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  2. Methylcyclopropane - Wikipedia

    en.wikipedia.org/wiki/Methylcyclopropane

    This colorless gas is the monomethyl derivative of cyclopropane. Reactions. Methylcyclopropane, like many other cyclopropanes, undergoes ring-opening reactions. Bond ...

  3. 1-Methylcyclopropene - Wikipedia

    en.wikipedia.org/wiki/1-Methylcyclopropene

    Methallyl chloride Phenyl lithium (base) LiCl + PhH 1-Methyl­cyclopropene The phenyllithium should be free of lithium halides. The corresponding reaction of allyl chloride and phenyllithium main affords cyclopropylbenzene. Isomers Methylcyclopropene can refer to either of two isomers, 1- methylcyclopropene covered in this article, or 3- methylcyclopropene which is not covered in this article ...

  4. Cyclopropane - Wikipedia

    en.wikipedia.org/wiki/Cyclopropane

    Cyclopropane is the cycloalkane with the molecular formula (CH 2) 3, consisting of three methylene groups (CH 2) linked to each other to form a triangular ring. The small size of the ring creates substantial ring strain in the structure.

  5. Walsh diagram - Wikipedia

    en.wikipedia.org/wiki/Walsh_diagram

    Walsh diagrams in conjunction with molecular orbital theory can also be used as a tool to predict reactivity. By generating a Walsh Diagram and then determining the HOMO/LUMO of that molecule, it can be determined how the molecule is likely to react. In the following example, the Lewis acidity of AH 3 molecules such as BH 3 and CH 3 + is predicted.

  6. Cyclopropanes - Wikipedia

    en.wikipedia.org/wiki/Cyclopropanes

    Cyclopropane derivatives are numerous. [4] Many biomolecules and pharmaceutical drugs feature the cyclopropane ring. Famous example is aminocyclopropane carboxylic acid, which is the precursor to ethylene, a plant hormone. [5] The pyrethroids are the basis of many insecticides. [6] Several cyclopropane fatty acids are known.

  7. Cyclopropanation - Wikipedia

    en.wikipedia.org/wiki/Cyclopropanation

    Structure of U-106305, a derivative of a cyclopropane fatty acid with six cyclopropane rings, isolated from Streptomyces sp. Although cyclopropanes are relatively rare in biochemistry, many cyclopropanation pathways have been identified in nature. The most common pathways involve ring closure reactions of carbocations in terpenoids.

  8. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    Norbornane (also called bicyclo[2.2.1]heptane). Unsubstituted cycloalkanes that contain a single ring in their molecular structure are typically named by adding the prefix "cyclo" to the name of the corresponding linear alkane with the same number of carbon atoms in its chain as the cycloalkane has in its ring.

  9. Methylenecyclopropane - Wikipedia

    en.wikipedia.org/wiki/Methylenecyclopropane

    It is a hydrocarbon which, as the name suggests, is derived from the addition of a methylene (=CH 2) substituent to a cyclopropane ring. It is a colourless, easily condensed gas that is used as a reagent in organic synthesis .