Works matching Diels-Alder reaction
Results: 3559
Concerted and stepwise mechanisms in the Diels–Alder and Michael reactions of furans with methyl 3-nitroacrylate — Experimental and theoretical studies.
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- Canadian Journal of Chemistry, 2006, v. 84, n. 3, p. 392, doi. 10.1139/V06-013
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Catalyst-free Diels-Alder reactions of vinylphosphonates with cyclopentadienones.
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- Canadian Journal of Chemistry, 2017, v. 95, n. 8, p. 871, doi. 10.1139/cjc-2017-0267
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Studies on chemo- and diastereo-selectivity of the Diels–Alder reactions of sulfinyltoluquinones with cyclopentadiene.
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- Canadian Journal of Chemistry, 2009, v. 87, n. 8, p. 1135, doi. 10.1139/V09-070
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Total synthesis of 14β-fluorosteroids via a transannular Diels–Alder reaction.
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- Canadian Journal of Chemistry, 2006, v. 84, n. 1, p. 29, doi. 10.1139/V05-259
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Exo selectivity and the effect of disubstitution in the Diels–Alder reactions of butadiene with 3,3-disubstituted cyclopropenes.
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- Canadian Journal of Chemistry, 2004, v. 82, n. 11, p. 1589, doi. 10.1139/V04-115
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Efficient and regioselective synthesis of bridged ring systems by domino Knoevenagel – hetero-Diels–Alder reaction.
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- Canadian Journal of Chemistry, 2001, v. 79, n. 11, p. 1511, doi. 10.1139/cjc-79-11-1511
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No Evidence Found for Diels-Alder Reaction Products in Soybean Oil Oxidized at the Frying Temperature by NMR Study.
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- Journal of the American Oil Chemists' Society (JAOCS), 2013, v. 90, n. 6, p. 825, doi. 10.1007/s11746-013-2229-9
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Development and Applications of Double Diels‐Alder Reaction in Organic Synthesis.
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- Asian Journal of Organic Chemistry, 2021, v. 10, n. 11, p. 2848, doi. 10.1002/ajoc.202100493
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Diels-Alder Reaction between Isoprene and Methyl Acrylate over Different Zeolites: Influence of Pore Topology and Acidity.
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- ChemPlusChem, 2013, v. 78, n. 9, p. 1134, doi. 10.1002/cplu.201300157
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Reactivity of 7-Azanorbornenes in Bioorthogonal Inverse Electron-Demand Diels-Alder Reactions.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 26, p. 3815, doi. 10.1002/ejoc.201700411
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Macromolecular materials based on the application of the Diels-Alder reaction to natural polymers and plant oils.
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- European Journal of Lipid Science & Technology, 2018, v. 120, n. 1, p. n/a, doi. 10.1002/ejlt.201700091
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Surfactant-assisted specific-acid catalysis of Diels–Alder reactions in aqueous media.
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- Journal of Physical Organic Chemistry, 2007, v. 20, n. 10, p. 764, doi. 10.1002/poc.1240
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Asymmetric Diels-Alder Reaction of α-Substituted and β,β-Disubstituted α,β-Enals via Diarylprolinol Silyl Ether for the Construction of All-Carbon Quaternary Stereocenters.
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- Chemistry - A European Journal, 2016, v. 22, n. 44, p. 15874, doi. 10.1002/chem.201602345
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Bioinspired Intramolecular Diels-Alder Reaction: A Rapid Access to the Highly-Strained Cyclopropane-Fused Polycyclic Skeleton.
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- Chemistry - A European Journal, 2014, v. 20, n. 9, p. 2425, doi. 10.1002/chem.201304839
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Catalyst-Free One-Pot Synthesis of 2,4,6-Triaryl-1,4-dihydropyridines in Ionic Liquid and Their Catalyzed Activity on Two Simple Diels-Alder Reactions.
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- Synthetic Communications, 2008, v. 38, n. 5, p. 666, doi. 10.1080/00397910701818446
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One-Pot Synthesis of 2-Arylthio-2-cyclohexenone Derivatives by the Diels-Alder Reaction of 4-Arylthio-3-hydroxy-2-pyrones.
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- Synthetic Communications, 2007, v. 37, n. 13, p. 2131, doi. 10.1080/00397910701392434
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Synthesis of Fused Tricyclic Systems from Cycloalkadienones via Diels–Alder Reaction: Sharpless Oxidation of bis Adducts.
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- Synthetic Communications, 2007, v. 37, n. 5, p. 775, doi. 10.1080/00397910601131445
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Quinones as Dienophiles in the Diels-Alder Reaction: History and Applications in Total Synthesis.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 8, p. 2056, doi. 10.1002/anie.201305908
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Unexpectedly Regioselective Diels‐Alder Reactions of New Unsymmetrical Benzoquinones: A Convenient Synthetic Entry to Uniquely Substituted Decalins.
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- Chemistry - A European Journal, 2024, v. 30, n. 55, p. 1, doi. 10.1002/chem.202401068
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Exo‐Selective Diels–Alder Reactions.
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- Chemistry - A European Journal, 2024, v. 30, n. 17, p. 1, doi. 10.1002/chem.202304371
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Front Cover: How Ionization Catalyzes Diels‐Alder Reactions (Chem. Eur. J. 40/2022).
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- Chemistry - A European Journal, 2022, v. 28, n. 40, p. 1, doi. 10.1002/chem.202201619
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How Ionization Catalyzes Diels‐Alder Reactions.
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- Chemistry - A European Journal, 2022, v. 28, n. 40, p. 1, doi. 10.1002/chem.202200987
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Highly Stereoselective Diels–Alder Reactions Catalyzed by Diboronate Complexes.
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- Angewandte Chemie, 2023, v. 135, n. 33, p. 1, doi. 10.1002/ange.202303075
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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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Self‐Accelerating Diels–Alder Reaction for Preparing Polymers of Intrinsic Microporosity.
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- Angewandte Chemie, 2023, v. 135, n. 24, p. 1, doi. 10.1002/ange.202302527
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Catalytic Asymmetric Inverse‐Electron‐Demand Diels–Alder Reactions of 2‐Pyrones with Indenes: Total Syntheses of Cephanolides A and B.
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- Angewandte Chemie, 2021, v. 133, n. 51, p. 26814, doi. 10.1002/ange.202112223
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An on‐surface Diels–Alder reaction.
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- Angewandte Chemie, 2021, v. 133, n. 50, p. 26550, doi. 10.1002/ange.202110311
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Catalytic Asymmetric Aza‐Diels–Alder Reaction of Ketimines and Unactivated Dienes.
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- Angewandte Chemie, 2021, v. 133, n. 32, p. 17749, doi. 10.1002/ange.202104788
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3‐(Methoxycarbonyl)Cyclobutenone as a Reactive Dienophile in Enantioselective Diels–Alder Reactions Catalyzed by Chiral Oxazaborolidinium Ions.
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- Angewandte Chemie, 2021, v. 133, n. 9, p. 4659, doi. 10.1002/ange.202014308
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Rolf Huisgen's Classic Studies of Cyclic Triene Diels–Alder Reactions Elaborated by Modern Computational Analysis.
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- Angewandte Chemie, 2020, v. 132, n. 30, p. 12606, doi. 10.1002/ange.202003279
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DABCO‐based chiral ionic liquids as recoverable and reusable organocatalyst for asymmetric Diels–Alder reaction.
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- Chirality, 2022, v. 34, n. 1, p. 134, doi. 10.1002/chir.23385
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Chiral Imidazolidin‐4‐one with catalytic amount of Dicationic ionic liquid act as a recoverable and reusable Organocatalyst for asymmetric Diels‐Alder reaction.
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- Chirality, 2020, v. 32, n. 1, p. 64, doi. 10.1002/chir.23137
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A theoretical study of the solvent effect on Diels-Alder reaction in room temperature ionic liquids using a supermolecular approach.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2009, v. 123, n. 3/4, p. 347, doi. 10.1007/s00214-009-0525-0
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Theoretical Study of Diels-Alder Reaction: Role of Substituent in Regioselectivity and Aromaticity.
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- Journal of the Iranian Chemical Society, 2010, v. 7, n. 3, p. 554, doi. 10.1007/BF03246043
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Multifunctional, robust, and self‐healable polyurethane coatings cross‐linked by Diels–Alder reaction of calix[4] arenes containing furan groups.
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- Journal of Applied Polymer Science, 2024, v. 141, n. 3, p. 1, doi. 10.1002/app.54825
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Catalytic and Enantioselective Diels‐Alder Reaction of Siloxydienes.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 6, p. 732, doi. 10.1002/ajoc.201900159
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Diels–Alder Reactions in Creating Complexity in Higher Order Isoprenoids: Proposed Biosynthesis and Biomimetic Total Syntheses.
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- Asian Journal of Organic Chemistry, 2018, v. 7, n. 8, p. 1488, doi. 10.1002/ajoc.201800158
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Inverse Electron‐Demanding Diels–Alder Reactions in the Chemical Synthesis of Prenylated Indole Alkaloids Containing a Bicycle[2.2.2]diazaoctane Moiety: A Theoretical Study.
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- Chemistry - An Asian Journal, 2023, v. 18, n. 7, p. 1, doi. 10.1002/asia.202300063
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Activation of the Unreactive Bond in C<sub>70</sub> Fullerene toward Diels‐Alder Reaction by Encapsulation of a Lithium Atom.
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- Chemistry - An Asian Journal, 2020, v. 15, n. 19, p. 3096, doi. 10.1002/asia.202000859
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How Alkali Cations Catalyze Aromatic Diels‐Alder Reactions.
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- Chemistry - An Asian Journal, 2020, v. 15, n. 7, p. 1167, doi. 10.1002/asia.202000009
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Front Cover: Water, an Essential Element for a Zn<sup>II</sup>‐Catalyzed Asymmetric Quinone Diels‐Alder Reaction: Multi‐Selective Construction of Highly Functionalized cis‐Decalins (Chem. Asian J. 19/2019).
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- Chemistry - An Asian Journal, 2019, v. 14, n. 19, p. 3221, doi. 10.1002/asia.201901196
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Hydrogen-Bonding Catalysis of Tetraalkylammonium Salts in an Aza-Diels-Alder Reaction.
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- Chemistry - An Asian Journal, 2016, v. 11, n. 15, p. 2126, doi. 10.1002/asia.201600781
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Bicyclic Guanidine Catalyzed Asymmetric Tandem Isomerization Intramolecular-Diels-Alder Reaction: The First Catalytic Enantioselective Total Synthesis of (+)-alpha-Yohimbine.
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- Chemistry - An Asian Journal, 2016, v. 11, n. 3, p. 390, doi. 10.1002/asia.201500246
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Overcoming Thermodynamically Driven Retro‐Diels–Alder Reaction through a Cascade One‐Pot Process Exemplified for a Bio‐Based Platform Chemical.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 21, p. 1, doi. 10.1002/ejoc.202300018
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The Diels-Alder reaction of 1,4-quinones in hexafluoroisopropanol.
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- ARKIVOC: Online Journal of Organic Chemistry, 2024, v. 2024, p. 1, doi. 10.24820/ark.5550190.p012.140
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Lewis acid-catalyzed Diels-Alder reaction of 2-cyclopentenones with Danishefsky's diene: double bond isomerization of tetrahydro-1Hindene- 1,5(7aH)-diones, and attempts on an asymmetric catalysis.
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- ARKIVOC: Online Journal of Organic Chemistry, 2012, p. 5
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Solid-phase cleavage by a thermal retro-Diels-Alder reaction: preparation of a small β-substituted α,β-ethylenic aldehydes library.
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- ARKIVOC: Online Journal of Organic Chemistry, 2009, p. 78
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Interfacial Thermoreversible Chemistry on Functional Coatings: A Focus on the Diels–Alder Reaction.
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- Advanced Functional Materials, 2019, v. 29, n. 10, p. N.PAG, doi. 10.1002/adfm.201806765
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Crosslinking starch with Diels–Alder reaction: water‐soluble materials and water‐mediated processes.
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- Polymer International, 2022, v. 71, n. 11, p. 1340, doi. 10.1002/pi.6438
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Switchable cholesterol recognition system with Diels–Alder reaction using molecular imprinting technique on self‐assembled monolayer.
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- Polymer International, 2019, v. 68, n. 10, p. 1722, doi. 10.1002/pi.5877
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