Works matching Dienophiles
Results: 613
Reactions of 5-(1,2-Dicarbadodecaboran-1-yl)-3-(2-pyridyl)-1,2,4-triazines with Dienophiles.
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- Russian Journal of General Chemistry, 2023, v. 93, n. 3, p. 500, doi. 10.1134/S1070363223030064
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- Article
Boron and Silicon-Substituted 1,3-Dienes and Dienophiles and Their Use in Diels-Alder Reactions.
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- Molecules, 2020, v. 25, n. 16, p. 3740, doi. 10.3390/molecules25163740
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- Article
Hydrazones as Productive Dienophiles in the Inverse Electron Demand Diels-Alder Reactions of 1,3,5-Triazines.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 20, p. 4344, doi. 10.1002/ejoc.201500499
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- Article
A Convenient Diels-Alder Approach toward Potential Polyketide-like Antibiotics Using α-Activated α,β-Unsaturated 4,4-Dimethyl-1-tetralones as Dienophiles.
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- Molecules, 2023, v. 28, n. 6, p. 2739, doi. 10.3390/molecules28062739
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An Optimized Protocol for the Synthesis of Peptides Containing trans‐Cyclooctene and Bicyclononyne Dienophiles as Useful Multifunctional Bioorthogonal Probes.
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- Chemistry - A European Journal, 2021, v. 27, n. 54, p. 13632, doi. 10.1002/chem.202102042
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- Article
Chinone als Dienophile in der Diels-Alder-Reaktion - historische Entwicklung und Anwendungen in der Totalsynthese.
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- Angewandte Chemie, 2014, v. 126, n. 8, p. 2086, doi. 10.1002/ange.201305908
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Diels‐Alder Reactivity of a Chiral Anthracene Template with Symmetrical and Unsymmetrical Dienophiles: A DFT Study.
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- ChemistryOpen, 2020, v. 9, n. 7, p. 748, doi. 10.1002/open.202000137
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Modulation of Reactivities of Dienophiles for DielsAlder Reactions via Complexation of α, β-Unsaturated Chelating Amides.
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- Helvetica Chimica Acta, 2015, v. 98, n. 3, p. 287, doi. 10.1002/hlca.201400224
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- Article
Phthalazine as a Diene in Diels–Alder Reactions With P‐ and As‐Containing Anionic Dienophiles: Comparison of Possible Reaction Channels.
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- ChemPlusChem, 2024, v. 89, n. 9, p. 1, doi. 10.1002/cplu.202400140
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- Article
Systematic Screening of Different Polyglycerin‐Based Dienophile Macromonomers for Efficient Nanogel Formation through IEDDA Inverse Nanoprecipitation.
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- Macromolecular Rapid Communications, 2020, v. 41, n. 1, p. N.PAG, doi. 10.1002/marc.201900510
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- Article
Design and Synthesis of Aza‐Bicyclononene Dienophiles for Rapid Fluorogenic Ligations.
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- Chemistry - A European Journal, 2018, v. 24, n. 10, p. 2426, doi. 10.1002/chem.201705188
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- Article
Radical Cation Diels-Alder Reactions of Non-Conjugated Alkenes as Dienophiles by Electrocatalysis.
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- Chinese Journal of Chemistry, 2019, v. 37, n. 6, p. 561, doi. 10.1002/cjoc.201900054
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- Article
Supramolecular Diversity of Oxabicyclo[2.2.2]octenes Formed between Substituted 2H-Pyran-2-ones and Vinyl-Moiety-Containing Dienophiles.
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- Symmetry (20738994), 2020, v. 12, n. 10, p. 1714, doi. 10.3390/sym12101714
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- Article
Effect of an α‐Methyl Substituent on the Dienophile on Diels‐Alder endo:exo Selectivity.
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- ChemistryOpen, 2019, v. 8, n. 1, p. 49, doi. 10.1002/open.201800237
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- Article
Masked Ketenes as Dienophiles in the Diels-Alder Reaction.
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- Australian Journal of Chemistry, 2016, v. 69, n. 12, p. 1365, doi. 10.1071/CH16428
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- Article
Synthesis of 3-trimethylsiloxy-1-(furan-3-yl)butadiene and its reactions with dienophiles.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 6, p. 364, doi. 10.1007/s10593-016-1897-4
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Reactions of triazines and tetrazines with dienophiles (Review).
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- Chemistry of Heterocyclic Compounds, 2012, v. 48, n. 8, p. 1153, doi. 10.1007/s10593-012-1117-9
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Iron(III) Chloride Catalyzed Synthesis of Highly Substituted Indolyl-Tetrahydroquinoline Derivatives by Using Indolylnitroalkene as Dienophiles and Its Application to the Synthesis of Indolo-Benzonaphthyridine Derivatives.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 18, p. 3849, doi. 10.1002/adsc.201400424
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Metal-Free Dehydrogenative Diels-Alder Reactions of 2-Methyl-3-Alkylindoles with Dienophiles: Rapid Access to Tetrahydrocarbazoles, Carbazoles, and Heteroacenes.
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- Angewandte Chemie, 2015, v. 127, n. 31, p. 9220, doi. 10.1002/ange.201503549
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Synthesis of polychlorinated mono- and bisimides of cyclic dicarboxylic acids containing diene-dienophile fragments.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 2, p. 211, doi. 10.1134/S1070428014020122
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Metal-Free Dehydrogenative Diels-Alder Reactions of 2-Methyl-3-Alkylindoles with Dienophiles: Rapid Access to Tetrahydrocarbazoles, Carbazoles, and Heteroacenes.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 31, p. 9092, doi. 10.1002/anie.201503549
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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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Origins of Endo Selectivity in Diels–Alder Reactions of Cyclic Allene Dienophiles.
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- Angewandte Chemie, 2021, v. 133, n. 27, p. 15116, doi. 10.1002/ange.202101809
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Erratum to: Reactions of 5-(1,2-Dicarbadodecaboran-1-yl)-3-(2-pyridyl)-1,2,4-triazines with Dienophiles.
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- 2023
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- Correction Notice
Stereoelectronic Effects on Dienophile Separation Influence the Diels-Alder Synthesis of Molecular Clefts.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 45, p. 6793, doi. 10.1002/ejoc.201701319
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- Article
Preparation of 3-(9-Anthryl)acrylates and 9-Aroylethenylanthracenes as Pi-Extended Anthracenes and Their Diels–Alder Type Adducts with Electron-Poor Dienophiles.
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- Polycyclic Aromatic Compounds, 2017, v. 37, n. 2/3, p. 148, doi. 10.1080/10406638.2016.1220962
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Diols as Dienophiles: Bridged Carbocycles via Ruthenium(0)-Catalyzed Transfer Hydrogenative Cycloadditions of Cyclohexadiene or Norbornadiene.
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- Angewandte Chemie, 2017, v. 129, n. 46, p. 14859, doi. 10.1002/ange.201708189
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- Article
A Bifunctional Fluorogenic Rhodamine Probe for Proximity-Induced Bioorthogonal Chemistry.
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- Chemistry - A European Journal, 2017, v. 23, n. 72, p. 18216, doi. 10.1002/chem.201703607
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- Article
Diels–Alder Reaction in the Synthesis of Fluorinated (Hetero)Aromatic Compounds.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 27/28, p. 3618, doi. 10.1002/ejoc.201800327
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- Article
Synthesis of Novel 8‐cyclo‐1,5,3,7‐Diazadiphosphocine Derivatives Via [4 + 2] Cycloaddition.
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- Bulletin of the Korean Chemical Society, 2021, v. 42, n. 1, p. 60, doi. 10.1002/bkcs.12154
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Total Synthesis of (−)‐Lepadin F based on a Stereoselective Diels–Alder Reaction Controlled by a Ketolactone‐type Dienophile.
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- Chemistry - A European Journal, 2021, v. 27, n. 12, p. 4141, doi. 10.1002/chem.202004778
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- Article
ETUDE THEORIQUE DU MECANISME DE LA REACTION D'ADDITION DU 4-NITROBENZODIFUROXANE SUR UNE SERIE DES DIENOPHILES.
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- Journal of the Algerian Chemical Society / Journal de Société Algérienne de Chimie, 2010, v. 20, n. 1, p. 1
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- Article
Origin of reversal of stereoselectivity for [4+2] cycloaddition reaction between cyclopentadiene and methyl methacrylate in the presence of the chloroloaluminate ionic liquid (1-ethyl-3-methyl-imidazolium chloride): in silico studies.
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- Canadian Journal of Chemistry, 2014, v. 92, n. 9, p. 862, doi. 10.1139/cjc-2014-0189
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- Article
Regioselective Transformation of Long π-Conjugated Backbones: From Oligofurans to Oligoarenes.
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- Angewandte Chemie, 2017, v. 129, n. 44, p. 13789, doi. 10.1002/ange.201705914
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- Article
Enantioselective oxa‐Diels–Alder Sequences of Dendralenes.
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- Angewandte Chemie, 2022, v. 134, n. 39, p. 1, doi. 10.1002/ange.202204872
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- Article
New Dienophiles: 1-Acetylvinyl Arenecarboxylates. Reactivity toward cyclopentadiene and exocyclic dienes.
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- Helvetica Chimica Acta, 1981, v. 64, n. 1, p. 188, doi. 10.1002/hlca.19810640121
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- Article
Cycloadditionen von 3,4-Dimethoxyfuran an Dienophile.
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- Helvetica Chimica Acta, 1979, v. 62, n. 7, p. 2202, doi. 10.1002/hlca.19790620717
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- Article
The Diels-Alder Approach towards Cannabinoid Derivatives and Formal Synthesis of Tetrahydrocannabinol (THC).
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- ChemistryOpen, 2021, v. 10, n. 5, p. 587, doi. 10.1002/open.202000343
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- Article
Regio- and stereoselective syntheses and cycloadditions of substituted 2H-pyran-2-ones and their fused derivatives.
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- ARKIVOC: Online Journal of Organic Chemistry, 2013, p. 333
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- Article
Theoretical design of new bridge-ring insensitive high energy compounds by selected normal Diels-Alder reactions between NH<sub>2</sub>- substituted oxazoles and NO<sub>2</sub>/NF<sub>2</sub>/NHNO<sub>2</sub>-substituted ethylenes/ acetylenes.
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- Defence Technology, 2021, v. 17, n. 5, p. 1731, doi. 10.1016/j.dt.2020.09.016
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Reductive Cycloisomerization of Diynes by Supported Palladium Catalysts and Subsequent [4+2] Cycloaddition for One‐Pot Synthesis of Cyclohexenes.
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- ChemCatChem, 2020, v. 12, n. 2, p. 455, doi. 10.1002/cctc.201901423
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- Article
Diels–Alder Additions to 2,2'‐Biaceanthrylene.
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- Helvetica Chimica Acta, 2023, v. 106, n. 2, p. 1, doi. 10.1002/hlca.202200126
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- Article
Mulberry Diels–Alder-type adducts: isolation, structure, bioactivity, and synthesis.
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- Natural Products & Bioprospecting, 2022, v. 12, n. 1, p. 1, doi. 10.1007/s13659-022-00355-y
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- Article
The Aza Diels-Alder Reaction on Brominated Conjugated Dienes.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 13, p. 2003, doi. 10.1002/ejoc.202100170
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- Article
2- and 3-Vinylindoles as 4p Components in Cycloaddition Reactions.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 31, p. 4512, doi. 10.1002/ejoc.201700120
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- Article
Origin of the endo Selectivity in the Diels-Alder Reaction between Cyclopentadiene and Maleic Anhydride.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 25, p. 4275, doi. 10.1002/ejoc.201600676
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- Article
An investigation of molecular mechanism and the role of Te-bridged-atom in the formation of polysubstituted pyridines via Hetero-Diels-Alder reaction of isotellurazole with acetylenic dienophile: a molecular electron density study.
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- Journal of Chemical Sciences, 2018, v. 130, n. 8, p. 1, doi. 10.1007/s12039-018-1459-7
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Study of the Deformation/Interaction Model: How Interactions Increase the Reaction Barrier.
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- Journal of Chemistry, 2018, p. 1, doi. 10.1155/2018/3106297
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- Article
Mechanism Controlling High‐Temperature Degradation of Sunflower Oil Triacylglycerols in the Absence of Oxygen.
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- European Journal of Lipid Science & Technology, 2021, v. 123, n. 3, p. 1, doi. 10.1002/ejlt.202000228
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- Article
tert -Butyl(2-oxo-2 H -pyran-5-yl)carbamate as the First Chameleon Diene Bearing an Electron-Donating Substituent.
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- Molecules, 2022, v. 27, n. 17, p. 5666, doi. 10.3390/molecules27175666
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- Article