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  2. Di-π-methane rearrangement - Wikipedia

    en.wikipedia.org/wiki/Di-π-methane_rearrangement

    Rearrangement of Mariano's diene. One example was the photolysis of Mariano's compound, 3,3‑dimethyl-1,1,5,5‑tetraphenyl-1,4‑pentadiene. In this symmetric diene, the active π bonds are conjugated to arenes, which does not inhibit the reaction. [4] [5] [6] Pratt's diene has two possibilities for rearrangement: a and b.

  3. Sigmatropic reaction - Wikipedia

    en.wikipedia.org/wiki/Sigmatropic_reaction

    The Cope rearrangement is an extensively studied organic reaction involving the [3,3] sigmatropic rearrangement of 1,5-dienes. [ 14 ] [ 15 ] [ 16 ] It was developed by Arthur C. Cope . For example, 3,4-dimethyl-1,5-hexadiene heated to 300 °C yields 2,6-octadiene.

  4. Cope rearrangement - Wikipedia

    en.wikipedia.org/wiki/Cope_rearrangement

    The rearrangement is widely used in organic synthesis. It is symmetry-allowed when it is suprafacial on all components. The transition state of the molecule passes through a boat or chair like transition state. An example of the Cope rearrangement is the expansion of a cyclobutane ring to a cycloocta-1,5-diene ring:

  5. Organic photochemistry - Wikipedia

    en.wikipedia.org/wiki/Organic_photochemistry

    Two further early examples were the rearrangement of 1,1,5,5-tetraphenyl-3,3-dimethyl-1,4-pentadiene (the "Mariano" molecule) [22] and the rearrangement of barrelene to semibullvalene. [23] We note that, in contrast to the cyclohexadienone reactions which used n- π * excited states, the di- π -methane rearrangements utilize π - π * excited ...

  6. Diels–Alder reaction - Wikipedia

    en.wikipedia.org/wiki/Diels–Alder_reaction

    Dienes with bulky terminal substituents (C1 and C4) decrease the rate of reaction, presumably by impeding the approach of the diene and dienophile. [28] An especially reactive diene is 1-methoxy-3-trimethylsiloxy-buta-1,3-diene, otherwise known as Danishefsky's diene. [29]

  7. Retro-Diels–Alder reaction - Wikipedia

    en.wikipedia.org/wiki/Retro-Diels–Alder_reaction

    Release of nitrogen from six-membered, cyclic diazenes is common and often spontaneous at room temperature. Such a reaction can be utilized in click reactions where alkanes react with a 1,2,4,5-tetrazine in a diels alder then retro diels alder reaction with the loss of nitrogen. In this another example, the epoxide shown undergoes rDA at 0 °C.

  8. NYT ‘Connections’ Hints and Answers Today, Tuesday, December 10

    www.aol.com/nyt-connections-hints-answers-today...

    December 10, 2024 at 12:25 AM. Spoilers ahead! We've warned you. We mean it. ... December 10, 2024. Today's NYT Connections puzzle for Tuesday, December 10, 2024The New York Times.

  9. Electrocyclic reaction - Wikipedia

    en.wikipedia.org/wiki/Electrocyclic_reaction

    In organic chemistry, an electrocyclic reaction is a type of pericyclic, rearrangement reaction where the net result is one pi bond being converted into one sigma bond or vice versa. [1] These reactions are usually categorized by the following criteria: Reactions can be either photochemical or thermal.

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