Works matching DE "BIRCH reduction"
Results: 33
Birch Reduction of Arenes as an Easy Entry to γ‐Spirolactones.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 46, p. 6383, doi. 10.1002/ejoc.202101018
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C2‐(1 N/2 N‐Methyl‐tetrazole)methyl Ether (MeTetMe) as a Stereodirecting Group for 1,2‐trans‐β‐O‐Glycosylation.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 41, p. 5732, doi. 10.1002/ejoc.202100973
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Synthesis of γ‐Spirolactams by Birch Reduction of Arenes.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 10, p. 1585, doi. 10.1002/ejoc.202100056
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Simple Synthesis of γ-Spirolactams by Birch Reduction of Benzoic Acids.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 6, p. 1074, doi. 10.1002/ejoc.201601650
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Reagent Control of a Birch Reduction for the Synthesis of a 2-Deoxyoligosaccharide Possessing a 1,4-Dialkylhydroquinone.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 22, p. 4939, doi. 10.1002/ejoc.201500515
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Graphane Nanostripes.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 45, p. 13965, doi. 10.1002/anie.201606852
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The crystal structure of methyl 4-((3,5-di-tert-butyl-4-oxocyclohexa-2,5-dien-1-ylidene)methyl) benzoate, C<sub>23</sub>H<sub>28</sub>O<sub>3</sub>.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2022, v. 237, n. 5, p. 857, doi. 10.1515/ncrs-2022-0283
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The Reactivity of Arylphosphorus Acid Amides Under Birch Reduction Conditions.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 20, p. 4351, doi. 10.1002/ejoc.201300344
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Reduction of Li<sup>+</sup> within a borate anion.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46948-8
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Birch and Benkeser Reductions: Application of Electride Salts in Organic Chemistry.
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- Resonance: Journal of Science Education, 2019, v. 24, n. 7, p. 735, doi. 10.1007/s12045-019-0835-z
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Dearomative di- and trifunctionalization of aryl sulfoxides via [5,5]-rearrangement.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32426-6
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Structural basis of enzymatic benzene ring reduction.
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- Nature Chemical Biology, 2015, v. 11, n. 8, p. 586, doi. 10.1038/nchembio.1849
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Enantioselective Synthesis of cis‐Decalins by Merging the Birch Reduction and Inverse‐Electron‐Demand Diels–Alder Reaction.
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- Angewandte Chemie, 2023, v. 135, n. 32, p. 1, doi. 10.1002/ange.202303876
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Total Syntheses of Polyhydroxylated Steroids by an Unsaturation‐Functionalization Strategy.
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- Angewandte Chemie, 2023, v. 135, n. 24, p. 1, doi. 10.1002/ange.202303639
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Mechanochemical Approach for Air‐Tolerant and Extremely Fast Lithium‐Based Birch Reductions in Minutes.
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- Angewandte Chemie, 2023, v. 135, n. 21, p. 1, doi. 10.1002/ange.202217723
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Josh Abbenseth.
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- Angewandte Chemie, 2021, v. 133, n. 46, p. 24556, doi. 10.1002/ange.202113158
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Total Synthesis of Haliclonin A.
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- Angewandte Chemie, 2021, v. 133, n. 17, p. 9752, doi. 10.1002/ange.202016343
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An Efficient Synthetic Approach for The Transition Metal-Free Preparation of 2-Bromo-3-(Bromomethyl)Naphthalene from Naphthalene.
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- Sakarya University Journal of Science (SAUJS) / Sakarya Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 2021, v. 25, n. 3, p. 714, doi. 10.16984/saufenbilder.909041
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Enantioselective Enzymatic Naphthoyl Ring Reduction.
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- Chemistry - A European Journal, 2018, v. 24, n. 48, p. 12505, doi. 10.1002/chem.201802683
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Ir‐Catalyzed Asymmetric and Regioselective Hydrogenation of Cyclic Allylsilanes and Generation of Quaternary Stereocenters via the Hosomi‐Sakurai Allylation.
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- Chemistry - A European Journal, 2018, v. 24, n. 7, p. 1681, doi. 10.1002/chem.201704684
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Recent Advances in Dearomative Partial Reduction of Benzenoid Arenes.
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- Angewandte Chemie, 2024, v. 136, n. 21, p. 1, doi. 10.1002/ange.202402819
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Mechanochemical Birch Reduction with Low Reactive Alkaline Earth Metals.
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- Angewandte Chemie, 2024, v. 136, n. 20, p. 1, doi. 10.1002/ange.202319449
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Chemoselective Quinoline and Isoquinoline Reduction by Energy Transfer Catalysis Enabled Hydrogen Atom Transfer.
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- Angewandte Chemie, 2023, v. 135, n. 48, p. 1, doi. 10.1002/ange.202312203
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Divergent Asymmetric Total Synthesis of Mulinane Diterpenoids.
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- Angewandte Chemie, 2017, v. 129, n. 41, p. 12882, doi. 10.1002/ange.201706994
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Graphane Nanostripes.
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- Angewandte Chemie, 2016, v. 128, n. 45, p. 14171, doi. 10.1002/ange.201606852
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- Article
trans-Hydrogenation: Application to a Concise and Scalable Synthesis of Brefeldin A.
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- Angewandte Chemie, 2015, v. 127, n. 13, p. 4050, doi. 10.1002/ange.201411618
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Synthesis of Octahydroperylene, the Framework of Altertoxin III.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 3, p. 1, doi. 10.1002/ejoc.202301053
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Near-Stoichiometric Bulk Graphane from Halogenated Graphenes (X = Cl/Br/I) by the Birch Reduction for High Density Energy Storage.
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- Advanced Functional Materials, 2017, v. 27, n. 13, p. n/a, doi. 10.1002/adfm.201605797
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Synthesis of 3-Amino-4-substituted Monocyclic ß-Lactams—Important Structural Motifs in Medicinal Chemistry.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 1, p. 360, doi. 10.3390/ijms23010360
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Iridium-catalyzed synthesis of pyrazolone fused 1,4-dihydrocinnolin-3-one employing α-diazotized Meldrum's acid.
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- ARKIVOC: Online Journal of Organic Chemistry, 2022, v. 2022, p. 1, doi. 10.24820/ark.5550190.p011.841
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Enantioselective synthesis of the aglycone of burnettramic acid A.
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- Bioscience, Biotechnology & Biochemistry, 2023, v. 87, n. 12, p. 1442, doi. 10.1093/bbb/zbad129
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The Hydronaphthalide Monoanion: Isolation of the "red transient" Birch Intermediate from liquid Ammonia.
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- Chemistry - A European Journal, 2024, v. 30, n. 54, p. 1, doi. 10.1002/chem.202401098
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Photoreduction of Anthracenes Catalyzed by peri‐Xanthenoxanthene: a Scalable and Sustainable Birch‐Type Alternative.
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- Chemistry - A European Journal, 2023, v. 29, n. 63, p. 1, doi. 10.1002/chem.202302129
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