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  2. Cyclopentadiene - Wikipedia

    en.wikipedia.org/wiki/Cyclopentadiene

    Cyclopentadiene is a highly reactive diene in the Diels–Alder reaction because minimal distortion of the diene is required to achieve the envelope geometry of the transition state compared to other dienes. [11] Famously, cyclopentadiene dimerizes. The conversion occurs in hours at room temperature, but the monomer can be stored for days at ...

  3. Cyclopentene - Wikipedia

    en.wikipedia.org/wiki/Cyclopentene

    Cyclopentene was first prepared by Carl Gärtner in 1893 from iodocyclopentane with potassium hydroxide.He named it pentamethenylene (German: Pentamethenylen). [3] ...

  4. Methylcyclopentadiene - Wikipedia

    en.wikipedia.org/wiki/Methylcyclopentadiene

    Methylcyclopentadiene is any of three isomeric cyclic dialkenes with the formula C 5 MeH 5 (Me = CH 3).These isomers are the organic precursor to the methylcyclopentadienyl ligand (C 5 H 4 Me, often denoted as Cp′), commonly found in organometallic chemistry.

  5. Trimethylsilyl group - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_group

    A trimethylsilyl group (abbreviated TMS) is a functional group in organic chemistry.This group consists of three methyl groups bonded to a silicon atom [−Si(CH 3) 3], which is in turn bonded to the rest of a molecule.

  6. List of isomers of tridecane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_tridecane

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  7. 1,2-Cyclopentanedione - Wikipedia

    en.wikipedia.org/wiki/1,2-Cyclopentanedione

    1,2-Cyclopentanedione is the organic compound with the formula (CH 2) 3 (CO) 2.It is one of two isomeric cyclopentanediones, the other being 1,3-cyclopentanedione.It was first prepared by base-induced condensation of di ethylglutarate with diethyloxalate, followed by hydrolysis of the resulting diketodiester followed by decarboxylation. [1]

  8. Pentamethylcyclopentadiene - Wikipedia

    en.wikipedia.org/wiki/Pentamethylcyclopentadiene

    1,2,3,4,5-Pentamethylcyclopentadiene is a cyclic diene with the formula C 5 (CH 3) 5 H, often written C 5 Me 5 H, where Me is CH 3. [3] It is a colorless liquid. [1]1,2,3,4,5-Pentamethylcyclopentadiene is the precursor to the ligand 1,2,3,4,5-pentamethylcyclopentadienyl, which is often denoted Cp* (C 5 Me 5) and read as "C P star", the "star" signifying the five methyl groups radiating from ...

  9. Di-tert-butylcyclopentadiene - Wikipedia

    en.wikipedia.org/wiki/Di-tert-butylcyclopentadiene

    Di-tert-butylcyclopentadiene is an organic compound with the formula (Me 3 C) 2 C 5 H 4, where Me = methyl.It is a colorless liquid that is soluble in organic solvents. The compound is the conjugate acid of the di-tert-butylcyclopentadienyl ligand, (Me 3 C) 2 C 5 H 3 − [1] (sometimes abbreviated Cp ‡−).