Статті в журналах з теми "C–X bond"
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Xu, Da-Zhen, Ren-Ming Hu, and Yi-Huan Lai. "Iron-Catalyzed Aerobic Oxidative Cross-Dehydrogenative C(sp3)–H/X–H (X = C, N, S) Coupling Reactions." Synlett 31, no. 18 (July 21, 2020): 1753–59. http://dx.doi.org/10.1055/s-0040-1707195.
Повний текст джерелаRobertson, Katherine N., Osvald Knop, and T. Stanley Cameron. "C-H···H-C interactions in organoammonium tetraphenylborates: another look at dihydrogen bonds." Canadian Journal of Chemistry 81, no. 6 (June 1, 2003): 727–43. http://dx.doi.org/10.1139/v03-080.
Повний текст джерелаLiu, Dong, Chao Liu, and Aiwen Lei. "Carbon-Centered Radical Addition to C=X Bonds for C−X Bond Formation." Chemistry - An Asian Journal 10, no. 10 (June 23, 2015): 2040–54. http://dx.doi.org/10.1002/asia.201500326.
Повний текст джерелаValentini, Federica, Oriana Piermatti, and Luigi Vaccaro. "Metal and Metal Oxide Nanoparticles Catalyzed C–H Activation for C–O and C–X (X = Halogen, B, P, S, Se) Bond Formation." Catalysts 13, no. 1 (December 22, 2022): 16. http://dx.doi.org/10.3390/catal13010016.
Повний текст джерелаAllwohn, Jürgen, Ralf Hunold, Monika Pilz, Rolf-Günter Müller, Werner Massa, and Armin Berndt. "Nachweis starker C – Sn-Hyperkonjugation über Kristallstruktur und NMR-Daten eines C-Stannylmethylenborans / Evidence for Strong C–Sn-Hyperconjugation by Crystal Structure and NMR Data of a C-Stannylmethyleneborane." Zeitschrift für Naturforschung B 45, no. 3 (March 1, 1990): 290–98. http://dx.doi.org/10.1515/znb-1990-0304.
Повний текст джерелаNagorny, Pavel, and Zhankui Sun. "New approaches to organocatalysis based on C–H and C–X bonding for electrophilic substrate activation." Beilstein Journal of Organic Chemistry 12 (December 23, 2016): 2834–48. http://dx.doi.org/10.3762/bjoc.12.283.
Повний текст джерелаLiu, Dong, Chao Liu, and Aiwen Lei. "ChemInform Abstract: Carbon-Centered Radical Addition to C=X Bonds for C-X Bond Formation." ChemInform 46, no. 46 (October 27, 2015): no. http://dx.doi.org/10.1002/chin.201546253.
Повний текст джерелаLuo, Tian, Shanghui Tian, Jie-Ping Wan, and Yunyun Liu. "Recent Advances in Transition Metal-Free Halogenation of C(sp2)-H Bonds." Current Organic Chemistry 25, no. 10 (June 1, 2021): 1180–93. http://dx.doi.org/10.2174/1385272825666210122094423.
Повний текст джерелаHao, Wenyan, and Yunyun Liu. "C–H bond halogenation catalyzed or mediated by copper: an overview." Beilstein Journal of Organic Chemistry 11 (November 9, 2015): 2132–44. http://dx.doi.org/10.3762/bjoc.11.230.
Повний текст джерелаLiu, Nan-nan, and Yi-hong Ding. "A metal–metal bond passing through the arene ligand: a theoretical study on inverse sandwiches X[Sc–C8H8–Sc]nX (X = F, Cl, Br; n = 1, 2)." New Journal of Chemistry 39, no. 3 (2015): 1558–62. http://dx.doi.org/10.1039/c4nj01832j.
Повний текст джерелаLykhach, Yaroslava, Viktor Johánek, Armin Neitzel, Tomáš Skála, Nataliya Tsud, Klára Beranová, Josef Mysliveček, Olaf Brummel, and Jörg Libuda. "Redox-mediated C–C bond scission in alcohols adsorbed on CeO2− x thin films." Journal of Physics: Condensed Matter 34, no. 19 (March 3, 2022): 194002. http://dx.doi.org/10.1088/1361-648x/ac5138.
Повний текст джерелаAguilar, David, Rafael Navarro, Tatiana Soler, and Esteban P. Urriolabeitia. "Regioselective functionalization of iminophosphoranes through Pd-mediated C–H bond activation: C–C and C–X bond formation." Dalton Transactions 39, no. 43 (2010): 10422. http://dx.doi.org/10.1039/c003241g.
Повний текст джерелаMarcos-Ayuso, Guillermo, Agustí Lledós, and Juan A. Casares. "Copper(i) activation of C–X bonds: bimolecular vs. unimolecular reaction mechanism." Chemical Communications 58, no. 16 (2022): 2718–21. http://dx.doi.org/10.1039/d1cc07027d.
Повний текст джерелаWang, Youliang, and Raymond A. Poirier. "Generalized valence bond study of rotational singlet structures and pi bond energies for systems containing C==C, Si==Si, and C==Si double bonds." Canadian Journal of Chemistry 76, no. 4 (April 1, 1998): 477–82. http://dx.doi.org/10.1139/v98-041.
Повний текст джерелаYan, Guobing, Xiangmei Wu, and Minghua Yang. "Transition-metal-catalyzed additions of C–H bonds to C–X (X = N, O) multiple bonds via C–H bond activation." Organic & Biomolecular Chemistry 11, no. 34 (2013): 5558. http://dx.doi.org/10.1039/c3ob40652k.
Повний текст джерелаBanerjee, 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 джерелаHan, Ying-Feng, and Guo-Xin Jin. "Cyclometalated [Cp*M(C^X)] (M = Ir, Rh; X = N, C, O, P) complexes." Chem. Soc. Rev. 43, no. 8 (2014): 2799–823. http://dx.doi.org/10.1039/c3cs60343a.
Повний текст джерелаGao, Han, Lingfei Hu, Yanlei Hu, Xiangying Lv, Yan-Bo Wu, and Gang Lu. "Origins of Lewis acid acceleration in nickel-catalysed C–H, C–C and C–O bond cleavage." Catalysis Science & Technology 11, no. 13 (2021): 4417–28. http://dx.doi.org/10.1039/d1cy00660f.
Повний текст джерелаParra, Rubén D., and Sławomir J. Grabowski. "Enhancing Effects of the Cyano Group on the C-X∙∙∙N Hydrogen or Halogen Bond in Complexes of X-Cyanomethanes with Trimethyl Amine: CH3−n(CN)nX∙∙∙NMe3, (n = 0–3; X = H, Cl, Br, I)." International Journal of Molecular Sciences 23, no. 19 (September 25, 2022): 11289. http://dx.doi.org/10.3390/ijms231911289.
Повний текст джерелаLinden, Anthony, Yuehui Zhou, and Heinz Heimgartner. "Intra- and intermolecular Se...X (X = Se, O) interactions in selenium-containing heterocycles: 3-benzoylimino-5-(morpholin-4-yl)-1,2,4-diselenazole." Acta Crystallographica Section C Structural Chemistry 70, no. 5 (April 18, 2014): 482–87. http://dx.doi.org/10.1107/s2053229614008237.
Повний текст джерелаOdoko, Mamiko, Min Yao, Eiki Yamashita, Ryosuke Nakashima, Kunio Hirata, Hiroshi Aoyama, Kazumasa Muramoto, Kyoko Shinzawa-Itoh, Shinya Yoshikawa та Tomitake Tsukihara. "Optimization of the energy constant of the methionine Sδ—C∊bond forX-PLORrefinement of protein structure". Journal of Applied Crystallography 34, № 1 (1 лютого 2001): 80–81. http://dx.doi.org/10.1107/s0021889800019944.
Повний текст джерелаLiu, Wen-Bo, Muhammad Usman, and Xiao-Wen Zhang. "Silicon-Tethered Frameworks as Directing Groups for Carbon–Carbon and Carbon–Heteroatom Bond Formation." Synthesis 51, no. 07 (March 5, 2019): 1529–44. http://dx.doi.org/10.1055/s-0037-1612123.
Повний текст джерелаLi, Chong, Juan Wang, and Shang-Dong Yang. "Visible-light-facilitated P-center radical addition to CX (X = C, N) bonds results in cyclizations." Chemical Communications 57, no. 65 (2021): 7997–8002. http://dx.doi.org/10.1039/d1cc02604f.
Повний текст джерелаWang, Yi, Anan Liu, Dongge Ma, Shuhong Li, Chichong Lu, Tao Li, and Chuncheng Chen. "TiO2 Photocatalyzed C–H Bond Transformation for C–C Coupling Reactions." Catalysts 8, no. 9 (August 27, 2018): 355. http://dx.doi.org/10.3390/catal8090355.
Повний текст джерелаYan, Guobing, Xiangmei Wu, and Minghua Yang. "ChemInform Abstract: Transition-Metal-Catalyzed Additions of C-H Bonds to C-X (X = N, O) Multiple Bonds via C-H Bond Activation." ChemInform 44, no. 44 (October 14, 2013): no. http://dx.doi.org/10.1002/chin.201344232.
Повний текст джерелаZeng, Qingle, Fuhai Li, and Xianjie Yin. "Transition metal-catalyzed construction of C-X bonds via cleavage of C-N bond of quaternary ammonium salts." AIMS Molecular Science 10, no. 3 (2023): 153–70. http://dx.doi.org/10.3934/molsci.2023011.
Повний текст джерелаYu, Bangkui, and Hanmin Huang. "Recent Advances in C—X Bond Metathesis Reactions." Chinese Journal of Organic Chemistry 42, no. 8 (2022): 2376. http://dx.doi.org/10.6023/cjoc202202003.
Повний текст джерелаAhmad, Muhammad Siddique, Po-Han Lin, Qing Zhang, Bing Zeng, Qifeng Wang, and Kamel Meguellati. "Visible Light Induced C-H/N-H and C-X Bonds Reactions." Reactions 4, no. 1 (March 2, 2023): 189–230. http://dx.doi.org/10.3390/reactions4010012.
Повний текст джерелаOrellana, Arturo, and Andrei Nikolaev. "Transition-Metal-Catalyzed C–C and C–X Bond-Forming Reactions Using Cyclopropanols." Synthesis 48, no. 12 (May 18, 2016): 1741–68. http://dx.doi.org/10.1055/s-0035-1560442.
Повний текст джерелаYuan, Kun, Hui Xue Li, Huian Tang, and Yuan Cheng Zhu. "Density Function Theory Study on the Recognition of the Urea-Based Involving Bromine Derivation Receptor for the Halogen Anions." Applied Mechanics and Materials 328 (June 2013): 850–54. http://dx.doi.org/10.4028/www.scientific.net/amm.328.850.
Повний текст джерелаQuentin, Jay, Eric W. Reinheimer, and Leonard R. MacGillivray. "Halogen-Bond Mediated [2+2] Photodimerizations: À la Carte Access to Unsymmetrical Cyclobutanes in the Solid State." Molecules 27, no. 3 (February 3, 2022): 1048. http://dx.doi.org/10.3390/molecules27031048.
Повний текст джерелаBaillargeon, Pierre, Tarik Rahem, Édouard Caron-Duval, Jacob Tremblay, Cloé Fortin, Étienne Blais, Victor Fan, Daniel Fortin, and Yves L. Dory. "Isomorphous crystal structures of chlorodiacetylene and iododiacetylene derivatives: simultaneous hydrogen and halogen bonds on carbonyl." Acta Crystallographica Section E Crystallographic Communications 73, no. 8 (July 17, 2017): 1175–79. http://dx.doi.org/10.1107/s2056989017010155.
Повний текст джерелаYang, Qi, Zongbin Jia, Longji Li, Long Zhang, and Sanzhong Luo. "Visible-light promoted arene C–H/C–X lactonizationviacarboxylic radical aromatic substitution." Organic Chemistry Frontiers 5, no. 2 (2018): 237–41. http://dx.doi.org/10.1039/c7qo00826k.
Повний текст джерелаGirgis, Adel S., Marian N. Aziz, ElSayed M. Shalaby, Fahmy M. Asaad, and I. S. Ahmed Farag. "Synthesis and X-ray Studies of Novel Azaphenanthrenes." Journal of Chemical Research 42, no. 2 (February 2018): 90–95. http://dx.doi.org/10.3184/174751918x15183538282993.
Повний текст джерелаLiu, Tao, Guo-Dong Liu, and Zhang-Yu Yu. "Ab initio study of hydrogen bond complexes of ring compounds containing the H2N-C=Y moiety with water." Open Chemistry 8, no. 5 (October 1, 2010): 1117–26. http://dx.doi.org/10.2478/s11532-010-0088-x.
Повний текст джерелаMani, Devendra, та Elangannan Arunan. "The X–C···π (X = F, Cl, Br, CN) Carbon Bond". Journal of Physical Chemistry A 118, № 43 (20 жовтня 2014): 10081–89. http://dx.doi.org/10.1021/jp507849g.
Повний текст джерелаLi, Wan-Di, Jia-Shuo Zhang, Lin-Yan Zhang, Zhong-Wen Liu, Juan Fan та Xian-Ying Shi. "Rhodium-Catalyzed Alkylation of Aromatic Ketones with Allylic Alcohols and α,β-Unsaturated Ketones". Catalysts 13, № 8 (26 липня 2023): 1157. http://dx.doi.org/10.3390/catal13081157.
Повний текст джерелаThimme Gowda, B., K. Jyothi, Jozef Kožíšek, and Hartmut Fuess. "Crystal Structure Studies on p-Substitutedbenzenesulphonamides 4-X-C6H4SO2NH2 (X = CH3, NH2 F, Cl or Br)." Zeitschrift für Naturforschung A 58, no. 11 (November 1, 2003): 656–60. http://dx.doi.org/10.1515/zna-2003-1110.
Повний текст джерелаFiore, Vito A., and Gerhard Maas. "Phospha-Michael reaction of tertiary phosphanes Ph2P–X (X=SiMe3, Cl) and N-triflyl-propiolamides." Zeitschrift für Naturforschung B 74, no. 9 (September 25, 2019): 671–76. http://dx.doi.org/10.1515/znb-2019-0100.
Повний текст джерелаTang, Ting-Hua, and Yun-Ping Cui. "A theoretical study of some hydrogen-bonded complexes using the theory of atoms in molecules." Canadian Journal of Chemistry 74, no. 6 (June 1, 1996): 1162–70. http://dx.doi.org/10.1139/v96-130.
Повний текст джерелаPurnachandar, Dalovai, Kanaparthy Suneel, Sridhar Balasubramanian, and Galla V. Karunakar. "Gold–carbene assisted formation of tetraarylmethane derivatives: double X–H activation by gold." Organic & Biomolecular Chemistry 17, no. 19 (2019): 4856–64. http://dx.doi.org/10.1039/c9ob00470j.
Повний текст джерелаBorpatra, Paran J., Bhaskar Deka, Mohit L. Deb, and Pranjal K. Baruah. "Recent advances in intramolecular C–O/C–N/C–S bond formation via C–H functionalization." Organic Chemistry Frontiers 6, no. 20 (2019): 3445–89. http://dx.doi.org/10.1039/c9qo00863b.
Повний текст джерелаQuentin, Jay, Dale C. Swenson, and Leonard R. MacGillivray. "Supramolecular Sandwiches: Halogen-Bonded Coformers Direct [2+2] Photoreactivity in Two-Component Cocrystals." Molecules 25, no. 4 (February 18, 2020): 907. http://dx.doi.org/10.3390/molecules25040907.
Повний текст джерелаGrabowsky, Simon, Manuela Weber, Jürgen Buschmann, and Peter Luger. "Experimental electron density study of ethylene oxide at 100 K." Acta Crystallographica Section B Structural Science 64, no. 3 (May 15, 2008): 397–400. http://dx.doi.org/10.1107/s0108768108010197.
Повний текст джерелаStarynowicz, Przemysław, Sławomir Berski, Nurbey Gulia, Karolina Osowska, Tadeusz Lis, and Sławomir Szafert. "Is It Conjugated or Not? The Theoretical and Experimental Electron Density Map of Bonding in p-CH3CH2COC6H4-C≡C-C≡C-p-C6H4COCH3CH2." Molecules 25, no. 19 (September 24, 2020): 4388. http://dx.doi.org/10.3390/molecules25194388.
Повний текст джерелаLu, Norman, Rong-Jyun Wei, Hsing-Fang Chiang, Joseph S. Thrasher, Yuh-Sheng Wen, and Ling-Kang Liu. "Weak hydrogen and halogen bonding in 4-[(2,2-difluoroethoxy)methyl]pyridinium iodide and 4-[(3-chloro-2,2,3,3-tetrafluoropropoxy)methyl]pyridinium iodide." Acta Crystallographica Section C Structural Chemistry 73, no. 9 (August 7, 2017): 682–87. http://dx.doi.org/10.1107/s2053229617011172.
Повний текст джерелаMurata, M. "ChemInform Abstract: C-B and C-Si Bond-Forming Reactions of C-X Electrophiles." ChemInform 44, no. 35 (August 8, 2013): no. http://dx.doi.org/10.1002/chin.201335228.
Повний текст джерелаSingh, Pallavi, Kishor Kumar Chouhan, and Arup Mukherjee. "Ruthenium Catalyzed Intramolecular C−X (X=C, N, O, S) Bond Formation via C−H Functionalization: An Overview." Chemistry – An Asian Journal 16, no. 17 (August 4, 2021): 2392–412. http://dx.doi.org/10.1002/asia.202100513.
Повний текст джерелаEngberts, J. B. F. N., Th A. J. W. Wajer, C. Kruk, and Th J. de Boer. "C-nitroso compounds. Part X: C-nitroso compounds as hydrogen bond acceptors." Recueil des Travaux Chimiques des Pays-Bas 88, no. 7 (September 2, 2010): 795–800. http://dx.doi.org/10.1002/recl.19690880704.
Повний текст джерелаMarkó, István E., and M. Lakshmi Kantam. "Catalytic CC bond formation using triorganothallium reagents." Tetrahedron Letters 32, no. 20 (May 1991): 2255–58. http://dx.doi.org/10.1016/s0040-4039(00)79695-x.
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