Works matching DE "METHOXYMETHYL compounds"
Results: 31
Two Possible Side Reaction Pathways during Furanic Etherification.
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- Catalysts (2073-4344), 2018, v. 8, n. 9, p. 383, doi. 10.3390/catal8090383
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- Article
Mass spectrometric investigation of the side-arm lariat effect of ortho- and para-methoxyphenoxymethyl-15-crown-5 in the gas phase.
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- Journal of Analytical Chemistry, 2013, v. 68, n. 14, p. 1178, doi. 10.1134/S1061934813140116
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Target site as the main mechanism of resistance to imazamox in a Euphorbia heterophylla biotype.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-51682-z
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Configuration and conformation of alfentanil hydrochloride. Conformational study by NMR and theoretical calculations.
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- Magnetic Resonance in Chemistry, 2014, v. 52, n. 8, p. 440, doi. 10.1002/mrc.4085
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New, Homochiral Synthons Obtained through Simple Manipulations of Enzymatically Derived 3-Halo-cis-1,2-dihydrocatechols.
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- Australian Journal of Chemistry, 2015, v. 68, n. 10, p. 1467, doi. 10.1071/CH15061
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Research on synthesis and thermodynamic properties of 2-methoxycyclohexanol.
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- Journal of Thermal Analysis & Calorimetry, 2018, v. 131, n. 3, p. 2197, doi. 10.1007/s10973-017-6784-4
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Optimal design of an intensified column with side-reactor configuration for the methoxy-methylheptane process.
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- Chemical Engineering Research & Design: Transactions of the Institution of Chemical Engineers Part A, 2018, v. 136, p. 11, doi. 10.1016/j.cherd.2018.05.006
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Enhancing Reactivity of Directly íObservable B-H-Pt Interactions through Conformational Rigidity.
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- European Journal of Inorganic Chemistry, 2016, v. 2016, n. 15/16, p. 2403, doi. 10.1002/ejic.201501305
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New methods for the synthesis of α,ω-bis-1,5,3-dithiazepanes on the basis of aliphatic α,ω-diamines.
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- Chemistry of Heterocyclic Compounds, 2013, v. 49, n. 8, p. 1237, doi. 10.1007/s10593-013-1368-0
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Furoyl phosphonates.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 5, p. 1046, doi. 10.1134/S107036321605011X
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An Alternative Approach to Isoganciclovir: A Prominent Impurity in the Antiviral Drug Ganciclovir.
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- Scientia Pharmaceutica, 2015, v. 83, n. 2, p. 233, doi. 10.3797/scipharm.1409-15
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An Alternative Approach to Isoganciclovir: A Prominent Impurity in the Antiviral Drug Ganciclovir.
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- Scientia Pharmaceutica, 2015, v. 83, n. 2, p. 233, doi. 10.3797/scipharm.1409-15
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- Article
Crystal structure of trans-3-chloro-4-[4-methyl-2-(1H-1,2,4-triazol-1- ylmethyl)-1,3-dioxolan-2-yl]phenyl-4-chlorophenyl ether, C<sub>19</sub>H<sub>17</sub>Cl<sub>2</sub>N<sub>3</sub>O<sub>3</sub>.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2014, v. 229, n. 3, p. 233, doi. 10.1515/ncrs-2014-0117
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Continuous usage of a hair dye product containing 2-methoxymethyl- para-phenylenediamine by hair-dye-allergic individuals.
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- British Journal of Dermatology, 2016, v. 174, n. 5, p. 1042, doi. 10.1111/bjd.14390
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Advice for patients with hair dye allergy remains 'stop using permanent hair dyes'.
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- British Journal of Dermatology, 2016, v. 174, n. 5, p. 957, doi. 10.1111/bjd.14591
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Cross-elicitation responses to 2-methoxymethyl- p-phenylenediamine under hair dye use conditions in p-phenylenediamine-allergic individuals.
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- British Journal of Dermatology, 2015, v. 172, n. 4, p. 976, doi. 10.1111/bjd.13412
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Gold(I)-Catalyzed Intramolecular Carbon-Oxygen Bond Cleavage Reaction via Gold Carbenes Derived from Vinylidenecyclopropanes.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 19, p. 3002, doi. 10.1002/adsc.201600483
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Alternative Access to Functionalized 2,8-Ethanonoradamantane Derivatives.
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- Molecules, 2017, v. 22, n. 6, p. 906, doi. 10.3390/molecules22060906
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Cross‐elicitation responses to 2‐methoxymethyl‐p‐phenylenediamine in p‐phenylenediamine‐allergic individuals: Results from open use testing and diagnostic patch testing.
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- Contact Dermatitis (01051873), 2018, v. 79, n. 5, p. 288, doi. 10.1111/cod.13078
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Asymmetric Cyclizative Dimerization of (ortho‐Alkynyl Phenyl) (Methoxymethyl) Sulfides with Palladium(II) Bisoxazoline Catalyst.
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- Chemistry - A European Journal, 2019, v. 25, n. 3, p. 733, doi. 10.1002/chem.201804779
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- Article
Optically Active Helical Poly[(S)-3-vinyl-2,2'-dihydroxy-1,1'- binaphthyl]: New Ligand for Asymmetric Addition of Diethylzinc to Aryl Aldehyde.
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- Chinese Journal of Chemistry, 2015, v. 33, n. 4, p. 463, doi. 10.1002/cjoc.201400819
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Photoactivated <italic>N</italic>‐Acyliminoiodinanes Applied to Amination: an <italic>ortho</italic>‐Methoxymethyl Group Stabilizes Reactive Precursors.
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- Angewandte Chemie, 2018, v. 130, n. 3, p. 701, doi. 10.1002/ange.201710277
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- Article
Synthesis and antiproliferative activity of 3α-hydroxyl-3β-methoxymethyl-5α-pregnan-20-one with a C-21 hydrophilic substituent.
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- Heteroatom Chemistry, 2017, v. 28, n. 3, p. n/a, doi. 10.1002/hc.21372
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Novel Intramolecular Cyclization of 2-(Buta-1,3-dienyl)benzyl Anions to 6,7(9)-Dihydro-5 H-benzocycloheptenyl Anions Leading to Successive Formation of 1,2-Dihydrocyclopropa[ a]naphthalenes.
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- Helvetica Chimica Acta, 2013, v. 96, n. 9, p. 1704, doi. 10.1002/hlca.201200653
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Efficient Synthesis of N-Aryl-substituted Nonathiatriaza-(1,4)-hexabenzocyclotetracosaphanes.
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- Russian Journal of Organic Chemistry, 2018, v. 54, n. 11, p. 1660, doi. 10.1134/S1070428018110064
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Low-Temperature Ozonolysis of 2-Alkenyl-1,1-dichlorocyclopropanes.
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- Russian Journal of Organic Chemistry, 2018, v. 54, n. 3, p. 377, doi. 10.1134/S1070428018030028
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Conformational analysis of 2-isopropyl-5-methyl-5-methoxymethyl-1,3,2-dioxaborinane.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 11, p. 1678, doi. 10.1134/S1070428017110112
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- Article
A new alkaloid from Chaetomium globosum.
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- Journal of Chinese Pharmaceutical Sciences, 2018, v. 27, n. 9, p. 617, doi. 10.5246/jcps.2018.09.063
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Axially phenoxy-derivative disubstituted phthalocyanine: synthesis, characterization and photophysical properties.
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- Research on Chemical Intermediates, 2018, v. 44, n. 10, p. 6197, doi. 10.1007/s11164-018-3485-y
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A New Pyrrole Alkaloid from Leccinum Extremiorientale.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 4, p. 730, doi. 10.1007/s10600-015-1394-5
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(S)-4-[(3aR,4S,7aR)-4-Methoxy-6-methyl-3-methylene-2-oxo-2,3,3a,4,7,7a-hexahydrobenzofuran-5-yl]pentyl Acetate.
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- Molbank, 2016, v. 2016, n. 1, p. m890, doi. 10.3390/M890
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- Article