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Self-Polyaddition of Six-Membered Cyclic Carbonate Having Fmoc-Protected Amino Group: Novel Synthetic Method of Polyhydroxyurethane

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/0471220574openalex-snapshot

Protective Groups in Organic Synthesis

inferredcites →https://doi.org/10.1002/apmc.1987.051480105openalex-snapshot

Epoxy resins modified by carbon dioxide

inferredcites →https://doi.org/10.1002/apmc.1989.051700117openalex-snapshot

Polyamines containing β‐hydroxyurethane linkages as curing agents for epoxy resin

inferredcites →https://doi.org/10.1002/app.1990.070410315openalex-snapshot

Epoxy resin modified by aliphatic cyclic carbonates

inferredcites →https://doi.org/10.1007/bf00863130openalex-snapshot

Heterochain polyesters. Communication 56. Mixed block polyesters prepared from polyethylene oxide, dihydric phenols, and aromatic dicarboxylic acid chlorides

inferredcites →https://doi.org/10.1021/jo00795a005openalex-snapshot

9-Fluorenylmethoxycarbonyl amino-protecting group

inferredcites →https://doi.org/10.1021/ma970878jopenalex-snapshot

Anionic Ring-Opening Polymerization of a Cyclic Carbonate Having a Norbornene Structure with Amine Initiators

inferredcites →https://doi.org/10.1139/v87-206openalex-snapshot

Diisopropylethylamine eliminates dipeptide formation during the acylation of amino acids using benzoyl chloride and some alkyl chloroformates

inferredcites →https://doi.org/10.14314/polimery.1989.141openalex-snapshot

Studies on the synthesis of poly(hydroxyurethane)s from diepoxides, carbon dioxide, and diamines

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.4844303openalex-extracted

Biobased, Catalyst-Free Non-Isocyanate Polythiourethane Foams:Highly Dynamic Nature Affords Fast Reprocessability, Extrudability and Refoamability

inferred← citeshttps://doi.org/10.1002/app.38215openalex-snapshot

Polyurethanes from soybean oil, aromatic, and cycloaliphatic diamines by nonisocyanate route

inferred← citeshttps://doi.org/10.1002/macp.201700043openalex-snapshot

Phosgene‐Free Syntheses and Hydrolytic Properties of Water‐Soluble Polyhydroxyurethanes with Ester–Carbonate–Ether Structures in Their Main Chains

inferred← citeshttps://doi.org/10.1002/pat.3522openalex-snapshot

Non‐isocyanate polyurethanes: synthesis, properties, and applications

inferred← citeshttps://doi.org/10.1002/pen.26425openalex-snapshot

High‐performance epoxy hybrid non‐isocyanate polyurethanes prepared from diol‐cyclocarbonation bisphenol A dicyclocarbonate

inferred← citeshttps://doi.org/10.1002/pola.27347openalex-snapshot

An efficient nonisocyanate route to polyurethanes via thiol‐ene self‐addition

inferred← citeshttps://doi.org/10.1007/s11746-011-1995-5openalex-snapshot

Aminolysis Reaction of Glycerol Carbonate in Organic and Hydroorganic Medium

inferred← citeshttps://doi.org/10.1016/b978-0-323-95486-0.00057-0openalex-snapshot

Polyhydroxyurethanes—Sustainable Materials With Broad Potential Applications

inferred← citeshttps://doi.org/10.1016/b978-0-444-53349-4.00107-2openalex-snapshot

ROP of Cyclic Carbonates and ROP of Macrocycles

inferred← citeshttps://doi.org/10.1016/j.cej.2024.154035openalex-snapshot

Biobased, catalyst-free non-isocyanate polythiourethane foams: Highly dynamic nature affords fast reprocessability, extrudability and refoamability

inferred← citeshttps://doi.org/10.1016/j.mtcomm.2022.105263openalex-snapshot

Epoxy-free synthesis of aromatic dicyclocarbonates and the related strong epoxy hybrid non-isocyanate polyurethanes

inferred← citeshttps://doi.org/10.1016/j.polymer.2008.01.025openalex-snapshot

Synthesis, characterization and ring-opening polymerization of a novel six-membered cyclic carbonate bearing pendent allyl ether group

inferred← citeshttps://doi.org/10.1016/j.progpolymsci.2005.01.005openalex-snapshot

Carbon dioxide and carbon disulfide as resources for functional polymers

inferred← citeshttps://doi.org/10.1016/j.reactfunctpolym.2010.11.031openalex-snapshot

Synthesis, characterization, and application of a bifunctional coupler containing a five- and a six-membered ring carbonate

inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00355openalex-snapshot

Isocyanate-Free Routes to Polyurethanes and Poly(hydroxy Urethane)s

inferred← citeshttps://doi.org/10.1021/acs.macromol.3c00220openalex-snapshot

Biobased, Reprocessable Non-isocyanate Polythiourethane Networks with Thionourethane and Disulfide Cross-Links: Comparison with Polyhydroxyurethane Network Analogues

inferred← citeshttps://doi.org/10.1021/acs.macromol.5c02932openalex-snapshot

Highly Efficient Approach to High-Molecular Weight Polyhydroxyurethanes

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00315openalex-snapshot

Modular Approach to 9-Monosubstituted Fluorene Derivatives Using MoV Reagents

inferred← citeshttps://doi.org/10.1021/acsapm.0c00183openalex-snapshot

Nanocomposites of Poly(hydroxyurethane)s with Multiwalled Carbon Nanotubes: Synthesis, Shape Memory, and Reprocessing Properties

inferred← citeshttps://doi.org/10.1021/bk-2013-1144.ch021openalex-snapshot

Biobased Industrial Products from Soybean Biorefinery

inferred← citeshttps://doi.org/10.1021/cr300195nopenalex-snapshot

On the Versatility of Urethane/Urea Bonds: Reversibility, Blocked Isocyanate, and Non-isocyanate Polyurethane

inferred← citeshttps://doi.org/10.1039/c3gc41821aopenalex-snapshot

α,ω-Di(glycerol carbonate) telechelic polyesters and polyolefins as precursors to polyhydroxyurethanes: an isocyanate-free approach

inferred← citeshttps://doi.org/10.3390/macromol5010012openalex-snapshot

Comparative Life Cycle Assessment of Recyclable Polyhydroxyurethanes Synthesized from Five- and Six-Membered Carbonates

inferred← citeshttps://doi.org/10.70675/807729cdz926ez4bdbz9523z5de89eefa168openalex-snapshot

Développement de nanoparticules de poly(hydroxy)uréthane pH- et thermo-stimulable par nanoprécipitation

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