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  2. Diels–Alder reaction - Wikipedia

    en.wikipedia.org/wiki/Diels–Alder_reaction

    Resonance structures of normal-demand dienes and dienophiles. In general, the regioselectivity found for both normal and inverse electron-demand Diels–Alder reaction follows the ortho-para rule, so named, because the cyclohexene product bears substituents in positions that are analogous to the ortho and para positions of disubstituted arenes ...

  3. Inverse electron-demand Diels–Alder reaction - Wikipedia

    en.wikipedia.org/wiki/Inverse_electron-demand...

    Other common classes of dienes are oxo- and aza- butadienes. [9] [11] The key quality of a good DA INV diene is a significantly lowered HOMO and LUMO, as compared to standard DA dienes. Below is a table showing a few commonly used DA INV dienes, their HOMO and LUMO energies, and some standard DA dienes, along with their respective MO energies.

  4. 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.

  5. Tetraphenylcyclopentadienone - Wikipedia

    en.wikipedia.org/wiki/Tetraphenylcyclopentadienone

    The central ring can serve as a diene in Diels–Alder reactions with various dienophiles. For example, reaction with benzyne leads to 1,2,3,4-tetraphenylnaphthalene and reaction with diphenylacetylene leads to hexaphenylbenzene. [5] In this way, it is a precursor to graphene-like molecules, [6] such as coronene.

  6. Aza-Diels–Alder reaction - Wikipedia

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

    The imine is often generated in situ from an amine and formaldehyde.An example is the reaction of cyclopentadiene with benzylamine to an aza norbornene. [9]The catalytic cycle starts with the reactions of the aromatic amine with formaldehyde to the imine and the reaction of the ketone with proline to the diene.

  7. Social Security Is Set to Run Out of Money in 2034. Here's ...

    www.aol.com/finance/social-security-set-run...

    Social Security has two other funding sources: benefit taxes on some seniors and interest income earned on money in the program's trust funds. But both of those are in danger right now. The ...

  8. Quinone - Wikipedia

    en.wikipedia.org/wiki/Quinone

    The quinones are a class of organic compounds that are formally "derived from aromatic compounds [such as benzene or naphthalene] by conversion of an even number of –CH= groups into –C(=O)– groups with any necessary rearrangement of double bonds", resulting in "a fully conjugated cyclic dione structure".

  9. Obesity in Cats: 5 Vet-Approved Ways to Help Them Lose Weight

    www.aol.com/obesity-cats-5-vet-approved...

    Risks Posed by Obesity in Cats. In the US, about 40% of the cat population is obese or overweight. Overweight cats have from 10 to 20% excess fat, and obese cats are 20 to 30% over their normal ...