Facile synthesis and antiproliferative activity of new 3-cyanopyridines.
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- BMC Chemistry, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s13065-019-0652-1
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Works in BMC Chemistry, 2019, Vol 13, Issue 1
Results: 142
1
2
Recent advances in the use of benzimidazoles as corrosion inhibitors.
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- BMC Chemistry, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s13065-019-0655-y
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- Article
3
Evaluation of an online, real-time, soft-photon ionisation time-of-flight mass spectrometer for mainstream tobacco smoke analysis.
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- BMC Chemistry, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s13065-019-0654-z
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- Article
4
Pressurized hot water extraction of hydrosable tannins from Phyllanthus tenellus Roxb.
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- BMC Chemistry, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s13065-019-0653-0
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5
Contribution of aroma compounds to the antioxidant properties of roasted white yam (Dioscorea rotundata).
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- BMC Chemistry, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s13065-019-0650-3
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6
A facile and one-pot synthesis of new tetrahydrobenzo[b]pyrans in water under microwave irradiation.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0651-2
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- Article
7
Potentiometric sensor for iron (III) quantitative determination: experimental and computational approaches.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0648-x
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8
Preparation of sub-microspherical Fe<sub>3</sub>O<sub>4</sub>@PDA-Pd NPs catalyst and application in catalytic hydroreduction reaction of halogenated aromatic nitro compounds to prepare halogenated aromatic amines.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0649-9
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- Article
9
A novel electrochemical aptasensor for fumonisin B<sub>1</sub> determination using DNA and exonuclease-I as signal amplification strategy.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0646-z
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- Article
10
Study of the mechanism of change in flavonoid composition in the processing of Chrysanthemum morifolium (Ramat.) Tzvel. 'Boju'.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0645-0
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11
Benzimidazole Schiff base derivatives: synthesis, characterization and antimicrobial activity.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0642-3
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- Article
12
Mechanistic formation of hazardous molecular heterocyclic amines from high temperature pyrolysis of model biomass materials: cellulose and tyrosine.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0644-1
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13
Direct analysis of volatile components from intact jujube by carbon fiber ionization mass spectrometry.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0641-4
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14
gem-Difluorobisarylic derivatives: design, synthesis and anti-inflammatory effect.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0640-5
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15
A green and facile synthesis of an industrially important quaternary heterocyclic intermediates for baricitinib.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0639-y
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- Article
16
Biorenewable triblock copolymers consisting of l-lactide and ε-caprolactone for removing organic pollutants from water: a lifecycle neutral solution.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0638-z
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17
New potentiometric sensors for methylphenidate detection based on host–guest interaction.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0634-3
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- Article
18
Crosslinked sulfonated polyacrylamide (Cross-PAA-SO<sub>3</sub>H) tethered to nano-Fe<sub>3</sub>O<sub>4</sub> as a superior catalyst for the synthesis of 1,3-thiazoles.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0637-0
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- Article
19
Green synthesis of spiro[indoline-3,4′-pyrano[2,3-c]pyrazoles] using Fe<sub>3</sub>O<sub>4</sub>@l-arginine as a robust and reusable catalyst.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0636-1
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- Article
20
Two novel UPLC methods utilizing two different analytical columns and different detection approaches for the simultaneous analysis of velpatasvir and sofosbuvir: application to their co-formulated tablet.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0635-2
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21
Construction of a novel quinoxaline as a new class of Nrf2 activator.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0633-4
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22
Design, efficient synthesis and molecular docking of some novel thiazolyl-pyrazole derivatives as anticancer agents.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0632-5
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23
Designing, synthesis and characterization of 2-aminothiazole-4-carboxylate Schiff bases; antimicrobial evaluation against multidrug resistant strains and molecular docking.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0631-6
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- Article
24
Chemical modification of Bombyx mori silk fibers with vinyl groups for thiol-ene click chemistry.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0630-7
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- Article
25
Synthesis, molecular docking and biological potentials of new 2-(4-(2-chloroacetyl) piperazin-1-yl)-N-(2-(4-chlorophenyl)-4-oxoquinazolin-3(4H)-yl)acetamide derivatives.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0629-0
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- Article
26
Graphene-based biosensors for the detection of prostate cancer protein biomarkers: a review.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0611-x
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27
A rapid and sensitive UPLC-MS/MS method for the determination of flibanserin in rat plasma: application to a pharmacokinetic study.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0620-9
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- Article
28
Atom transfer radical polymer-modified paper for improvement in protein fixation in paper-based ELISA.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0622-7
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29
Design, synthesis, and preliminary biological evaluation of catalpol propionates as antiaging drugs.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0626-3
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30
Treatment and characterization of phosphorus from synthetic wastewater using aluminum plate electrodes in the electrocoagulation process.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0628-1
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31
A review of bioanalytical techniques for evaluation of cannabis (Marijuana, weed, Hashish) in human hair.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0627-2
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32
Chemical constituents and coagulation activity of Syringa oblata Lindl flowers.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0621-8
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33
Thermodynamic properties of some isomeric 5-(nitrophenyl)-furyl-2 derivatives.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0619-2
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34
Protective effect of blackthorn fruits (Prunus spinosa) against tartrazine toxicity development in albino Wistar rats.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0610-y
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- Article
35
Secondary metabolites from the Aspergillus sp. in the rhizosphere soil of Phoenix dactylifera (Palm tree).
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0624-5
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36
Pharmacological significance of heterocyclic 1H-benzimidazole scaffolds: a review.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0625-4
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37
Identification of novel antifungal agents: antimicrobial evaluation, SAR, ADME–Tox and molecular docking studies of a series of imidazole derivatives.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0623-6
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- Article
38
Three smart spectrophotometric methods for resolution of severely overlapped binary mixture of Ibuprofen and Paracetamol in pharmaceutical dosage form.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0618-3
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39
Synthesis, anti-leishmanial and molecular docking study of bis-indole derivatives.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0617-4
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- Article
40
Sulfonic acid-functionalized polyallylamine (sevelamer) as an efficient reusable strong solid acid catalyst for the synthesis of xanthenes derivatives.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0609-4
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- Article
41
Binding interaction of sodium benzoate food additive with bovine serum albumin: multi-spectroscopy and molecular docking studies.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0615-6
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- Article
42
Computational approaches: discovery of GTPase HRas as prospective drug target for 1,3-diazine scaffolds.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0613-8
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- Article
43
Peanut shell as a green biomolecule support for anchoring Cu<sub>2</sub>O: a biocatalyst for green synthesis of 1,2,3-triazoles under ultrasonic irradiation.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0612-9
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- Article
44
Identification of C-glycosyl flavones by high performance liquid chromatography electrospray ionization mass spectrometry and quantification of five main C-glycosyl flavones in Flickingeria fimbriata.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0616-5
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45
Analysis of chemical constituents in mainstream bidi smoke.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0614-7
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- Article
46
Oligosaccharide-based quality evaluation of Atractylodis rhizome and a strategy for simplifying its quality control.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0605-8
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47
In-silico molecular design of heterocyclic benzimidazole scaffolds as prospective anticancer agents.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0608-5
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- Article
48
A minireview of hydroamination catalysis: alkene and alkyne substrate selective, metal complex design.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0606-7
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49
Design, synthesis, and biological evaluation of novel N<sup>4</sup>-substituted sulfonamides: acetamides derivatives as dihydrofolate reductase (DHFR) inhibitors.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0603-x
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50
Electrodeposition of amorphous molybdenum sulfide thin film for electrochemical hydrogen evolution reaction.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0600-0
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