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  2. 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 ...

  3. Dewar–Chatt–Duncanson model - Wikipedia

    en.wikipedia.org/wiki/Dewar–Chatt–Duncanson...

    Main group elements can also form π-complexes with alkenes and alkynes. The β-diketiminato aluminum(I) complex Al{HC(CMeNAr) 2 } (Ar = 2,6-diisopropylphenyl), which bears an Al-based sp x lone pair, reacts with alkenes and alkynes to give alumina (III) cyclopropanes and alumina (III) cyclopropenes in a process analogous to the formation of π ...

  4. Oxidation with dioxiranes - Wikipedia

    en.wikipedia.org/wiki/Oxidation_with_dioxiranes

    Diastereoselective epoxidation may be achieved through the use of alkene starting materials with diastereotopic faces. When racemic 3-isopropylcyclohexene was subjected to DMD oxidation, the trans epoxide, which resulted from attack on the less hindered face of the double bond, was the major product.

  5. α,β-Unsaturated carbonyl compound - Wikipedia

    en.wikipedia.org/wiki/Α,β-Unsaturated_carbonyl...

    An enal (or alkenal) is an organic compound containing both alkene and aldehyde functional groups. In an α,β-unsaturated enal, the alkene is conjugated to the carbonyl group of the aldehyde (formyl group). [3] The simplest enal is acrolein (CH 2 =CHCHO). Other examples include cis-3-hexenal (essence of mowed lawns) and cinnamaldehyde (essence ...

  6. Selenoxide elimination - Wikipedia

    en.wikipedia.org/wiki/Selenoxide_elimination

    Selenoxide elimination (also called α-selenation) [1] is a method for the chemical synthesis of alkenes from selenoxides. It is most commonly used to synthesize α,β-unsaturated carbonyl compounds from the corresponding saturated analogues. [ 2 ]

  7. Why the Royal Kids Might Not Be Allowed to Keep Some of Their ...

    www.aol.com/why-royal-kids-might-not-130400241.html

    Prince William and Kate Middleton joined the rest of the royals for their annual walk around Sandringham on Christmas Day, and brought their kids along for the occasion. And before you ask, yes ...

  8. Hydrosilylation - Wikipedia

    en.wikipedia.org/wiki/Hydrosilylation

    Idealized mechanism for metal-catalysed hydrosilylation of an alkene. Hydrosilylation of alkenes represents a commercially important method for preparing organosilicon compounds. The process is mechanistically similar to the hydrogenation of alkenes. In fact, similar catalysts are sometimes employed for the two catalytic processes.

  9. 24 hours that exposed a schism between Trump and Johnson and ...

    www.aol.com/news/24-hours-exposed-schism-between...

    President-elect Donald Trump has long supported House Speaker Mike Johnson — hosting him on election night, bringing him to the Army-Navy college football game last weekend and backing him ...

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