Works matching DE "ATROPISOMERS"
Results: 212
Synthesis of trans,trans-2,3,4-trisubstituted chromans from 3-nitro-2 Н-chromenes and enamines of acetoacetic ester and acetylacetone. A new type of configurationally stable atropisomers.
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- Chemistry of Heterocyclic Compounds, 2015, v. 51, n. 6, p. 531, doi. 10.1007/s10593-015-1733-2
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- Article
Cobalt-catalyzed atroposelective C−H activation/annulation to access N−N axially chiral frameworks.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-40978-4
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Atropisomeric determination of chiral hydroxylated metabolites of polychlorinated biphenyls using HPLC-MS.
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- Chemistry Central Journal, 2013, v. 7, n. 1, p. 1, doi. 10.1186/1752-153X-7-183
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Strategic Synthesis of 'Picket Fence' Porphyrins Based on Nonplanar Macrocycles**.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 12, p. 1871, doi. 10.1002/ejoc.202100154
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Analysis of Interconversion between Atropisomers of Chiral Substituted 9,9'‐Bicarbazole.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 3, p. 449, doi. 10.1002/ejoc.202001385
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Stereochemistry and Recent Applications of Axially Chiral Organic Molecules.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 27, p. 4070, doi. 10.1002/ejoc.201901918
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Brønsted Acid Promoted Thermal‐Ring‐Rearrangement of Fluorenopyrans to 2‐(1H‐Inden‐3‐yl)‐9H‐fluoren‐3‐ols Bearing Two All‐Carbon‐Quaternary Centres.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 15, p. 2199, doi. 10.1002/ejoc.202000251
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Synthesis of Enantiopure Isosteres of Amino Acids Containing a Quaternary Stereocenter: Experimental and Computational Evaluation of a Novel Class of Atropisomers.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 46, p. 6524, doi. 10.1002/ejoc.201801213
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Stereochemical Stability and Absolute Configuration of Atropisomeric Alkylthioporphyrazines by Dynamic NMR and HPLC Studies and Computational Analysis of HPLC‐ECD Recorded Spectra.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 29, p. 4029, doi. 10.1002/ejoc.201800553
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- Article
First Total Synthesis of the Bioactive Arylnaphthyl Lignan 4-O-Glycosides Phyllanthusmin D and 4"-O-Acetylmananthoside B.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 25, p. 3674, doi. 10.1002/ejoc.201700556
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- Article
Atropoisomerism in Mono- and Diaryl-Substituted 4-Amino-2,6-lutidines.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 17, p. 2966, doi. 10.1002/ejoc.201600456
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- Article
Access to Atropisomerically Enriched Biaryls by the Coupling of Aryllithiums with Arynes under Control by Homochiral Oxazolines.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 4, p. 725, doi. 10.1002/ejoc.201501503
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Spectroscopic Characterization of 1-Naphthyl Isocyanate Anion Radical and of Tris(1-naphthyl) Isocyanurate Atropisomers.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 27, p. 6040, doi. 10.1002/ejoc.201500863
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- Article
Conformational Studies and Atropisomerism Kinetics of the ALK Clinical Candidate Lorlatinib (PF-06463922) and Desmethyl Congeners.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 11, p. 3590, doi. 10.1002/anie.201509240
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Exploiting Atropisomerism to Increase the Target Selectivity of Kinase Inhibitors.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 40, p. 11754, doi. 10.1002/anie.201506085
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Concise and Practical Asymmetric Synthesis of a Challenging Atropisomeric HIV Integrase Inhibitor.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 24, p. 7144, doi. 10.1002/anie.201501575
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Aromatic Amide-Derived Non-Biaryl Atropisomers as Highly Efficient Ligands in Silver-Catalyzed Asymmetric Cycloaddition Reactions.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 17, p. 5255, doi. 10.1002/anie.201501100
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The Atropomer Composition of Iopromide as an Indicator for Assessment of the Quality of its Substance and Medincal Formulations.
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- Pharmaceutical Chemistry Journal, 2014, v. 48, n. 3, p. 186, doi. 10.1007/s11094-014-1075-x
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Halogenase-Targeted Genome Mining Leads to the Discovery of (±) Pestalachlorides A1a, A2a, and Their Atropisomers.
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- Antibiotics (2079-6382), 2022, v. 11, n. 10, p. N.PAG, doi. 10.3390/antibiotics11101304
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Synthesis of Epimethanetriyloxazoloand Epimethanetriylimidazobenzazocinones and -benzazoninones from syn- and anti-Atropisomers of N-Acyl-N-[2-(cycloalk-2-en-1-yl)-6-methylphenyl]glycines.
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- Russian Journal of Organic Chemistry, 2018, v. 54, n. 10, p. 1519, doi. 10.1134/S1070428018100147
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Atropisomeric N-acyl- N-(cyclopentenylphenyl)glycines in the synthesis of oxazolo[3,4- a]benzoxazocinones.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 5, p. 697, doi. 10.1134/S1070428017050098
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Synthesis, structure, and heck cyclization of the <i>syn</i>- and <i>anti</i>-atropisomers of <i>N</i>-acyl-<i>N</i>-(4-methyl-3,6-dihydro-2<i>H</i>-pyran-3-yl)-2-iodo-4,6-dimethylaniline.
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- Russian Journal of Organic Chemistry, 2013, v. 49, n. 10, p. 1486, doi. 10.1134/S107042801310014X
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Preparation and Crystal Structure of the 1,3-alternate Atropisomer of a Calix[4]radialene.
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- European Journal of Organic Chemistry, 2015, p. 3221, doi. 10.1002/ejoc.201500319
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- Article
Tetrahydroanthraquinone Derivatives from the Endophytic Fungus Stemphylium globuliferum.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 12, p. 2646, doi. 10.1002/ejoc.201500079
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- Article
Elucidating the Structural Isomerism of Fluorescent Strigolactone Analogue CISA-1.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 6, p. 1211, doi. 10.1002/ejoc.201403457
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- Article
Atropisomerism in 3,4,5-Tri-(2-methoxyphenyl)-2,6-lutidine.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 35, p. 7867, doi. 10.1002/ejoc.201301378
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- Article
Ph-tetraMe-Bithienine, the First Member of the Class of Chiral Heterophosphepines: Synthesis, Electronic and Steric Properties, Metal Complexes and Catalytic Activity.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 36, p. 8174, doi. 10.1002/ejoc.201301098
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Application of aromatic amide‐derived atropisomers as chiral solvating agents for discrimination of optically active mandelic acid derivatives in <sup>1</sup>H nuclear magnetic resonance spectroscopy.
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- Magnetic Resonance in Chemistry, 2022, v. 60, n. 1, p. 86, doi. 10.1002/mrc.5185
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Controlled interconversion of macrocyclic atropisomers via defined intermediates.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-50739-6
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Organocatalytic diastereo- and atroposelective construction of N–N axially chiral pyrroles and indoles.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-44743-z
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- Article
Organocatalytic diastereo- and atroposelective construction of N–N axially chiral pyrroles and indoles.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-44743-z
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- Article
Amide C–N bonds activation by A new variant of bifunctional N-heterocyclic carbene.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-44756-8
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Thermally-induced atropisomerism promotes metal-organic cage construction.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-43756-4
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Identifying absolute configurations of PCB atropisomers by comparison of their experimental specific rotations with their DFT calculated values.
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- Canadian Journal of Chemistry, 2019, v. 97, n. 5, p. 325, doi. 10.1139/cjc-2018-0458
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Separation of 2-naphthol atropisomers on cyclofructan-based chiral stationary phases.
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- Journal of Liquid Chromatography & Related Technologies, 2016, v. 39, n. 15, p. 710, doi. 10.1080/10826076.2016.1234395
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- Article
Sterically hindered 5,15-tetraphenylbenzene-porphyrins: syntheses, structures, atropisomerism and photophysical properties.
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- Journal of Chemical Sciences, 2018, v. 130, n. 7, p. 1, doi. 10.1007/s12039-018-1485-5
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Three atropisomers of biphenyl: twist by tunable para substituents.
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- Journal of Chemical Sciences, 2018, v. 130, n. 7, p. 1, doi. 10.1007/s12039-018-1482-8
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- Article
Atropisomerism about the C(1)-N single bond in N,N-disubstituted-1-aminoanthracenes: isolation of conformational diastereomers.
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- Journal of Chemical Sciences, 2018, v. 130, n. 6, p. 1, doi. 10.1007/s12039-018-1473-9
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DIFLUORPHOS and SYNPHOS in asymmetric catalysis: Synthetic applications.
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- Journal of Chemical Sciences, 2014, v. 126, n. 2, p. 325, doi. 10.1007/s12039-014-0571-6
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- Article
Synthesis of Indolophanes by Photochemical Macrocyclization.
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- Chemistry - A European Journal, 2016, v. 22, n. 25, p. 8444, doi. 10.1002/chem.201600835
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- Article
Enzymatic Desymmetrising Redox Reactions for the Asymmetric Synthesis of Biaryl Atropisomers.
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- Chemistry - A European Journal, 2014, v. 20, n. 41, p. 13084, doi. 10.1002/chem.201404509
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- Article
Inside Front Cover Image, Volume 44, Issue 5.
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- Medicinal Research Reviews, 2024, v. 44, n. 5, p. ii, doi. 10.1002/med.22067
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Bioactive atropisomers: Unraveling design strategies and synthetic routes for drug discovery.
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- Medicinal Research Reviews, 2024, v. 44, n. 5, p. 1971, doi. 10.1002/med.22037
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Synthesis of a Conformationally Stable Atropisomeric Pair of Biphenyl Scaffold Containing Additional Stereogenic Centers.
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- Molecules, 2019, v. 24, n. 3, p. 643, doi. 10.3390/molecules24030643
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Highly stable atropisomers by electrophilic amination of a chiral γ-lactam within the synthesis of an elusive conformationally restricted analogue of α-methylhomoserine.
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- Amino Acids, 2016, v. 48, n. 2, p. 461, doi. 10.1007/s00726-015-2100-4
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Conformational enantiodiscrimination for asymmetric construction of atropisomers.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32432-8
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- Article
Atroposelective P<sup>III</sup>/P<sup>V</sup>=O Redox Catalysis for the Isoquinoline‐Forming Staudinger–aza‐Wittig Reaction.
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- Angewandte Chemie, 2023, v. 135, n. 39, p. 1, doi. 10.1002/ange.202309053
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- Article
Enantioselective Synthesis of N−N Biaryl Atropisomers through Iridium(I)‐Catalyzed C−H Alkylation with Acrylates.
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- Angewandte Chemie, 2023, v. 135, n. 37, p. 1, doi. 10.1002/ange.202305067
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Enantioselective Strategies for The Synthesis of N−N Atropisomers.
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- Angewandte Chemie, 2023, v. 135, n. 31, p. 1, doi. 10.1002/ange.202303966
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- Article
Synthesis of a Blue‐Emissive Azaborathia[9]helicene by Silicon‐Boron Exchange from Unusual Atropisomeric Teraryls.
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- Angewandte Chemie, 2023, v. 135, n. 30, p. 1, doi. 10.1002/ange.202304291
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