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  2. Trimethylolpropane triglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Trimethylolpropane...

    As the molecule has 3 oxirane functionalities, a key use is modifying and reducing the viscosity of epoxy resins. [11] These reactive diluent modified epoxy resins may then be further formulated into CASE applications: Coatings, [12] Adhesives, [13] Sealants, [14] Elastomers. The use of the diluent does effect mechanical properties and ...

  3. Sharpless epoxidation - Wikipedia

    en.wikipedia.org/wiki/Sharpless_epoxidation

    The Sharpless epoxidation is viable with a large range of primary and secondary alkenic alcohols. Furthermore, with the exception noted above, a given dialkyl tartrate will preferentially add to the same face independent of the substitution on the alkene.To demonstrate the synthetic utility of the Sharpless epoxidation, the Sharpless group created synthetic intermediates of various natural ...

  4. Trimethylolethane triglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Trimethylolethane...

    As the molecule has 3 oxirane functionalities, a key use is modifying and reducing the viscosity of epoxy resins but giving higher functionality. [7] These reactive diluent modified epoxy resins may then be further formulated into CASE applications: Coatings, Adhesives, Sealants, and Elastomers. The use of the diluent does effect mechanical ...

  5. 1,4-Cyclohexanedimethanol diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/1,4-Cyclohexanedimethanol...

    These reactive diluent modified epoxy resins may then be further formulated into which may then be formulated into CASE applications: Coatings, [10] Adhesives, Sealants, [11] Elastomers, and electronic encapsulant. [12] The use of the diluent does affect mechanical properties and microstructure of epoxy resins. [13] [14]

  6. Poly(propylene glycol) diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Poly(propylene_glycol...

    The molecule has 2 oxirane functionalities, and so a key use is modifying and reducing the viscosity of epoxy resins. [9] [10] These reactive diluent modified epoxy resins may then be further formulated into CASE applications: coatings, [11] adhesives, sealants, and elastomers. It produces epoxy coatings with high impact resistance. [12]

  7. Asymmetric nucleophilic epoxidation - Wikipedia

    en.wikipedia.org/wiki/Asymmetric_nucleophilic_ep...

    Lithium, magnesium, and calcium [12] alkylperoxides have also been employed as asymmetric nucleophilic epoxidation reagents. Simple tartrate and pseudoephedrine ligands are effective in combination with these metals; however, little detailed information about the precise mechanisms of these systems is known.

  8. Epoxide - Wikipedia

    en.wikipedia.org/wiki/Epoxide

    A compound containing the epoxide functional group can be called an epoxy, epoxide, oxirane, and ethoxyline. Simple epoxides are often referred to as oxides. Thus, the epoxide of ethylene (C 2 H 4) is ethylene oxide (C 2 H 4 O). Many compounds have trivial names; for instance, ethylene oxide is called "oxirane".

  9. Payne rearrangement - Wikipedia

    en.wikipedia.org/wiki/Payne_rearrangement

    The Payne rearrangement is the isomerization, under basic conditions, of 2,3-epoxy alcohols to isomeric 1,2-epoxy alcohols with inversion of configuration. Aza- and thia-Payne rearrangements of aziridines and thiiraniums, respectively, are also known. [1]