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A 1,3-Diaza-Claisen Rearrangement that Affords Guanidines
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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/cber.19660990924openalex-snapshot
Über N‐Acyl‐imidsäureester, I. N‐Sulfonyl‐iminodithiokohlensäureester und N‐Sulfonyl‐dithiourethane
inferredcites →https://doi.org/10.1016/0040-4020(95)01019-xopenalex-snapshot
The invention of radical reactions. Part XXXV. A novel radical fission reaction of N-sulfonylthioxocarbamates
inferredcites →https://doi.org/10.1016/s0040-4020(98)00900-4openalex-snapshot
Solid phase synthesis of oligomeric guanidiniums
inferredcites →https://doi.org/10.1016/s0040-4039(00)01410-6openalex-snapshot
One-pot synthesis of sulfamoylguanidines and sulfonylguanidines
inferredcites →https://doi.org/10.1016/s0040-4039(00)70685-xopenalex-snapshot
A facile synthesis of cyanoguanidines from thioureas
inferredcites →https://doi.org/10.1021/ja00253a053openalex-snapshot
Retro aza Diels-Alder reactions: acid catalyzed heterocycloreversion of 2-azanorbornenes in water at ambient temperature
inferredcites →https://doi.org/10.1021/ja00292a057openalex-snapshot
Aza Diels-Alder reactions in aqueous solution: cyclocondensation of dienes with simple iminium salts generated under Mannich conditions
inferredcites →https://doi.org/10.1021/jo00235a021openalex-snapshot
Immonium ion based synthetic methodology: a novel method for the N-methylation of dipeptides and amino acid derivatives via retro aza Diels-Alder reactions
inferredcites →https://doi.org/10.1021/jo9810617openalex-snapshot
Solid-Phase Synthesis of Trisubstituted Bicyclic Guanidines via Cyclization of Reduced N-Acylated Dipeptides
inferredcites →https://doi.org/10.1021/ol0069711openalex-snapshot
Solid-Phase Guanidinylation as a Diversification Strategy of Poly- l -proline Type II Peptide Mimic Scaffolds
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4676572openalex-extracted
A Formal Pd0-Catalyzed 1,3-Diaza-Claisen Rearrangement
inferred← citeshttps://doi.org/10.1002/047084289x.re062.pub2openalex-snapshot
1-Ethyl-3-(3′-dimethylaminopropyl)carbodiimide Hydrochloride
inferred← citeshttps://doi.org/10.1002/ange.201911156openalex-snapshot
One‐Step Synthesis of 2,5‐Diaminoimidazoles and Total Synthesis of Methylglyoxal‐Derived Imidazolium Crosslink (MODIC)
inferred← citeshttps://doi.org/10.1002/anie.201911156openalex-snapshot
One‐Step Synthesis of 2,5‐Diaminoimidazoles and Total Synthesis of Methylglyoxal‐Derived Imidazolium Crosslink (MODIC)
inferred← citeshttps://doi.org/10.1002/chin.200502157openalex-snapshot
A 1,3‐Diaza‐Claisen Rearrangement that Affords Guanidines.
inferred← citeshttps://doi.org/10.1016/b978-0-08-100017-5.00001-7openalex-snapshot
Recent Developments in the Synthesis of Cyclic Guanidine Alkaloids
inferred← citeshttps://doi.org/10.1016/j.bioorg.2015.01.006openalex-snapshot
Guanidines from ‘toxic substances’ to compounds with multiple biological applications – Detailed outlook on synthetic procedures employed for the synthesis of guanidines
inferred← citeshttps://doi.org/10.1016/j.tet.2005.08.052openalex-snapshot
The first synthesis of pyridinium N-benzoylguanidines by bismuth- and mercury-promoted guanylation of N-iminopyridinium ylide with thioureas
inferred← citeshttps://doi.org/10.1016/j.tet.2025.135035openalex-snapshot
Cationic 1-thia-3-aza-Claisen rearrangement entry to cyclic S-allylic isothioureas
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.02.132openalex-snapshot
Synthesis of highly substituted ureas and thioureas through 1,3-diaza-Claisen rearrangements
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.07.138openalex-snapshot
The first bismuth(III)-catalyzed guanylation of thioureas
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.04.064openalex-snapshot
Optimization of methods for the generation of carbodiimides for zwitterionic 1,3-diaza-Claisen rearrangements
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.154954openalex-snapshot
A formal Pd0-catalyzed 1,3-diaza-Claisen rearrangement
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02721openalex-snapshot
Asymmetric Aza-Claisen Rearrangement between Enantioenriched α-Chiral Allylamines and Allenones
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00667openalex-snapshot
Broadening the Scope of the Zwitterionic 1,3-Diaza-Claisen Rearrangement through a Tethering Strategy
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02524openalex-snapshot
1,3-Diaza-Claisen Rearrangements of Vinyl Pyrrolidines Tethered to In Situ Generated Carbodiimides Afford Ring-Expanded [9,5]- and [9,6]-Bicyclic Guanidines
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00941openalex-snapshot
Boron-Catalyzed Silylative Reduction of Nitriles in Accessing Primary Amines and Imines
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02655openalex-snapshot
Modular Synthesis of Enantioenriched α-Chiral Homoallylic Amidines Enabled by Relay Ir/Cu Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01746openalex-snapshot
Intramolecular Formation of Zwitterionic Intermediates in 1,3-Diaza-Claisen Rearrangements
inferred← citeshttps://doi.org/10.1021/jo401810popenalex-snapshot
Structure–Reactivity Relationships of Zwitterionic 1,3-Diaza-Claisen Rearrangements
inferred← citeshttps://doi.org/10.1021/jp910173dopenalex-snapshot
Theoretical Study on the Reaction Mechanism between 6-Benzyl-6-azabicyclo[2.2.1]hept-2-ene and Benzoyl Isocyanate to Urea and Isourea
inferred← citeshttps://doi.org/10.1021/ol802577zopenalex-snapshot
Facile 1,3-diaza-Claisen Rearrangements of Tertiary Allylic Amines Bearing an Electron-Deficient Alkene
inferred← citeshttps://doi.org/10.3390/molecules170910178openalex-snapshot
A Synthetic Method to Access Symmetric and Non-Symmetric 2-(N,N'-disubstituted)guanidinebenzothiazoles
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