Статті в журналах з теми "C-P Bond Formation"
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Li, Lili, Wenbin Huang, Lijin Chen, Jiaxing Dong, Xuebing Ma, and Yungui Peng. "Silver-Catalyzed Oxidative C(sp3 )−P Bond Formation through C−C and P−H Bond Cleavage." Angewandte Chemie 129, no. 35 (July 21, 2017): 10675–80. http://dx.doi.org/10.1002/ange.201704910.
Повний текст джерелаLi, Lili, Wenbin Huang, Lijin Chen, Jiaxing Dong, Xuebing Ma, and Yungui Peng. "Silver-Catalyzed Oxidative C(sp3 )−P Bond Formation through C−C and P−H Bond Cleavage." Angewandte Chemie International Edition 56, no. 35 (July 21, 2017): 10539–44. http://dx.doi.org/10.1002/anie.201704910.
Повний текст джерелаZagidullin, Almaz A., Il’yas F. Sakhapov, Vasili A. Miluykov, and Dmitry G. Yakhvarov. "Nickel Complexes in C‒P Bond Formation." Molecules 26, no. 17 (August 31, 2021): 5283. http://dx.doi.org/10.3390/molecules26175283.
Повний текст джерелаBudnikova, Yulia H., Tatyana V. Gryaznova, Valeriya V. Grinenko, Yulia B. Dudkina, and Mikhail N. Khrizanforov. "Eco-efficient electrocatalytic C–P bond formation." Pure and Applied Chemistry 89, no. 3 (March 1, 2017): 311–30. http://dx.doi.org/10.1515/pac-2016-1001.
Повний текст джерелаWauters, Iris, Wouter Debrouwer, and Christian V. Stevens. "Preparation of phosphines through C–P bond formation." Beilstein Journal of Organic Chemistry 10 (May 9, 2014): 1064–96. http://dx.doi.org/10.3762/bjoc.10.106.
Повний текст джерелаHIDAKA, Tomomi, and Haruo SETO. "Studies on C-P Bond Forming Enzymes. Biochemical Mechanisms of C-P Bond Formation in Bialaphos." Journal of the agricultural chemical society of Japan 65, no. 10 (1991): 1497–500. http://dx.doi.org/10.1271/nogeikagaku1924.65.1497.
Повний текст джерелаCai, Bao-Gui, Jun Xuan, and Wen-Jing Xiao. "Visible light-mediated C P bond formation reactions." Science Bulletin 64, no. 5 (March 2019): 337–50. http://dx.doi.org/10.1016/j.scib.2019.02.002.
Повний текст джерелаKhrizanforov, M. N., S. O. Strekalova, V. V. Grinenko, A. I. Kononov, E. L. Dolengovski, and Y. H. Budnikova. "C-P bond formation via selective electrocatalytic C-H phosphorylation." Phosphorus, Sulfur, and Silicon and the Related Elements 194, no. 4-6 (January 9, 2019): 384–85. http://dx.doi.org/10.1080/10426507.2018.1555538.
Повний текст джерелаOnys'ko, Petro, Yuliya Rassukana, and Anatoly Sinitsa. "Phosphorylation of α-Haloimines: P-C vs. P-N Bond Formation." Current Organic Chemistry 12, no. 1 (January 1, 2008): 2–24. http://dx.doi.org/10.2174/138527208783330091.
Повний текст джерелаHidaka, Tomomi, Kazuma Kamigiri, Satoshi Imai, and Haruo Seto. "Biosynthetic Mechanisms of C-P Bond Formation of Bialaphos." Actinomycetologica 5, no. 2 (1991): 112–18. http://dx.doi.org/10.3209/saj.5_112.
Повний текст джерелаBorger, Jaap E., Andreas W. Ehlers, J. Chris Slootweg, and Koop Lammertsma. "Functionalization of P4 through Direct P−C Bond Formation." Chemistry - A European Journal 23, no. 49 (July 27, 2017): 11738–46. http://dx.doi.org/10.1002/chem.201702067.
Повний текст джерелаZhang, Ji-Shu, Tieqiao Chen, Jia Yang, and Li-Biao Han. "Nickel-catalysed P–C bond formation via P–H/C–CN cross coupling reactions." Chemical Communications 51, no. 35 (2015): 7540–42. http://dx.doi.org/10.1039/c5cc01182e.
Повний текст джерелаChen, Lijin, Zhenfei Zhou, Saifei Zhang, Xiaoqian Li, Xuebing Ma, and Jiaxing Dong. "Palladium(ii)-catalyzed oxidative C(sp3)–P bond formation via C(sp3)–H bond activation." Chemical Communications 55, no. 91 (2019): 13693–96. http://dx.doi.org/10.1039/c9cc07637a.
Повний текст джерелаHari, Durga Prasad, and Burkhard König. "Eosin Y Catalyzed Visible Light Oxidative C–C and C–P bond Formation." Organic Letters 13, no. 15 (August 5, 2011): 3852–55. http://dx.doi.org/10.1021/ol201376v.
Повний текст джерелаGeer, Ana M., Ángel L. Serrano, Bas de Bruin, Miguel A. Ciriano, and Cristina Tejel. "Terminal Phosphanido Rhodium Complexes Mediating Catalytic PP and PC Bond Formation." Angewandte Chemie 127, no. 2 (November 19, 2014): 482–85. http://dx.doi.org/10.1002/ange.201407707.
Повний текст джерелаBanerjee, Indrani, and Tarun K. Panda. "Recent advances in the carbon–phosphorus (C–P) bond formation from unsaturated compounds by s- and p-block metals." Organic & Biomolecular Chemistry 19, no. 30 (2021): 6571–87. http://dx.doi.org/10.1039/d1ob01019k.
Повний текст джерелаHIDAKA, Tomomi, Osamu KARA, Satoshi IMAI, Hiroyuki ANZAI, Takeshi MURAKAMI, Kozo NAGAOKA, and Haruo SETO. "Biochemical mechanism of C-P bond formation of bialaphos: Use of gene manipulation for the analysis of the C-P bond formation step." Agricultural and Biological Chemistry 54, no. 8 (1990): 2121–25. http://dx.doi.org/10.1271/bbb1961.54.2121.
Повний текст джерелаHidaka, Tomomi, Osamu Hara, Satoshi Imai, Hiroyuki Anzai, Takeshi Murakami, Kozo Nagaoka, and Haruo Seto. "Biochemical Mechanism of C–P Bond Formation of Bialaphos: Use of Gene Manipulation for the Analysis of the C–P Bond Formation Step." Agricultural and Biological Chemistry 54, no. 8 (August 1990): 2121–25. http://dx.doi.org/10.1080/00021369.1990.10870254.
Повний текст джерелаYorimitsu, Hideki. "Homolytic substitution at phosphorus for C–P bond formation in organic synthesis." Beilstein Journal of Organic Chemistry 9 (June 28, 2013): 1269–77. http://dx.doi.org/10.3762/bjoc.9.143.
Повний текст джерелаZhao, Xiuli, Mengmeng Huang, Yabo Li, Jianye Zhang, Jung Keun Kim, and Yangjie Wu. "Stepwise photosensitized C(sp3)–C(CO) bond cleavage and C–P bond formation of 1,3-dicarbonyls with arylphosphine oxides." Organic Chemistry Frontiers 6, no. 9 (2019): 1433–37. http://dx.doi.org/10.1039/c9qo00075e.
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 джерелаXie, Peizhong, Lei Guo, Lanlan Xu, and Teck-Peng Loh. "Asymmetric P−C Bond Formation: Diastereoselective Synthesis of Adjacent P,C-Stereogenic Allylic Phosphorus Compounds." Chemistry - An Asian Journal 11, no. 9 (March 29, 2016): 1353–56. http://dx.doi.org/10.1002/asia.201600108.
Повний текст джерелаWicht, Denyce K., Igor V. Kourkine, Ivan Kovacik, David S. Glueck, Thomas E. Concolino, Glenn P. A. Yap, Christopher D. Incarvito, and Arnold L. Rheingold. "Platinum-Catalyzed Acrylonitrile Hydrophosphination. P−C Bond Formation via Olefin Insertion into a Pt−P Bond." Organometallics 18, no. 25 (December 1999): 5381–94. http://dx.doi.org/10.1021/om990745h.
Повний текст джерелаHidaka, Tomomi, and Haruo Seto. "Studies on the C-P Bond Formation Mechanisms in Bialaphos." Actinomycetologica 6, no. 2 (1992): 105–12. http://dx.doi.org/10.3209/saj.6_105.
Повний текст джерелаJayaraman, Arumugam, Tyler V. Jacob, Jeff Bisskey, and Brian T. Sterenberg. "Sequential electrophilic P–C bond formation in metal-coordinated chlorophosphines." Dalton Transactions 44, no. 19 (2015): 8788–91. http://dx.doi.org/10.1039/c5dt01281c.
Повний текст джерелаHidaka, T., S. Imai, O. Hara, H. Anzai, T. Murakami, K. Nagaoka, and H. Seto. "Carboxyphosphonoenolpyruvate phosphonomutase, a novel enzyme catalyzing C-P bond formation." Journal of Bacteriology 172, no. 6 (1990): 3066–72. http://dx.doi.org/10.1128/jb.172.6.3066-3072.1990.
Повний текст джерелаHosseinian, Akram, Fatemeh Alsadat Hosseini Nasab, Sheida Ahmadi, Zahra Rahmani, and Esmail Vessally. "Decarboxylative cross-coupling reactions for P(O)–C bond formation." RSC Advances 8, no. 46 (2018): 26383–98. http://dx.doi.org/10.1039/c8ra04557g.
Повний текст джерелаYang, Shang-Dong, and Ya-Min Li. "New Strategies for Transition-Metal-Catalyzed C-P Bond Formation." Synlett 24, no. 14 (July 26, 2013): 1739–44. http://dx.doi.org/10.1055/s-0033-1339341.
Повний текст джерелаZhang, Hui, Xue-Yan Zhang, Dao-Qing Dong, and Zu-Li Wang. "Copper-catalyzed cross-coupling reactions for C–P bond formation." RSC Advances 5, no. 65 (2015): 52824–31. http://dx.doi.org/10.1039/c5ra08858e.
Повний текст джерелаWauters, Iris, Wouter Debrouwer, and Christian V. Stevens. "ChemInform Abstract: Preparation of Phosphines Through C-P Bond Formation." ChemInform 46, no. 14 (March 19, 2015): no. http://dx.doi.org/10.1002/chin.201514320.
Повний текст джерелаHeinl, Sebastian, Sabine Reisinger, Christoph Schwarzmaier, Michael Bodensteiner, and Manfred Scheer. "Selective Functionalization of P4by Metal-Mediated CP Bond Formation." Angewandte Chemie International Edition 53, no. 29 (May 30, 2014): 7639–42. http://dx.doi.org/10.1002/anie.201403295.
Повний текст джерелаJablonkai, Erzsebet, and Gyorgy Keglevich. "ChemInform Abstract: P-C Bond Formation by Coupling Reactions Utilizing." ChemInform 45, no. 34 (August 7, 2014): no. http://dx.doi.org/10.1002/chin.201434255.
Повний текст джерелаLi, Yuanming, Shyamal Chakrabarty, Christian Mück-Lichtenfeld, and Armido Studer. "Ortho -Trialkylstannyl Arylphosphanes by C-P and C-Sn Bond Formation in Arynes." Angewandte Chemie International Edition 55, no. 2 (December 3, 2015): 802–6. http://dx.doi.org/10.1002/anie.201509329.
Повний текст джерелаZhang, Ji-Shu, Tieqiao Chen, Jia Yang, and Li-Biao Han. "ChemInform Abstract: Nickel-Catalyzed P-C Bond Formation via P-H/C-CN Cross Coupling Reactions." ChemInform 46, no. 34 (August 2015): no. http://dx.doi.org/10.1002/chin.201534225.
Повний текст джерелаZhang, Bo, Constantin Gabriel Daniliuc, and Armido Studer. "6-Phosphorylated Phenanthridines from 2-Isocyanobiphenyls via Radical C–P and C–C Bond Formation." Organic Letters 16, no. 1 (December 9, 2013): 250–53. http://dx.doi.org/10.1021/ol403256e.
Повний текст джерелаHari, Durga Prasad, and Burkhard Koenig. "ChemInform Abstract: Eosin Y Catalyzed Visible Light Oxidative C-C and C-P Bond Formation." ChemInform 42, no. 50 (November 17, 2011): no. http://dx.doi.org/10.1002/chin.201150136.
Повний текст джерелаWan, Boshun, Haolong Wang, Xincheng Li, and Fan Wu. "Direct Oxidative C-P Bond Formation of Indoles with Dialkyl Phosphites." Synthesis 44, no. 06 (February 14, 2012): 941–45. http://dx.doi.org/10.1055/s-0031-1289700.
Повний текст джерелаGiffin, Kaitie A., Lorraine A. Pua, Ilia Korobkov, and R. Tom Baker. "Formation and C–F bond functionalization of [P,N]-ligated perfluoronickelacyclopentanes." Polyhedron 157 (January 2019): 458–66. http://dx.doi.org/10.1016/j.poly.2018.10.024.
Повний текст джерелаIsshiki, Ryota, Kei Muto, and Junichiro Yamaguchi. "Decarbonylative C–P Bond Formation Using Aromatic Esters and Organophosphorus Compounds." Organic Letters 20, no. 4 (February 2, 2018): 1150–53. http://dx.doi.org/10.1021/acs.orglett.8b00080.
Повний текст джерелаZhang, Yan, and Chengjian Zhu. "Gold complex-catalyzed C P bond formation by Kabachnik–Fields reactions." Catalysis Communications 28 (November 2012): 134–37. http://dx.doi.org/10.1016/j.catcom.2012.08.001.
Повний текст джерелаGlueck, David S. "ChemInform Abstract: Recent Advances in Metal-Catalyzed C-P- Bond Formation." ChemInform 42, no. 18 (April 7, 2011): no. http://dx.doi.org/10.1002/chin.201118202.
Повний текст джерелаBlum, Ofer, Felix Frolow, and David Milstein. "C–F bond activation by iridium(I). A unique process involving P–C bond cleavage, P–F bond formation and net retention of oxidation state." J. Chem. Soc., Chem. Commun., no. 4 (1991): 258–59. http://dx.doi.org/10.1039/c39910000258.
Повний текст джерелаDas, Deepankar, та Daniel Seidel. "Redox-Neutral α-C–H Bond Functionalization of Secondary Amines with Concurrent C–P Bond Formation/N-Alkylation". Organic Letters 15, № 17 (19 серпня 2013): 4358–61. http://dx.doi.org/10.1021/ol401858k.
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 джерелаXiong, Yunkui, Jianye Zhang, Liping Qi, Yu Zhang, and Tao Wang. "Oxidative C(SP2)‐P Formation: Direct Construction of C‐P Bond on Quinoxalines via Aromatic Phosphorous Oxide." ChemistrySelect 6, no. 4 (January 25, 2021): 657–62. http://dx.doi.org/10.1002/slct.202004036.
Повний текст джерелаDiaz, Armando A., Bryan Buster, Daniel Schomisch, Masood A. Khan, J. Clayton Baum, and Rudolf J. Wehmschulte. "Size Matters: Room Temperature P−C Bond Formation Through C−H Activation inm-Terphenyldiiodophosphines." Inorganic Chemistry 47, no. 7 (April 2008): 2858–63. http://dx.doi.org/10.1021/ic702105s.
Повний текст джерелаBlades, Kevin, Sunita T. Patel, Jonathan M. Percy, and Robin D. Wilkes. "Facile [2,3]-rearrangements of difluoroallylic alcohols with CP and CS bond formation." Tetrahedron Letters 37, no. 35 (August 1996): 6403–6. http://dx.doi.org/10.1016/0040-4039(96)01358-5.
Повний текст джерелаSrinivas, Katam, and Ganesan Prabusankar. "Role of C, S, Se and P donor ligands in copper(i) mediated C–N and C–Si bond formation reactions." RSC Advances 8, no. 56 (2018): 32269–82. http://dx.doi.org/10.1039/c8ra06057f.
Повний текст джерелаLi, Xue, Tieqiao Chen, Yuta Saga та Li-Biao Han. "Iron-catalyzed cross coupling of P–H/C–O bonds: efficient synthesis of α-alkoxyphosphorus compounds". Dalton Transactions 45, № 5 (2016): 1877–80. http://dx.doi.org/10.1039/c5dt02454d.
Повний текст джерелаKeweloh, Lukas, Niklas Aders, Alexander Hepp, Damian Pleschka, Ernst-Ulrich Würthwein, and Werner Uhl. "A P–H functionalized Al/P-based frustrated Lewis pair – hydrophosphination of nitriles, ring opening with cyclopropenones and evidence of PC double bond formation." Dalton Transactions 47, no. 25 (2018): 8402–17. http://dx.doi.org/10.1039/c8dt01836g.
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