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Study on products and reaction paths for synthesis of 3,4-dihydro-2H-3-phenyl-1,3-benzoxazine from phenol, aniline and formaldehyde
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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)1521-3935(19990701)200:7<1745::aid-macp1745>3.0.co;2-dopenalex-snapshot
1,3,5-Triphenylhexahydro-1,3,5-triazine - active intermediate and precursor in the novel synthesis of benzoxazine monomers and oligomers
inferredcites →https://doi.org/10.1002/chin.197709197openalex-snapshot
ChemInform Abstract: EQUILIBRIUMS AND KINETICS OF N‐HYDROXYMETHYLAMINE FORMATION FROM AROMATIC EXOCYCLIC AMINES AND FORMALDEHYDE. EFFECTS OF NUCLEOPHILICITY AND CATALYST STRENGTH UPON MECHANISMS OF CATALYSIS OF CARBINOLAMINE FORMATION
inferredcites →https://doi.org/10.1002/jhet.130openalex-snapshot
Self termination of ring opening reaction of p‐substituted phenol‐based benzoxazines: An obstructive effect via intramolecular hydrogen bond
inferredcites →https://doi.org/10.1002/pola.1994.080320614openalex-snapshot
Phenolic materials via ring‐opening polymerization: Synthesis and characterization of bisphenol‐A based benzoxazines and their polymers
inferredcites →https://doi.org/10.1002/pola.20428openalex-snapshot
Preparation and properties of novel benzoxazine and polybenzoxazine with maleimide groups
inferredcites →https://doi.org/10.1002/pola.24566openalex-snapshot
Influence of electronic effects from bridging groups on synthetic reaction and thermally activated polymerization of bisphenol‐based benzoxazines
inferredcites →https://doi.org/10.1002/pola.25993openalex-snapshot
Synthesis of 9,9‐bis(4‐aminophenyl)fluorene‐based benzoxazine and properties of its high‐performance thermoset
inferredcites →https://doi.org/10.1016/b978-0-444-53790-4.00050-3openalex-snapshot
Using Molecular Simulation to Predict the Physical and Mechanical Properties of Polybenzoxazines
inferredcites →https://doi.org/10.1016/c2010-0-66598-9openalex-snapshot
Handbook of Benzoxazine Resins
inferredcites →https://doi.org/10.1016/j.cclet.2009.12.012openalex-snapshot
Synthesis of a novel benzoxazine containing benzoxazole structure
inferredcites →https://doi.org/10.1016/j.cclet.2010.01.007openalex-snapshot
Synthesis of benzoxazine-based phenolic resin containing furan groups
inferredcites →https://doi.org/10.1016/j.polymer.2007.12.042openalex-snapshot
Aromatic diamine-based benzoxazines and their high performance thermosets
inferredcites →https://doi.org/10.1016/j.progpolymsci.2007.07.002openalex-snapshot
Polybenzoxazines—New high performance thermosetting resins: Synthesis and properties
inferredcites →https://doi.org/10.1021/cr60085a001openalex-snapshot
A Summary of the Reactions of Aldehydes with Amines.
inferredcites →https://doi.org/10.1021/ie402978sopenalex-snapshot
Kinetics of 3,4-Dihydro-2H-3-phenyl-1,3-benzoxazine Synthesis from Mannich Base and Formaldehyde
inferredcites →https://doi.org/10.1021/ja004048oopenalex-snapshot
Asymmetric Mono-oxazine: An Inevitable Product from Mannich Reaction of Benzoxazine Dimers
inferredcites →https://doi.org/10.1021/ja00440a052openalex-snapshot
Equilibriums and kinetics of N-hydroxymethylamine formation from aromatic exocyclic amines and formaldehyde. Effects of nucleophilicity and catalyst strength upon mechanisms of catalysis of carbinolamine formation
inferredcites →https://doi.org/10.1021/ja01123a007openalex-snapshot
N,N-Bis-(hydroxybenzyl)-amines: Synthesis from Phenols, Formaldehyde and Primary Amines1
inferredcites →https://doi.org/10.1021/ja01126a050openalex-snapshot
Monomeric Products from the Condensation of Phenol with Formaldehyde and Primary Amines
inferredcites →https://doi.org/10.1021/ja01134a039openalex-snapshot
Condensation of Naphthols with Formaldehyde and Primary Amines1
inferredcites →https://doi.org/10.1021/ja01166a094openalex-snapshot
3,4-Dihydro-1,3,2H-Benzoxazines. Reaction of Polyhydroxybenzenes with N-Methylolamines1
inferredcites →https://doi.org/10.1021/ja01170a063openalex-snapshot
3,4-Dihydro-1,3,2H-Benzoxazines. Reaction of p -Substituted Phenols with N,N-Dimethylolamines
inferredcites →https://doi.org/10.1021/ja01239a022openalex-snapshot
Condensation Products of Aldehydes and Ketones with o-Aminobenzyl Alcohol and o-Hydroxybenzylamine
inferredcites →https://doi.org/10.1021/ja01635a065openalex-snapshot
Condensation of Hydroxyaromatic Compounds with Formaldehyde and Primary Aromatic Amines
inferredcites →https://doi.org/10.1021/jo01027a038openalex-snapshot
Condensation of Halophenols with Formaldehyde and Primary Amines 1
inferredcites →https://doi.org/10.1021/jo01039a058openalex-snapshot
Mono-1,3-benzoxazines from Hydroquinone1
inferredcites →https://doi.org/10.1021/jo01069a053openalex-snapshot
Bis-m-oxazines from Hydroquinone1
inferredcites →https://doi.org/10.1021/la303730mopenalex-snapshot
Synthesis and Surface Properties of Low Surface Free Energy Silane-Functional Polybenzoxazine Films
inferredcites →https://doi.org/10.1021/ma202694popenalex-snapshot
Cross-Linked Benzoxazine–Benzimidazole Copolymer Electrolyte Membranes for Fuel Cells at Elevated Temperature
inferredcites →https://doi.org/10.1021/ma3004218openalex-snapshot
Synthesis and Properties of Highly Cross-Linked Thermosetting Resins of Benzocyclobutene-Functionalized Benzoxazine
inferredcites →https://doi.org/10.1021/ma902416hopenalex-snapshot
A Highly Reactive Benzoxazine Monomer, 1-(2-Hydroxyethyl)-1,3-Benzoxazine: Activation of Benzoxazine by Neighboring Group Participation of Hydroxyl Group
inferredcites →https://doi.org/10.1039/c39820000469openalex-snapshot
Behaviour of an N-(o-hydroxybenzyl)-β-amino-acid in the presence of dehydrating agents. Synthesis of a 3,4-dihydro-2H-1,3-benzoxazine
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.4688349openalex-extracted
Studies on Catalyst Assisted Low-Temperature Curing of Benzoxazines
inferred← citeshttps://doi.org/10.1002/app.45408openalex-snapshot
Remarkable improvement of thermal stability of main‐chain benzoxazine oligomer by incorporating o‐norbornene as terminal functionality
inferred← citeshttps://doi.org/10.1002/ceat.70002openalex-snapshot
Impact of Ring‐Closed Ratio on Properties of Benzoxazine via Solvent‐Free Continuous Flow Synthesis
inferred← citeshttps://doi.org/10.1002/pola.28755openalex-snapshot
Microwave‐assisted solvent‐free synthesis of novel benzoxazines: A faster and environmentally friendly route to the development of bio‐based thermosetting resins
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2021.110671openalex-snapshot
Synthesis and properties of the bio-based isomeric benzoxazine resins: Revealing the effect of the neglected short alkyl substituents
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2026.115079openalex-snapshot
Dynamic covalent strategies and structure–property relationships of reprocessable Polybenzoxazines
inferred← citeshttps://doi.org/10.1016/j.matchemphys.2025.130959openalex-snapshot
The novel benzoxazine olefin copolymer forms composite phase change materials with excellent heat storage, insulation, and flame retardant properties
inferred← citeshttps://doi.org/10.1016/j.polymer.2017.10.053openalex-snapshot
Synthesis of artificial urushi via ring-opening reaction of benzoxazine with renewable cardanol
inferred← citeshttps://doi.org/10.1016/j.reactfunctpolym.2024.105880openalex-snapshot
Studies on catalyst assisted low-temperature curing of benzoxazines
inferred← citeshttps://doi.org/10.1016/j.rineng.2025.104023openalex-snapshot
Efficient scale-up of benzoxazinone derivative-deferasirox intermediate synthesis: A study on cyanuric chloride as a chlorinating agent
inferred← citeshttps://doi.org/10.1021/acs.jpca.9b05065openalex-snapshot
Benzoxazine Formation Mechanism Evaluation by Direct Observation of Reaction Intermediates
inferred← citeshttps://doi.org/10.1021/acsomega.5c07831openalex-snapshot
Strategies to Enhance the Reaction Efficiency: A Model Study Using Bisphenol A, Hexylamine, and Formaldehyde for the Synthesis of 1,3-Benzoxazine Monomer
inferred← citeshttps://doi.org/10.1038/s41428-022-00664-6openalex-snapshot
CHCl3/triethanolamine: a new mixed solvent for preparing high-molecular-weight main-chain benzoxazines through Mannich-type polycondensation
inferred← citeshttps://doi.org/10.1039/c5ra17395gopenalex-snapshot
Effect of phenol on the synthesis of benzoxazine
inferred← citeshttps://doi.org/10.11606/t.46.2022.tde-26102022-103622openalex-snapshot
Estudo de reações catalíticas por espectroscopia de ação e mobilidade iônica acopladas à espectrometria de massas
inferred← citeshttps://doi.org/10.1557/jmr.2019.92openalex-snapshot
Synthesis and electrochemical properties of benzoxazine-based heteroatom-doped carbon materials
inferred← citeshttps://doi.org/10.2298/jsc180530001sopenalex-snapshot
3,4-Dihydro-2H-1,3-benzoxazines and their oxo-derivatives - Chemistry and bioactivities
inferred← citeshttps://doi.org/10.3390/app10010422openalex-snapshot
Synthesis of Benzoxazine-Based N-Doped Mesoporous Carbons as High-Performance Electrode Materials
inferred← citeshttps://doi.org/10.58837/chula.the.2022.61openalex-snapshot
Scale up of benzoxazinone derivative synthesis in batch reactor
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