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  2. 1-Bromododecane - Wikipedia

    en.wikipedia.org/wiki/1-bromododecane

    Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene, which is 1-dodecene in the case of 1-bromododecane. These conditions lead to anti-Markovnikov addition, giving the 1-bromo derivative. [2] 1-Bromododecane can also be prepared by treating dodecanol with hydrobromic acid and sulfuric acid. [3]

  3. Organobromine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organobromine_chemistry

    Free-radical substitution with bromine is commonly used to prepare organobromine compounds. Carbonyl-containing, benzylic, allylic substrates are especially prone to this reactions. For example, the commercially significant bromoacetic acid is generated directly from acetic acid and bromine in the presence of phosphorus tribromide catalyst:

  4. 1-Bromopentane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopentane

    Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene, which is 1-pentene in the case of 1-bromopentane. These conditions lead to anti-Markovnikov addition, giving the 1-bromo derivative. [2] It is also formed by the reaction of 1-pentanol with hydrogen bromide.

  5. Wittig reaction - Wikipedia

    en.wikipedia.org/wiki/Wittig_reaction

    Wittig reactions are most commonly used to convert aldehydes and ketones to alkenes. [1] [2] [3] Most often, the Wittig reaction is used to introduce a methylene group using methylenetriphenylphosphorane (Ph 3 P=CH 2). Using this reagent, even a sterically hindered ketone such as camphor can be converted to its methylene derivative.

  6. Category:Bromoalkenes - Wikipedia

    en.wikipedia.org/wiki/Category:Bromoalkenes

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  7. 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 ...

  8. Julia olefination - Wikipedia

    en.wikipedia.org/wiki/Julia_olefination

    The Julia olefination (also known as the Julia–Lythgoe olefination) is the chemical reaction used in organic chemistry of phenyl sulfones (1) with aldehydes (or ketones) to give alkenes (olefins)(3) after alcohol functionalization and reductive elimination using sodium amalgam or SmI 2. The reaction is named after the French chemist Marc Julia.

  9. 2-Bromohexane - Wikipedia

    en.wikipedia.org/wiki/2-Bromohexane

    2-Bromohexane is the organobromine compound with the formula CH 3 CH(Br)(CH 2) 3 CH 3. It is a colorless liquid. The compound is chiral. Most 2-bromoalkanes are prepared by addition of hydrogen bromide to the 1-alkene. Markovnikov addition proceeds in the absence of free-radicals, i.e. give the 2-bromo derivatives. [2]