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  2. Epoxide - Wikipedia

    en.wikipedia.org/wiki/Epoxide

    A generic epoxide. In organic chemistry, an epoxide is a cyclic ether, where the ether forms a three-atom ring: two atoms of carbon and one atom of oxygen. This triangular structure has substantial ring strain, making epoxides highly reactive, more so than other ethers. They are produced on a large scale for many applications.

  3. Fosfomycin - Wikipedia

    en.wikipedia.org/wiki/Fosfomycin

    The fosfomycin molecule has an epoxide or oxirane ring, which is highly strained and thus very reactive. [citation needed] Fosfomycin has broad antibacterial activity against both Gram-positive and Gram-negative pathogens, with useful activity against E. faecalis, E. coli, and various Gram-negatives such as Citrobacter and Proteus. Given a ...

  4. Ring strain - Wikipedia

    en.wikipedia.org/wiki/Ring_strain

    In alkanes, optimum overlap of atomic orbitals is achieved at 109.5°. The most common cyclic compounds have five or six carbons in their ring. [6] Adolf von Baeyer received a Nobel Prize in 1905 for the discovery of the Baeyer strain theory, which was an explanation of the relative stabilities of cyclic molecules in 1885.

  5. Episulfide - Wikipedia

    en.wikipedia.org/wiki/Episulfide

    In organic chemistry, episulfides are a class of organic compounds that contain a saturated, heterocyclic ring consisting of two carbon atoms and one sulfur atom. It is the sulfur analogue of an epoxide or aziridine. They are also known as thiiranes, olefin sulfides, thioalkylene oxides, and thiacyclopropanes. Episulfides are less common and ...

  6. Base-promoted epoxide isomerization - Wikipedia

    en.wikipedia.org/wiki/Base-promoted_epoxide...

    In reactions of chiral, non-racemic epoxides, the configuration of the allylic alcohol product matches that of the epoxide substrate at the carbon whose C–O bond does not break (the starred carbon below). Besides β-elimination some other reactions [2] [3] are possible, as metalation of the epoxide ring can take place competitively.

  7. Fürst-Plattner Rule - Wikipedia

    en.wikipedia.org/wiki/Fürst-Plattner_Rule

    Nucleophilic ring-opening of this class of epoxides can occur by an attack at either the C1 or C2-position. It is well known that nucleophilic ring-opening reactions of these substrates can proceed with excellent regioselectivity. The Fürst-Plattner rule attributes this regiochemical control to a large preference for the reaction pathway that ...

  8. EBay to pay $59 million to settle US charges over illegal ...

    www.aol.com/news/ebay-pay-59-million-settle...

    (Reuters) -EBay agreed to pay $59 million and upgrade compliance measures to resolve U.S. Department of Justice allegations it didn't try hard enough to stop criminals from buying devices for ...

  9. Category:Epoxides - Wikipedia

    en.wikipedia.org/wiki/Category:Epoxides

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