Artigos de revistas sobre o tema "Organohalides"
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Maucourt, Bruno, Stéphane Vuilleumier e Françoise Bringel. "Transcriptional regulation of organohalide pollutant utilisation in bacteria". FEMS Microbiology Reviews 44, n.º 2 (3 de fevereiro de 2020): 189–207. http://dx.doi.org/10.1093/femsre/fuaa002.
Texto completo da fonteLee, Matthew, Chris Marquis, Bat-Erdene Judger e Mike Manefield. "Anaerobic microorganisms and bioremediation of organohalide pollution". Microbiology Australia 36, n.º 3 (2015): 125. http://dx.doi.org/10.1071/ma15044.
Texto completo da fonteBolandi, Ali, Setare Tahmasebi Nick e Sherine O. Obare. "Nanoscale materials for organohalide degradation via reduction pathways". Nanotechnology Reviews 1, n.º 2 (1 de março de 2012): 147–71. http://dx.doi.org/10.1515/ntrev-2012-0003.
Texto completo da fonteBertolini, Martina, Sarah Zecchin, Giovanni Pietro Beretta, Patrizia De Nisi, Laura Ferrari e Lucia Cavalca. "Effectiveness of Permeable Reactive Bio-Barriers for Bioremediation of an Organohalide-Polluted Aquifer by Natural-Occurring Microbial Community". Water 13, n.º 17 (5 de setembro de 2021): 2442. http://dx.doi.org/10.3390/w13172442.
Texto completo da fonteFutagami, Taiki, Yuki Morono, Takeshi Terada, Anna H. Kaksonen e Fumio Inagaki. "Distribution of dehalogenation activity in subseafloor sediments of the Nankai Trough subduction zone". Philosophical Transactions of the Royal Society B: Biological Sciences 368, n.º 1616 (19 de abril de 2013): 20120249. http://dx.doi.org/10.1098/rstb.2012.0249.
Texto completo da fonteIto, Hajime, Eiji Yamamoto, Satoshi Maeda e Tetsuya Taketsugu. "Transition-Metal-Free Boryl Substitution Using Silylboranes and Alkoxy Bases". Synlett 28, n.º 11 (26 de abril de 2017): 1258–67. http://dx.doi.org/10.1055/s-0036-1588772.
Texto completo da fonteSpurling, TH, e DA Winkler. "CNDO/2 Calculations for Organohalides". Australian Journal of Chemistry 39, n.º 2 (1986): 233. http://dx.doi.org/10.1071/ch9860233.
Texto completo da fonteWigginton, Nicholas S. "How bacteria break down organohalides". Science 346, n.º 6208 (23 de outubro de 2014): 435.9–436. http://dx.doi.org/10.1126/science.346.6208.435-i.
Texto completo da fonteRupakula, Aamani, Thomas Kruse, Sjef Boeren, Christof Holliger, Hauke Smidt e Julien Maillard. "The restricted metabolism of the obligate organohalide respiring bacterium Dehalobacter restrictus: lessons from tiered functional genomics". Philosophical Transactions of the Royal Society B: Biological Sciences 368, n.º 1616 (19 de abril de 2013): 20120325. http://dx.doi.org/10.1098/rstb.2012.0325.
Texto completo da fonteLi, Sheng-Jun, Lu Han e Shi-Kai Tian. "1,2-Aminohalogenation of arynes with amines and organohalides". Chemical Communications 55, n.º 75 (2019): 11255–58. http://dx.doi.org/10.1039/c9cc05505c.
Texto completo da fonteDenk, Michael K., Nicholas S. Milutinović, Katherine M. Marczenko, Natalie M. Sadowski e Athanasios Paschos. "Nature's hydrides: rapid reduction of halocarbons by folate model compounds". Chemical Science 8, n.º 3 (2017): 1883–87. http://dx.doi.org/10.1039/c6sc04314c.
Texto completo da fonteGhasemi, Mehri, Miaoqiang Lyu, Md Roknuzzaman, Jung-Ho Yun, Mengmeng Hao, Dongxu He, Yang Bai et al. "Phenethylammonium bismuth halides: from single crystals to bulky-organic cation promoted thin-film deposition for potential optoelectronic applications". Journal of Materials Chemistry A 7, n.º 36 (2019): 20733–41. http://dx.doi.org/10.1039/c9ta07454f.
Texto completo da fonteKim, Hyejin, e Chulbom Lee. "Nickel-Catalyzed Reductive Cyclization of Organohalides". Organic Letters 13, n.º 8 (15 de abril de 2011): 2050–53. http://dx.doi.org/10.1021/ol200455n.
Texto completo da fonteXiao, Shuhuan, Chen Liu, Bin Song, Liang Wang, Yan Qi e Yongjun Liu. "Samarium-based Grignard-type addition of organohalides to carbonyl compounds under catalysis of CuI". Chemical Communications 57, n.º 50 (2021): 6169–72. http://dx.doi.org/10.1039/d1cc00965f.
Texto completo da fonteKareem, Rzgar Tawfeeq, Bayan Azizi, Manzarbanou Asnaashariisfahani, Abdolghaffar Ebadi e Esmail Vessally. "Vicinal halo-trifluoromethylation of alkenes". RSC Advances 11, n.º 25 (2021): 14941–55. http://dx.doi.org/10.1039/d0ra06872a.
Texto completo da fonteSun, Baozhen, Shuang Liu, Mengru Zhang, Jinbo Zhao e Qian Zhang. "Pd-Catalyzed carboannulation of γ,δ-alkenyl oximes: efficient access to 5-membered cyclic nitrones and dihydroazines". Organic Chemistry Frontiers 6, n.º 3 (2019): 388–92. http://dx.doi.org/10.1039/c8qo01076e.
Texto completo da fonteZhang, Haoxiang, Mengze Liang, Xiao Zhang, Meng-Ke He, Chao Yang, Lin Guo e Wujiong Xia. "Electrochemical synthesis of functionalized gem-difluoroalkenes with diverse alkyl sources via a defluorinative alkylation process". Organic Chemistry Frontiers 9, n.º 1 (2022): 95–101. http://dx.doi.org/10.1039/d1qo01460a.
Texto completo da fonteXu, Qing, Huamei Xie, Pingliang Chen, Lei Yu, Jianhui Chen e Xingen Hu. "Organohalide-catalyzed dehydrative O-alkylation between alcohols: a facile etherification method for aliphatic ether synthesis". Green Chemistry 17, n.º 5 (2015): 2774–79. http://dx.doi.org/10.1039/c5gc00284b.
Texto completo da fonteFagin, Anatolii A., Tatyana V. Balashova, Dmitrii M. Kusyaev, Tatyana I. Kulikova, Tatyana A. Glukhova, Natalya P. Makarenko, Yurii A. Kurskii, William J. Evans e Mikhail N. Bochkarev. "Reactions of neodymium(II) iodide with organohalides". Polyhedron 25, n.º 5 (março de 2006): 1105–10. http://dx.doi.org/10.1016/j.poly.2005.08.050.
Texto completo da fonteChu, Xue-Qiang, Dan Liu, Zhen-Hua Xing, Xiao-Ping Xu e Shun-Jun Ji. "Palladium-Catalyzed Cyclization of Alkenes with Organohalides". Organic Letters 18, n.º 4 (2 de fevereiro de 2016): 776–79. http://dx.doi.org/10.1021/acs.orglett.6b00035.
Texto completo da fonteRoot, Douglas P., Gerald Pitz e Namal Priyantha. "Electrocatalytic metalloporphyrin electrode for detection of organohalides". Electrochimica Acta 36, n.º 5-6 (janeiro de 1991): 855–58. http://dx.doi.org/10.1016/0013-4686(91)85285-f.
Texto completo da fontePri-Bar, Ilan, e Ouri Buchman. "Homogeneous, palladium-catalyzed, selective hydrogenolysis of organohalides". Journal of Organic Chemistry 51, n.º 5 (março de 1986): 734–36. http://dx.doi.org/10.1021/jo00355a029.
Texto completo da fonteBoateng, Sakyiwaa. "Assessing conceptual difficulties experienced by pre-service chemistry teachers in organic chemistry". Eurasia Journal of Mathematics, Science and Technology Education 20, n.º 2 (1 de fevereiro de 2024): em2398. http://dx.doi.org/10.29333/ejmste/14156.
Texto completo da fonteBauman, Lew, e Michael K. Stenstrom. "Observations of the reaction between organohalides and sulfite". Environmental Science & Technology 23, n.º 2 (fevereiro de 1989): 232–36. http://dx.doi.org/10.1021/es00179a017.
Texto completo da fonteKim, Hyejin, e Chulbom Lee. "Visible-Light-Induced Photocatalytic Reductive Transformations of Organohalides". Angewandte Chemie 124, n.º 49 (4 de novembro de 2012): 12469–72. http://dx.doi.org/10.1002/ange.201203599.
Texto completo da fonteLekkala, Ravindar, Revathi Lekkala, Balakrishna Moku, K. P. Rakesh e Hua-Li Qin. "Recent Developments in Radical-Mediated Transformations of Organohalides". European Journal of Organic Chemistry 2019, n.º 17 (12 de abril de 2019): 2769–806. http://dx.doi.org/10.1002/ejoc.201900098.
Texto completo da fonteKim, Hyejin, e Chulbom Lee. "Visible-Light-Induced Photocatalytic Reductive Transformations of Organohalides". Angewandte Chemie International Edition 51, n.º 49 (4 de novembro de 2012): 12303–6. http://dx.doi.org/10.1002/anie.201203599.
Texto completo da fonteKim, Hyejin, e Chulbom Lee. "ChemInform Abstract: Nickel-Catalyzed Reductive Cyclizaton of Organohalides." ChemInform 42, n.º 30 (30 de junho de 2011): no. http://dx.doi.org/10.1002/chin.201130030.
Texto completo da fonteAbbaspourtamijani, Ali, Nicholas Vitti, Henry White e Yue Qi. "Electrochemical Reduction of Organohalides: Insights from First Principles Calculations". ECS Meeting Abstracts MA2021-02, n.º 48 (19 de outubro de 2021): 1940. http://dx.doi.org/10.1149/ma2021-02481940mtgabs.
Texto completo da fonteHe, Haozheng, Yiyang Li, Rui Shen, Hojae Shim, Yanhong Zeng, Siyan Zhao, Qihong Lu, Bixian Mai e Shanquan Wang. "Environmental occurrence and remediation of emerging organohalides: A review". Environmental Pollution 290 (dezembro de 2021): 118060. http://dx.doi.org/10.1016/j.envpol.2021.118060.
Texto completo da fonteLu, Qihong, Lan Qiu, Ling Yu, Shangwei Zhang, Renata Alves de Toledo, Hojae Shim e Shanquan Wang. "Microbial transformation of chiral organohalides: Distribution, microorganisms and mechanisms". Journal of Hazardous Materials 368 (abril de 2019): 849–61. http://dx.doi.org/10.1016/j.jhazmat.2019.01.103.
Texto completo da fonteWallner, Olov A., e Kálmán J. Szabó. "Employment of Palladium Pincer-Complexes in Phenylselenylation of Organohalides". Journal of Organic Chemistry 70, n.º 23 (novembro de 2005): 9215–21. http://dx.doi.org/10.1021/jo051266x.
Texto completo da fonteCheung, Man Sing, Todd B. Marder e Zhenyang Lin. "Mechanisms of Reactions of a Lithium Boryl with Organohalides". Organometallics 30, n.º 11 (13 de junho de 2011): 3018–28. http://dx.doi.org/10.1021/om200115y.
Texto completo da fonteZanaroli, Giulio, Andrea Negroni, Max M. Häggblom e Fabio Fava. "Microbial dehalogenation of organohalides in marine and estuarine environments". Current Opinion in Biotechnology 33 (junho de 2015): 287–95. http://dx.doi.org/10.1016/j.copbio.2015.03.013.
Texto completo da fonteNijenhuis, Ivonne, e Hans H. Richnow. "Stable isotope fractionation concepts for characterizing biotransformation of organohalides". Current Opinion in Biotechnology 41 (outubro de 2016): 108–13. http://dx.doi.org/10.1016/j.copbio.2016.06.002.
Texto completo da fonteLi, Yuqiang, e Guoyin Yin. "Bathocuproine-Enabled Nickel-Catalyzed Selective Ullmann Cross-Coupling of Two sp2-Hybridized Organohalides". Synlett 32, n.º 16 (24 de agosto de 2021): 1657–61. http://dx.doi.org/10.1055/a-1608-5693.
Texto completo da fonteWackett, Lawrence P. "Recruitment of Co-Metabolic Enzymes for Environmental Detoxification of Organohalides". Environmental Health Perspectives 103 (junho de 1995): 45. http://dx.doi.org/10.2307/3432478.
Texto completo da fonteWackett, L. P. "Recruitment of co-metabolic enzymes for environmental detoxification of organohalides." Environmental Health Perspectives 103, suppl 5 (junho de 1995): 45–48. http://dx.doi.org/10.1289/ehp.95103s445.
Texto completo da fonteCristofoli, Walter A., e Brian A. Keay. "A palladium catalyzed cross-coupling between furylborates (generated ) and organohalides". Tetrahedron Letters 32, n.º 42 (outubro de 1991): 5881–84. http://dx.doi.org/10.1016/s0040-4039(00)79416-0.
Texto completo da fonteZheng, Kewang, Guanlin Xiao, Tao Guo, Yalan Ding, Chengdong Wang, Teck-Peng Loh e Xiaojin Wu. "Intermolecular Reductive Heck Reaction of Unactivated Aliphatic Alkenes with Organohalides". Organic Letters 22, n.º 2 (8 de janeiro de 2020): 694–99. http://dx.doi.org/10.1021/acs.orglett.9b04474.
Texto completo da fonteJugder, Bat-Erdene, Haluk Ertan, Matthew Lee, Michael Manefield e Christopher P. Marquis. "Reductive Dehalogenases Come of Age in Biological Destruction of Organohalides". Trends in Biotechnology 33, n.º 10 (outubro de 2015): 595–610. http://dx.doi.org/10.1016/j.tibtech.2015.07.004.
Texto completo da fonteKim, Hyejin, e Chulbom Lee. "ChemInform Abstract: Visible Light Induced Photocatalytic Reductive Transformations of Organohalides." ChemInform 44, n.º 22 (13 de maio de 2013): no. http://dx.doi.org/10.1002/chin.201322033.
Texto completo da fonteHuang, Yu, Ruizhi Yang e Wenbo H. Liu. "Recent advances of the Grignard-type reactions without involving organohalides". Tetrahedron Chem 9 (março de 2024): 100069. http://dx.doi.org/10.1016/j.tchem.2024.100069.
Texto completo da fonteTang, Shuang-Qi, Martine Schmitt e Frédéric Bihel. "POxAP Precatalysts and the Negishi Cross-Coupling Reaction". Synthesis 52, n.º 01 (28 de outubro de 2019): 51–59. http://dx.doi.org/10.1055/s-0039-1690728.
Texto completo da fonteKohn, Tamar, e A. Lynn Roberts. "Interspecies Competitive Effects in Reduction of Organohalides in Connelly Iron Columns". Environmental Engineering Science 23, n.º 5 (setembro de 2006): 874–85. http://dx.doi.org/10.1089/ees.2006.23.874.
Texto completo da fonteLiu, Yongjun, Shuhuan Xiao, Yan Qi e Feng Du. "Reductive Homocoupling of Organohalides Using Nickel(II) Chloride and Samarium Metal". Chemistry - An Asian Journal 12, n.º 6 (21 de fevereiro de 2017): 673–78. http://dx.doi.org/10.1002/asia.201601712.
Texto completo da fonteGilbert, Bruce C., Richard J. Harrison, Chris I. Lindsay, P. Terry McGrail, Andrew F. Parsons, Richard Southward e Derek J. Irvine. "Polymerization of Methyl Methacrylate Using Dimanganese Decacarbonyl in the Presence of Organohalides". Macromolecules 36, n.º 24 (dezembro de 2003): 9020–23. http://dx.doi.org/10.1021/ma034712w.
Texto completo da fonteFalck, J. R., Rama K. Bhatt e Jianhua Ye. "Tin-Copper Transmetalation: Cross-Coupling of .alpha.-Heteroatom-Substituted Alkyltributylstannanes with Organohalides". Journal of the American Chemical Society 117, n.º 22 (junho de 1995): 5973–82. http://dx.doi.org/10.1021/ja00127a010.
Texto completo da fonteShrestha, Bijay, Surendra Thapa, Santosh K. Gurung, Ryan A. S. Pike e Ramesh Giri. "General Copper-Catalyzed Coupling of Alkyl-, Aryl-, and Alkynylaluminum Reagents with Organohalides". Journal of Organic Chemistry 81, n.º 3 (20 de janeiro de 2016): 787–802. http://dx.doi.org/10.1021/acs.joc.5b02077.
Texto completo da fonteZhang, Ting-Ting, Mu-Jia Luo, Yang Li, Ren-Jie Song e Jin-Heng Li. "Electrochemical Alkoxyhalogenation of Alkenes with Organohalides as the Halide Sources via Dehalogenation". Organic Letters 22, n.º 18 (27 de agosto de 2020): 7250–54. http://dx.doi.org/10.1021/acs.orglett.0c02582.
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