Artigos de revistas sobre o tema "Dibenzocyclooctyne"
Crie uma referência precisa em APA, MLA, Chicago, Harvard, e outros estilos
Veja os 50 melhores artigos de revistas para estudos sobre o assunto "Dibenzocyclooctyne".
Ao lado de cada fonte na lista de referências, há um botão "Adicionar à bibliografia". Clique e geraremos automaticamente a citação bibliográfica do trabalho escolhido no estilo de citação de que você precisa: APA, MLA, Harvard, Chicago, Vancouver, etc.
Você também pode baixar o texto completo da publicação científica em formato .pdf e ler o resumo do trabalho online se estiver presente nos metadados.
Veja os artigos de revistas das mais diversas áreas científicas e compile uma bibliografia correta.
He, Yinming, Li Liu e Liang Cheng. "A Short Review of Research Progress on the Synthesis Approaches of Aza-Dibenzocyclooctyne Derivatives". Molecules 28, n.º 9 (25 de abril de 2023): 3715. http://dx.doi.org/10.3390/molecules28093715.
Texto completo da fonteNarayanam, Maruthi Kumar, Yong Liang, K. N. Houk e Jennifer M. Murphy. "Discovery of new mutually orthogonal bioorthogonal cycloaddition pairs through computational screening". Chemical Science 7, n.º 2 (2016): 1257–61. http://dx.doi.org/10.1039/c5sc03259h.
Texto completo da fonteShenje, Learnmore, Yingqi Qu, Vladimir Popik e Susanne Ullrich. "Femtosecond photodecarbonylation of photo-ODIBO studied by stimulated Raman spectroscopy and density functional theory". Physical Chemistry Chemical Physics 23, n.º 45 (2021): 25637–48. http://dx.doi.org/10.1039/d1cp03512f.
Texto completo da fonteAdronov, Alex, Kelvin Li e Stuart McNelles. "Preparation and Properties of a Hydrolytically Stable Cyclooctyne-Containing Polymer". Synlett 29, n.º 19 (3 de setembro de 2018): 2535–41. http://dx.doi.org/10.1055/s-0037-1610636.
Texto completo da fonteWang, Mengzhe, Christopher D. McNitt, Hui Wang, Xiaofen Ma, Sarah M. Scarry, Zhanhong Wu, Vladimir V. Popik e Zibo Li. "The efficiency of 18F labelling of a prostate specific membrane antigen ligand via strain-promoted azide–alkyne reaction: reaction speed versus hydrophilicity". Chemical Communications 54, n.º 56 (2018): 7810–13. http://dx.doi.org/10.1039/c8cc03999b.
Texto completo da fonteKardelis, Vladimir, Ryan C. Chadwick e Alex Adronov. "Click Functionalization of a Dibenzocyclooctyne-Containing Conjugated Polyimine". Angewandte Chemie International Edition 55, n.º 3 (8 de dezembro de 2015): 945–49. http://dx.doi.org/10.1002/anie.201508639.
Texto completo da fonteKardelis, Vladimir, Ryan C. Chadwick e Alex Adronov. "Click Functionalization of a Dibenzocyclooctyne-Containing Conjugated Polyimine". Angewandte Chemie 128, n.º 3 (8 de dezembro de 2015): 957–61. http://dx.doi.org/10.1002/ange.201508639.
Texto completo da fonteMoran, Joseph, Craig S. McKay e John Paul Pezacki. "Strain-promoted 1,3-dipolar cycloadditions of diazo compounds with cyclooctynes". Canadian Journal of Chemistry 89, n.º 2 (fevereiro de 2011): 148–51. http://dx.doi.org/10.1139/v10-112.
Texto completo da fonteKettenbach, K., e T. L. Ross. "A 18F-labeled dibenzocyclooctyne (DBCO) derivative for copper-free click labeling of biomolecules". MedChemComm 7, n.º 4 (2016): 654–57. http://dx.doi.org/10.1039/c5md00508f.
Texto completo da fonteDjurdjevic, Sinisa, e James R. Green. "Nicholas Reactions in the Synthesis of Dicobalt Dibenzocyclooctyne Complexes". Organic Letters 15, n.º 21 (14 de outubro de 2013): 5468–71. http://dx.doi.org/10.1021/ol402617a.
Texto completo da fonteAndo, Takehiro, Yukio Takamori, Takumi Yokoyama, Mizuki Yamamoto e Takashi Kawakami. "Directed evolution of dibenzocyclooctyne-reactive peptide tags for protein labeling". Biochemical and Biophysical Research Communications 534 (janeiro de 2021): 27–33. http://dx.doi.org/10.1016/j.bbrc.2020.12.002.
Texto completo da fonteZeng, Zhiying, Changying Li, Yupeng Zhu, Lan Yang, Shuangquan Shi, Fengyuan Yang e Xuli Feng. "Dibenzocyclooctyne linked lysine-cyclodextrin for efficient intranucleus delivery of proteins". Journal of Controlled Release 352 (dezembro de 2022): 759–65. http://dx.doi.org/10.1016/j.jconrel.2022.11.001.
Texto completo da fonteYang, Xiaoke, Shuangshuang Wang, Yechao Yan, Ying Wu, Ke Zhang e Yongming Chen. "Well-defined dibenzocyclooctyne end functionalized polymers from atom transfer radical polymerization". Polymer 55, n.º 5 (março de 2014): 1128–35. http://dx.doi.org/10.1016/j.polymer.2014.01.022.
Texto completo da fonteMcNitt, Christopher D., e Vladimir V. Popik. "Photochemical generation of oxa-dibenzocyclooctyne (ODIBO) for metal-free click ligations". Organic & Biomolecular Chemistry 10, n.º 41 (2012): 8200. http://dx.doi.org/10.1039/c2ob26581h.
Texto completo da fonteLo, Kenneth Kam-Wing, Bruce Ting-Ngok Chan, Hua-Wei Liu, Kenneth Yin Zhang, Steve Po-Yam Li e Tommy Siu-Ming Tang. "Cyclometalated iridium(iii) polypyridine dibenzocyclooctyne complexes as the first phosphorescent bioorthogonal probes". Chem. Commun. 49, n.º 39 (2013): 4271–73. http://dx.doi.org/10.1039/c2cc36907a.
Texto completo da fonteSun, Peng, Guowei Yan, Qingquan Tang, Yongming Chen e Ke Zhang. "Well-defined cyclopropenone-masked dibenzocyclooctyne functionalized polymers from atom transfer radical polymerization". Polymer 64 (maio de 2015): 202–9. http://dx.doi.org/10.1016/j.polymer.2014.10.041.
Texto completo da fonteQu, Lin, Ying Wu, Peng Sun, Ke Zhang e Zhengping Liu. "Cyclopropenone-masked dibenzocyclooctyne end-functionalized polymers from reversible addition-fragmentation chain transfer polymerization". Polymer 114 (abril de 2017): 36–43. http://dx.doi.org/10.1016/j.polymer.2017.02.071.
Texto completo da fonteTang, Tommy Siu-Ming, Alex Man-Hei Yip, Kenneth Yin Zhang, Hua-Wei Liu, Po Lam Wu, King Fai Li, Kok Wai Cheah e Kenneth Kam-Wing Lo. "Bioorthogonal Labeling, Bioimaging, and Photocytotoxicity Studies of Phosphorescent Ruthenium(II) Polypyridine Dibenzocyclooctyne Complexes". Chemistry - A European Journal 21, n.º 30 (19 de junho de 2015): 10729–40. http://dx.doi.org/10.1002/chem.201501040.
Texto completo da fonteDing, Jin, Hang Su, Fan Wang e Taiwei Chu. "A pre-targeting strategy for imaging glucose metabolism using technetium-99m labelled dibenzocyclooctyne derivative". Bioorganic & Medicinal Chemistry Letters 29, n.º 14 (julho de 2019): 1791–98. http://dx.doi.org/10.1016/j.bmcl.2019.05.012.
Texto completo da fonteChoi, Alex Wing-Tat, Hua-Wei Liu e Kenneth Kam-Wing Lo. "Rhenium(I) polypyridine dibenzocyclooctyne complexes as phosphorescent bioorthogonal probes: Synthesis, characterization, emissive behavior, and biolabeling properties". Journal of Inorganic Biochemistry 148 (julho de 2015): 2–10. http://dx.doi.org/10.1016/j.jinorgbio.2015.02.018.
Texto completo da fonteOsuofa, Joshua, e Scott M. Husson. "Preparation of Protein A Membrane Adsorbers Using Strain-Promoted, Copper-Free Dibenzocyclooctyne (DBCO)-Azide Click Chemistry". Membranes 13, n.º 10 (6 de outubro de 2023): 824. http://dx.doi.org/10.3390/membranes13100824.
Texto completo da fonteErickson, Patrick W., James M. Fulcher, Paul Spaltenstein e Michael S. Kay. "Traceless Click-Assisted Native Chemical Ligation Enabled by Protecting Dibenzocyclooctyne from Acid-Mediated Rearrangement with Copper(I)". Bioconjugate Chemistry 32, n.º 10 (8 de outubro de 2021): 2233–44. http://dx.doi.org/10.1021/acs.bioconjchem.1c00403.
Texto completo da fontePorcello, Alexandre, Paula Gonzalez-Fernandez, Olivier Jordan e Eric Allémann. "Nanoforming Hyaluronan-Based Thermoresponsive Hydrogels: Optimized and Tunable Functionality in Osteoarthritis Management". Pharmaceutics 14, n.º 3 (17 de março de 2022): 659. http://dx.doi.org/10.3390/pharmaceutics14030659.
Texto completo da fonteKutovyi, Yurii, Jie Li, Ihor Zadorozhnyi, Hanna Hlukhova, Nazarii Boichuk, Dmytro Yehorov, Marcus Menger e Svetlana Vitusevich. "Highly Sensitive and Fast Detection of C-Reactive Protein and Troponin Biomarkers Using Liquid-gated Single Silicon Nanowire Biosensors". MRS Advances 5, n.º 16 (2020): 835–46. http://dx.doi.org/10.1557/adv.2020.60.
Texto completo da fonteDharmatti, Miyatake, Nandakumar, Ueda, Kobayashi, Kiga, Yamamura e Ito. "Enhancement of Binding Affinity of Folate to Its Receptor by Peptide Conjugation". International Journal of Molecular Sciences 20, n.º 9 (30 de abril de 2019): 2152. http://dx.doi.org/10.3390/ijms20092152.
Texto completo da fonteAu, Kin Man, Andrew Z. Wang e Steven I. Park. "Pretargeted delivery of PI3K/mTOR small-molecule inhibitor–loaded nanoparticles for treatment of non-Hodgkin’s lymphoma". Science Advances 6, n.º 14 (abril de 2020): eaaz9798. http://dx.doi.org/10.1126/sciadv.aaz9798.
Texto completo da fonteDadfar, Seyed Mohammad Mahdi, Sylwia Sekula-Neuner, Vanessa Trouillet, Hui-Yu Liu, Ravi Kumar, Annie K. Powell e Michael Hirtz. "Evaluation of click chemistry microarrays for immunosensing of alpha-fetoprotein (AFP)". Beilstein Journal of Nanotechnology 10 (16 de dezembro de 2019): 2505–15. http://dx.doi.org/10.3762/bjnano.10.241.
Texto completo da fonteYang, Bingquan, Yangxin Wang, Mariia Vorobii, Eric Sauter, Meike Koenig, Ravi Kumar, Cesar Rodriguez‐Emmenegger e Michael Hirtz. "Evaluation of Dibenzocyclooctyne and Bicyclononyne Click Reaction on Azido‐Functionalized Antifouling Polymer Brushes via Microspotting (Adv. Mater. Interfaces 16/2022)". Advanced Materials Interfaces 9, n.º 16 (junho de 2022): 2270092. http://dx.doi.org/10.1002/admi.202270092.
Texto completo da fonteGolkowski, Martin, e Thomas Ziegler. "Synthesis of Tetra(2-hydroxyethoxy)-Substituted Dibenzocyclooctyne Derivatives as Novel, Highly Hydrophilic Tool Compounds for Strain-Promoted Alkyne-Azide Cycloaddition Applications". Synthesis 45, n.º 09 (28 de março de 2013): 1207–14. http://dx.doi.org/10.1055/s-0032-1316875.
Texto completo da fonteKarsten, Lennard, Nils Janson, Vadim Le Joncour, Sarfaraz Alam, Benjamin Müller, Jayendrakishore Tanjore Ramanathan, Pirjo Laakkonen, Norbert Sewald e Kristian M. Müller. "Bivalent EGFR-Targeting DARPin-MMAE Conjugates". International Journal of Molecular Sciences 23, n.º 5 (23 de fevereiro de 2022): 2468. http://dx.doi.org/10.3390/ijms23052468.
Texto completo da fontePorcello, Alexandre, Paula Gonzalez-Fernandez, Annick Jeannerat, Cédric Peneveyre, Philippe Abdel-Sayed, Corinne Scaletta, Wassim Raffoul et al. "Thermo-Responsive Hyaluronan-Based Hydrogels Combined with Allogeneic Cytotherapeutics for the Treatment of Osteoarthritis". Pharmaceutics 15, n.º 5 (18 de maio de 2023): 1528. http://dx.doi.org/10.3390/pharmaceutics15051528.
Texto completo da fonteHellwinkel, Dieter, e Siegbert Bohnet. "Dibenzocycloocten-, Dibenzochalcocin- und Diarenochalconindione". Chemische Berichte 120, n.º 7 (julho de 1987): 1151–73. http://dx.doi.org/10.1002/cber.19871200711.
Texto completo da fonteChen, Min, Zhixin Liao e Daofeng Chen. "Four New Dibenzocyclooctene Lignans fromKadsura renchangiana". Helvetica Chimica Acta 87, n.º 6 (junho de 2004): 1368–76. http://dx.doi.org/10.1002/hlca.200490124.
Texto completo da fonteMa, Wen-Hui, Yan Lu e Dao-Feng Chen. "Dibenzocyclooctane Lignans from the Stems of Schisandra wilsoniana". Planta Medica 79, n.º 12 (9 de julho de 2013): 1051–55. http://dx.doi.org/10.1055/s-0032-1328747.
Texto completo da fonteMa, Wen-Hui, Jian-Cheng He, Peng-Shan Duan, Ting Han, Cheng-Jian Zheng e Lu-Ping Qin. "Dibenzocyclooctane lignans from the stems of Schisandra bicolor". Biochemical Systematics and Ecology 38, n.º 6 (dezembro de 2010): 1156–59. http://dx.doi.org/10.1016/j.bse.2010.10.011.
Texto completo da fonteMoore, J. A., e T. D. Mitchell. "REGIOSELECTIVE FORMATION OF β-KETOAMIDES IN THE DIBENZOCYCLOOCTANE FAMILY". Organic Preparations and Procedures International 20, n.º 2 (abril de 1988): 135–43. http://dx.doi.org/10.1080/00304948809355801.
Texto completo da fonteLu, Hua, e Geng-Tao Liu. "Anti-Oxidant Activity of Dibenzocyclooctene Lignans Isolated from Schisandraceae". Planta Medica 58, n.º 04 (agosto de 1992): 311–13. http://dx.doi.org/10.1055/s-2006-961473.
Texto completo da fonteCarroll, AR, e WC Taylor. "Intramolecular Oxidative Coupling of Aromatic Compounds. VI. An Efficient Synthesis of Some Dibenzocyclooctene Lignans". Australian Journal of Chemistry 47, n.º 5 (1994): 937. http://dx.doi.org/10.1071/ch9940937.
Texto completo da fonteChen, Min, Xiumei Xu, Zhihua Liao, Li Dong, Lei Li e Chengzhi Huang. "Neglschisandrins A-B: Two New Dibenzocyclooctene Lignans from Schisandra neglecta". Molecules 13, n.º 3 (3 de março de 2008): 548–55. http://dx.doi.org/10.3390/molecules13030548.
Texto completo da fonteJia, Zhengwei, Zhixin Liao e Daofeng Chen. "Two New Dibenzocyclooctene Lignans from the Water Extract ofKadsura spp." Helvetica Chimica Acta 88, n.º 8 (agosto de 2005): 2288–93. http://dx.doi.org/10.1002/hlca.200590163.
Texto completo da fonteFriscourt, Frédéric, Petr A. Ledin, Ngalle Eric Mbua, Heather R. Flanagan-Steet, Margreet A. Wolfert, Richard Steet e Geert-Jan Boons. "Polar Dibenzocyclooctynes for Selective Labeling of Extracellular Glycoconjugates of Living Cells". Journal of the American Chemical Society 134, n.º 11 (9 de março de 2012): 5381–89. http://dx.doi.org/10.1021/ja3002666.
Texto completo da fonteLiu, Xiaojun, Jian Zhang, Lin Shen, Jieqiong Liu, Jian Huang, Zhixiang Zhuang, Yongmei Yin, Xiang Wang, Xian Wang e Jiong Wu. "Evaluation of the safety, pharmacokinetics, and efficacy of JSKN003 in patients with advanced solid tumors: A phase I/II clinical study." Journal of Clinical Oncology 42, n.º 16_suppl (1 de junho de 2024): 3031. http://dx.doi.org/10.1200/jco.2024.42.16_suppl.3031.
Texto completo da fontete Grotenhuis, Colet, Naudin van den Heuvel, Jarl Ivar van der Vlugt e Bas de Bruin. "Catalytic Dibenzocyclooctene Synthesis via Cobalt(III)-Carbene Radical and ortho -Quinodimethane Intermediates". Angewandte Chemie 130, n.º 1 (6 de dezembro de 2017): 146–51. http://dx.doi.org/10.1002/ange.201711028.
Texto completo da fonteLi, Liang, Hai-Ying Ren, Xiao-Dong Yang, Jing-Feng Zhao, Gan-Peng Li e Hong-Bin Zhang. "Rubriflorin A and B, Two Novel Partially Saturated Dibenzocyclooctene Lignans fromSchisandra rubriflora". Helvetica Chimica Acta 87, n.º 11 (novembro de 2004): 2943–47. http://dx.doi.org/10.1002/hlca.200490265.
Texto completo da fonteLu, Yan, e Daofeng Chen. "Kadsutherins A–C: Three New Dibenzocyclooctane Lignans from the Stems ofKadsura Species". Helvetica Chimica Acta 89, n.º 5 (maio de 2006): 895–901. http://dx.doi.org/10.1002/hlca.200690092.
Texto completo da fontete Grotenhuis, Colet, Naudin van den Heuvel, Jarl Ivar van der Vlugt e Bas de Bruin. "Catalytic Dibenzocyclooctene Synthesis via Cobalt(III)-Carbene Radical and ortho -Quinodimethane Intermediates". Angewandte Chemie International Edition 57, n.º 1 (6 de dezembro de 2017): 140–45. http://dx.doi.org/10.1002/anie.201711028.
Texto completo da fonteYang, Bing-You, Jiang-Tao Guo, Zu-Yi Li, Chang-Fu Wang, Zhi-Bin Wang, Qiu-Hong Wang e Hai-Xue Kuang. "New Thymoquinol Glycosides and Neuroprotective Dibenzocyclooctane Lignans from the Rattan Stems ofSchisandra chinensis". Chemistry & Biodiversity 13, n.º 9 (setembro de 2016): 1118–25. http://dx.doi.org/10.1002/cbdv.201500311.
Texto completo da fontePelter, Andrew, Peter Satchwell, Robert S. Ward e Keith Blake. "Effective, direct biomimetic synthesis of dibenzocyclooctene lignans by hypervalent iodine oxidation of phenolic dibenzylbutyrolactones". Journal of the Chemical Society, Perkin Transactions 1, n.º 18 (1995): 2201. http://dx.doi.org/10.1039/p19950002201.
Texto completo da fonteXUE, J., G. LIU, H. WEI e Y. PAN. "Antioxidant activity of two dibenzocyclooctene lignans on the aged and ischemic brain in rats☆". Free Radical Biology and Medicine 12, n.º 2 (1992): 127–35. http://dx.doi.org/10.1016/0891-5849(92)90006-3.
Texto completo da fonteTerzic, Vida, Guillaume Pousse, Rachel Méallet-Renault, Philippe Grellier e Joëlle Dubois. "Dibenzocyclooctynes: Effect of Aryl Substitution on Their Reactivity toward Strain-Promoted Alkyne–Azide Cycloaddition". Journal of Organic Chemistry 84, n.º 13 (3 de junho de 2019): 8542–51. http://dx.doi.org/10.1021/acs.joc.9b00895.
Texto completo da fonte