Добірка наукової літератури з теми "C-H bonds functionalisation"
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Статті в журналах з теми "C-H bonds functionalisation"
Banerjee, Arghya, Satavisha Sarkar, and Bhisma K. Patel. "C–H functionalisation of cycloalkanes." Organic & Biomolecular Chemistry 15, no. 3 (2017): 505–30. http://dx.doi.org/10.1039/c6ob01975g.
Повний текст джерелаPrakash, Gaurav, Nilanjan Paul, Gwyndaf A. Oliver, Daniel B. Werz, and Debabrata Maiti. "C–H deuteration of organic compounds and potential drug candidates." Chemical Society Reviews 51, no. 8 (2022): 3123–63. http://dx.doi.org/10.1039/d0cs01496f.
Повний текст джерелаPatrick, Scott R., Ine I. F. Boogaerts, Sylvain Gaillard, Alexandra M. Z. Slawin, and Steven P. Nolan. "The role of silver additives in gold-mediated C–H functionalisation." Beilstein Journal of Organic Chemistry 7 (July 1, 2011): 892–96. http://dx.doi.org/10.3762/bjoc.7.102.
Повний текст джерелаChe, Chi-Ming, Vanessa Kar-Yan Lo, Cong-Ying Zhou, and Jie-Sheng Huang. "Selective functionalisation of saturated C–H bonds with metalloporphyrin catalysts." Chemical Society Reviews 40, no. 4 (2011): 1950. http://dx.doi.org/10.1039/c0cs00142b.
Повний текст джерелаCrowe, Charlotte, Samuel Molyneux, Sunil V. Sharma, Ying Zhang, Danai S. Gkotsi, Helen Connaris, and Rebecca J. M. Goss. "Halogenases: a palette of emerging opportunities for synthetic biology–synthetic chemistry and C–H functionalisation." Chemical Society Reviews 50, no. 17 (2021): 9443–81. http://dx.doi.org/10.1039/d0cs01551b.
Повний текст джерелаVellakkaran, Mari, Jagadish Das, Sourajit Bera, and Debasis Banerjee. "Nickel-catalysed alkylation of C(sp3)–H bonds with alcohols: direct access to functionalised N-heteroaromatics." Chemical Communications 54, no. 87 (2018): 12369–72. http://dx.doi.org/10.1039/c8cc06370b.
Повний текст джерелаGulzar, Naeem, Bertrand Schweitzer-Chaput, and Martin Klussmann. "Oxidative coupling reactions for the functionalisation of C–H bonds using oxygen." Catalysis Science & Technology 4, no. 9 (June 16, 2014): 2778. http://dx.doi.org/10.1039/c4cy00544a.
Повний текст джерелаShaikh, Mohammed Umar M., Sulochana S. Mudaliar, and Kishor H. Chikhalia. "An efficient alkynylation of 4-thiazolidinone with terminal alkyne under C–H functionalisation." RSC Advances 6, no. 56 (2016): 50780–85. http://dx.doi.org/10.1039/c6ra05015h.
Повний текст джерелаSt John-Campbell, Sahra, and James A. Bull. "Transient imines as ‘next generation’ directing groups for the catalytic functionalisation of C–H bonds in a single operation." Organic & Biomolecular Chemistry 16, no. 25 (2018): 4582–95. http://dx.doi.org/10.1039/c8ob00926k.
Повний текст джерелаGulzar, Naeem, Bertrand Schweitzer-Chaput, and Martin Klussmann. "ChemInform Abstract: Oxidative Coupling Reactions for the Functionalisation of C-H Bonds Using Oxygen." ChemInform 45, no. 41 (September 25, 2014): no. http://dx.doi.org/10.1002/chin.201441235.
Повний текст джерелаДисертації з теми "C-H bonds functionalisation"
Davis, Holly. "Harnessing non-covalent interactions to control regioselectivity in the functionalisation of arene C-H bonds." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/277900.
Повний текст джерелаYahaya, N. P. "Cyclometallation at Pd, Mn and Co : functionalisation of C-H and C≡C bonds involving cyclisation, rearrangement and isomerisation processes." Thesis, University of York, 2016. http://etheses.whiterose.ac.uk/12566/.
Повний текст джерелаTruscott, Fiona Rosemary. "Transition metal catalysed C-C bond formation via C-H functionalisation." Thesis, University of Oxford, 2012. http://ora.ox.ac.uk/objects/uuid:6a1ef296-8d63-470d-96bd-3e01a887c81f.
Повний текст джерелаTeskey, Christopher. "Strategic use of transition metals for selective C-H bond functionalisation." Thesis, University of Manchester, 2016. https://www.research.manchester.ac.uk/portal/en/theses/strategic-use-of-transition-metals-for-selective-ch-bond-functionalisation(496828e4-75db-428e-afb5-0138d55c3258).html.
Повний текст джерелаWilliams, Thomas. "Understanding C-H bond functionalisation at heterocycles and biomolecules : a synthetic and mechanistic study." Thesis, University of York, 2013. http://etheses.whiterose.ac.uk/4133/.
Повний текст джерелаBeck, Elizabeth Mary. "New strategies for chemical synthesis : metal-catalyzed C-H bond functionalisation for complex molecule synthesis." Thesis, University of Cambridge, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.596508.
Повний текст джерелаReay, Alan. "Development of Pd-catalysed C–H bond functionalisation methodologies for the accession of molecular complexity." Thesis, University of York, 2016. http://etheses.whiterose.ac.uk/13161/.
Повний текст джерелаChen, Lu. "Palladium-catalysed C-C bond construction in virtue of C-H functionalisation : direct arylation of heteroaromatics tolerant to reactive functional groups." Thesis, Rennes 1, 2013. http://www.theses.fr/2013REN1S011.
Повний текст джерелаDuring my thesis, I focused on condition for the activation / functionalisation of C-H bonds for the construction of biaryl derivatives tolerant to the reactive functional groups such as silyl, alkenes, esters or amides. Compared to classic cross-coupling protocols (Suzuki, Stille or Negishi), C-H bond functionalisation provides a costly effective and environmentally attractive procedures. At first, we observed that the silyl-substituted thiophenes can be directly arylated with aryl bromides without desilylation, using the simple Pd(OAc)2/dppb precatalyst for both conversion and desilylation inhibition. Then, we have demonstrated that the Pd(OAc)2/KOAc catalyst system without phosphine ligand, even using as few as 0.1 mol% of Pd catalyst, promotes the direct arylation of heteroaromatics and inhibits the Heck type reaction with 1,2-disubstituted alkenes. In addition, we demonstrated that easily accessible esters on heteroaromatics can be advantageously employed as blocking groups in the course of the direct arylation of several heteroaromatic derivatives. Finally, the palladium-catalyzed direct heteroarylation of 2- or 4-bromobenzamide with heteroarenes was studied. In the presence of KOAc as the base, no formation of C-N or C-C bonds by coupling of two bromobenzamide was observed
Haffemayer, Benjamin. "Development of novel amine-directed Pd(II)-catalysed sp2 and sp3 C-H bond functionalisation processes." Thesis, University of Cambridge, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607792.
Повний текст джерелаPlatt, George. "Mechanistic investigation into the Pd-catalysed C–H bond functionalisation of fluoroarenes : reaction kinetics and intermediate characterisation." Thesis, University of York, 2016. http://etheses.whiterose.ac.uk/17253/.
Повний текст джерелаЧастини книг з теми "C-H bonds functionalisation"
Bruneau, Christian, and Pierre H. Dixneuf. "Ruthenium(II)-Catalysed Functionalisation of C–H Bonds with Alkenes: Alkenylation versus Alkylation." In C-H Bond Activation and Catalytic Functionalization I, 137–88. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_134.
Повний текст джерелаBruneau, Christian, and Pierre H. Dixneuf. "Erratum to: Ruthenium(II)-Catalysed Functionalisation of C–H Bonds with Alkenes: Alkenylation versus Alkylation." In C-H Bond Activation and Catalytic Functionalization I, 259–60. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_150.
Повний текст джерелаHaber, Jerzy. "Theoretical Basis of the Activation of C-H Bond." In Catalytic Activation and Functionalisation of Light Alkanes, 157–87. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-017-0982-8_7.
Повний текст джерелаCarr, Kevin J. T., Stuart A. Macgregor, and Claire L. McMullin. "Computational Studies on Heteroatom-Assisted C–H Activation and Functionalisation at Group 8 and 9 Metal Centres." In C-H Bond Activation and Catalytic Functionalization I, 53–76. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_125.
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