On the public citation graph
A Mild and Efficient Modified Hofmann Rearrangement
0 signed · 81 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1021/ja00096a082openalex-snapshot
Nature of N-Bromosuccinimide in Basic Media: The True Oxidizing Species in the Hofmann Rearrangement
inferredcites →https://doi.org/10.1021/jo00061a022openalex-snapshot
Preparation of methyl carbamates from primary alkyl- and arylcarboxamides using hypervalent iodine
inferredcites →https://doi.org/10.1021/jo00912a019openalex-snapshot
Reactions of amines. XVIII. Oxidative rearrangement of amides with lead tetraacetate
inferredcites →https://doi.org/10.1107/s0108768187010541openalex-snapshot
Crystal structure of 2-bromo-5-hydroxyethoxy-7,7,8,8-tetracyanoquinodimethane, BHTCNQ
inferredcites →https://doi.org/10.1246/bcsj.61.1401openalex-snapshot
Halogenation Using Quaternary Ammonium Polyhalides. IX. One-Step Syntheses of Acylureas and Carbamates from Amides by Use of Tetrabutylammonium Tribromide and DBU
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/0471264180.os078.26openalex-snapshot
Methyl Carbamate Formation Via Modified H ofmann Rearrangement Reactions: Methyl N‐(p‐Methoxyphenyl)Carbamate
inferred← citeshttps://doi.org/10.1002/advs.74920openalex-snapshot
Electrochemical Hofmann Rearrangement for Modular Synthesis of Unsymmetrical Ureas and Late‐Stage Modification of Drugs
inferred← citeshttps://doi.org/10.1002/asia.202000092openalex-snapshot
Synthesis of (R)‐3‐(tert‐Butoxycarbonylamino)‐4‐(2,4,5‐trifluorophenyl)butanoic Acid, a Key Intermediate, and the Formal Synthesis of Sitagliptin Phosphate
inferred← citeshttps://doi.org/10.1002/asia.70859openalex-snapshot
Redefining N ‐Bromosuccinimide: Chemistry Beyond Allylic Bromination
inferred← citeshttps://doi.org/10.1002/chem.202300675openalex-snapshot
Spectroscopic and Computational Study of the Organocatalytic Umpolung of Bromocations: An Accelerated Stereoselective Dibromination Protocol**
inferred← citeshttps://doi.org/10.1002/chin.199811068openalex-snapshot
ChemInform Abstract: A Mild and Efficient Modified Hofmann Rearrangement.
inferred← citeshttps://doi.org/10.1002/cjoc.201090071openalex-snapshot
Design and Synthesis of Two Aromatic Amines with Dendritic Structure
inferred← citeshttps://doi.org/10.1002/ejoc.202300767openalex-snapshot
A New Strategy for the Preparation of 3‐Amino‐4‐hydroxypyrrolidinone‐4‐acetic Acid, an Unusual γ‐Amino Acid found in Microsclerodermins
inferred← citeshttps://doi.org/10.1007/978-3-662-04835-1_134openalex-snapshot
Hofmann rearrangement (Hofmann degradation reaction)
inferred← citeshttps://doi.org/10.1007/s10593-011-0660-0openalex-snapshot
NitropyridineS. 9*. Synthesis of substituted 3-amino-5-nitropyridines
inferred← citeshttps://doi.org/10.1007/s10967-009-0005-yopenalex-snapshot
Synthesis of a carbon-14 analogue of aryl N-alkoxycarbamates and its application for synthesis of unsymmetrical N,N′-urea derivatives
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00037-4openalex-snapshot
Vinyl- and Arylnitrogen Compounds
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00623-6openalex-snapshot
6.15 Hofmann, Curtius, Schmidt, Lossen, and Related Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-323-95948-3.00006-4openalex-snapshot
Rearrangements, participation, and fragmentation reactions
inferred← citeshttps://doi.org/10.1016/b978-012059475-7/50008-9openalex-snapshot
Running the Reaction
inferred← citeshttps://doi.org/10.1016/j.rechem.2026.103447openalex-snapshot
An alternative synthetic route to Nepicastat enabled by palladium catalyzed cyclization
inferred← citeshttps://doi.org/10.1016/j.tet.2011.10.001openalex-snapshot
Perspectives on the synthesis of organic carbamates
inferred← citeshttps://doi.org/10.1016/j.tet.2017.10.073openalex-snapshot
Mechanistic study on iodine-catalyzed aromatic bromination of aryl ethers by N -Bromosuccinimide
inferred← citeshttps://doi.org/10.1016/j.tet.2019.01.055openalex-snapshot
Preparation of a novel bromine complex and its application in organic synthesis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.11.134openalex-snapshot
An efficient modification of the Hofmann rearrangement: synthesis of methyl carbamates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.07.147openalex-snapshot
Application of α-chloroaldoxime O-methanesulfonates to one-pot synthesis of N,N′,N″-substituted guanidines via Tiemann rearrangement
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.01.126openalex-snapshot
TBCA mediated microwave-assisted Hofmann rearrangement
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.04.011openalex-snapshot
Efficient synthesis of methyl carbamate via Hofmann rearrangement in the presence of TsNBr2
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.07.036openalex-snapshot
Direct α-amination of nitrones achieved by DBU-activated N -haloimides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.01.025openalex-snapshot
Hofmann rearrangement of primary carboxamides and cyclic imides using DCDMH and application to the synthesis of gabapentin and its potential peptide prodrugs
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154683openalex-snapshot
AgF-mediated Hofmann-type reaction of N-tosyl cyclic imides with silicate esters
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)00985-6openalex-snapshot
A convenient route to 1-benzyl 3-aminopyrrolidine and 3-aminopiperidine
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)02433-4openalex-snapshot
Synthesis of chiral α-amino acids
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00400openalex-snapshot
Use of Bromine and Bromo-Organic Compounds in Organic Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01133openalex-snapshot
Interrupted Curtius Rearrangements of Quaternary Proline Derivatives: A Flow Route to Acyclic Ketones and Unsaturated Pyrrolidines
inferred← citeshttps://doi.org/10.1021/acs.joc.5c03064openalex-snapshot
Fine-Tuned Imino-Diels–Alder Reaction for the Sustainable Synthesis of Nicotinonitriles via Push–Pull Vinylogous Enamino Nitriles
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00329openalex-snapshot
Palladium-Catalyzed Carbamate-Directed Regioselective Halogenation: A Route to Halogenated Anilines
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01530openalex-snapshot
Synthesis of Azobenzenes Using N-Chlorosuccinimide and 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU)
inferred← citeshttps://doi.org/10.1021/acs.oprd.1c00440openalex-snapshot
Continuous-Flow Hofmann Rearrangement Using Trichloroisocyanuric Acid for the Preparation of 2-Benzoxazolinone
inferred← citeshttps://doi.org/10.1021/acs.oprd.3c00332openalex-snapshot
Multigram Electrochemical Hofmann Rearrangement Using a Spinning Three-Dimensional Anode
inferred← citeshttps://doi.org/10.1021/acs.oprd.4c00197openalex-snapshot
Micelle-Enabled Hofmann Rearrangement in Water
inferred← citeshttps://doi.org/10.1021/acs.oprd.5c00234openalex-snapshot
Hectogram-Scale Synthesis of Carbamates Using Electrochemical Hofmann Rearrangement in Flow
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03925openalex-snapshot
Harnessing Dual Reactivity of N-Chloroamides for Cascade C–H Amidation/Chlorination of Indoles under Cobalt-Catalysis: Overriding Hofmann Rearrangement Pathway Leading to Aminocarbonylation
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04418openalex-snapshot
Polyfluoroalkanoic Acids as Fluoroalkylating Reagents: Strategy for Direct Access to Rf-Embedded Amides
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c01122openalex-snapshot
Asymmetric Synthesis of Small Molecule Inhibitors of IL-17A via Crystallization-Induced Diastereoselective Strecker Reaction
inferred← citeshttps://doi.org/10.1021/acsomega.3c04797openalex-snapshot
Electrooxidative Hofmann Rearrangement of Phthalimides to Access Anthranilate Derivatives
inferred← citeshttps://doi.org/10.1021/jo101504eopenalex-snapshot
Synthesis of Methyl-1-(tert-butoxycarbonylamino)-2-vinylcyclopropanecarboxylate via a Hofmann Rearrangement Utilizing Trichloroisocyanuric Acid as an Oxidant
inferred← citeshttps://doi.org/10.1021/ma301448bopenalex-snapshot
Direct Probing of Regioregularity for Polycarbodiimide Systems via15N NMR Analysis
inferred← citeshttps://doi.org/10.1021/ma301639mopenalex-snapshot
Determining the Regioregularity in Alkyne Polycarbodiimides and Their Orthogonal Modification of Side Chains To Yield Perfectly Alternating Functional Polymers
inferred← citeshttps://doi.org/10.1021/mz3001836openalex-snapshot
Resolving the Regioregularity of Poly(N-n-hexyl-N′-phenylcarbodiimide) via Nitrogen-15 Labeling
inferred← citeshttps://doi.org/10.1021/op2000699openalex-snapshot
Multijet Oscillating Disc Millireactor: A Novel Approach for Continuous Flow Organic Synthesis
inferred← citeshttps://doi.org/10.1034/j.1399-3011.1999.00005.xopenalex-snapshot
Synthesis and characterization of a series of novel glutamic γ‐15N‐anilide dipeptides
inferred← citeshttps://doi.org/10.1038/s42004-026-02131-2openalex-snapshot
Metal-free strategy for C–N cross-coupling of benzamide with sulfonamide enabled by a Smiles rearrangement
inferred← citeshttps://doi.org/10.1039/b801909fopenalex-snapshot
Synthesis of imidazolidin-2-one-4-carboxylate and of (tetrahydro)pyrimidin-2-one-5-carboxylate via an efficient modification of the Hofmann rearrangement
inferred← citeshttps://doi.org/10.1039/c2cc33914eopenalex-snapshot
Effect of catalytic alkali metal bromide on Hofmann-type rearrangement of imides
inferred← citeshttps://doi.org/10.1039/c3gc40440dopenalex-snapshot
Sustainable routes to polyurethane precursors
inferred← citeshttps://doi.org/10.1039/c5ra13708jopenalex-snapshot
Metal-free C–N cross-coupling of electrophilic compounds and N-haloimides
inferred← citeshttps://doi.org/10.1039/c5ra14528gopenalex-snapshot
4-Dodecylbenzenesulfonic acid (DBSA) promoted solvent-free diversity-oriented synthesis of primary carbamates, S-thiocarbamates and ureas
inferred← citeshttps://doi.org/10.1039/c6gc03123dopenalex-snapshot
Development of a concise, scalable synthesis of a CCR1 antagonist utilizing a continuous flow Curtius rearrangement
inferred← citeshttps://doi.org/10.1039/c8ob01059eopenalex-snapshot
Electrochemical Hofmann rearrangement mediated by NaBr: practical access to bioactive carbamates
inferred← citeshttps://doi.org/10.1039/d1cc00116gopenalex-snapshot
Electrochemical rearrangement protocols towards the construction of diverse molecular frameworks
inferred← citeshttps://doi.org/10.1039/d3gc04355jopenalex-snapshot
Unified and green oxidation of amides and aldehydes for the Hofmann and Curtius rearrangements
inferred← citeshttps://doi.org/10.1039/d3py00594aopenalex-snapshot
An electrochemical Hofmann rearrangement on acrylamide copolymers
inferred← citeshttps://doi.org/10.1039/d4gc05807kopenalex-snapshot
A novel electrochemical Hofmann-type rearrangement enables facile access to α-oxoisocyanates for the synthesis of N -carbamoylacetamides
inferred← citeshttps://doi.org/10.1039/d4qo02437kopenalex-snapshot
Recent progress in electrochemical rearrangement reactions
inferred← citeshttps://doi.org/10.1080/10426500802446710openalex-snapshot
Novel Phosphoranes Containing Urea Derivatives: Synthesis and Characterization
inferred← citeshttps://doi.org/10.1081/scc-120014028openalex-snapshot
1,8-DIAZABICYCLO[5.4.0]UNDEC-7-ENE (DBU): A POWERFUL CATALYST FOR THE MICHAEL ADDITION REACTION OF β-KETOESTERS TO ACRYLATES AND ENONES
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4010880/v1openalex-snapshot
Separation of OH-containing compounds from the essential oil mixture via a one-pot synthesis of carbamates, antimicrobial evaluation and dynamic 1H NMR study of their derivatives
inferred← citeshttps://doi.org/10.2174/138527211795378173openalex-snapshot
Recent Developments on the Carbamation of Amines
inferred← citeshttps://doi.org/10.2174/1385272823666191023115842openalex-snapshot
Recent Advances in the Applications of the Intramolecular Suzuki Cross-coupling Reaction in Cyclization and Heterocyclization: An Update
inferred← citeshttps://doi.org/10.30707/etd2023.20230711063203283312.999937openalex-snapshot
An ( R )-4-Phenyl-1,3-oxazolidine-2-Thione Mediated Approach to 2, 3-Disubstituted Oxetanes and the Key Hydroxyethyl Isostere of the Hiv Protease Inhibitor Darunavir. Preparation of Non-evans Syn Glycolate Aldol Addition Products. a New Direction for the Curtius Rearrangement in the Dehomologation…
inferred← citeshttps://doi.org/10.30707/etd2024.20240827063557736135.999970openalex-snapshot
Redefining the Scope of the Curtius Reaction via a Dehomologation of Carboxylic Acids Bearing an Alpha Leaving Group. Determining the Stereoelectronic Limitations of the Crimmins Anti-selective Asymmetric Glycolate Aldol Addition Reaction.
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.