enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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. 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.

  4. Retro-Diels–Alder reaction - Wikipedia

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

    If isolation or reaction of an elusive diene or dienophile is the goal, one of two strategies may be used. Flash vacuum pyrolysis of Diels–Alder adducts synthesized by independent means can provide extremely reactive, short-lived dienophiles (which can then be captured by a unique diene). [11]

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

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

    The inverse electron demand Diels–Alder reaction, or DA INV or IEDDA [1] is an organic chemical reaction, in which two new chemical bonds and a six-membered ring are formed. It is related to the Diels–Alder reaction , but unlike the Diels–Alder (or DA) reaction, the DA INV is a cycloaddition between an electron-rich dienophile and an ...

  6. Sulfolene - Wikipedia

    en.wikipedia.org/wiki/Sulfolene

    In the presence of very reactive dienes (for example 1,3-diphenylisobenzofuran) butadienesulfone behaves as a dienophile and forms the corresponding Diels-Alder adduct. [ 21 ] As early as 1938, Kurt Alder and co-workers reported Diels-Alder adducts from the isomeric 2-sulfolene with 1,3-butadiene and 2-sulfolene with cyclopentadiene .

  7. Cycloisomerization - Wikipedia

    en.wikipedia.org/wiki/Cycloisomerization

    Intramolecular Diels–Alder (IMDA) reactions pair tethered dienes and dienophiles in a [4+2] fashion, the most common being terminal substitution. These transformations are popular in total synthesis and have seen a wide spread use in advance to numerous difficult synthetic targets. [6]

  8. Member of US government employee appeals board sues over ...

    www.aol.com/news/member-us-government-employee...

    (Reuters) -A Democrat who served at the U.S. agency that hears appeals by federal government employees when they are fired or disciplined has filed a lawsuit challenging Republican U.S. President ...

  9. (4+3) cycloaddition - Wikipedia

    en.wikipedia.org/wiki/(4+3)_cycloaddition

    Neutral dienes and cationic allyl systems (most commonly oxyallyl cations) may react in a concerted or stepwise fashion to give seven-membered rings. A number of dienes have been employed in the reaction, although cyclic, electron-rich dienes such as those found in the cyclopentadiene and furan ring systems are the best 4π systems for this ...