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  2. Cyclobutane - Wikipedia

    en.wikipedia.org/wiki/Cyclobutane

    Cyclobutane is a cycloalkane and organic compound with the formula (CH 2) 4. Cyclobutane is a colourless gas and is commercially available as a liquefied gas. Derivatives of cyclobutane are called cyclobutanes. Cyclobutane itself is of no commercial or biological significance, but more complex derivatives are important in biology and ...

  3. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    Ball-and-stick model of cyclobutane In organic chemistry , the cycloalkanes (also called naphthenes , but distinct from naphthalene ) are the monocyclic saturated hydrocarbons . [ 1 ] In other words, a cycloalkane consists only of hydrogen and carbon atoms arranged in a structure containing a single ring (possibly with side chains ), and all of ...

  4. Cyclobutanone - Wikipedia

    en.wikipedia.org/wiki/Cyclobutanone

    Kischner synthesized cyclobutanone from cyclobutanecarboxylic acid. The Russian chemist Nikolai Kischner first prepared cyclobutanone in a low yield from cyclobutanecarboxylic acid.

  5. Category:Cyclobutanes - Wikipedia

    en.wikipedia.org/wiki/Category:Cyclobutanes

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  6. Cyclobutanol - Wikipedia

    en.wikipedia.org/wiki/Cyclobutanol

    Cyclobutanol is an organic compound with the chemical formula C 4 H 8 O; it is defined as a cyclobutyl group with a hydroxyl group pendant and thus a cycloalkanol. Physically, it is a yellowish clear liquid [1] that crystallizes orthorhombically at low-temperatures.

  7. Pyrimidine dimer - Wikipedia

    en.wikipedia.org/wiki/Pyrimidine_dimer

    Cyclobutane dimer (CPD) (left), 6,4-dimer (6-4PP) (right) Pyrimidine dimers encompass several types, each with distinct structures and implications for DNA integrity. [citation needed] Cyclobutane pyrimidine dimer (CPD) is a dimer which features a four-membered ring formed by the fusion of two double-bonded carbons from adjacent pyrimidines.

  8. Ladderane - Wikipedia

    en.wikipedia.org/wiki/Ladderane

    The final cyclobutane is formed by a Wolff rearrangement, and the alkyl chain is installed by a Wittig olefination. Synthesis of [5]-ladderane lipid pentacycloannamoxic acid In 2016, Burns and co-workers at Stanford University reported an enantioselective synthesis of both the [3]- and [5]-ladderane lipid tails and their incorporation into a ...

  9. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Acyclic aliphatic/non-aromatic compound Cyclic aliphatic/non-aromatic compound (cyclobutane)In organic chemistry, hydrocarbons (compounds composed solely of carbon and hydrogen) are divided into two classes: aromatic compounds and aliphatic compounds (/ ˌ æ l ɪ ˈ f æ t ɪ k /; G. aleiphar, fat, oil).