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Epoxy Compounds

Known as: Epoxy Compounds [Chemical/Ingredient], Oxiranes, Epoxides 
Organic compounds that include a cyclic ether with three ring atoms in their structure. They are commonly used as precursors for POLYMERS such as… 
National Institutes of Health

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Narrower (46)

1,2-dichloro-3,4-epoxybutane1,2-epoxy-5-hexene1,3-diphenylpropene oxide2,2-bis(4-glycidyloxyphenyl)propane
In Bloodagonistsantagonists & inhibitorschemical synthesis

Papers overview

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Review
2011
Review
2011
Gold α-oxo carbenoids in catalysis: catalytic oxygen-atom transfer to alkynes.
An overview of reactive gold α-oxo carbenoid intermediates in the gold-catalyzed functionalization of alkynes is presented. Such… 
Highly Cited
2004
Highly Cited
2004
Chiral ionic liquids as stationary phases in gas chromatography.
Recently, it has been found that room-temperature ionic liquids can be used as stable, unusual selectivity stationary phases… 
Highly Cited
1998
Highly Cited
1998
Viscoelastic Responses of Polyhedral Oligosilsesquioxane Reinforced Epoxy Systems.
The properties of nanostructured plastics are determined by complex relationships between the type and size of the… 
Highly Cited
1989
Highly Cited
1989
Roles of individual human cytochrome P-450 enzymes in the bioactivation of benzo(a)pyrene, 7,8-dihydroxy-7,8-dihydrobenzo(a)pyrene, and other dihydrodiol derivatives of polycyclic aromatic…
Human liver microsomes oxidized 7,8-dihydroxy-7,8-dihydrobenzo(a)pyrene [B(a)P-7,8-diol] to products that yield DNA adduct… 
Highly Cited
1985
Highly Cited
1985
4‐Hydroxyalk‐2‐enals are substrates for glutathione transferase
Highly Cited
1982
Highly Cited
1982
Inhibition of the mutagenicity of bay-region diol epoxides of polycyclic aromatic hydrocarbons by naturally occurring plant phenols: exceptional activity of ellagic acid.
Ferulic, caffeic, chlorogenic, and ellagic acids, four naturally occurring plant phenols, inhibit the mutagenicity and… 
Highly Cited
1978
Highly Cited
1978
Binding of benzo[a]pyrene 7,8-diol-9,10-epoxides to DNA, RNA, and protein of mouse skin occurs with high stereoselectivity.
The formation, stereostructure, and cellular reactions of the 7,8-diol-9,10-epoxide metabolites of the carcinogen benzo[a]pyrene… 
Highly Cited
1976
Highly Cited
1976
Metabolism of benzo(a)pyrene and benzo (a)pyrene derivatives to mutagenic products by highly purified hepatic microsomal enzymes.
Highly Cited
1976
Highly Cited
1976
Enzymatic conversion of benzo(a)pyrene leading predominantly to the diol-epoxide r-7,t-8-dihydroxy-t-9,10-oxy-7,8,9,10-tetrahydrobenzo(a)pyrene through a single enantiomer of r-7, t-8-dihydroxy-7,8…
Benzo(a)pyrene is metabolically and stereospecifically converted by mixed-function oxidases of rat liver microsomes and epoxide… 
Highly Cited
1971
Highly Cited
1971
A radiometric assay for hepatic epoxide hydrase activity with [7-3H] styrene oxide.
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