Literatura académica sobre el tema "C - hetero"
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Artículos de revistas sobre el tema "C - hetero"
Zhao, Yating y Wujiong Xia. "Photochemical C–H bond coupling for (hetero)aryl C(sp2)–C(sp3) bond construction". Organic & Biomolecular Chemistry 17, n.º 20 (2019): 4951–63. http://dx.doi.org/10.1039/c9ob00244h.
Texto completoHucthagowder, Vishwanathan, Chelsea D. Mullins, Rekha Meyer, Rakesh Nagarajan, John F. DiPersio, Ravi Vij, Michael H. Tomasson y Shashikant Kulkarni. "Resequencing Analysis of the Human Candidate Ras and Receptor Tyrosine Kinase Gene Family In Multiple Myeloma". Blood 116, n.º 21 (19 de noviembre de 2010): 301. http://dx.doi.org/10.1182/blood.v116.21.301.301.
Texto completoChoy, Pui Ying, Shun Man Wong, Anant Kapdi y Fuk Yee Kwong. "Recent developments in palladium-catalysed non-directed coupling of (hetero)arene C–H bonds with C–Z (Z = B, Si, Sn, S, N, C, H) bonds in bi(hetero)aryl synthesis". Organic Chemistry Frontiers 5, n.º 2 (2018): 288–321. http://dx.doi.org/10.1039/c7qo00693d.
Texto completoXiao, Fang, Jin-Hong Lin, Fei Hao, Xing Zheng, Yu Guo y Ji-Chang Xiao. "Visible light mediated C–H trifluoromethylation of (hetero)arenes". Organic Chemistry Frontiers 9, n.º 7 (2022): 1982–85. http://dx.doi.org/10.1039/d2qo00067a.
Texto completoRan, You, Yudong Yang, Huansha You y Jingsong You. "RhCl3-Catalyzed Oxidative C–H/C–H Cross-Coupling of (Hetero)aromatic Sulfonamides with (Hetero)arenes". ACS Catalysis 8, n.º 3 (30 de enero de 2018): 1796–801. http://dx.doi.org/10.1021/acscatal.7b04298.
Texto completoVerrier, Cécile, Pierrik Lassalas, Laure Théveau, Guy Quéguiner, François Trécourt, Francis Marsais y Christophe Hoarau. "Recent advances in direct C–H arylation: Methodology, selectivity and mechanism in oxazole series". Beilstein Journal of Organic Chemistry 7 (29 de noviembre de 2011): 1584–601. http://dx.doi.org/10.3762/bjoc.7.187.
Texto completoLiu, Yahu, Xuebin Liao y Lu Hu. "Recent Progress in Methylation of (Hetero)Arenes by Cross-Coupling or C–H Activation". Synlett 29, n.º 04 (5 de febrero de 2018): 375–82. http://dx.doi.org/10.1055/s-0037-1609093.
Texto completoPahovnik, David, Uroš Uršič, Uroš Grošelj, Anton Meden, Jurij Svete y Branko Stanovnik. "Synthesis of Dimethyl 1-(Hetero)aryl-4-oxo-1,4-dihydropyridazine- 3,5-dicarboxylates from Dimethyl 3-Oxopentane-1,5-dioates". Zeitschrift für Naturforschung B 63, n.º 4 (1 de abril de 2008): 407–14. http://dx.doi.org/10.1515/znb-2008-0407.
Texto completoArani, A. Ghorbanpour y R. Kolahchi. "Exact solution for nonlocal axial buckling of linear carbon nanotube hetero-junctions". Proceedings of the Institution of Mechanical Engineers, Part C: Journal of Mechanical Engineering Science 228, n.º 2 (25 de marzo de 2013): 366–77. http://dx.doi.org/10.1177/0954406213483647.
Texto completoGui, Yong-Yuan, Li-Li Liao, Liang Sun, Zhen Zhang, Jian-Heng Ye, Guo Shen, Zhi-Peng Lu, Wen-Jun Zhou y Da-Gang Yu. "Coupling of C(sp3)–H bonds with C(sp2)–O electrophiles: mild, general and selective". Chemical Communications 53, n.º 6 (2017): 1192–95. http://dx.doi.org/10.1039/c6cc09685a.
Texto completoTesis sobre el tema "C - hetero"
Devaraj, Karthik. "Ruthenium-catalyzed C-H Functionalization of (Hetero)arenes". Doctoral thesis, Uppsala universitet, Organisk kemi, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-310998.
Texto completoSubba, Raju. "Studies on the reactions of C - hetero bond formation". Thesis, University of North Bengal, 2015. http://ir.nbu.ac.in/handle/123456789/1854.
Texto completoSaha, Bittu. "Development of Novel methodologies for the construction of c-hetero bond". Thesis, University of North Bengal, 2018. http://ir.nbu.ac.in/handle/123456789/2823.
Texto completoLi, Haoran. "Pd-catalyzed C-H bond functionalizations of (hetero)arenes and alkenes : A one step access to poly(hetero)aromatics and styrene derivatives". Thesis, Rennes, Ecole nationale supérieure de chimie, 2020. http://www.theses.fr/2020ENCR0068.
Texto completoIn order to explain the background of my research work, in the first chapter, I summarized general mechanistic information on palladium-catalyzed C-H bond arylation and detailed some literature on direct arylation related to my research work. My objectives were to study the reactivity of new synthetic units allowing the straightforward access to bi-(hetero)aryls compounds or styrene derivatives using aryl halides or benzenesulfonyl chloride derivatives as the aryl-sources. Then, in the chapters 2-6, I summarized my research work. I studied the regiocontrolled palladium-catalyzed direct C2-arylations of Methoxsalen using benzenesulfonyl chlorides and C2,C3-diarylations using aryl bromides as the aryl sources. These results are summarized in the chapter 2. Then, I found that Pd-catalyzed direct arylation reaction allows the easy access to Ticlopidine derivatives arylated at the C5-position of the thienyl ring in one step. These results are reported in the chapter 3. In the chapter 4, we studied the reactivity of Diflufenican which contains a 1,3-difluorobenzene ring and a pyridine unit using Ru and Pd catalysis. Under appropriate conditions, two different C-H bonds of Diflufenican could be arylated. In the chapter 5, I employed different aryl sources to functionalize the C10- and C11-positions of dibenzo[b,f]azepines, and obtained asymmetric products. Through these reactions, a wide diversity of functional group were introduced on the dibenzo[b,f]azepine derivatives. Finally, in the Chapter 6, I report the first method allowing to prepare C10-arylated Cyproheptadine derivatives
Zhao, Liqin. "Palladium-catalyzed direct arylation via sp² and sp³ C-H activation of hetero(aromatics) and hydrocarbons for C-C bond formation". Thesis, Rennes 1, 2014. http://www.theses.fr/2014REN1S038/document.
Texto completoDuring this thesis, we were interested in the sp² and sp³ C-H bond activation catalyzed by palladium catalysts for the preparation of (hetero)aryl-aryls and biaryls. This method is considered as cost effective and environmentally attractive compared to the classical couplings such as Suzuki, Heck, or Negishi. First we described the palladium-catalyzed direct C2-arylation of benzothiophene in the absence of phosphine ligand with high selectivity. We also demonstrated that it is possible to active both C2 and C5 C-H bonds for access to 2,5-diarylated compounds in one step, and also to non-symmetrically substituted 2,5-diarylpyrroles via sequential C2 arylation followed by C5 arylation. We also studied the reactivity of polychlorobenzenes via palladium-catalyzed C-H activation. We finally examined the palladium-catalysed selective sp² and sp³ C-H bond activation of guaiazulene. The selectivity depends on the solvent and base: sp² C2-arylation (KOAc in ethylbenzene), sp² C3-arylation (KOAc in DMAc) and sp³ C4-Me arylation (CsOAc/K₂CO₃ in DMAc). Through this method, a challenging sp³ C-H bond was activated
Öhlenschläger, Kim K. [Verfasser] y C. [Akademischer Betreuer] Barner-Kowollik. "Hetero Diels-Alder Reactions in Material Science / Kim K. Öhlenschläger. Betreuer: C. Barner-Kowollik". Karlsruhe : KIT-Bibliothek, 2014. http://d-nb.info/1082294411/34.
Texto completoKirchberg, Sylvia [Verfasser]. "Palladium-katalysierte C-H-Arylierungen von (Hetero)-Arenen mit Arylboronsäuren und TEMPO / Sylvia Kirchberg". München : Verlag Dr. Hut, 2011. http://d-nb.info/1017353379/34.
Texto completoSala, Fernanda Angélica. "Estudo da interação entre domínios C-terminais de septinas humanas: implicação na formação e estabilidade do filamento". Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/75/75133/tde-10082015-140053/.
Texto completoSeptins comprise a conserved protein family that binds guanidine nucleotide and forms heterofilaments. In structural terms they have a common organization: a central GTPase domain, a N-terminal domain and a C-terminal domain, this last one is predicted to form coiled coil structures. Currently, the human septin heterocomplex best characterized (SEPT2/SEPT6/SEPT7) reveals the importance of the GTPase domain in filament assembly, however the absence of electron density for the C-terminal domains makes its function still unknown. Studies with mammals septins, and of others organisms like C. elegans and S. cerevisea suggests that some septins groups (e.g. II e IV in mammals) interact via its C-terminal domains and this could act in a determinative way to correct filament assembly. In this way, this project aimed to study the homo/heterotypical affinity for the C-terminal domains of human septins belonging to groups II (SEPT6C/8C/10C/11C) e IV (SEPT7C), investigating whether this domain contributes with the preference of septins to interact with proteins of different groups during assembly of the heterofilament. The C-terminal domains were expressed in E. coli and purificated. It was carried out studies using analytical ultracentrifugation and circular dichroism spectropolarimetry tecniques which allowed identification of major affinity and stability in the heterotypical association compared to homotypical. It was measured apparent dissociation constants for homodimers of low µM range while for heterodimers our group\'s data shows dissociation constants in the nM range. To understand at atomic level the factors responsible for this significant preference in the C-terminal domains interaction between groups II and IV was performed molecular modelling studies and analysis of the primary sequence. These analysis suggests the presence of a high number of charged residues in position a of the coiled coil as responsible for selectivity. Consequently, the heterodimer would be therefore favoured because of the minor repulsive effect coming from the staggered of charged residues in a. Thus, these results indicate the crucial or cooperative action of C-terminal domains in preferential organization of septins during filament assembly, favouring the NC interface between septins of groups II and IV.
Clouston, Laurel L. "The design and synthesis of C¦3 symmetric ligands for lanthanide Lewis acid catalysis of the inverse demand hetero Diels-Alder reaction". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp02/NQ37336.pdf.
Texto completoO'Connor, Sean M. J. "Application of Tridentate Schiff Base Chromium (III) Complex Catalysts Towards the Total Synthesis of (-)- Lasonolide A and C-Disaccharide Mimics". Thesis, Griffith University, 2012. http://hdl.handle.net/10072/366217.
Texto completoThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
School of Biomolecular and Physical Sciences
Science, Environment, Engineering and Technology
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Libros sobre el tema "C - hetero"
Rodd, E. H. Rodd's Chemistry of Carbon Compounds: Heterocyclic Compounds, Part C 5 Membered Heterocyclic Compounds With 2 Hetero Atoms in the Ring (Rodd's Chemistry of Carbon Compounds 2nd Edition). 2a ed. Elsevier Science Ltd, 1986.
Buscar texto completoAnsell, Martin F. Supplements to the 2nd Edition of Rodd's Chemistry of Carbon Compounds : Heterocyclic Compounds : Part C: Five-Membered Heterocyclic Compounds with Two Hetero-Atoms in the Ring from Groups V and/or VI of the Periodic Table. Part D: Five-Membered Heterocyclic Compounds with More than Two Hetero-Atoms in the Ring. Not Avail, 1994.
Buscar texto completoCapítulos de libros sobre el tema "C - hetero"
Vopsaroiu, M., V. Kuncser, J. Bartolome, V. M. Meriacre, K. I. Turta, I. Prisecaru y G. Filoti. "Mössbauer and magnetic evidence for spin frustration in hetero-trinuclear clusters". En Hyperfine Interactions (C), 213–16. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0281-3_53.
Texto completoGang, Peng, Wang Xiaojing, Tang Pengju, Zhou Wenli y Yu Jun. "Simulation and Optimization of A-Si:H/C-Si Hetero-Junction Solar Cells". En Proceedings of ISES World Congress 2007 (Vol. I – Vol. V), 1159–63. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75997-3_230.
Texto completoGupta, Aniket, Sreedhar Gundekari y Sukalyan Bhadra. "C(sp3)–H Bond Hetero-functionalization of Aliphatic Carboxylic Acid Equivalents Enabled by Transition Metals". En Catalysis for Clean Energy and Environmental Sustainability, 383–427. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-65017-9_13.
Texto completoDeka, Himangshu, Arun Kumar Sunaniya y Pratima Agarwal. "A Numerical Study on a c-Si(P) Substrate-Based Homo-Hetero Junction Solar Cell". En Sustainable Energy Generation and Storage, 91–99. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-2088-4_7.
Texto completoCabezas-Gómez, Luben, Hélio Aparecido Navarro y José Maria Saíz-Jabardo. "Computational Code HETE (Standard C Programming Language)". En SpringerBriefs in Applied Sciences and Technology, 63–67. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-09671-1_5.
Texto completoHemingway, Richard W., Seiji Ohara, Jan P. Steynberg, E. Vincent Brandt y Daneel Ferreira. "C-H Hetcor NMR Studies of Proanthocyanidins and their Derivatives". En Plant Polyphenols, 321–37. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3476-1_18.
Texto completoLiu, B., C. Renaud, J. Kowynia, K. K. Nelson, E. Roudachevski, D. Snyder, J. Timar y K. V. Honn. "Activation Of Protein Kinase C by 12(S)-HETE: Role in Tumor Cell Metastasis". En Eicosanoids and Other Bioactive Lipids in Cancer, Inflammation and Radiation Injury, 629–34. Boston, MA: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-3520-1_123.
Texto completoTang, Dean G. y Kenneth V. Honn. "Role of Protein Kinase C and Phosphatases in 12(S)-Hete-Induced Tumor Cell Cytoskeletal Reorganization". En Advances in Experimental Medicine and Biology, 349–61. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-5325-0_48.
Texto completoIshihara, K. y A. Sakakura. "Hetero-Diels–Alder Reactions". En Stereoselective Pericyclic Reactions, Cross Coupling, and C—H and C—X Activation, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-203-00060.
Texto completoIshihara, K. y A. Sakakura. "Enantioselective Hetero-Diels–Alder Reactions of Carbonyl Compounds". En Stereoselective Pericyclic Reactions, Cross Coupling, and C—H and C—X Activation, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-203-00061.
Texto completoActas de conferencias sobre el tema "C - hetero"
Hun-Soo Kim, Chang-Ho Lee, Doo-Bong Lee, Se-Young Oh y Jeong-Woo Choi. "Bio electroluminescent device composed of cytochrome c/chlorophyll a hetero-structure". En 2006 IEEE Nanotechnology Materials and Devices Conference. IEEE, 2006. http://dx.doi.org/10.1109/nmdc.2006.4388762.
Texto completoKunishima, I., K. Suguro, T. Aoyama y J. Matsunaga. "Homogeneous Hetero-Epitaxial NiSi2 Formation on (100)Si". En 1990 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 1990. http://dx.doi.org/10.7567/ssdm.1990.c-10-7.
Texto completoChoi, Sang H. y Adam J. Duzik. "Rhombohedral super hetero epitaxy of cubic SiGe on trigonal c-plane sapphire". En 2017 IEEE Photonics Society Summer Topical Meeting Series (SUM). IEEE, 2017. http://dx.doi.org/10.1109/phosst.2017.8012670.
Texto completoJeong-Woo Choi, Doo-Bong Lee y Bumhwan Lee. "Rectified photocurrent of biophodiode composed of cytochrome c/chlorophyll a hetero-structure". En 2006 IEEE Nanotechnology Materials and Devices Conference. IEEE, 2006. http://dx.doi.org/10.1109/nmdc.2006.4388761.
Texto completoTagmatarchis, Nikos. "Hetero- and homo- [70] fullerene dimers: (C[sub 69]N)[sub 2] and (C[sub 70])[sub 2]". En ELECTRONIC PROPERTIES OF MOLECULAR NANOSTRUCTURES: XV International Winterschool/Euroconference. AIP, 2001. http://dx.doi.org/10.1063/1.1426814.
Texto completoSchmidt, M., H. Angermann, E. Conrad, L. Korte, A. Laades, K. Maydell, Ch Schubert y R. Stangl. "Physical and Technological Aspects of a-Si:H/c-Si Hetero-Junction Solar Cells". En 2006 IEEE 4th World Conference on Photovoltaic Energy Conference. IEEE, 2006. http://dx.doi.org/10.1109/wcpec.2006.279722.
Texto completoRusop, M., Mohamad Rusop y Tetsuo Soga. "Photovoltaic Characteristics of Fabricated Carbon Based P-C∕N-Si Hetero-Junction Solar Cells". En NANOSCIENCE AND NANOTECHNOLOGY: International Conference on Nanoscience and Nanotechnology—2008. AIP, 2009. http://dx.doi.org/10.1063/1.3160226.
Texto completoUeda, Koji, Yuichiro Ando, Mamoru Kumano, Taizoh Sadoh, Kazumasa Narumi, Yoshihito Maeda y Masanobu Miyao. "Atomically Controlled Hetero-Epitaxy of DO3-type Fe3Si on Ge(111) Substrate". En 2007 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2007. http://dx.doi.org/10.7567/ssdm.2007.c-2-1.
Texto completoShen, G. D., D. X. Xu, M. Willander y G. V. Hansson. "Multi-step Bidirectional NDR Characteristics in Si/Si1-xGex/Si Double Hetero-Structures". En 1988 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 1988. http://dx.doi.org/10.7567/ssdm.1988.c-3-2.
Texto completoZhang, G., K. Tateno, H. Gotoh y T. Sogawa. "InAsP-InAs-InAsP hetero-nanowires grown via the self-assisted vapor-liquid-solid mode". En 2012 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2012. http://dx.doi.org/10.7567/ssdm.2012.c-2-2.
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