Recent advances using cyclopropanols and cyclobutanols in ring-opening asymmetric synthesis

Due to high ring strain energies, cyclopropanols and cyclobutanols have a strong tendency of breaking the endocyclic C-C bonds to participate in versatile organic transformations. With an inherent three-dimensional structure, cyclopropanols and cyclobutanols have the advantage of synthesizing linear or cyclic molecules with stereogenic centers via ring-opening asymmetric synthesis. There are three strategies for the ring-opening of cyclopropanols and cyclobutanols usually involved in asymmetric synthesis: 1) fl-carbon elimination of metal alkoxide; 2) radical ring-opening; 3) ring-opening via semipinacol rearrangement. The present review has highlighted the progress developed in the last five years.

Automated summary

Due to high ring strain energies, cyclopropanols and cyclobutanols have a strong tendency of breaking the endocyclic C-C bonds to participate in versatile organic transformations. Ring-opening asymmetric synthesis of these compounds allows for the synthesis of linear or cyclic molecules with stereogenic centers.