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  2. Sharpless asymmetric dihydroxylation - Wikipedia

    en.wikipedia.org/wiki/Sharpless_asymmetric_di...

    In the example shown below, the para-methoxybenzoyl substituent serves primarily as a source of steric bulk to allow the catalyst to differentiate the two faces of the alkene. [23] SAD scheme 3. It is often difficult to obtain high diastereoselectivity on cis-disubstituted alkenes when both ends of the olefin have similar steric environments.

  3. Grieco elimination - Wikipedia

    en.wikipedia.org/wiki/Grieco_elimination

    The Grieco elimination is an organic reaction describing the elimination reaction of an aliphatic primary alcohol through a selenide to a terminal alkene. [1] [2] It is named for Paul Grieco. The alcohol first reacts with o-nitrophenylselenocyanate and tributylphosphine to form a selenide via a nucleophilic substitution on the electron ...

  4. Horner–Wadsworth–Emmons reaction - Wikipedia

    en.wikipedia.org/wiki/Horner–Wadsworth–Emmons...

    The final elimination of oxaphosphetanes 4a and 4b yield (E)-alkene 5 and (Z)-alkene 6, with the by-product being a dialkyl-phosphate. The mechanism of the Horner-Wadsworth-Emmons reaction The ratio of alkene isomers 5 and 6 is not dependent upon the stereochemical outcome of the initial carbanion addition and upon the ability of the ...

  5. Ring-closing metathesis - Wikipedia

    en.wikipedia.org/wiki/Ring-closing_metathesis

    In addition to terminal alkenes, tri- and tetrasubstituted alkenes have been used in RCM reactions to afford substituted cyclic olefin products. [32] Ring-closing metathesis has also been used to cyclize rings containing an alkyne to produce a new terminal alkene , or even undergo a second cyclization to form bicycles.

  6. Terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Terminal_alkene

    In organic chemistry, terminal alkenes (alpha-olefins, α-olefins, or 1-alkenes) are a family of organic compounds which are alkenes (also known as olefins) with a chemical formula C x H 2x, distinguished by having a double bond at the primary, alpha (α), or 1-position. [1]

  7. Riley oxidation - Wikipedia

    en.wikipedia.org/wiki/Riley_oxidation

    Allylic oxidation can be predicted by the substitution pattern on the olefin. In the case of 1,2-disubstituted olefins, reaction rates follow CH > CH 2 > CH 3: Geminally-substituted olefins react in the same order of reaction rates as above: [2] Trisubstituted alkenes experience reactivity at the more substituted end of the double bond.

  8. Straight-chain terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Straight-chain_terminal_alkene

    Straight-chain terminal alkenes, also called linear alpha olefins (LAO) or normal alpha olefins (NAO), are alkenes (olefins) having a chemical formula C n H 2n, distinguished from other alkenes with a similar molecular formula by being terminal alkenes, in which the double bond occurs at the alpha (α-, 1-or primary) position, and by having a linear (unbranched) hydrocarbon chain.

  9. Wilkinson's catalyst - Wikipedia

    en.wikipedia.org/wiki/Wilkinson's_catalyst

    In practice, terminal and disubstituted alkenes are good substrates, but more hindered alkenes are slower to hydrogenate. The hydrogenation of alkynes is troublesome to control since alkynes tend to be reduced to alkanes, via intermediacy of the cis-alkene. [ 14 ]