rektaanides

Rektaanides are a class of organic compounds that are characterized by the presence of a single carbon-carbon triple bond within a cyclic structure. These molecules are also known as cyclic alkynes. The nomenclature for rektaanides follows standard IUPAC rules, with the triple bond being assigned the lowest possible locant within the ring. The presence of the triple bond in a ring introduces significant ring strain, especially in smaller rings, which affects their chemical reactivity and physical properties.

The synthesis of rektaanides can be challenging due to the inherent strain. Common methods involve cyclization reactions where a precursor containing a triple bond or functionalities that can be converted into a triple bond are brought together. For instance, the intramolecular coupling of diynes or the dehydrohalogenation of dihaloalkanes within a cyclic framework can lead to the formation of rektaanides. The feasibility of forming these compounds is highly dependent on the ring size. Smaller rings (less than eight members) are generally very difficult to synthesize and are often unstable.

Rektaanides exhibit reactivity typical of alkynes, including addition reactions across the triple bond. However, the cyclic constraint can influence the stereochemistry and regiochemistry of these reactions. Due to the strain, some rektaanides can undergo ring-opening reactions or act as strained alkyne precursors for further synthetic transformations. Their applications are primarily found in academic research, serving as interesting targets for studying strain effects in organic chemistry and as building blocks for more complex molecules.