1,2-Disubstituted 1,2-Dihydro-1,2,4,5-tetrazine-3,6-dione as a Dynamic Covalent Bonding Unit at Room Temperature
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Title
1,2-Disubstituted 1,2-Dihydro-1,2,4,5-tetrazine-3,6-dione as a Dynamic Covalent Bonding Unit at Room Temperature
Authors
Keywords
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Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 144, Issue 3, Pages 1370-1379
Publisher
American Chemical Society (ACS)
Online
2022-01-19
DOI
10.1021/jacs.1c11665
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- (2017) Christian S. Diercks et al. SCIENCE
- Design of a thermally controlled sequence of triazolinedione-based click and transclick reactions
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- Triazolinediones as Highly Enabling Synthetic Tools
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- Dearomative dihydroxylation with arenophiles
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- Macromolecular Coupling in Seconds of Triazolinedione End-Functionalized Polymers Prepared by RAFT Polymerization
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- Dynamic combinatorial chemistry: a tool to facilitate the identification of inhibitors for protein targets
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- Dynamic Covalent Chemistry Approaches Toward Macrocycles, Molecular Cages, and Polymers
- (2014) Yinghua Jin et al. ACCOUNTS OF CHEMICAL RESEARCH
- Controlling a Polymer Adhesive Using Light and a Molecular Switch
- (2014) Amir Mahmoud Asadirad et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Triazolinediones enable ultrafast and reversible click chemistry for the design of dynamic polymer systems
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- Dynamic combinatorial/covalent chemistry: a tool to read, generate and modulate the bioactivity of compounds and compound mixtures
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- The furan/maleimide Diels–Alder reaction: A versatile click–unclick tool in macromolecular synthesis
- (2012) Alessandro Gandini PROGRESS IN POLYMER SCIENCE
- Dynamic Covalent Chemistry: A Facile Room-Temperature, Reversible, Diels-Alder Reaction between Anthracene Derivatives and N-Phenyltriazolinedione
- (2011) Nabarun Roy et al. Chemistry-An Asian Journal
- Substituent Effects on the Reversibility of Furan–Maleimide Cycloadditions
- (2011) Robert C. Boutelle et al. JOURNAL OF ORGANIC CHEMISTRY
- Diels–Alder “click” reactions: recent applications in polymer and material science
- (2011) Mehmet Atilla Tasdelen Polymer Chemistry
- Tyrosine Bioconjugation through Aqueous Ene-Type Reactions: A Click-Like Reaction for Tyrosine
- (2010) Hitoshi Ban et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
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- (2008) Mohammad Ali Zolfigol et al. MONATSHEFTE FUR CHEMIE
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