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Nucleophilic Attack on Nitrogen in Tetrazines by Silyl-Enol Ethers
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-987x(19990115)20:1<114::aid-jcc12>3.0.co;2-lopenalex-snapshot
Understanding reactivity with Kohn-Sham molecular orbital theory: E2-SN2 mechanistic spectrum and other concepts
inferredcites →https://doi.org/10.1002/(sici)1099-0690(199812)1998:12<2885::aid-ejoc2885>3.0.co;2-lopenalex-snapshot
1,2,4,5-Tetrazine: Synthesis and Reactivity in [4+2] Cycloadditions
inferredcites →https://doi.org/10.1002/anie.201400135openalex-snapshot
In Situ Synthesis of Alkenyl Tetrazines for Highly Fluorogenic Bioorthogonal Live‐Cell Imaging Probes
inferredcites →https://doi.org/10.1002/anie.201501385openalex-snapshot
From Carbanions to Organometallic Compounds: Quantification of Metal Ion Effects on Nucleophilic Reactivities
inferredcites →https://doi.org/10.1002/anie.201601082openalex-snapshot
Ortho ‐Functionalized Aryltetrazines by Direct Palladium‐Catalyzed C−H Halogenation: Application to Fast Electrophilic Fluorination Reactions
inferredcites →https://doi.org/10.1002/anie.201701486openalex-snapshot
Analyzing Reaction Rates with the Distortion/Interaction‐Activation Strain Model
inferredcites →https://doi.org/10.1002/anie.201804878openalex-snapshot
Metal‐Free Synthetic Approach to 3‐Monosubstituted Unsymmetrical 1,2,4,5‐Tetrazines Useful for Bioorthogonal Reactions
inferredcites →https://doi.org/10.1002/anie.201903839openalex-snapshot
Lewis Acid Directed Regioselective Metalations of Pyridazine
inferredcites →https://doi.org/10.1002/anie.201911947openalex-snapshot
Bridge‐Clamp Bis(tetrazine)s with [N]8 π‐Stacking Interactions and Azido‐s‐Aryl Tetrazines: Two Classes of Doubly Clickable Tetrazines
inferredcites →https://doi.org/10.1002/anie.202005569openalex-snapshot
Divergent Synthesis of Monosubstituted and Unsymmetrical 3,6‐Disubstituted Tetrazines from Carboxylic Ester Precursors
inferredcites →https://doi.org/10.1002/cber.189302602188openalex-snapshot
Ueber die Einwirkung von Hydrazin auf Imidoäther
inferredcites →https://doi.org/10.1002/cber.19851180602openalex-snapshot
1,2,4,5‐Tetrazin‐1(2H)‐yl‐Radikale
inferredcites →https://doi.org/10.1002/cber.19901230715openalex-snapshot
Nucleophilic Attack at Heterocyclic Nitrogen: Unusual Reactivity of the Benzotriazole Heterocyclic Ring
inferredcites →https://doi.org/10.1002/chem.201705962openalex-snapshot
Which Factors Control the Nucleophilic Reactivities of Enamines?
inferredcites →https://doi.org/10.1002/wcms.1221openalex-snapshot
The activation strain model and molecular orbital theory
inferredcites →https://doi.org/10.1002/zfch.19750150607openalex-snapshot
Synthese und Reaktivität von 4H‐1,3,4‐Oxadiazolo[2,3‐c]‐asymm.‐triazinen
inferredcites →https://doi.org/10.1016/j.jphotochemrev.2020.100372openalex-snapshot
1,2,4,5-Tetrazines: An intriguing heterocycles family with outstanding characteristics in the field of luminescence and electrochemistry
inferredcites →https://doi.org/10.1016/j.tet.2004.01.013openalex-snapshot
The azaphilic addition of organometallic reagents on tetrazines: scope and limitations
inferredcites →https://doi.org/10.1021/acs.accounts.6b00532openalex-snapshot
Holy Grails for Computational Organic Chemistry and Biochemistry
inferredcites →https://doi.org/10.1021/acs.accounts.8b00062openalex-snapshot
Advances in Tetrazine Bioorthogonal Chemistry Driven by the Synthesis of Novel Tetrazines and Dienophiles
inferredcites →https://doi.org/10.1021/acs.bioconjchem.0c00052openalex-snapshot
Synthesis and Application of 3-Bromo-1,2,4,5-Tetrazine for Protein Labeling to Trigger Click-to-Release Biorthogonal Reactions
inferredcites →https://doi.org/10.1021/acs.orglett.0c04113openalex-snapshot
Nucleophilic Attack on Nitrogen in Tetrazines by Silyl-Enol Ethers
inferredcites →https://doi.org/10.1021/acs.orglett.7b02868openalex-snapshot
Preparation of Unsymmetrical 1,2,4,5-Tetrazines via a Mild Suzuki Cross-Coupling Reaction
inferredcites →https://doi.org/10.1021/cr900357eopenalex-snapshot
s -Tetrazines as Building Blocks for New Functional Molecules and Molecular Materials
inferredcites →https://doi.org/10.1021/ja0734086openalex-snapshot
Distortion/Interaction Energy Control of 1,3-Dipolar Cycloaddition Reactivity
inferredcites →https://doi.org/10.1021/jacs.0c09775openalex-snapshot
Selective N1/N4 1,4-Cycloaddition of 1,2,4,5-Tetrazines Enabled by Solvent Hydrogen Bonding
inferredcites →https://doi.org/10.1021/jacs.9b08677openalex-snapshot
Installation of Minimal Tetrazines through Silver-Mediated Liebeskind–Srogl Coupling with Arylboronic Acids
inferredcites →https://doi.org/10.1021/jo00338a009openalex-snapshot
Occurrence of the SN(ANRORC) mechanism in the hydrazination of 1,2,4,5-tetrazines
inferredcites →https://doi.org/10.1038/s41596-019-0265-0openalex-snapshot
Understanding chemical reactivity using the activation strain model
inferredcites →https://doi.org/10.1039/c3ra46893copenalex-snapshot
New unsymmetrical alkyl-s-tetrazines: original syntheses, fluorescence and electrochemical behaviour
inferredcites →https://doi.org/10.1039/c4cs00055bopenalex-snapshot
The activation strain model and molecular orbital theory: understanding and designing chemical reactions
inferredcites →https://doi.org/10.1039/c7cs00184copenalex-snapshot
Inverse electron demand Diels–Alder reactions in chemical biology
inferredcites →https://doi.org/10.1039/c7qo00172jopenalex-snapshot
Synthesis of 2,3-diaza-anthraquinones via the bidentate Lewis acid catalysed inverse electron-demand Diels–Alder (IEDDA) reaction
inferredcites →https://doi.org/10.1039/c8sc01796dopenalex-snapshot
The mechanism of the triple aryne–tetrazine reaction cascade: theory and experiment
inferredcites →https://doi.org/10.1039/c9sc06169jopenalex-snapshot
3-Bromotetrazine: labelling of macromolecules via monosubstituted bifunctional s -tetrazines
inferredcites →https://doi.org/10.1039/d0cc01647kopenalex-snapshot
Iridium-catalyzed C–H amidation of s -tetrazines
inferredcites →https://doi.org/10.1039/p19840002779openalex-snapshot
Termal rearrangement of 1-alkyl-3,6-diaryl-1,4-dihydro-s-tetrazines to 1-alkylamino-3,5-diaryl-1,2,4-triazoles
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/asia.202100562openalex-snapshot
One‐Pot and Two‐Chamber Methodologies for Using Acetylene Surrogates in the Synthesis of Pyridazines and Their D‐Labeled Derivatives
inferred← citeshttps://doi.org/10.1002/ejic.202100998openalex-snapshot
(Spectro)Electrochemistry of 3‐(Pyrid‐2‐yl)‐s‐Tetrazine‐ and 1,2‐ (Dihydro)pyridazine Tricarbonylrhenium(I)chloride
inferred← citeshttps://doi.org/10.1002/ejoc.202100486openalex-snapshot
Mechanistic Study of Domino Processes Involving the Bidentate Lewis Acid Catalyzed Inverse Electron‐Demand Diels−Alder Reaction
inferred← citeshttps://doi.org/10.1002/hlca.202200198openalex-snapshot
Preparation of 3‐Bromo‐1,2,4,5‐tetrazine
inferred← citeshttps://doi.org/10.1002/open.70317openalex-snapshot
1,2,4,5‐Tetrazine‐Boron Halide Adduct Formation Unraveled in Solution and Solid State
inferred← citeshttps://doi.org/10.1007/s11244-021-01516-yopenalex-snapshot
Closer Look at Inverse Electron Demand Diels–Alder and Nucleophilic Addition Reactions on s-Tetrazines Using Enhanced Sampling Methods
inferred← citeshttps://doi.org/10.1016/b978-0-443-18939-5.00019-6openalex-snapshot
Triazines, tetrazines, and fused ring polyaza systems
inferred← citeshttps://doi.org/10.1016/j.fpc.2022.09.005openalex-snapshot
Recent advances in the synthesis and performance of 1,2,4,5-tetrazine-based energetic materials
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.138680openalex-snapshot
Novel 1,2,4-triazole-maleamic acid derivatives: synthesis and evaluation as anticancer agents with carbonic anhydrase inhibitory activity
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01384openalex-snapshot
Boron Trifluoride-Mediated Cycloaddition of 3-Bromotetrazine and Silyl Enol Ethers: Synthesis of 3-Bromo-pyridazines
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00543openalex-snapshot
N1/N4 1,4-Cycloaddition of 1,2,4,5-Tetrazines with Enamines Promoted by the Lewis Acid ZnCl2
inferred← citeshttps://doi.org/10.1021/jacs.1c03257openalex-snapshot
Azine Activation via Silylium Catalysis
inferred← citeshttps://doi.org/10.1039/d3ra08712copenalex-snapshot
Discovery of new tetrazines for bioorthogonal reactions with strained alkenes via computational chemistry
inferred← citeshttps://doi.org/10.1080/00268976.2026.2615022openalex-snapshot
DFT-based structural and energetic characterisation of nitrogen-rich tetrazine/triazine derivatives with Kamlet-Jacobs performance predictions
inferred← citeshttps://doi.org/10.3390/molecules27185891openalex-snapshot
An Alliance of Polynitrogen Heterocycles: Novel Energetic Tetrazinedioxide-Hydroxytetrazole-Based Materials
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