Добірка наукової літератури з теми "C-C bonds"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "C-C bonds".
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.
Статті в журналах з теми "C-C bonds"
RITTER, STEPHEN K. "EXTREME C–C BONDS." Chemical & Engineering News 87, no. 19 (May 11, 2009): 32–33. http://dx.doi.org/10.1021/cen-v087n019.p032.
Повний текст джерелаHuntley, Deborah R., Georgios Markopoulos, Patrick M. Donovan, Lawrence T. Scott, and Roald Hoffmann. "Squeezing CC Bonds." Angewandte Chemie 117, no. 46 (November 25, 2005): 7721–25. http://dx.doi.org/10.1002/ange.200502721.
Повний текст джерелаHuntley, Deborah R., Georgios Markopoulos, Patrick M. Donovan, Lawrence T. Scott, and Roald Hoffmann. "Squeezing CC Bonds." Angewandte Chemie International Edition 44, no. 46 (November 25, 2005): 7549–53. http://dx.doi.org/10.1002/anie.200502721.
Повний текст джерелаZeng, Xiaoming, and Xuefeng Cong. "Chromium-Catalyzed Cross-Coupling Reactions by Selective Activation of Chemically Inert Aromatic C–O, C–N, and C–H Bonds." Synlett 32, no. 13 (May 11, 2021): 1343–53. http://dx.doi.org/10.1055/a-1507-4153.
Повний текст джерелаEgami, Hiromichi. "Fluorofunctionalizations of C–C Multiple Bonds and C–H Bonds." Chemical and Pharmaceutical Bulletin 68, no. 6 (June 1, 2020): 491–511. http://dx.doi.org/10.1248/cpb.c19-00856.
Повний текст джерелаMeng, Ge, Pengfei Li, Kai Chen, and Linghua Wang. "Recent Advances in Transition-Metal-Free Aryl C–B Bond Formation." Synthesis 49, no. 21 (September 26, 2017): 4719–30. http://dx.doi.org/10.1055/s-0036-1590913.
Повний текст джерелаLuh, Tien-Yau. "Chelation Assisted Conversion of C-S Bonds into C-C Bonds." Phosphorus, Sulfur, and Silicon and the Related Elements 120, no. 1 (January 1, 1997): 259–73. http://dx.doi.org/10.1080/10426509708545523.
Повний текст джерелаHamel, Jean-Denys, та Jean-François Paquin. "Activation of C–F bonds α to C–C multiple bonds". Chemical Communications 54, № 73 (2018): 10224–39. http://dx.doi.org/10.1039/c8cc05108a.
Повний текст джерелаKaupp, Gerd, and Jürgen Boy. "Overlong CC Single Bonds." Angewandte Chemie International Edition in English 36, no. 12 (February 3, 1997): 48–49. http://dx.doi.org/10.1002/anie.199700481.
Повний текст джерелаWang, Chang-Sheng, Pierre H. Dixneuf, and Jean-François Soulé. "Photoredox Catalysis for Building C–C Bonds from C(sp2)–H Bonds." Chemical Reviews 118, no. 16 (July 16, 2018): 7532–85. http://dx.doi.org/10.1021/acs.chemrev.8b00077.
Повний текст джерелаДисертації з теми "C-C bonds"
Correia, Camille. "Oxidative C-C bond formation via metal-catalyzed coupling of two C-H bonds." Thesis, McGill University, 2013. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=114441.
Повний текст джерелаCette thèse décrit la formation de nouvelles liaisons C-C par activation oxydative directe de deux liaisons C-H grâce à l'utilisation de métaux de transition comme catalyseurs. La première partie présentera trois différentes réactions de Cross-Dehydrogenative-Coupling (CDC) oxydantes. Dans un premier temps, sera présentée dans le chapitre 2, la réaction d'alkylation de liens C-H benzylique par 1,3-dicarbonyles et cétones. Ce system a démontré son efficacité sur une large variété de substrats contenant des liaisons C-H enolysable. De plus il a été rendu possible, grâce à l'utilisation d'un co-catalyseur organique, le N-Hydroxyphthalimide (NHPI), d'utiliser l'oxygène moléculaire comme oxydant terminal. Dans un second temps, nous étudierons l'utilisation du 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) comme médiateur pour l'alkynylation de liaisons sp3 C-H. Une nouvelle CDC réaction catalysée par le triflate de cuivre (I) sera présentée dans le chapitre 3, entre un alcyne et une liaison C-H benzylique. Le chapitre 4 présentera le développement de cette réaction à l'alcynation d'éthers benzyliques en présence d'une quantité catalytique de triflate d'argent (I). Ces deux procédures sont seulement applicables pour les alcynes vrais aromatiques. Finalement, le chapitre 6 portera sur la réaction de Minisci catalysée par le palladium. Le peroxyde radical α-hydroxyalkyl généré lors de la réaction est capable de réagir avec les azines. La quantité stœchiométrique d'acide nécessaire lors de la traditionnelle réaction de Minisci, a été remplacée par une quantité catalytique de dichloro palladium.
Rix, Kathryn. "Electrochemical reduction of amides and c=c bonds." Thesis, Imperial College London, 2012. http://hdl.handle.net/10044/1/39846.
Повний текст джерелаKanuru, Vijaykumar. "Understanding surface mediated C-C and C-N bond forming reactions." Thesis, University of Cambridge, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.608956.
Повний текст джерелаBowen, John George. "C-H activation in the formation of C-N and C-O Bonds." Thesis, University of Bristol, 2015. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.685335.
Повний текст джерелаLee, Kang-sang. "New Concepts and Catalysts for Enantioselective Synthesis of C-C, C-Si, and C-B Bonds." Thesis, Boston College, 2010. http://hdl.handle.net/2345/1739.
Повний текст джерелаChapter 1. The development of chiral monodentate N-heterocyclic carbenes (NHCs) is presented. Structurally varied twenty-eight new chiral imidazolinim salts, NHC precursors, were synthesized and characterized. Chapter 2. The first example of Cu-catalyzed enantioselective conjugate additions of alkyl- and arylzinc reagents to unactivated cyclic enones is presented. Transformations are promoted in the presence of 2.5-15 mol % of a readily available chiral NHC-based Cu complex, affording the desired products bearing all-carbon quaternary stereogenic centers in 67-98% yield and in up to 97% ee. Catalytic enantioselective reactions can be carried out on a benchtop, with undistilled solvent and commercially available (not further purified) Cu salts. Chapter 3. A new class of enantioselective conjugate addition (ECA) reactions that involve aryl- or alkenylsilylfluoride reagents and are catalyzed by chiral non-C2-symmetric Cu-based NHC complexes are presented. Transformations have been designed based on the principle that a catalytically active chiral NHC-Cu-aryl or NHC-Cu-alkenyl complex can be accessed from reaction of a Cu-halide precursor with in situ-generated aryl- or alkenyl-tetrafluorosilicate. Reactions proceed in the presence of 1.5 equivalents of the aryl- or alkenylsilane reagents and 1.5 equivalents of tris(dimethylamino)sulfonium difluorotrimethylsilicate. Desired products are isolated in 63-97% yield and 73.5:26.5-98.5:1.5 enantiomeric ratio (47%-97% ee). Chapter 4. An efficient Cu-catalyzed protocol for enantioselective addition of a dimethylphenylsilanyl group to a wide range of cyclic and acyclic unsaturated ketones, esters, acrylonitriles and dienones is presented. Reactions are performed in the presence of 1-5 mol % of commercially available and inexpensive CuCl, a readily accessible monodentate imidazolinium salt as well as commercially available (dimethylphenylsilyl)pinacolatoboron. Cu-catalyzed 1,4- and 1,6-conjugate additions afford the enantiomerically enriched silanes in 72%-98% yield and 90:10->99:1 enantiomeric ratio (er) with up to >25:1 of Z:E selectivity. Chapter 5. A Cu-catalyzed method for enantioselective boronate conjugate additions to trisubstituted alkenes of acyclic a,b-unsaturated carboxylic esters, ketones, and thioesters is presented. All transformations are promoted by 5 mol % of a chiral monodentate NHC-Cu complex, derived from a readily available C1-symmetric imidazolinium salt, and in the presence of commercially available bis(pinacolato)diboron. Reactions are efficient (typically, 60% to >98% yield after purification) and deliver the desired boryl carbonyls in up to >98:2 enantiomer ratio (er). In addition, metal-free, nucleophilic activation of a B-B bond has been exploited in the development of a highly efficient method for conjugate additions of commercially available bis(pinacolato)diboron to cyclic or acyclic a,b-unsaturated carbonyls. Reactions are readily catalyzed by 2.5-10 mol % of a simple NHC. A variety of cyclic and acyclic unsaturated ketones and esters can serve as substrates. Transformations deliver boryl carbonyls bearing tertiary as well as quaternary B-substituted carbons in up to >98% yield
Thesis (PhD) — Boston College, 2010
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Owen, Gareth Richard. "Palladium-mediated transformationand activation of unsaturated C-N, C-S and C-O bonds." Thesis, Imperial College London, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.408281.
Повний текст джерелаJiang, Tuo. "Palladium(II)-Catalyzed Oxidative Carbocyclization : Stereoselective Formation of C–C and C–B Bonds." Doctoral thesis, Stockholms universitet, Institutionen för organisk kemi, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-108669.
Повний текст джерелаAt the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 4: Manuscript.
Ziadi, Asraa. "Metal-catalyzed functionalization of c-c bonds in four-membered rings." Doctoral thesis, Universitat Rovira i Virgili, 2014. http://hdl.handle.net/10803/320185.
Повний текст джерелаRecientemente la funcionalización catalítica de enlaces C-C ha suscitado un gran interés en la comunidad científica a pesar de los retos que conlleva. Esta tesis doctoral se ha basado en diseñar nuevos procesos catalíticos para la funcionalización de enlaces C-C en anillos de cuatro miembros. Específicamente, se ha demostrado la viabilidad de preparar cetonas con grupos arilo en posición γ usando precatalizadores de Pd para promover la rotura de enlaces C-C en anillos de tert-ciclobutanol utilizando cloruros de arilo y tosilatos como agentes arilantes (Capítulo 2). La transformación se caracteriza por su amplia generalidad y baja carga de catalizador. La selectividad de la reacción puede ser fácilmente controlada por la naturaleza del ligando, en la que fosfinas con grupos ricos en electrones y voluminosos dan los mejores resultados, evitando la β-eliminación de hidrógeno de las especies organometálicas intermedias. Considerando los precedentes del Capítulo 2, se ha extendido esta metodología al acoplamiento con haloacetilenos para preparar cetonas con grupos alquino en posición γ (Capítulo 3). Curiosamente, los substituyentes del grupo alquino juegan un papel fundamental en la reactividad, pudiéndose controlar mediante la utilización de un cierto ligando. En el Capítulo 4, se ha desarrollado una nueva transformación basada en una reacción catalizada por compuestos de Ni para efectuar la síntesis de anillos de ocho eslabones mediante una reacción formal de cicloadición [4+4] de benzociclobutanonas y dienos simples. Curiosamente, dicho método muestra una especial preferencia para formar anillos de ocho eslabones sobre los, a priori, anillos de 6 eslabones que son más estables termodinámicamente. En la presente tesis doctoral se ha estudiado también la viabilidad de llevar a cabo una fijación catalítica de CO2 y la formación de enlaces C-F mediante una rotura de enlaces C-C (Capítulo 5) aunque no se han encontrado las condiciones óptimas para llevar a cabo tales transformaciones.
The means to promote catalytic C-C bond-functionalization has gained a considerable attention in recent years and probably can be considered one of the most challenging and vibrant subjects in organometallic chemistry. This PhD thesis deals with the design of new metal-catalyzed functionalization of C-C bonds in four-membered ring frameworks. Specifically, we have demonstrated the viability of preparing γ-arylated ketones via Pd-catalyzed cleavage of C-C bonds in tert-cyclobutanol using aryl chloride or tosylate counterparts (Chapter 2). The transformation possesses a wide substrate scope and remarkable low catalyst loadings. Selectivity was controlled by the ligand in which electron-rich and sterically-hindered phosphine ligands provided a unique reaction outcome that avoided the proclivity of alkyl metal species towards destructive β−hydride elimination. Prompted by the precedents in Chapter 2, we successfully extended the scope of the metal-catalyzed C-C bond-cleavage of tert-cyclobutanols by using halo acetylene counterparts giving γ-alkynylated ketones (Chapter 3). Interestingly, substituents on the alkyne motif showed a remarkable influence on reactivity. Of particular interest is the application profile of such methodology since γ-alkynylated ketones could promote consecutive metal-catalyzed transformations into valuable synthetic intermediates. In Chapter 4, we extended the interest for C-C bond-cleavage beyond the use of tert-cycñobutanols. Specifically, we developed a Ni-catalyzed C-C bond-cleavage event in benzocyclobutenones for preparing eight-membered rings via formal [4+4]-cycloaddition with dienes (Chapter 4). The method shows a specific preference for eight-membered rings over thermodynamically more stable six-membered rings. This PhD thesis has also studied the development of catalytic CO2 fixation and C-F bond-formation via C-C bond-cleavage (Chapter 5). While we have not found reaction conditions to effect the desired transformations, our research group is actively involved in related catalytic endeavors and it is expected that such research will shed light into the targeted CO2 fixation or C-F bond-forming reactions via C-C bond-cleavage.
Sau, Roca Míriam. "From Click Chemistry to catalytic cleavage of unstrained C-C bonds." Doctoral thesis, Universitat Rovira i Virgili, 2016. http://hdl.handle.net/10803/396080.
Повний текст джерелаÉsta tesis doctoral está basada principalmente en la síntesis de moléculas pequeñas potencialmente útiles para investigaciones avanzadas. Se han empleado diferentes metodologías para obtenerlas: 1) Cicloadiciones intramoleculares entre un alkino y una azida libres de cobre para la obtención de derivados de benzodiazepinas. Se han obtenido una gran variedad de triazoles fusionados a heterociclos de siete miembros. Posteriormente se han realizado pruebas de actividad biológica de las moléculas resultantes. 2) a) Escisión de enlaces carbono-carbono no activados de amino alcoholes y utilitzación de éstos como nucleófilos conjuntamente con bromuros de arilo para una reacción de acoplamiento catalizada por paladio para la obtención de derivados de dibenzil aminas. Se ha realizado una gran optimización de las condiciones de reacción; base, disolvente, electrófilo, temperatura, catalizador y ligando. b) Escisión de enlaces carbono-carbono no activados de N-alilo amino alcoholes y la utilización de éste como nucleófilo conjuntamente con bromuros de arilo en una reacción de acoplamiento catalizada por paladio para la obtención de aldehídos arilados en posición beta. Se ha realizado la síntesis de un gran numero de amino alcoholes nuevos y éstos se han sometido a las condiciones optimizadas de reacción. Demostrando que ésta transformación es útil para una gran variedad de sustratos (bromuros de arilo y amino alcoholes). La enamina resultante de la reacción de acoplamiento se ha alquilado con vinil metil cetona con buenos rendimientos pero pobres diastereoselectividades aunque se ha demostrado que la reacción es factible. Para finalizar, se ha desarrollado la versión enantioselectiva de la anterior transformación obteniendo buenos excesos enantioméricos aunque con bajos rendimientos.
This PhD thesis is based basically on synthesis of small molecules potentially useful for further investigations. Different strategies have been used to obtain them; 1) Copper free intramolecular cycloadditions between an azide and an akyne for the obtention of benzodiazepine derivatives. A wide range of triazoles fused to seven membered heterocycles rings have been obtained. Later, biological studies have been carried out. 2)a) Carbon-carbon bond cleavage of amino alcohols has been carried out with the subsequent use of them as a nucleophile together with aryl bromides to develop a cross-coupling reaction for the obtention of dibenzyl amines. A wide optimization of the reaction parameters was carried out; base, ligand, catalyst, electrophile, temperatura, and solent. b) Carbon-carbon bond cleavage of N- allyl amino alcohols has been carried out with the subsequent use of them as a nucleophile together with aryl bromides to develop a cross-coupling reaction for the obtention of beta arylated aldehydes. An important number of new amino alcohols have been synthesized and these have been subjected to the optimized reaction conditions. It has been demonstrated that this transformation is useful for a wide range of substrates (amino alcohols and aryl bromides). The resultant enamine has been alkylated with methyl vinyl ketone with good yields but poor diastereoselectivity. To finish the enantioselective version of beta functionalization of aldehydes has been developed obtaining good enantioselectivity but poor yields
Chudasama, V. "The use of aerobic aldehyde C-H activation for the construction of C-C and C-N bonds." Thesis, University College London (University of London), 2011. http://discovery.ucl.ac.uk/1324525/.
Повний текст джерелаКниги з теми "C-C bonds"
Li, Chao-Jun, ed. From C-H to C-C Bonds. Cambridge: Royal Society of Chemistry, 2014. http://dx.doi.org/10.1039/9781782620082.
Повний текст джерелаShimajiri, Takuya. The Nature of Ultralong C–C Bonds. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-0670-3.
Повний текст джерелаLu, Wenjun, and Lihong Zhou. Oxidation of C─H Bonds. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2017. http://dx.doi.org/10.1002/9781119092490.
Повний текст джерелаYou, Shu-Li, ed. Asymmetric Functionalization of C-H Bonds. Cambridge: Royal Society of Chemistry, 2015. http://dx.doi.org/10.1039/9781782621966.
Повний текст джерелаGoldberg, Karen I., and Alan S. Goldman, eds. Activation and Functionalization of C—H Bonds. Washington, DC: American Chemical Society, 2004. http://dx.doi.org/10.1021/bk-2004-0885.
Повний текст джерелаC-X bond formation. Heidelberg: Springer, 2010.
Знайти повний текст джерелаTaillefer, Marc, and Dawei Ma, eds. Amination and Formation of sp2 C-N Bonds. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-40546-4.
Повний текст джерела1945-, Fuchs Philip L., ed. Reagents for direct functionalization of C-H bonds. Chichester, England: John Wiley, 2007.
Знайти повний текст джерелаZucherman, Jerry J. The Formation of bonds to C, Si, Ge, Sn, Pb (part 2). New York, N.Y: VCH Publishers, 1989.
Знайти повний текст джерелаCatalyst Design for the Ionic Hydrogenation of C=N Bonds. [New York, N.Y.?]: [publisher not identified], 2015.
Знайти повний текст джерелаЧастини книг з теми "C-C bonds"
Kakiuchi, Fumitoshi. "Catalytic Addition of C – H Bonds to C – C Multiple Bonds." In Topics in Organometallic Chemistry, 1–33. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/3418_2007_064.
Повний текст джерелаTreichel, P. M. "Reactions Involving C-H and C-C Bonds." In Inorganic Reactions and Methods, 230–32. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145296.ch199.
Повний текст джерелаBougioukou, Despina J., and Jon D. Stewart. "Reduction of CC Double Bonds." In Enzyme Catalysis in Organic Synthesis, 1111–63. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527639861.ch27.
Повний текст джерелаBühler, Bruno, Katja Bühler, and Frank Hollmann. "Oxyfunctionalization of CC Multiple Bonds." In Enzyme Catalysis in Organic Synthesis, 1269–324. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527639861.ch31.
Повний текст джерелаRios, Ramon, Jorge Esteban, and Xavier Companyó. "Cascade Reactions Forming C-C Bonds." In Stereoselective Organocatalysis, 351–80. Hoboken, New Jersey: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118604755.ch10.
Повний текст джерелаShimajiri, Takuya. "Discovery of Flexible Bonds Based on an Extremely Elongated C–C Single Bond." In The Nature of Ultralong C–C Bonds, 41–78. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-0670-3_3.
Повний текст джерелаGhosh, Pradip, Marc-Etienne Moret, and Robertus J. M. Klein Gebbink. "Catalytic Oxygenation of CC and CH Bonds." In Non-Noble Metal Catalysis, 355–89. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527699087.ch14.
Повний текст джерела"4. C–C bonds." In High Pressure Organic Synthesis, 93–128. Berlin, Boston: De Gruyter, 2019. http://dx.doi.org/10.1515/9783110556841-004.
Повний текст джерела"C–C Bond Formation." In Biocatalysis in Organic Synthesis: The Retrosynthesis Approach, 217–53. The Royal Society of Chemistry, 2018. http://dx.doi.org/10.1039/bk9781782625308-00217.
Повний текст джерела"C." In Encyclopedia of Municipal Bonds, 28–42. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118531624.ch3.
Повний текст джерелаТези доповідей конференцій з теми "C-C bonds"
Mbomson, Ifeoma G., Scott McMeekin, Richard De La Rue, and Nigel P. Johnson. "Matching plasmon resonances to the C=C and C-H bonds in estradiol." In SPIE BiOS, edited by Tuan Vo-Dinh and Joseph R. Lakowicz. SPIE, 2015. http://dx.doi.org/10.1117/12.2081409.
Повний текст джерелаParsch, Jörg, and Joachim W. Engels. "C–F···H–C hydrogen bonds in crystals of fluorobenzene ribonucleosides." In XIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 1999. http://dx.doi.org/10.1135/css199902011.
Повний текст джерелаTHORPE, M. F., BRANDON M. HESPENHEIDE, YI YANG, and LESLIE A. KUHN. "FLEXIBILITY AND CRITICAL HYDROGEN BONDS IN CYTOCHROME C." In Proceedings of the Pacific Symposium. WORLD SCIENTIFIC, 1999. http://dx.doi.org/10.1142/9789814447331_0018.
Повний текст джерелаSiewert, Inke. "Electroreduction of C=O Bonds in CO2, Ketones, and Aldehydes." In MATSUS23 & Sustainable Technology Forum València (STECH23). València: FUNDACIO DE LA COMUNITAT VALENCIANA SCITO, 2022. http://dx.doi.org/10.29363/nanoge.matsus.2023.032.
Повний текст джерелаŽENÍŠEK, Jaroslav, Pavel SOUČEK, Pavel ONDRAČKA, and Petr VAŠINA. "STUDY OF W-X BONDS IN AMORPHOUS W-B-C." In NANOCON 2021. TANGER Ltd., 2021. http://dx.doi.org/10.37904/nanocon.2021.4380.
Повний текст джерелаsaki, zeinab, Nahla Talebi, Abedin Zabardasti, and Ali Kakanejadifard. "The B–C and C–C bonds as preferred electron source for H-bondand Li-bond interactions in complex pairing of C4B2H6 with HFand LiH molecules." In The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-e018.
Повний текст джерелаRollier, Floriane, Marta Costa Figueiredo, and Emiel Hensen. "The influence of copper particle size on the electrochemical reduction of CO to products with C-C bonds." In Materials for Sustainable Development Conference (MAT-SUS). València: FUNDACIO DE LA COMUNITAT VALENCIANA SCITO, 2022. http://dx.doi.org/10.29363/nanoge.nfm.2022.074.
Повний текст джерелаZárate, Cayetana, and Rubén Martin. "Ni-Catalyzed Silylation of Inert C-O Bonds under Mild Conditions." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013101312526.
Повний текст джерелаMarco de Lucas, M. C., J. M. Chappé, L. Cunha, C. Moura, J. F. Pierson, L. Imhoff, V. Potin, et al. "Structure and Chemical Bonds in Black Ti(C, N, O) Thin Films." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482693.
Повний текст джерелаCosta, Roberta L. da, and Simon J. Garden. "Phenanthridine derivatives via palladium catalyzed intramolecular functionalization of C(sp2)-H bonds." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013819134214.
Повний текст джерелаЗвіти організацій з теми "C-C bonds"
Novoa, J. J., Myung-Hwan Whangbo, and J. M. Williams. Intermolecular interactions involving C-H bonds, 3, Structure and energetics of the interaction between CH{sub 4} and CN{sup {minus}}. Office of Scientific and Technical Information (OSTI), December 1991. http://dx.doi.org/10.2172/10187953.
Повний текст джерелаGland, J. L. Hydrogen induced C-C, C-N, and C-S bond activation on Pt and Ni surfaces. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/10102894.
Повний текст джерелаGland, J. L. Hydrogen induced C-C, C-N, and C-S bond activation on Pt and Ni surfaces. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/6915688.
Повний текст джерелаGland, J. L. Hydrogen Induced C-C, C-N, & C-S Bond Activation on Pt & Ni Surfaces. Office of Scientific and Technical Information (OSTI), July 2004. http://dx.doi.org/10.2172/830711.
Повний текст джерелаGland, J. L. [Hydrogen induced C-C, C-N, and C-S bond activities on Pi and Ni surfaces]: Summary. Office of Scientific and Technical Information (OSTI), December 1994. http://dx.doi.org/10.2172/10110807.
Повний текст джерелаBiermann, Ursula, and Jürgen O. Metzger. Functionalization of Unsaturated Fatty Compounds Across the C,C Double Bond. AOCS, May 2011. http://dx.doi.org/10.21748/lipidlibrary.39193.
Повний текст джерелаLees, Alistair J. Photochemistry of Intermolecular C-H Bond Activation Reactions. Office of Scientific and Technical Information (OSTI), June 2000. http://dx.doi.org/10.2172/761218.
Повний текст джерелаMcFarland, Eric, Horia Metiu, and Michael Gordon. Fundamental Mechanisms of C-X bond Transformations on Complex Molten Surfaces. Office of Scientific and Technical Information (OSTI), July 2019. http://dx.doi.org/10.2172/1580080.
Повний текст джерелаAsplund, M. C. Time resolved infrared studies of C-H bond activation by organometallics. Office of Scientific and Technical Information (OSTI), June 1998. http://dx.doi.org/10.2172/290889.
Повний текст джерелаKimura, Mineo. Correlation between shape resonance energies and C-C bond length in carbon-containing molecules: Elastic electron scattering and carbon K-shell excitation by photons. Office of Scientific and Technical Information (OSTI), June 1994. http://dx.doi.org/10.2172/10159440.
Повний текст джерела