The Diels-Alder-Reaction with inverse-Electron-Demand, a very efficient versatile Click-Reaction Concept for proper Ligation of variable molecular Partners

International Journal of Medical Sciences ◽

10.7150/ijms.7.19 ◽

2010 ◽

pp. 19-28 ◽

Cited By ~ 20

Author(s):

Manfred Wiessler ◽

Waldemar Waldeck ◽

Christian Kliem ◽

Ruediger Pipkorn ◽

Klaus Braun

Keyword(s):

Click Reaction ◽

Alder Reaction ◽

Diels Alder ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Electron Demand

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ChemInform Abstract: The Diels-Alder-Reaction with Inverse-Electron-Demand - A Review of an Efficient & Attractive Click-Reaction Concept

ChemInform ◽

10.1002/chin.201441278 ◽

2014 ◽

Vol 45 (41) ◽

pp. no-no

Author(s):

Manfred Wiessler ◽

Waldemar Waldeck ◽

Ruediger Pipkorn ◽

Peter Lorenz ◽

Juergen Debus ◽

...

Keyword(s):

Click Reaction ◽

Alder Reaction ◽

Diels Alder ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Electron Demand

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Synthesis of Medium-Sized Carbocycles via a Bidentate Lewis Acid-Catalyzed Inverse Electron-Demand Diels–Alder Reaction Followed by Photoinduced Ring-Opening

Organic Letters ◽

10.1021/acs.orglett.1c00249 ◽

2021 ◽

Author(s):

Julia Ruhl ◽

Sebastian Ahles ◽

Marcel A. Strauss ◽

Christopher M. Leonhardt ◽

Hermann A. Wegner

Keyword(s):

Lewis Acid ◽

Ring Opening ◽

Alder Reaction ◽

Diels Alder ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Acid Catalyzed ◽

Electron Demand

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Organocatalytic Strategies for the Development of the Enantioselective Inverse‐electron‐demand Hetero‐Diels‐Alder Reaction

Chemistry - A European Journal ◽

10.1002/chem.202101696 ◽

2021 ◽

Author(s):

José Alemán ◽

Víctor Laina-Martín ◽

Jose A. Fernández-Salas

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Electron Demand

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PPh3-catalyzed synthesis of dicyano-2-methylenebut-3-enoates as efficient dienes in catalytic asymmetric inverse-electron-demand Diels–Alder reaction

Chemical Communications ◽

10.1039/c1cc12834e ◽

2011 ◽

Vol 47 (29) ◽

pp. 8289 ◽

Cited By ~ 37

Author(s):

Xianxing Jiang ◽

Dan Fu ◽

Xiaomei Shi ◽

Shoulei Wang ◽

Rui Wang

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Catalytic Asymmetric ◽

Electron Demand

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Highly Enantioselective Catalytic Hetero-Diels-Alder Reaction with Inverse Electron Demand

Angewandte Chemie International Edition ◽

10.1002/(sici)1521-3773(19980918)37:17<2404::aid-anie2404>3.0.co;2-d ◽

1998 ◽

Vol 37 (17) ◽

pp. 2404-2406 ◽

Cited By ~ 95

Author(s):

Jacob Thorhauge ◽

Mogens Johannsen ◽

Karl Anker Jørgensen

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Electron Demand

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Racemic and enantiopure 4-(piperidine-2′-yl)-pyridazines: novel synthesis of anabasine-analogues with potential nicotinic acetylcholine receptor agonist activity—a new approach via Diels–Alder reaction with inverse electron demand

Tetrahedron ◽

10.1016/s0040-4020(01)01236-4 ◽

2002 ◽

Vol 58 (7) ◽

pp. 1343-1354 ◽

Cited By ~ 28

Author(s):

Astrid Stehl ◽

Gunther Seitz ◽

Karen Schulz

Keyword(s):

Receptor Agonist ◽

Alder Reaction ◽

Diels Alder ◽

Agonist Activity ◽

Nicotinic Acetylcholine ◽

New Approach ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Novel Synthesis ◽

Electron Demand

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Studies on inverse electron demand hetero Diels–Alder reaction of perfluoroalkyl 2(1H) pyridones with different dienophiles under microwave irradiation

Journal of Fluorine Chemistry ◽

10.1016/s0022-1139(01)00494-8 ◽

2002 ◽

Vol 113 (1) ◽

pp. 133-137 ◽

Cited By ~ 11

Author(s):

A Krishnaiah ◽

B Narsaiah

Keyword(s):

Microwave Irradiation ◽

Alder Reaction ◽

Diels Alder ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Electron Demand

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Single wall carbon nanotube (SWCNT)–gold nanorod (AuNR) conjugates via thermally-mild reaction conditions

New Journal of Chemistry ◽

10.1039/c7nj02619f ◽

2017 ◽

Vol 41 (21) ◽

pp. 12392-12396 ◽

Cited By ~ 3

Author(s):

Siting Ni ◽

Jun Zhu ◽

Mohamed Amine Mezour ◽

R. Bruce Lennox

Keyword(s):

Carbon Nanotube ◽

Covalent Binding ◽

Alder Reaction ◽

Diels Alder ◽

Gold Nanorod ◽

Reaction Conditions ◽

Single Wall Carbon ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Electron Demand

A thermally-mild method for covalent binding of SWCNTs to AuNRs, based on an inverse-electron-demand Diels–Alder reaction, is established and discussed.

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Front Cover Picture: Stereoselective Synthesis of Hydropyrano[3,2-b]indolesviaOrganocatalytic Asymmetric Inverse-Electron-Demand Oxa-Diels-Alder Reaction (Adv. Synth. Catal. 18/2016)

Advanced Synthesis & Catalysis ◽

10.1002/adsc.201600890 ◽

2016 ◽

Vol 358 (18) ◽

pp. 2861-2861

Author(s):

Lei Yang ◽

Wei Huang ◽

Xiang-Hong He ◽

Ming-Cheng Yang ◽

Xiang Li ◽

...

Keyword(s):

Stereoselective Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Front Cover ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Electron Demand

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Total syntheses of ericifolione and analogues via a biomimetic inverse-electron-demand Diels-Alder reaction

Chemical Communications ◽

10.1039/d1cc06361h ◽

2021 ◽

Author(s):

Tingting Zhou ◽

Anquan Zheng ◽

Luqiong Huo ◽

Changgeng Li ◽

Haibo Tan ◽

...

Keyword(s):

Sodium Acetate ◽

Alder Reaction ◽

Diels Alder ◽

Total Syntheses ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Sterically Hindered ◽

Electron Demand

Driven by bioinspiration and appreciation of the structure of ericifolione, a biomimetic tautomerization/intermolecular inverse-electron-demand hetero Diels-Alder reaction cascade sequence promoted by sodium acetate to rapidly construct sterically hindered dihydropyran scaffolds...

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