Статті в журналах з теми "Heteroatomic radical"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Heteroatomic radical".
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.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Han, Yuxuan, and Xiuling Cui. "Copper-Catalyzed Enantioselective Radical Heteroatomic S—O Cross-Coupling." Chinese Journal of Organic Chemistry 43, no. 3 (2023): 1201. http://dx.doi.org/10.6023/cjoc202300013.
Повний текст джерелаLinker, Torsten. "Addition of Heteroatom Radicals to endo-Glycals †." Chemistry 2, no. 1 (February 20, 2020): 80–92. http://dx.doi.org/10.3390/chemistry2010008.
Повний текст джерелаDi Vaira, Massimo, Piero Stoppioni, Stefano Midollini, Franco Laschi, and Piero Zanello. "H+ addition to the heteroatomic CoP3 cluster. Synthesis of the radical CoP3+ cluster and electrochemical study." Polyhedron 10, no. 18 (January 1991): 2123–29. http://dx.doi.org/10.1016/s0277-5387(00)86131-8.
Повний текст джерелаRhodes, Christopher J., Harry Morris, Hikmet Agirbas, Mark Standing, and Yaming Zhang. "Distonic isomerisations of imine radical cations: aspects of the reactivity of heteroatomic subunits damaged by ionising radiation." Journal of the Chemical Society, Perkin Transactions 2, no. 6 (1998): 1375–80. http://dx.doi.org/10.1039/a801066h.
Повний текст джерелаTaniguchi, Tsuyoshi. "Recent Advances in Reactions of Heteroatom-Centered Radicals." Synthesis 49, no. 16 (July 26, 2017): 3511–34. http://dx.doi.org/10.1055/s-0036-1588481.
Повний текст джерелаOgawa, Akiya, and Yuki Yamamoto. "Multicomponent Reactions between Heteroatom Compounds and Unsaturated Compounds in Radical Reactions." Molecules 28, no. 17 (August 30, 2023): 6356. http://dx.doi.org/10.3390/molecules28176356.
Повний текст джерелаRenaud, Philippe, Alice Beauseigneur, Andrea Brecht-Forster, Barbara Becattini, Vincent Darmency, Sarkunam Kandhasamy, Florian Montermini, et al. "Boron: A key element in radical reactions." Pure and Applied Chemistry 79, no. 2 (January 1, 2007): 223–33. http://dx.doi.org/10.1351/pac200779020223.
Повний текст джерелаKawaguchi, Shin-ichi, Akiya Ogawa, Yuki Sato, and Akihiro Nomoto. "Photoinduced Coupling Reaction of Diphenyl(2,4,6-trimethylbenzoyl)phosphine Oxide with Interelement Compounds: Application to the Synthesis of Thio- or Selenophosphinates." Synthesis 49, no. 16 (July 4, 2017): 3558–67. http://dx.doi.org/10.1055/s-0036-1588867.
Повний текст джерелаGuo, Weisi, Qian Wang, and Jieping Zhu. "Visible light photoredox-catalysed remote C–H functionalisation enabled by 1,5-hydrogen atom transfer (1,5-HAT)." Chemical Society Reviews 50, no. 13 (2021): 7359–77. http://dx.doi.org/10.1039/d0cs00774a.
Повний текст джерелаKubo, Takashi. "Synthesis, Physical Properties, and Reactivity of Stable, π-Conjugated, Carbon-Centered Radicals". Molecules 24, № 4 (13 лютого 2019): 665. http://dx.doi.org/10.3390/molecules24040665.
Повний текст джерелаXiao, Tiebo, Lei Zhou, Hongtai Huang, and Devireddy Anand. "Iminyl-Radical-Triggered C–C Bond Cleavage of Cycloketone Oxime Derivatives: Generation of Distal Cyano-Substituted Alkyl Radicals and Their Functionalization." Synthesis 52, no. 11 (March 5, 2020): 1585–601. http://dx.doi.org/10.1055/s-0039-1690844.
Повний текст джерелаPaick, Jihun, Seunghee Hong, Jy-Young Jyoung, Eun-Sook Lee, and Doohwan Lee. "Comparative Studies on Effects of Metal Cation (La) and Non-Metal Anion (N) Doping on CeO2 Nanoparticles for Regenerative Scavenging of Reactive Oxygen Radicals." Catalysts 13, no. 3 (March 11, 2023): 572. http://dx.doi.org/10.3390/catal13030572.
Повний текст джерелаYamamoto, Yuki, Qiqi Chen, and Akiya Ogawa. "Diphenyl Diselenide-Assisted Radical Addition Reaction of Diphenyl Disulfide to Unsaturated Bonds upon Photoirradiation." Molecules 28, no. 6 (March 7, 2023): 2450. http://dx.doi.org/10.3390/molecules28062450.
Повний текст джерелаMozafari, Mina, Lalangi Chandrasena, Iain McKenzie, Kerim Samedov, and Paul W. Percival. "Characterization of free radicals in clathrate hydrates of pyrrole, thiophene, and isoxazole by muon spin spectroscopy." Canadian Journal of Chemistry 96, no. 2 (February 2018): 217–25. http://dx.doi.org/10.1139/cjc-2017-0313.
Повний текст джерелаKatritzky, Alan R., Baozhen Yang, and Naresh S. Dalal. "Novel Heteroatom-Linked Analogues of Trityl Radicals: Diaryl(benzotriazol-1-yl)methyl Radical Dimers." Journal of Organic Chemistry 63, no. 5 (March 1998): 1467–72. http://dx.doi.org/10.1021/jo9715229.
Повний текст джерелаKaur, Rupinder preet, Damanjit Kaur, and Ritika Sharma. "Substituent effect on N–H bond dissociation enthalpies of carbamates: a theoretical study." Canadian Journal of Chemistry 93, no. 3 (March 2015): 279–88. http://dx.doi.org/10.1139/cjc-2014-0326.
Повний текст джерелаWan, Zhonghao, Yuqing Sun, Daniel C. W. Tsang, Iris K. M. Yu, Jiajun Fan, James H. Clark, Yaoyu Zhou, Xinde Cao, Bin Gao, and Yong Sik Ok. "A sustainable biochar catalyst synergized with copper heteroatoms and CO2 for singlet oxygenation and electron transfer routes." Green Chemistry 21, no. 17 (2019): 4800–4814. http://dx.doi.org/10.1039/c9gc01843c.
Повний текст джерелаSCHUCHMANN, H. P., and C. VON SONNTAG. "ChemInform Abstract: Heteroatom Peroxyl Radicals." ChemInform 29, no. 22 (June 22, 2010): no. http://dx.doi.org/10.1002/chin.199822209.
Повний текст джерелаZhang, Kai, Benjamin B. Noble, Adam C. Mater, Michael J. Monteiro, Michelle L. Coote, and Zhongfan Jia. "Effect of heteroatom and functionality substitution on the oxidation potential of cyclic nitroxide radicals: role of electrostatics in electrochemistry." Physical Chemistry Chemical Physics 20, no. 4 (2018): 2606–14. http://dx.doi.org/10.1039/c7cp07444a.
Повний текст джерелаMieden, Oliver J., and Clemens von Sonntag. "Peptide Free-Radicals: The Reactions of OH Radicals with Glycine Anhydride and its Methyl Derivatives Sarcosine and Alanine Anhydride. A Pulse Radiolysis and Product Study." Zeitschrift für Naturforschung B 44, no. 8 (August 1, 1989): 959–74. http://dx.doi.org/10.1515/znb-1989-0818.
Повний текст джерелаRoss, Philip L., Scott E. Van Bramer, and Murray V. Johnston. "Ultraviolet Photodissociation of Gas-Phase Alcohols, Amines, and Nitroalkanes." Applied Spectroscopy 50, no. 5 (May 1996): 608–13. http://dx.doi.org/10.1366/0003702963905862.
Повний текст джерелаde la Vega-Hernández, Karen, Elise Romain, Anais Coffinet, Kajetan Bijouard, Geoffrey Gontard, Fabrice Chemla, Franck Ferreira, Olivier Jackowski та Alejandro Perez-Luna. "Radical Germylzincation of α-Heteroatom-Substituted Alkynes". Journal of the American Chemical Society 140, № 50 (29 листопада 2018): 17632–42. http://dx.doi.org/10.1021/jacs.8b09851.
Повний текст джерелаZhi, Sanjun, Hongjun Yao, and Wei Zhang. "Difunctionalization of Dienes, Enynes and Related Compounds via Sequential Radical Addition and Cyclization Reactions." Molecules 28, no. 3 (January 23, 2023): 1145. http://dx.doi.org/10.3390/molecules28031145.
Повний текст джерелаHuang, Min-Hua, Wen-Juan Hao, Guigen Li, Shu-Jiang Tu, and Bo Jiang. "Recent advances in radical transformations of internal alkynes." Chemical Communications 54, no. 77 (2018): 10791–811. http://dx.doi.org/10.1039/c8cc04618b.
Повний текст джерелаYateem, Ali Hussain. "Rotational Barrier and Bond Dissociation Energy and Enthalpy: Computational Study of the Substituent Effects in <i>Para</i>-Substituted Anilines and Phenols." Indonesian Journal of Chemistry 22, no. 1 (January 8, 2022): 179. http://dx.doi.org/10.22146/ijc.68687.
Повний текст джерелаDemay-Drouhard, Paul, H. Y. Vincent Ching, Christophe Decroos, Régis Guillot, Yun Li, Leandro C. Tabares, Clotilde Policar, Helene C. Bertrand, and Sun Un. "Understanding the g-tensors of perchlorotriphenylmethyl and Finland-type trityl radicals." Physical Chemistry Chemical Physics 22, no. 36 (2020): 20792–800. http://dx.doi.org/10.1039/d0cp03626a.
Повний текст джерелаMukhopadhyay, Anamika, Lilit Jacob, and Sugumar Venkataramani. "Dehydro-oxazole, thiazole and imidazole radicals: insights into the electronic structure, stability and reactivity aspects." Physical Chemistry Chemical Physics 19, no. 1 (2017): 394–407. http://dx.doi.org/10.1039/c6cp05677f.
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 джерелаDénès, Fabrice. "Intermolecular Radical C–H Bond Activation: A Powerful Tool for Late Stage Functionalization." CHIMIA International Journal for Chemistry 74, no. 1 (February 26, 2020): 23–32. http://dx.doi.org/10.2533/chimia.2020.23.
Повний текст джерелаNaito, Takeaki. "Heteroatom Radical Addition-Cyclization and Its Synthetic Application." HETEROCYCLES 50, no. 1 (1999): 505. http://dx.doi.org/10.3987/rev-98-sr(h)2.
Повний текст джерелаCoote, Michelle L., Ching Yeh Lin, and Andreas A. Zavitsas. "Inherent and transferable stabilization energies of carbon- and heteroatom-centred radicals on the same relative scale and their applications." Phys. Chem. Chem. Phys. 16, no. 18 (2014): 8686–96. http://dx.doi.org/10.1039/c4cp00537f.
Повний текст джерелаYu, Jing-Miao, та Chun Cai. "Iodine(iii)-mediated intramolecular sulfeno- and selenofunctionalization of β,γ-unsaturated tosyl hydrazones and oximes". Organic & Biomolecular Chemistry 16, № 3 (2018): 490–98. http://dx.doi.org/10.1039/c7ob02892j.
Повний текст джерелаKirchhoff, Dirk, Hans-Friedrich Grützmacher, and Hansjörg Grützmacher. "Trends in the Periodic System: The Mass Spectrum of Dimethylphenyl Phosphane and a Comparison of the Gas Phase Reactivity of Dimethylphenyl Pnictogene Radical Cations C6H5E(CH3)2•+, (E = N, P, As)." European Journal of Mass Spectrometry 15, no. 2 (April 2009): 131–44. http://dx.doi.org/10.1255/ejms.940.
Повний текст джерелаBlank, Lena, Maurizio Fagnoni, Stefano Protti, and Magnus Rueping. "Visible Light-Promoted Formation of C–B and C–S Bonds under Metal- and Photocatalyst-Free Conditions." Synthesis 51, no. 05 (February 6, 2019): 1243–52. http://dx.doi.org/10.1055/s-0037-1611648.
Повний текст джерелаHendon, Christopher H., David R. Carbery, and Aron Walsh. "Three-electron two-centred bonds and the stabilisation of cationic sulfur radicals." Chem. Sci. 5, no. 4 (2014): 1390–95. http://dx.doi.org/10.1039/c3sc53432d.
Повний текст джерелаSchier, Jan E. S., David Cohen-Sacal, and Robin A. Hutchinson. "Hydrogen bonding in radical solution copolymerization kinetics of acrylates and methacrylates: a comparison of hydroxy- and methoxy-functionality." Polymer Chemistry 8, no. 12 (2017): 1943–52. http://dx.doi.org/10.1039/c7py00185a.
Повний текст джерелаRussell, Glen A., Preecha Ngoviwatchai, Hasan I. Tashtoush, Anna Pla-Dalmau, and Rajive K. Khanna. "Reactions of alkylmercurials with heteroatom-centered acceptor radicals." Journal of the American Chemical Society 110, no. 11 (May 1988): 3530–38. http://dx.doi.org/10.1021/ja00219a030.
Повний текст джерелаRANAUD, P. "ChemInform Abstract: Heteroatom-Substituted Radicals: 1,2-Asymmetric Induction." ChemInform 27, no. 40 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199640268.
Повний текст джерелаSerwinski, Paul R., Burak Esat, Paul M. Lahti, Yi Liao, Richard Walton, and Jiang Lan. "Photolysis and Oxidation of Azidophenyl-Substituted Radicals: Delocalization in Heteroatom-Based Radicals." Journal of Organic Chemistry 69, no. 16 (August 2004): 5247–60. http://dx.doi.org/10.1021/jo049500r.
Повний текст джерелаMiyabe, Hideto, and Yoshiji Takemoto. "Cascade radical reactions via carbon-carbon/heteroatom bond-forming process." Universal Organic Chemistry 2, no. 1 (2014): 1. http://dx.doi.org/10.7243/2053-7670-2-1.
Повний текст джерелаNaito, Takeaki. "ChemInform Abstract: Heteroatom Radical Addition-Cyclization and Its Synthetic Application." ChemInform 30, no. 20 (June 15, 2010): no. http://dx.doi.org/10.1002/chin.199920279.
Повний текст джерелаErfan, Abeer, Emad Yousif, Ahmed Neama Alshanon, Dina Saadi Ahmed, Muna Bufaroosha, and Gamal El-Hiti. "Organotin(IV) Complexes as Promising Potential Drug Candidates in the Field of Cancer Chemotherapy: A Narrative Review." Al-Rafidain Journal of Medical Sciences ( ISSN 2789-3219 ) 5 (July 15, 2023): 48–56. http://dx.doi.org/10.54133/ajms.v5i.146.
Повний текст джерелаBuntinx, G., and O. Poizat. "Time-Resolved Resonance Raman Spectroscopy of Photochemical Reactive Intermediates: Radical Cation of Fluorene and Triplet State of Fluorene, Dibenzofuran and Dibenzothiophen." Laser Chemistry 10, no. 5-6 (January 1, 1990): 333–47. http://dx.doi.org/10.1155/1990/28350.
Повний текст джерелаPyszka, Ilona, and Beata Jędrzejewska. "Acenaphthoquinoxaline Derivatives as Dental Photoinitiators of Acrylates Polymerization." Materials 14, no. 17 (August 27, 2021): 4881. http://dx.doi.org/10.3390/ma14174881.
Повний текст джерелаKamijo, Shin, Kaori Kamijo, and Toshihiro Murafuji. "Aryl Ketone Mediated Photoinduced Radical Coupling for the Alkylation of Benzazoles Employing Saturated Heterocyclic Compounds." Synthesis 51, no. 20 (July 31, 2019): 3859–64. http://dx.doi.org/10.1055/s-0037-1611895.
Повний текст джерелаKatritzky, Alan R., Baozhen Yang, and David P. M. Pleynet. "Novel Heteroatom-Substituted Trityl Radical Analogues: Preparation and Properties of Diaryl(benzotriazol-2-yl)methyl Radical Dimers‡." Journal of Organic Chemistry 63, no. 26 (December 1998): 9992–94. http://dx.doi.org/10.1021/jo980618f.
Повний текст джерелаLi, Ping, Boon Chong Lee, Ming Joo Koh, and Xiaoxiang Zhang. "Base-Mediated Site-Selective Hydroamination of Alkenes." Synthesis 54, no. 06 (October 28, 2021): 1566–76. http://dx.doi.org/10.1055/a-1681-4720.
Повний текст джерелаSchiesser, Carl H., and Lisa M. Wild. "Free-radical homolytic substitution: New methods for formation of bonds to heteroatoms." Tetrahedron 52, no. 42 (October 1996): 13265–314. http://dx.doi.org/10.1016/0040-4020(96)00809-5.
Повний текст джерелаSonawane, Amol D., Rohini A. Sonawane, Masayuki Ninomiya, and Mamoru Koketsu. "Synthesis of Seleno‐Heterocycles via Electrophilic/Radical Cyclization of Alkyne Containing Heteroatoms." Advanced Synthesis & Catalysis 362, no. 17 (July 9, 2020): 3485–515. http://dx.doi.org/10.1002/adsc.202000490.
Повний текст джерелаOgawa, Akiya, Taichi Tamai, Takenori Mitamura, and Akihiro Nomoto. "Highly selective introduction of heteroatom groups to isocyanides and its application to electrocyclic reactions." Pure and Applied Chemistry 85, no. 4 (December 7, 2012): 785–99. http://dx.doi.org/10.1351/pac-con-12-07-01.
Повний текст джерела