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1. Full Text Catalytic reductive [4+1]-cycloadditions of vinylidenes and dienes
by Zhou, You-Yun and Uyeda, Christopher
Science (American Association for the Advancement of Science), ISSN 0036-8075, 02/2019, Volume 363, Issue 6429, pp. 857 - 862
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Chemistry, Organic | Ring formation (Chemistry) | Research | Diels-Alder reaction | Chemical research | Vinylidene | Alkenes | Catalysts | Metals | Chemical reactions | Enantiomers | Carbon | Carbenes | Zinc | Diels-Alder reactions | Cycloaddition | Cycloalkanes | Cyclopropane | Chemical bonds | Nickel | Catalysis | Dienes | Carbon sources
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2. Full Text Catalytic Asymmetric Intramolecular [4+2] Cycloaddition of In Situ Generated ortho‐Quinone Methides
by Xie, Youwei and List, Benjamin
Angewandte Chemie (International ed.), ISSN 1433-7851, 04/2017, Volume 56, Issue 18, pp. 4936 - 4940
organocatalysis | cycloadditions | asymmetric catalysis | hetero-Diels–Alder reactions | Brønsted acids | Quinone | Catalysis
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3. Full Text Cycloadditions of Alkenylboronic Derivatives
by Grygorenko, Oleksandr O and Moskvina, Viktoriia S and Hryshchuk, Oleksandr V and Tymtsunik, Andriy V
Synthesis (Stuttgart), ISSN 0039-7881, 10/2020, Volume 52, Issue 19, pp. 2761 - 2780
short review | cyclobutanes | cycloaddition | Diels-Alder reaction | cyclopropanation | organoboron compounds | 1,3-dipolar cycloaddition | Physical Sciences | Chemistry | Chemistry, Organic | Science & Technology
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4. Full Text Catalytic Asymmetric [4+2]‐Cycloadditions Using Tropolones: Developments, Scope, Transformations, and Bioactivity
by Hammer, Niels and Erickson, Jeremy D and Lauridsen, Vibeke H and Jakobsen, Joakim B and Hansen, Bente K and Jacobsen, Kristian M and Poulsen, Thomas B and Jørgensen, Karl Anker
Angewandte Chemie (International ed.), ISSN 1433-7851, 10/2018, Volume 57, Issue 40, pp. 13216 - 13220
organocatalysis | photoisomerization | cycloaddition | tropolone | bioactivity | Diels-Alder reaction | Catalysis | Stereoselectivity | Biomedical materials | Cycloaddition | Biocompatibility | Transformations | In vivo methods and tests | Biological activity | Cancer | Index Medicus
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5. Full Text Click chemistry beyond metal-catalyzed cycloaddition
by Becer, C.R and Hoogenboom, R and Schubert, U.S
Angewandte Chemie (International ed.), ISSN 0570-0833, 2009, Volume 48, Issue 27, pp. 4900 - 4908
Journal Article | thio‐click reaction | click chemistry | cycloaddition | Diels–Alder reaction | catalyst‐free method | Thio-click reaction | Cycloaddition | Catalyst-free method | Click chemistry | Diels-Alder reaction | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology
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6. Full Text An Unexpected Transannular [4+2] Cycloaddition during the Total Synthesis of (+)‐Norcembrene 5
by Breunig, Michael and Yuan, Po and Gaich, Tanja
Angewandte Chemie (International ed.), ISSN 1433-7851, 03/2020, Volume 59, Issue 14, pp. 5521 - 5525
terpenoids | total synthesis | Diels–Alder reaction | ring-closing metathesis | transannular cycloaddition | Diterpenes | Cycloaddition | Synthesis | Metathesis | Index Medicus | Communications | Communication
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7. Full Text Substituent Effects on the Reversibility of Furan–Maleimide Cycloadditions
by Boutelle, Robert C and Northrop, Brian H
Journal of organic chemistry, ISSN 0022-3263, 10/2011, Volume 76, Issue 19, pp. 7994 - 8002
Physical Sciences | Chemistry | Chemistry, Organic | Science & Technology | Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives | Organic chemistry | Heterocyclic compounds | Heterocyclic compounds with only one n hetero atom and condensed derivatives | Reactivity and mechanisms | Exact sciences and technology | Chemical reactivity | Preparations and properties | Thermodynamics | Magnetic Resonance Spectroscopy | Maleimides - chemistry | Furans - chemistry | Stereoisomerism | Electrons | Usage | Analysis | Nuclear magnetic resonance spectroscopy | Furans | Ring formation (Chemistry) | Diels-Alder reaction | Chemical properties | Index Medicus
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8. Full Text Biomimetic Dehydrogenative Diels–Alder Cycloadditions: Total Syntheses of Brosimones A and B
by Qi, Chao and Cong, Huan and Cahill, Katharine J and Müller, Peter and Johnson, Richard P and Porco, John A
Angewandte Chemie (International ed.), ISSN 1433-7851, 08/2013, Volume 52, Issue 32, pp. 8345 - 8348
dehydrogenative cycloaddition | brosimone | nanoparticle catalysts | natural product synthesis | Diels‐Alder cycloaddition | Diels-Alder cycloaddition | Cyclization | Flavonoids - chemical synthesis | Stereoisomerism | Molecular Structure | Cycloaddition Reaction | Flavonoids - chemistry | Biomimetic Materials - chemistry | Index Medicus | nanoparticle catalyst | Diels-Alder
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9. Full Text Diels–Alder Cycloaddition‐Cycloreversion: A Powerful Combo in Materials Design
by Sanyal, Amitav
Macromolecular chemistry and physics, ISSN 1022-1352, 07/2010, Volume 211, Issue 13, pp. 1417 - 1425
retro Diels–Alder cycloreversion | Diels–Alder cycloaddition | maleimide polymers | dendrimers | dendronized polymers | diblock copolymers | Dendrimers | Retro Diels-Alder cycloreversion | Dendronized polymers | Diblock copolymers | Diels-Alder cycloaddition | Maleimide polymers | Polymer Science | Physical Sciences | Science & Technology | Polymerization | Applied sciences | Organic polymers | Physicochemistry of polymers | Preparation, kinetics, thermodynamics, mechanism and catalysts | Exact sciences and technology | Polymer chemistry | Enzymes | Cycloaddition | Construction | Synthesis | Architecture | Immobilization | Polymers
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10. Full Text Mechanism‐Based Fluorogenic trans‐Cyclooctene–Tetrazine Cycloaddition
by Vázquez, Arcadio and Dzijak, Rastislav and Dračínský, Martin and Rampmaier, Robert and Siegl, Sebastian J and Vrabel, Milan
Angewandte Chemie (International ed.), ISSN 1433-7851, 01/2017, Volume 56, Issue 5, pp. 1334 - 1337
bioorthogonal chemistry | cycloaddition | click reactions | imaging agents | heterocycles | Diels-Alder reaction | Cycloaddition | Medical imaging | Nuclear magnetic resonance--NMR | Atmospheric chemistry | Reagents | Computer applications | Fluorescence | Photochemicals | Isomers | Communications | Communication
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