0000000001309930

AUTHOR

Grzegorz Schroeder

showing 12 related works from this author

Biomass and Extracts of Algae as Material for Cosmetics

2015

Algae biomassAlgaemedia_common.quotation_subjectBotanyBiomassBiologybiology.organism_classificationCosmeticsmedia_common
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The influence of fluorine position on the properties of fluorobenzoxaboroles

2015

5-Fluoro-2,1-benzoxaborol-1(3H)-ol, a potent antifungal drug also known as Tavaborole or AN2690, has been compared with its three isomers in terms of its activity against several fungi as well as pKa and multinuclear NMR characterization. The molecular and crystal structure of 6-fluoro-2,1-benzoxaborol-1(3H)-ol was determined and compared with that of AN2690.

Boron CompoundsModels Molecularcrystal structureAntifungal AgentsMagnetic Resonance SpectroscopyHalogenationStereochemistryAntifungal drugchemistry.chemical_elementCrystal structureCrystallography X-RayBiochemistrybenzoxaborolesIsomerismDrug DiscoveryHumansMolecular BiologytavaboroleTavaboroleChemistryOrganic Chemistryantifungal activityFungiFluorineBridged Bicyclo Compounds HeterocyclicMycosesFluorineBioorganic Chemistry
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Novel 2,6-disubstituted phenylboronic compounds - Synthesis, crystal structures, solution behaviour and reactivity

2015

Abstract 2,6-Diformylphenylboronic acid has been synthesized and characterized both in the solid state as well as in solution. In crystal, an unusual structural pattern has been found with the formation of intermolecular hydrogen bonds by B(OH) 2 and CHO groups as well as water molecules. In solution tautomeric equilibrium with the formation of oxaborole ring by one of the formyl groups was proved on the basis of multinuclear NMR spectroscopy. The title compound reacts with secondary mono- and diamines to form various types of substituted benzoxaboroles, which have been characterized by XRD and spectroscopic methods.

crystal structureboronic acidsChemistryHydrogen bondOrganic ChemistryCrystal structureNuclear magnetic resonance spectroscopyRing (chemistry)BiochemistryTautomerreductive aminationtautomeric equilibriaInorganic ChemistryCrystalbenzoxaborolesPolymer chemistryMaterials ChemistryMoleculeReactivity (chemistry)Physical and Theoretical ChemistryJournal of Organometallic Chemistry
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Supercritical Algal Extracts: A Source of Biologically Active Compounds from Nature

2015

The paper discusses the potential applicability of the process of supercritical fluid extraction (SFE) in the production of algal extracts with the consideration of the process conditions and yields. State of the art in the research on solvent-free isolation of biologically active compounds from the biomass of algae was presented. Various aspects related with the properties of useful compounds found in cells of microalgae and macroalgae were discussed, including their potential applications as the natural components of plant protection products (biostimulants and bioregulators), dietary feed and food supplements, and pharmaceuticals. Analytical methods of determination of the natural compou…

biologyChemistrySupercritical fluid extractionBiomassBiological activityGeneral ChemistryPulp and paper industrybiology.organism_classificationSupercritical fluidProcess conditionslcsh:ChemistryAlgaelcsh:QD1-999Environmental chemistryEconomic analysisJournal of Chemistry
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Analysis of Green Algae Extracts

2015

biologyChemistryBotanyBiomassGreen algaebiology.organism_classification
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Supercritical fluid extraction of algae enhances levels of biologically active compounds promoting plant growth

2016

The aim of this research was to screen plant growth biostimulant properties of supercritical CO2 macroalgal extracts. To this end secondary metabolites were isolated from the biomass of marine macroalgae from the Baltic Sea (species of Polysiphonia, Ulva and Cladophora). Chemical characteristics of the algal extracts were determined by inductively coupled plasma atomic emission spectroscopy for inorganic constituents and high-performance liquid chromatography and spectrophotometry for organic constituents. Inorganic (macro- and microelements) and organic (plant hormones: auxins and cytokinins; polyphenols) compounds were detected in the extract. Algal extracts were tested primarily on garde…

0106 biological scienceschemistry.chemical_classification010401 analytical chemistrySupercritical fluid extractionBiomassPlant ScienceAquatic ScienceBiologyplant biostimulants01 natural sciences0104 chemical sciencesLepidium sativumchemistry.chemical_compoundchemistryAuxinPolyphenol010608 biotechnologyChlorophyllBotanyShootactive compoundsPoaceaebaltic macroalgaesupercritical fluid extractionbioregulatorsEuropean Journal of Phycology
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Identification and Ecology of Macroalgae Species Existing in Poland

2015

Ecologybusiness.industryEcology (disciplines)Distribution (economics)Identification (biology)Biologybusiness
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“Twin” phosphorous atoms of tetraethyl 2-methyl-piperyd-1-ylmethylenebisphosphonates

2007

Recently, bisaminophosphonates found applications as therapeutic agents for curing bone disorders. When trying to relate the structures of substituted piperid-1-ylmethylenebisphosphonic with their biological properties, non-typical findings that in 31P NMR spectra of 2-methyl-piperid-1-ylmethylenebisphosphonic and 2-ethyl-piperid-1-ylmethylenebisphosphonic acids, two separate singlets from each of the phosphonic groups were observed, while their analogues bearing substituent in position 3 exhibit only one signal. Their presence was explained by freezing of the molecular motions by strong hydrogen bonding between NH and P = O atoms. In this work, synthesis as well as spectroscopic and theore…

31p nmr spectraCrystallographychemistry.chemical_compoundChemistryStereochemistryHydrogen bondBiological propertyHeteroatomMolecular motionSubstituentMoleculeGeneral ChemistryCuring (chemistry)Heteroatom Chemistry
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Valuable natural products from marine and freshwater macroalgae obtained from supercritical fluid extracts

2017

The biologically active compounds (fatty acids, pigments, phenolics, and flavonoid content) were studied in supercritical fluid extracts from the biomass of marine (Ulva clathrata, Cladophora glomerata, Polysiphonia fucoides, and their multi-species mixture) and freshwater (C. glomerata) macroalgae. Different extraction techniques were used in order to compare differences in the biologically active compound composition of the macroalgal extracts. The results indicated that the saturated and unsaturated fatty acids ranged from C9:0 to C22:0. The analysis of differences in the composition of unsaturated to saturated fatty acids in extracts showed that palmitic acid (C16:0) and oleic acid (C18…

0106 biological sciencesPlant ScienceAquatic ScienceBiology01 natural sciencesfatty acidsArticlePalmitic acidchemistry.chemical_compoundAlgaeBotanyFood scienceCarotenoidpolyphenolschemistry.chemical_classificationbioactive compounds010405 organic chemistry010604 marine biology & hydrobiologyExtraction (chemistry)Supercritical fluid extractionfood and beveragesUlva clathratabiology.organism_classificationantioxidant properties0104 chemical sciencesOleic acidchemistryPolyphenolsupercritical fluid extractionDPPHJournal of Applied Phycology
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CCDC 1029677: Experimental Crystal Structure Determination

2015

Related Article: Agnieszka Adamczyk-Woźniak, Krzysztof Ejsmont, Błażej Gierczyk, Ewa Kaczorowska, Alicja Matuszewska, Grzegorz Schroeder, Andrzej Sporzyński, Bartosz Zarychta|2015|J.Organomet.Chem.|788|36|doi:10.1016/j.jorganchem.2015.04.026

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(26-Diformylphenyl)boronic acid monohydrateExperimental 3D Coordinates
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CCDC 1029678: Experimental Crystal Structure Determination

2015

Related Article: Agnieszka Adamczyk-Woźniak, Krzysztof Ejsmont, Błażej Gierczyk, Ewa Kaczorowska, Alicja Matuszewska, Grzegorz Schroeder, Andrzej Sporzyński, Bartosz Zarychta|2015|J.Organomet.Chem.|788|36|doi:10.1016/j.jorganchem.2015.04.026

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters7-(Morpholin-4-ylmethyl)-13-dihydro-1-hydroxybenzo[c][21]oxaboroleExperimental 3D Coordinates
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CCDC 1027467: Experimental Crystal Structure Determination

2015

Related Article: Agnieszka Adamczyk-Woźniak, Małgorzata K. Cabaj, Paulina M. Dominiak, Patrycja Gajowiec, Błażej Gierczyk, Jacek Lipok, Łukasz Popenda, Grzegorz Schroeder, Ewelina Tomecka, Piotr Urbański, Dorota Wieczorek, Andrzej Sporzyński|2015|Bioorg.Chem.|60|130|doi:10.1016/j.bioorg.2015.05.004

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates6-fluoro-21-benzoxaborol-1(3H)-ol
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