The ‘inverse electron-demand' Diels–Alder reaction in polymer synthesis. Part 4.1 The preparation and crystal structures of some bis(1,2,4,5-tetrazines)

Journal of the Chemical Society Perkin Transactions 2 ◽

10.1039/a607646g ◽

1997 ◽

pp. 1167-1174 ◽

Cited By ~ 26

Author(s):

Christopher Glidewell ◽

Philip Lightfoot ◽

Brodyck J. L. Royles ◽

David M. Smith

Keyword(s):

Crystal Structures ◽

Polymer Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Electron Demand

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The ‘inverse electron-demand’ Diels–Alder reaction in polymer synthesis. Part 1. A convenient synthetic route to diethynyl aromatic compounds

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19940000355 ◽

1994 ◽

pp. 355-358 ◽

Cited By ~ 18

Author(s):

Brodyck J. L. Royles ◽

David M. Smith

Keyword(s):

Aromatic Compounds ◽

Polymer Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Synthetic Route ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Electron Demand

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ChemInform Abstract: The “Inverse Electron-Demand” Diels-Alder Reaction in Polymer Synthesis. Part 3. Model Diels-Alder Reactions of Some Bis(1,2,4- triazines) with Dienophiles and Some Bisdienophiles with Heterocyclic Dienes.

ChemInform ◽

10.1002/chin.199705069 ◽

2010 ◽

Vol 28 (5) ◽

pp. no-no

Author(s):

G. A. MCLEAN ◽

B. J. L. ROYLES ◽

D. M. SMITH ◽

M. J. BRUCE

Keyword(s):

Polymer Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Electron Demand

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ChemInform Abstract: The “Inverse Electron-Demand” Diels-Alder Reaction in Polymer Synthesis. Part 1. A Convenient Synthetic Route to Diethynyl Aromatic Compounds.

ChemInform ◽

10.1002/chin.199424073 ◽

2010 ◽

Vol 25 (24) ◽

pp. no-no

Author(s):

B. J. L. ROYLES ◽

D. M. SMITH

Keyword(s):

Aromatic Compounds ◽

Polymer Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Synthetic Route ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Electron Demand

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The ‘inverse electron-demand’ Diels–Alder reaction in polymer synthesis. Part 2. Some bis(1,2,4-triazines) as potential bis-diene monomers

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19950001789 ◽

1995 ◽

pp. 1789-1795 ◽

Cited By ~ 9

Author(s):

Michael J. Bruce ◽

Gillian A. McLean ◽

Brodyck J. L. Royles ◽

David M. Smith ◽

Paul N. Standring

Keyword(s):

Polymer Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Electron Demand

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The ‘inverse electron-demand’ Diels–Alder reaction in polymer synthesis. Part 5: Preparation and model reactions of some electron-rich bis-dienamines

Tetrahedron ◽

10.1016/j.tet.2004.02.035 ◽

2004 ◽

Vol 60 (15) ◽

pp. 3421-3425 ◽

Cited By ~ 13

Author(s):

András Kotschy ◽

János Faragó ◽

Antal Csámpai ◽

David M Smith

Keyword(s):

Polymer Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Electron Demand ◽

Model Reactions

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ChemInform Abstract: The “Inverse Electron-Demand” Diels-Alder Reaction in Polymer Synthesis. Part 2. Some Bis(1,2,4-triazines) as Potential Bis-Diene Monomers.

ChemInform ◽

10.1002/chin.199545197 ◽

2010 ◽

Vol 26 (45) ◽

pp. no-no

Author(s):

M. J. BRUCE ◽

G. A. MCLEAN ◽

B. J. L. ROYLES ◽

D. M. SMITH ◽

P. N. STANDRING

Keyword(s):

Polymer Synthesis ◽

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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