Thermally stable Diels–Alder polymer using an azodicarbonyl compound as the dienophile-Reference-Cited by-同舟云学术

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Thermally stable Diels–Alder polymer using an azodicarbonyl compound as the dienophile

Published:2019-03 Issue: Volume:167 Page:60-66
ISSN:0032-3861
Container-title:Polymer
language:en
Short-container-title:Polymer

Author:

Sakurai Masayoshi,Kihara Nobuhiro^ORCID

Funder

Research Foundation

Publisher

Elsevier BV

Subject

Polymers and Plastics,Materials Chemistry,Organic Chemistry

Reference36 articles.

1. The diels–alder reaction with maleic anhydride;Kloetzel,1948

2. The diels–alder reaction: ethylenic and acetylenic dienophiles;Holmes,1948

3. Dienes in the Diels–Alder Reaction;Fringuelli,1990

4. The retro-diels–alder reaction. Part I. C–C dienophiles;Rickborn,1998

5. The retro-diels–alder reaction. Part II. Dienophiles with one or more heteroatoms;Rickborn,1998

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1. Construction of the Red‐Green‐Blue Luminescence Conversion System Based on Donor‐Acceptor Dyes Exchange with Diels‐Alder Dynamic Covalent Bonds;ChemPhotoChem;2024-05-26

2. A Semiflexible Tetrahydrazone Macrocycle for Binding of Pyrophosphate and Smaller Anions;The Journal of Organic Chemistry;2024-04-25

3. Nickel-Catalyzed Azide–Alkyne Click Polymerization toward 1,5-Regioregular Polytriazoles;Macromolecules;2023-12-07

4. Self-correcting energy transfer Diels-Alder adduct dyes;Dyes and Pigments;2022-07

5. Criegee Intermediates Beyond Ozonolysis: Synthetic and Mechanistic Insights;Angewandte Chemie International Edition;2021-03-09

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