Статті в журналах з теми "Morpholino Monomers"
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Ознайомтеся з топ-29 статей у журналах для дослідження на тему "Morpholino Monomers".
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Paul, Sibasish, Bappaditya Nandi, Sankha Pattanayak, and Surajit Sinha. "Synthesis of 5-alkynylated uracil–morpholino monomers using Sonogashira coupling." Tetrahedron Letters 53, no. 32 (August 2012): 4179–83. http://dx.doi.org/10.1016/j.tetlet.2012.05.141.
Повний текст джерелаPaul, Sibasish, Santanu Jana, Jhuma Bhadra, and Surajit Sinha. "Photophysical studies and submicron ring formation of morpholino U-nucleoside monomers." Chemical Communications 49, no. 96 (2013): 11278. http://dx.doi.org/10.1039/c3cc45082a.
Повний текст джерелаPaul, Sibasish, Bappaditya Nandi, Sankha Pattanayak, and Surajit Sinha. "ChemInform Abstract: Synthesis of 5-Alkynylated Uracil-Morpholino Monomers Using Sonogashira Coupling." ChemInform 43, no. 47 (October 30, 2012): no. http://dx.doi.org/10.1002/chin.201247164.
Повний текст джерелаVejlegaard, Kim, Sibasish Paul, Tamer Kosbar, Jesper Wengel, and Marvin H. Caruthers. "Oligodeoxynucleotides containing 2′-amino-LNA nucleotides as constrained morpholino phosphoramidate and phosphorodiamidate monomers." Bioorganic & Medicinal Chemistry Letters 27, no. 14 (July 2017): 3173–76. http://dx.doi.org/10.1016/j.bmcl.2017.05.023.
Повний текст джерелаPattanayak, Sankha, Sibasish Paul, Bappaditya Nandi, and Surajit Sinha. "Improved Protocol for the Synthesis of Flexibly Protected Morpholino Monomers from Unprotected Ribonucleosides." Nucleosides, Nucleotides and Nucleic Acids 31, no. 11 (November 2012): 763–82. http://dx.doi.org/10.1080/15257770.2012.724491.
Повний текст джерелаCale, Jessica M., Kane Greer, Sue Fletcher, and Steve D. Wilton. "Proof-of-Concept: Antisense Oligonucleotide Mediated Skipping of Fibrillin-1 Exon 52." International Journal of Molecular Sciences 22, no. 7 (March 27, 2021): 3479. http://dx.doi.org/10.3390/ijms22073479.
Повний текст джерелаNandi, Bappaditya, Sankha Pattanayak, Sibasish Paul, and Surajit Sinha. "Synthesis of Nucleobase-Functionalized Morpholino-Modified Nucleoside Monomers Through Palladium-Catalyzed Cross-Coupling Reactions." European Journal of Organic Chemistry 2013, no. 7 (January 18, 2013): 1271–86. http://dx.doi.org/10.1002/ejoc.201201384.
Повний текст джерелаPattanayak, Sankha, Sibasish Paul, Bappaditya Nandi, and Surajit Sinha. "ChemInform Abstract: Improved Protocol for the Synthesis of Flexibly Protected Morpholino Monomers from Unprotected Ribonucleosides." ChemInform 44, no. 17 (April 4, 2013): no. http://dx.doi.org/10.1002/chin.201317042.
Повний текст джерелаNandi, Bappaditya, Sankha Pattanayak, Sibasish Paul, and Surajit Sinha. "ChemInform Abstract: Synthesis of Nucleobase-Functionalized Morpholino-Modified Nucleoside Monomers Through Palladium-Catalyzed Cross-Coupling Reactions." ChemInform 44, no. 35 (August 8, 2013): no. http://dx.doi.org/10.1002/chin.201335159.
Повний текст джерелаGrigale-Soročina, Zane, Elina Vindedze, Julija Kozela, and Ingmārs Birks. "Evaluation of Reactive Diluent Impact on Stability of Systems Viscosity in UV-Curable Compositions." Solid State Phenomena 320 (June 30, 2021): 150–54. http://dx.doi.org/10.4028/www.scientific.net/ssp.320.150.
Повний текст джерелаHuang, Weiwei, and Jin-Ho Jang. "Photografting of PET Fabrics with Vinyl Pyrrolidone and Acryloyl Morpholine Monomers." Textile Coloration and Finishing 20, no. 5 (October 27, 2008): 28–34. http://dx.doi.org/10.5764/tcf.2008.20.5.028.
Повний текст джерелаOzcan, Fatma, Zekeriya Dogruyol, and Sevnur Keskin Dogruyol. "4-methyl-4-[2-(naphthalene)-2-oxoethyl] morpholin-4-ium iodide as a water soluble photoinitiator." Polimery 68, no. 4 (June 27, 2023): 215–20. http://dx.doi.org/10.14314/polimery.2023.4.3.
Повний текст джерелаPeng, Xingzhou, Marc Behl, Pengfei Zhang, Magdalena Mazurek-Budzyńska, Yakai Feng, and Andreas Lendlein. "Synthesis and Characterization of Multiblock Poly(Ester-Amide-Urethane)s." MRS Advances 2, no. 47 (2017): 2551–59. http://dx.doi.org/10.1557/adv.2017.486.
Повний текст джерелаAldea, Anca, Ana-Maria Albu, Alina Nicolescu, and Victorita Tecuceanu. "Kinetics of Free Radical Polymerization of N-Substituted Amides and Their Structural Implications." Advances in Materials Science and Engineering 2016 (2016): 1–9. http://dx.doi.org/10.1155/2016/6430416.
Повний текст джерелаInce, Ahmet, and Niyazi Bicak. "Crosslinking Copolymerization of Vinyl Monomers Using Non-Vinyl Crosslinker: Morpholine Substituted Poly (vinyl methyl ketone)." Macromolecular Symposia 352, no. 1 (June 2015): 38–41. http://dx.doi.org/10.1002/masy.201400149.
Повний текст джерелаSameni, Farzaneh, Basar Ozkan, Sarah Karmel, Daniel S. Engstrøm, and Ehsan Sabet. "Large Scale Vat-Photopolymerization of Investment Casting Master Patterns: The Total Solution." Polymers 14, no. 21 (October 29, 2022): 4593. http://dx.doi.org/10.3390/polym14214593.
Повний текст джерелаLi, Shao-Lu, Pengfei Wu, Juntao Wang, Jing Wang, and Yunxia Hu. "Fabrication of high performance polyamide reverse osmosis membrane from monomer 4-morpholino-m-phenylenediamine and tailoring with zwitterions." Desalination 473 (January 2020): 114169. http://dx.doi.org/10.1016/j.desal.2019.114169.
Повний текст джерелаVejjasilpa, Ketpat, Iram Maqsood, Michaela Schulz-Siegmund, and Michael C. Hacker. "Adjustable Thermo-Responsive, Cell-Adhesive Tissue Engineering Scaffolds for Cell Stimulation through Periodic Changes in Culture Temperature." International Journal of Molecular Sciences 24, no. 1 (December 29, 2022): 572. http://dx.doi.org/10.3390/ijms24010572.
Повний текст джерелаClay, Anthony M., Joshua R. Mitchell, Zachary R. Boelter, and John J. La Scala. "Superior Properties through Feedstock Development for Vat Photopolymerization Additive Manufacturing of High-Performance Biobased Feedstocks." Materials 14, no. 17 (August 26, 2021): 4843. http://dx.doi.org/10.3390/ma14174843.
Повний текст джерелаSielaff, Bernhard, and Jan R. Andreesen. "Analysis of the nearly identical morpholine monooxygenase-encoding mor genes from different Mycobacterium strains and characterization of the specific NADH : ferredoxin oxidoreductase of this cytochrome P450 system." Microbiology 151, no. 8 (August 1, 2005): 2593–603. http://dx.doi.org/10.1099/mic.0.28039-0.
Повний текст джерелаShi, Chang-Xia, Yu-Ting Guo, Yu-Huan Wu, Zhao-Yue Li, Yao-Zong Wang, Fu-Sheng Du, and Zi-Chen Li. "Synthesis and Controlled Organobase-Catalyzed Ring-Opening Polymerization of Morpholine-2,5-Dione Derivatives and Monomer Recovery by Acid-Catalyzed Degradation of the Polymers." Macromolecules 52, no. 11 (May 29, 2019): 4260–69. http://dx.doi.org/10.1021/acs.macromol.8b02498.
Повний текст джерелаAngira, Deekshi, Althaf Shaik, Sivapriya Kirubakaran, and Vijay Thiruvenkatam. "Exploring a solvated dimer of Gefitinib: a quantitative analysis." Acta Crystallographica Section C Structural Chemistry 74, no. 8 (July 19, 2018): 944–50. http://dx.doi.org/10.1107/s2053229618009671.
Повний текст джерелаMorozova, Sofia M., Alexander S. Shaplov, Elena I. Lozinskaya, Petr S. Vlasov, Haritz Sardon, David Mecerreyes, and Yakov S. Vygodskii. "Poly(ionic liquid)-based polyurethanes having imidazolium, ammonium, morpholinium or pyrrolidinium cations." High Performance Polymers 29, no. 6 (April 10, 2017): 691–703. http://dx.doi.org/10.1177/0954008317701551.
Повний текст джерелаVenediktov, E. A., E. Yu Tulikova та V. E. Maizlish. "Photogeneration of singlet molecular oxygen (1O2, 1Δ g ) using monomeric and aggregated forms of copper tetra-4-(morpholine-4-yl)-tetra-5-(2-naphthoxy)phthalocyanine in organic solvents". Russian Journal of General Chemistry 82, № 6 (червень 2012): 1145–52. http://dx.doi.org/10.1134/s1070363212060187.
Повний текст джерелаPapis, Marta, Camilla Loro, Michele Penso, Gianluigi Broggini, and Francesca Foschi. "Synthesis of Morpholino Nucleosides Starting From Enantiopure Glycidol." Organic Chemistry Frontiers, 2022. http://dx.doi.org/10.1039/d2qo00400c.
Повний текст джерелаBhadra, Jhuma, Sankha Pattanayak, and Surajit Sinha. "Synthesis of Morpholino Monomers, Chlorophosphoramidate Monomers, and Solid‐Phase Synthesis of Short Morpholino Oligomers." Current Protocols in Nucleic Acid Chemistry 62, no. 1 (September 2015). http://dx.doi.org/10.1002/0471142700.nc0465s62.
Повний текст джерелаDas, Arnab, Atanu Ghosh, and Surajit Sinha. "C5-Pyrimidine-Functionalized Morpholino Oligonucleotides Exhibit Differential Binding Affinity, Target Specificity and Lipophilicity." Organic & Biomolecular Chemistry, 2023. http://dx.doi.org/10.1039/d2ob01759h.
Повний текст джерелаKundu, Jayanta, Ujjwal Ghosh, Atanu Ghosh, Sankha Pattanayak, Arnab Das, and Surajit Sinha. "Synthesis of Chlorophosphoramidate Monomer Morpholinos and PMOs." Current Protocols 3, no. 2 (February 2023). http://dx.doi.org/10.1002/cpz1.686.
Повний текст джерелаDU PREEZ, J. G. H., T. I. A. GERBER, and O. KNOESEN. "ChemInform Abstract: THE CHEMISTRY OF RHENIUM AND TECHNETIUM. PART IV. FACILE CLEAVAGE OF THE TECHNETIUM-OXYGEN DOUBLE BOND IN THE OXOTETRACHLOROTECHNETIUM(V) ANION BY MORPHOLINE-N-CARBODITHIOATE TO YIELD THE EIGHT-COORDINATE MONOMERIC TETRACARBODITHIOATE." Chemischer Informationsdienst 16, no. 36 (September 10, 1985). http://dx.doi.org/10.1002/chin.198536273.
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