Works matching DE "PROTECTIVE groups (Chemistry)"
Results: 35
Solid phase synthesis of two muramyl pentapeptide derivatives.
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- Journal of Carbohydrate Chemistry, 2016, v. 35, n. 3, p. 161, doi. 10.1080/07328303.2016.1154153
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- Article
Identification of a GDI displacement factor that releases endosomal Rab GTPases from Rab-GDI.
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- EMBO Journal, 1997, v. 16, n. 3, p. 465, doi. 10.1093/emboj/16.3.465
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Immuno–spin trapping of DNA radicals.
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- Nature Methods, 2006, v. 3, n. 2, p. 123, doi. 10.1038/nmeth852
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Biomass/adsorbent electrostatic interactions in expanded bed adsorption: A zeta potential study.
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- Biotechnology & Bioengineering, 2003, v. 83, n. 2, p. 149, doi. 10.1002/bit.10654
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- Article
Understanding Tetrahydropyranyl as a Protecting Group in Peptide Chemistry.
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- ChemistryOpen, 2017, v. 6, n. 2, p. 168, doi. 10.1002/open.201600156
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Synthesis of 2-[2-(3,4,5-Trimethoxybenzoyloxy)ethyl]pyrrolidine Hydrochloride Controlled by GC-MS, <sup>1</sup>H and <sup>13</sup>C NMR Analyses.
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- Turkish Journal of Chemistry, 2005, v. 29, n. 6, p. 641
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No need for protection.
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- TCE: The Chemical Engineer, 2007, n. 791, p. 17
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A cost-effective deprotection catalyst.
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- Chemical Engineering, 2008, v. 115, n. 7, p. 18
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- Article
Professor Horst Kunz: A Tribute.
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- ARKIVOC: Online Journal of Organic Chemistry, 2021, v. 2021, p. 1, doi. 10.24820/ark.5550190.p001.481
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- Article
Antioxidants in eggs of great tits Parus major from Chernobyl and hatching success.
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- Journal of Comparative Physiology B: Biochemical, Systemic & Environmental Physiology, 2008, v. 178, n. 6, p. 735, doi. 10.1007/s00360-008-0262-z
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Blocking Resistance of Membrane during Cake Filtration of Dilute Suspensions.
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- AIChE Journal, 2005, v. 51, n. 9, p. 2609, doi. 10.1002/aic.10550
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Ionic Liquids for the Chemical Recycling of Polymeric Materials and Control of Their Solubility.
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- Chemical Record, 2023, v. 23, n. 8, p. 1, doi. 10.1002/tcr.202200269
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- Article
Application of the site blocking method to the investigation of the kinetics of carbon monoxide electrooxidation on nanostructured Pt.
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- Journal of Solid State Electrochemistry, 2014, v. 18, n. 5, p. 1195, doi. 10.1007/s10008-013-2251-8
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Chloroglycidate Synthesis of a Precursor of Natural 3-Deoxy-D-manno-octulosonic Acid with Combined Protective Groups.
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- Russian Journal of General Chemistry, 2004, v. 74, n. 2, p. 225, doi. 10.1023/B:RUGC.0000025507.24993.c6
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- Article
The Cyanopivaloyl Ester: A Protecting Group in the Assembly of Oligorhamnans.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 31, p. 5282, doi. 10.1002/ejoc.201600956
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Labeled Nucleoside Triphosphates with Reversibly Terminating Aminoalkoxyl Groups.
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- Nucleosides, Nucleotides & Nucleic Acids, 2010, v. 29, n. 11/12, p. 879, doi. 10.1080/15257770.2010.536191
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- Article
Tetraindole Derivatives of Porphyrins as Building Blocks in the Synthesis of Monodisperse Polyphenols.
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- Doklady Chemistry, 2018, v. 478, n. 1, p. 1, doi. 10.1134/S0012500818010020
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Współczesne perspektywy rozwoju lakierów proszkowych.
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- Polimery, 2008, v. 53, n. 7/8, p. 513
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Enrichment and Purification of Polyphenol Extract from Sphallerocarpus gracilis Stems and Leaves and in Vitro Evaluation of DNA Damage-Protective Activity and Inhibitory Effects of α-Amylase and α-Glucosidase.
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- Molecules, 2015, v. 20, n. 12, p. 21442, doi. 10.3390/molecules201219780
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- Article
JNK Contributes to Hif-1α Regulation in Hypoxic Neurons.
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- Molecules, 2010, v. 15, n. 1, p. 114, doi. 10.3390/molecules15010114
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- Article
Why are most phospholipidosis inducers also hERG blockers?
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- Archives of Toxicology, 2017, v. 91, n. 12, p. 3885, doi. 10.1007/s00204-017-1995-9
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Effect of macrocyclic nickel(II) and copper(II) complexes on the reaction of trypsin with a soybean bioinhibitor.
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- Theoretical & Experimental Chemistry, 2008, v. 44, n. 4, p. 260, doi. 10.1007/s11237-008-9033-x
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Blocking and pseudoblocking: The reply of Rattus norvegicus to Apis mellifera.
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- Quarterly Journal of Experimental Psychology, 2008, v. 61, n. 8, p. 1186, doi. 10.1080/17470210701480238
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Direct synthesis of cellulose adipate derivatives using adipic anhydride.
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- Cellulose, 2012, v. 19, n. 4, p. 1279, doi. 10.1007/s10570-012-9724-2
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- Article
A Synthesis Route of an Oral Antidiabetic Drug-Linagliptin based on the Removal of Protective Group.
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- Acta Microscopica, 2020, v. 29, n. 1, p. 244
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- Article
Use of Cleavable Coordinating Rings as Protective Groups in the Synthesis of a Rotaxane with an Axis that Incorporates More Chelating Groups Than Threaded Macrocycles.
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- Chemistry - A European Journal, 2013, v. 19, n. 38, p. 12815, doi. 10.1002/chem.201301717
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A Novel Base-Induced Isomerization Gives Access to Unprecedented ( E)- exo-Glycals.
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- Chemistry - A European Journal, 2013, v. 19, n. 35, p. 11547, doi. 10.1002/chem.201300969
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Protectors against doxorubicin-induced cardiotoxicity: Flavonoids.
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- Cell Biology & Toxicology, 2007, v. 23, n. 1, p. 39, doi. 10.1007/s10565-006-0139-4
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'Moth-eaten effect' driven by Pauli blocking, revealed for cooper pairs.
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- JETP Letters, 2010, v. 92, n. 7, p. 484, doi. 10.1134/S0021364010190112
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- Article
Cyclopentyl: A Novel Protective Group for Phenols.
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- Synthetic Communications, 2007, v. 37, n. 24, p. 4309, doi. 10.1080/00397910701575855
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Cyclopentyl: A Novel Protective Group for Phenols.
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- Synthetic Communications, 2007, v. 37, n. 17, p. 2877, doi. 10.1080/00397910701471253
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Selective Reductions of C ‐(4,6‐ O ‐Benzylidene‐β‐d‐glucopyranosyl) Nitromethane.
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- Synthetic Communications, 2005, v. 35, n. 12, p. 1589, doi. 10.1081/SCC-200061554
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Protective Agent-free Preparation of Gold Nanoplates and Nanorods in Aqueous HAuC1<sub>4</sub> Solutions Using Gas-Liquid Interface Discharge.
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- Chemistry Letters, 2007, v. 36, n. 9, p. 1088, doi. 10.1246/cl.2007.1088
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A structural link between inactivation and block of a K<sup>+</sup> channel.
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- Nature Structural & Molecular Biology, 2008, v. 15, n. 6, p. 605, doi. 10.1038/nsmb.1430
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Acetylation serves as a protective group in noscapine biosynthesis in opium poppy.
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- Nature Chemical Biology, 2015, v. 11, n. 2, p. 104, doi. 10.1038/nchembio.1717
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