ChemInform Abstract: 1,4-Dialkyl-1,4-diazabutadienes: Their Reactions with Aluminum and Indium Halides." ChemInform 45, no. 20 (April 28, 2014): no. http://dx.doi.org/10.1002/chin.201420111.
Повний текст джерелаDiel, Bruce N., Peter J. Deardorff та Catherine M. Zelenski. "ChemInform Abstract: Synthesis of New 2,3-Perfluoroalkyl- and Perfluoroaryl-1,4-diazabutadienes (α-Diimines)". ChemInform 31, № 9 (10 червня 2010): no. http://dx.doi.org/10.1002/chin.200009078.
Повний текст джерелаBarluenga, José, Miguel Tomás, Alfredo Ballesteros, and Luis A. López. "1,4-Cycloaddition of 1,3-diazabutadienes with enamines: An efficient route to the pyrimidine ring." Tetrahedron Letters 30, no. 34 (January 1989): 4573–76. http://dx.doi.org/10.1016/s0040-4039(01)80748-6.
Повний текст джерелаBooth, Corwin H., Marc D. Walter, Daniel Kazhdan, Yung-Jin Hu, Wayne W. Lukens, Eric D. Bauer, Laurent Maron, Odile Eisenstein, and Richard A. Andersen. "Decamethylytterbocene Complexes of Bipyridines and Diazabutadienes: Multiconfigurational Ground States and Open-Shell Singlet Formation." Journal of the American Chemical Society 131, no. 18 (May 13, 2009): 6480–91. http://dx.doi.org/10.1021/ja809624w.
Повний текст джерелаHe, Jingyu, Hongxing Xin, Hong Yan, Xiuqing Song, and Rugang Zhong. "ChemInform Abstract: Synthesis of 1,4-Diazabutadienes (=N,N′-Ethane-1,2-diylidenebis[amines]) by Grinding." ChemInform 42, no. 17 (March 31, 2011): no. http://dx.doi.org/10.1002/chin.201117055.
Повний текст джерелаFaust, Rüdiger, Bernd Göbelt, and Christian Weber. "Triisopropylsilyl Protected Hexa-1,5-diyne-3,4-dione: A Convenient Precursor to 2,3-Dialkynyl 1,4-Diazabutadienes." Synlett 1998, no. 01 (January 1998): 64–66. http://dx.doi.org/10.1055/s-1998-1559.
Повний текст джерелаFaust, Rüdiger, and Bernd Göbelt. "First 2,3-Dialkynyl-1,4-diazabutadienes by Pd-Catalyzed Cross-Coupling of Bis(imidoyl chlorides) and Alkynylstannanes." Tetrahedron Letters 38, no. 46 (November 1997): 8017–20. http://dx.doi.org/10.1016/s0040-4039(97)10218-0.
Повний текст джерелаJanich, Simon, Roland Fröhlich, Andrea Wilken, Jan von Zamory, Atsushi Wakamiya, Shigehiro Yamaguchi, and Ernst-Ulrich Würthwein. "3,4-Dihydro-3H-pyrrol-2-imines as Conformationally Restrained 1,3-Diazabutadienes: Synthesis, Structural Properties and Protonation." European Journal of Organic Chemistry 2009, no. 13 (May 2009): 2077–87. http://dx.doi.org/10.1002/ejoc.200900045.
Повний текст джерелаImhof, Wolfgang, and Ernst Anders. "Regioselectivity in Iron-Catalyzed [2+2+1] Cycloadditions: A DFT Investigation of Substituent Effects in 1,4-Diazabutadienes." Chemistry - A European Journal 10, no. 22 (November 19, 2004): 5717–29. http://dx.doi.org/10.1002/chem.200400215.
Повний текст джерелаFAUST, R., B. GOEBELT, and C. WEBER. "ChemInform Abstract: Triisopropylsilyl Protected Hexa-1,5-diyne-3,4-dione: A Convenient Precursor to 2,3-Dialkynyl 1,4-Diazabutadienes." ChemInform 29, no. 17 (June 23, 2010): no. http://dx.doi.org/10.1002/chin.199817087.
Повний текст джерелаBootz, Konrad, and Wilhelm P. Neumann. "The first synthesis of aza-germacyclopentenes: Cycloadditions of 1-aza- and 1,4-diazabutadienes with free singlet dimethyl germylene." Tetrahedron Letters 30, no. 48 (1989): 6669–72. http://dx.doi.org/10.1016/s0040-4039(00)70646-0.
Повний текст джерелаFAUST, R., and B. GOEBELT. "ChemInform Abstract: First 2,3-Dialkynyl-1,4-diazabutadienes by Pd-Catalyzed Cross-Coupling of Bis(imidoyl chlorides) and Alkynylstannanes." ChemInform 29, no. 7 (June 24, 2010): no. http://dx.doi.org/10.1002/chin.199807041.
Повний текст джерелаSingh, G. S., and K. Kopo. "ChemInform Abstract: Synthesis of 1,1,4,4-Tetraryl-1,3-diazabutadienes (II) by Oxidation of Hydrazones (I) Using Bis(acetylacetonato)copper(II)." ChemInform 33, no. 46 (May 19, 2010): no. http://dx.doi.org/10.1002/chin.200246113.
Повний текст джерелаBarluenga, José, Miguel Tomás, Alfredo Ballesteros, and Luis A. López. "A Simple, Regioselective Synthesis of 5,6-Dihydro-1,3,5-triazine-2,4(1H,3H)-dione Derivatives fromN-Trimethylsilyl Imines via 1,3-Diazabutadienes." Synthesis 1989, no. 03 (1989): 228–29. http://dx.doi.org/10.1055/s-1989-27212.
Повний текст джерелаBaker, Robert J., Robert D. Farley, Cameron Jones, Marc Kloth, and Damien M. Murphy. "The reactivity of diazabutadienes toward low oxidation state Group 13 iodides and the synthesis of a new gallium(i) carbene analogue." Journal of the Chemical Society, Dalton Transactions, no. 20 (2002): 3844. http://dx.doi.org/10.1039/b206605j.
Повний текст джерелаDas, Samir, Indranil Chakraborty, and Animesh Chakravorty. "Rhenium Chemistry of Diazabutadienes and Derived Iminoacetamides Spanning the Valence Domain II−VI. Synthesis, Characterization, and Metal-Promoted Regiospecific Imine Oxidation." Inorganic Chemistry 42, no. 20 (October 2003): 6545–55. http://dx.doi.org/10.1021/ic034586c.
Повний текст джерелаKia, Reza, and Azadeh Kalaghchi. "Intra- and intermolecular interactions in a series of chlorido-tricarbonyl-diazabutadienerhenium(I) complexes: structural and theoretical studies." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 76, no. 3 (May 16, 2020): 417–26. http://dx.doi.org/10.1107/s2052520620004333.
Повний текст джерелаKia, Reza, and Azadeh Kalaghchi. "Structural, Non-Covalent Interaction, and Natural Bond Orbital Studies on Bromido-Tricarbonyl Rhenium(I) Complexes Bearing Alkyl-Substituted 1,4-Diazabutadiene (DAB) Ligands." Crystals 10, no. 4 (April 1, 2020): 267. http://dx.doi.org/10.3390/cryst10040267.
Повний текст джерелаZhao, Jie, Jianchao Yuan, Weibing Xu, Jingjing Chen, and Yanqiong Mu. "2,3-Bis{[2,3-dimethyl-6-(phenylvinyl)phenyl]imino}butane." Acta Crystallographica Section E Structure Reports Online 70, no. 2 (January 11, 2014): o130. http://dx.doi.org/10.1107/s1600536814000440.
Повний текст джерелаPott, Thomas, Peter Jutzi, Beate Neumann, and Hans-Georg Stammler. "Differing Reactivities of Cp*Ga toward Diazabutadienes: Synthesis of Novel 1-Galla-2,5-diazoles and of the Known Radical Ga[But-DAB]2." Organometallics 20, no. 10 (May 2001): 1965–67. http://dx.doi.org/10.1021/om001045b.
Повний текст джерелаSain, Bir, Satyendra P. Singh, and Jagir S. Sandhu. "Diazabutadienes in heterocyclic syntheses. Preparation of pyrimidin-6-ones by reaction of 4-dialkylamino-1,3-diaza-1,3-butadienes with 2-oxazolin-5-ones." Tetrahedron 48, no. 22 (January 1992): 4567–78. http://dx.doi.org/10.1016/s0040-4020(01)81230-8.
Повний текст джерелаWeber, Lothar, Jan Förster, Hans-Georg Stammler, and Beate Neumann. "Contribution to the Reactivity ofN,N′-Diaryl-1,4-diazabutadienes Aryl–N=CH–CH=N–Aryl (Aryl = 2,6-Dimethylphenyl; 2,4,6-Trimethylphenyl) Towards Boron Trichloride." European Journal of Inorganic Chemistry 2006, no. 24 (December 2006): 5048–56. http://dx.doi.org/10.1002/ejic.200600728.
Повний текст джерелаLv, Wen-Xian, Jian Li, Yu-Lai Hu, Ying-Peng Su, and Dan-Feng Huang. "(Z)-N-[(Z)-3-(2,5-Dimethylphenylimino)butan-2-ylidene]-2,5-dimethylaniline." Acta Crystallographica Section E Structure Reports Online 70, no. 2 (January 22, 2014): o175. http://dx.doi.org/10.1107/s1600536814001020.
Повний текст джерелаUhl, Werner, Jens Molter, and Bernhard Neumüller. "Synthesis of Aluminum Hydrazides by Hydroalumination of 2,3-Diazabutadienes—Formation of an Al4(N2)3 Cage Compound and an Al3(N2)3 Macrocyclic Ligand." Chemistry 7, no. 7 (April 1, 2001): 1510–15. http://dx.doi.org/10.1002/1521-3765(20010401)7:7<1510::aid-chem1510>3.0.co;2-p.
Повний текст джерелаSAIN, B., S. P. SINGH, and J. S. SANDHU. "ChemInform Abstract: Diazabutadienes in Heterocyclic Syntheses. Preparation of Pyrimidin-6- ones by Reaction of 4-Dialkylamino-1,3-diaza-1,3-butadienes with 2- Oxazolin-5-ones." ChemInform 23, no. 39 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199239208.
Повний текст джерелаTrifonov, Alexander A., Elena A. Fedorova, Georgy K. Fukin, Evgenii V. Baranov, Nikolai O. Druzhkov та Mikhail N. Bochkarev. "Bridging μ-η5:η4-Coordination of an Indenyl Ligand and Reductive Coupling of Diazabutadienes in the Assembly of Di- and Tetranuclear Mixed-Valent Ytterbium Indenyldiazabutadiene Complexes". Chemistry - A European Journal 12, № 10 (20 березня 2006): 2752–57. http://dx.doi.org/10.1002/chem.200501181.
Повний текст джерелаWEIDENBRUCH, M., A. LESCH, and K. PETERS. "ChemInform Abstract: Silicon Compounds with Strongly Intramolecular Steric Interactions. Part 44. (4 +1) Versus (4 + 2) Cycloaddition of Di-tert.-butylsilylene and Tetra-tert.-butyldisilene to 1,4-Diazabutadienes." ChemInform 22, no. 26 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199126221.
Повний текст джерела