Английская Википедия:Cyclopropanes

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Cyclopropanes are a family of organic compounds containing the cyclopropyl group. The parent is cyclopropane (Шаблон:Chem2).

Synthesis and reactions

Most cyclopropanes are not prepared from the parent cyclopropane, which is somewhat inert. Cyclopropyl groups are often prepared by cyclization of 1,3-difunctional alkanes. An example of the former, cyclopropyl cyanide is prepared by the reaction of 4-chlorobutyronitrile with a strong base.[1] Phenylcyclopropane is produced analogously from the 1,3-dibromide.[2]

A second major route to cyclopropanes entails addition of methylene (or its substituted derivatives) to an alkene, a process called cyclopropanation.[3]

Substituted cyclopropanes undergo the reactions associated with the cyclopropyl ring or the substituents. Vinylcyclopropanes are a special case as they undergo vinylcyclopropane rearrangement.

Applications and occurrence

Файл:(R,R)-(+)-trans-chrysanthemic acid.svg
(1R,3R)- or (+)-trans-chrysanthemic acid.

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.

Файл:1-aminocyclopropanecarboxylic acid 200.svg
1-Aminocyclopropane-1-carboxylic acid plays an important role in the biosynthesis of the plant hormone ethylene.[5]

Cyclopropane derivatives are numerous.[7] Many biomolecules and pharmaceutical drugs feature the cyclopropane ring. Famous example is aminocyclopropane carboxylic acid, which is the precursor to ethylene, a plant hormone.

References

Шаблон:Cycloalkanes