Artículos de revistas sobre el tema "N-Aryl aldimines"
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Beng, Timothy K., Jorge Garcia, Jane Eichwald, and Claire Borg. "Introducing a sulfone-embedded anhydride to the anhydride-imine reaction for the modular synthesis of N-heterocyclic sulfones bearing vicinal stereocenters." RSC Advances 13, no. 21 (2023): 14355–60. http://dx.doi.org/10.1039/d3ra01812a.
Texto completoRohit, Kumar, Paul Piyali, and Bhattacharya Samaresh. "N-(Aryl)pyrrole-2-aldimine complexes of ruthenium: Synthesis, characterization and catalytic transfer-hydrogenation." Journal of Indian Chemical Society Vol. 95, Jul 2018 (2018): 721–28. https://doi.org/10.5281/zenodo.5638362.
Texto completoKostryukov, S. G., V. A. Kalyazin, P. S. Petrov, E. V. Bezrukova, and N. V. Somov. "1,3-dipolar cycloaddition as a method for the synthesis of dipyrrolidinyl- and dipyrrolylketones." Журнал общей химии 94, no. 4 (2024): 469–88. http://dx.doi.org/10.31857/s0044460x24040028.
Texto completoDenmark, Scott, and Hyung Chi. "Synthesis of 2-Alkenyl-Tethered Anilines." Synthesis 49, no. 13 (2017): 2873–88. http://dx.doi.org/10.1055/s-0036-1589002.
Texto completoLi, Yang, Bi-Jie Li, Wen-Hua Wang, et al. "Rhodium-Catalyzed Direct Addition of Aryl CH Bonds to N-Sulfonyl Aldimines." Angewandte Chemie International Edition 50, no. 9 (2011): 2115–19. http://dx.doi.org/10.1002/anie.201007464.
Texto completoLi, Yang, Bi-Jie Li, Wen-Hua Wang, et al. "Rhodium-Catalyzed Direct Addition of Aryl CH Bonds to N-Sulfonyl Aldimines." Angewandte Chemie 123, no. 9 (2011): 2163–67. http://dx.doi.org/10.1002/ange.201007464.
Texto completoSeth, Dipravath Kumar, and Samaresh Bhattacharya. "Copper(I) complexes of N-(aryl)pyridine-2-aldimines: Spectral, electrochemical and catalytic properties." Polyhedron 30, no. 15 (2011): 2438–43. http://dx.doi.org/10.1016/j.poly.2011.05.037.
Texto completoLi, Yang, Bi-Jie Li, Wen-Hua Wang, et al. "ChemInform Abstract: Rhodium-Catalyzed Direct Addition of Aryl C-H Bonds to N-Sulfonyl Aldimines." ChemInform 42, no. 26 (2011): no. http://dx.doi.org/10.1002/chin.201126087.
Texto completoJit, Karmakar, Barua Trisha, Paul Piyali, and Bhattacharya Samaresh. "Interaction of N-(aryl)pyrrole-2-aldimines with Ru(0) : Synthesis, structure and, spectral and electrochemical properties of the resulting complexes." Journal of Indian Chemical Society Vol. 92, Dec 2015 (2015): 1993–99. https://doi.org/10.5281/zenodo.5602564.
Texto completoZhao, Gui-Ling, and Min Shi. "Baylis–Hillman reactions of N-tosyl aldimines and aryl aldehydes with 3-methylpenta-3,4-dien-2-one." Organic & Biomolecular Chemistry 3, no. 20 (2005): 3686. http://dx.doi.org/10.1039/b510572b.
Texto completoPaul, Piyali, and Samaresh Bhattacharya. "Iridium mediated N–H and C–H bond activation of N-(aryl)pyrrole-2-aldimines. Synthesis, structure and, spectral and electrochemical properties." Journal of Organometallic Chemistry 713 (August 2012): 72–79. http://dx.doi.org/10.1016/j.jorganchem.2012.04.023.
Texto completoMitra, Kamala, Subhendu Biswas, Shyamal Kumar Chattopadhyay, C. Robert Lucas, and Bibhutosh Adhikary. "Synthesis and X-ray Crystal Structures of Two Luminescent Imidazopyridinium Derivatives from the Corresponding N-(aryl)-Pyridine-2-aldimines." Journal of Chemical Crystallography 37, no. 8 (2007): 567–71. http://dx.doi.org/10.1007/s10870-007-9212-y.
Texto completoCurti, Claudio, Lucia Battistini, Beatrice Ranieri, et al. "ChemInform Abstract: anti-Selective, Catalytic Asymmetric Vinylogous Mukaiyama Mannich Reactions of Pyrrole-Based Silyl Dienolates with N-Aryl Aldimines." ChemInform 42, no. 27 (2011): no. http://dx.doi.org/10.1002/chin.201127115.
Texto completoIshiyama, Tatsuo, and John Hartwig. "ChemInform Abstract: A Heck-Type Reaction Involving Carbon-Heteroatom Double Bonds. Rhodium(I)-Catalyzed Coupling of Aryl Halides with N-Pyrazyl Aldimines." ChemInform 32, no. 16 (2001): no. http://dx.doi.org/10.1002/chin.200116114.
Texto completoTomaszewski, MJ, J. Warkentin, and NH Werstiuk. "Free-Radical Chemistry of Imines." Australian Journal of Chemistry 48, no. 2 (1995): 291. http://dx.doi.org/10.1071/ch9950291.
Texto completoDey, Bikash Kali, Jayita Dutta, Michael G. B. Drew, and Samaresh Bhattacharya. "Chloro-ruthenium complexes with carbonyl and N-(aryl)pyridine-2-aldimines as ancillary ligands. Synthesis, characterization and catalytic application in C–C cross-coupling of arylaldehydes with arylboronic acids." Journal of Organometallic Chemistry 750 (January 2014): 176–84. http://dx.doi.org/10.1016/j.jorganchem.2013.11.019.
Texto completoDey, Bikash Kali, Jayita Dutta, Michael G. B. Drew, and Samaresh Bhattacharya. "ChemInform Abstract: Chloro-Ruthenium Complexes with Carbonyl and N-(Aryl)pyridine-2-aldimines as Ancillary Ligands. Synthesis, Characterization and Catalytic Application in C-C Cross-Coupling of Arylaldehydes with Arylboronic Acids." ChemInform 45, no. 30 (2014): no. http://dx.doi.org/10.1002/chin.201430081.
Texto completoKpoezoun, Amavi, Gnon Baba, and Jean-Claude Guillemin. "Primary Pyrrolimines and Pyridinimines." Molecules 30, no. 6 (2025): 1239. https://doi.org/10.3390/molecules30061239.
Texto completoCrousse, Benoît, Jean-Pierre Bégué, and Danièle Bonnet-Delpon. "Synthesis of 2-CF3-Tetrahydroquinoline and Quinoline Derivatives from CF3-N-Aryl-aldimine." Journal of Organic Chemistry 65, no. 16 (2000): 5009–13. http://dx.doi.org/10.1021/jo9918807.
Texto completoGoswami, Sreebrata, Wancydora Kharmawphlang, Alok K. Deb, and Shie-Ming Peng. "Monovalent copper complexes of N-aryl-pyridine-2-aldimine. synthesis, characterization and structure." Polyhedron 15, no. 20 (1996): 3635–41. http://dx.doi.org/10.1016/0277-5387(96)00065-4.
Texto completoWang, Shang-Hua, and Rong-Jie Chein. "(Thiolan-2-yl)diphenylmethyl benzyl ether/N,N′-diarylurea cocatalyzed asymmetric aziridination of cinnamyl bromide and aryl aldimine." Tetrahedron 72, no. 21 (2016): 2607–15. http://dx.doi.org/10.1016/j.tet.2014.12.063.
Texto completoLucas, C. Robert, Kamala Mitra, Subhendu Biswas, Shyamal Kumar Chattopadhyay, and Bibhutosh Adhikary. "Synthesis, spectroscopy and redox properties of mononuclear manganese(II) and manganese(IV) complexes with N-(aryl)-pyridine-2-aldimine (L) and its amide derivatives. X-ray structural characterization of [Mn(MeL)2(NCS)2] (MeL = N-(4-methylphenyl)-pyridine-2-aldimine)." Transition Metal Chemistry 30, no. 2 (2005): 185–90. http://dx.doi.org/10.1007/s11243-004-3225-6.
Texto completoNath Mitra, Kedar, Subrata Choudhury, Sreebrata Goswami, and Shie-Ming Peng. "A family of mixed ligand complexes of RuII-L [L = N-aryl-pyridine-2-aldimine], their reactions, isolation and characterization. X-ray crystal structure of [Ru(pic)(L1)2][ClO4]· CH2Cl2 [pic= 2-picolinate ion]." Polyhedron 16, no. 10 (1997): 1605–14. http://dx.doi.org/10.1016/s0277-5387(96)00482-2.
Texto completoMishra, Dipankar, Subhendu Naskar, Bibhutosh Adhikary, Raymond J. Butcher, and Shyamal Kumar Chattopadhyay. "Synthesis, spectroscopic and electrochemical properties of some heteroleptic tris-chelates of ruthenium (II) involving 2,2′-bipyridine (bpy) and N-(aryl) pyridine-2-aldimine(L): X-ray crystal structures of [Ru(bpy)(L2)2](ClO4)2·H2O and 3-N(4-tolyl) imidazo [1,5a] pyridinium perchlorate." Polyhedron 24, no. 2 (2005): 201–8. http://dx.doi.org/10.1016/j.poly.2004.11.011.
Texto completo"Stereoselective Vinylation of Aryl N-(2-Pyridylsulfonyl) Aldimines." Synfacts 8, no. 03 (2012): 0308. http://dx.doi.org/10.1055/s-0031-1290214.
Texto completoChandra, Anushri, Papu Dhibar, Pragna Dutta, Piyali Paul, and Samaresh Bhattacharya. "N-(aryl)pyrrole-2-aldimine complexes of ruthenium: Synthesis, structure and, spectral and electrochemical properties." New Journal of Chemistry, 2023. http://dx.doi.org/10.1039/d2nj05295d.
Texto completoDeng, Yu-Qin, Qi-Qi Yan, Ting-Ting Zhang, Yi Zhou, Cheng-Yu He, and Quan-Zhong Liu. "Copper-Catalyzed Asymmetric Allylation of N-Aryl Aldimines." Journal of Organic Chemistry, December 11, 2023. http://dx.doi.org/10.1021/acs.joc.3c02035.
Texto completoLasri, Jamal, Naser E. Eltayeb, Saied M. Soliman, et al. "Synthesis and X‐Ray Structural Analyses Combined Anticancer Efficacy and Molecular Docking for N‐Aryl‐(2‐pyridyl)aldimines." ChemistrySelect 9, no. 36 (2024). http://dx.doi.org/10.1002/slct.202402236.
Texto completoLi, Zhenjiang, Xinhua Ren, Yuhu Shi, and Pingkai Ouyang. "Practical and General Entry to N-Tosyl Aryl Aldimines Promoted by Sulfamic Acid in Water and Alcohol." ChemInform 38, no. 31 (2007). http://dx.doi.org/10.1002/chin.200731059.
Texto completoEsquivias, Jorge, Ramon Gomez Arrayas, and Juan Carlos Carretero. "ChemInform Abstract: Alkylation of Aryl N-(2-Pyridylsulfonyl)aldimines with Organozinc Halides: Conciliation of Reactivity and Chemoselectivity." ChemInform 39, no. 15 (2008). http://dx.doi.org/10.1002/chin.200815070.
Texto completoGrooms, Alexander J., Robert T. Huttner, Mackenzie Stockwell, et al. "Programmable C–N Bond Formation through Radical‐Mediated Chemistry in Plasma‐Microdroplet Fusion." Angewandte Chemie, October 25, 2024. http://dx.doi.org/10.1002/ange.202413122.
Texto completoGrooms, Alexander J., Robert T. Huttner, Mackenzie Stockwell, et al. "Programmable C–N Bond Formation through Radical‐Mediated Chemistry in Plasma‐Microdroplet Fusion." Angewandte Chemie International Edition, October 25, 2024. http://dx.doi.org/10.1002/anie.202413122.
Texto completoChen, Donghuang, Clément Lepori, Régis Guillot, Richard Gil, Sophie Bezzenine, and Jérôme Hannedouche. "A Rationally Designed Iron(II) Catalyst for C(sp3)−C(sp2) and C(sp3)−C(sp3) Suzuki−Miyaura Cross‐Coupling." Angewandte Chemie International Edition, May 22, 2024. http://dx.doi.org/10.1002/anie.202408419.
Texto completoChen, Donghuang, Clément Lepori, Régis Guillot, Richard Gil, Sophie Bezzenine, and Jérôme Hannedouche. "A Rationally Designed Iron(II) Catalyst for C(sp3)−C(sp2) and C(sp3)−C(sp3) Suzuki−Miyaura Cross‐Coupling." Angewandte Chemie, May 22, 2024. http://dx.doi.org/10.1002/ange.202408419.
Texto completoWang, Shang-Hua, and Rong-Jie Chein. "ChemInform Abstract: (Thiolan-2-yl)diphenylmethyl Benzyl Ether/N,N′-Diarylurea Cocatalyzed Asymmetric Aziridination of Cinnamyl Bromide and Aryl Aldimine." ChemInform 47, no. 38 (2016). http://dx.doi.org/10.1002/chin.201638022.
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