Recent advances in the applications of [1.1.1]-propellane in organic synthesis

Abstract As a highly strained small molecule, [1.1.1]-propellane has been widely used in various synthetic transformations owing to the exceptional reactivity of the central bond between the two bridgehead carbons. Utilizing strain-release approaches, the rapid development of strategies for the construction of bicyclo[1.1.1]pentane (BCP) and cyclobutane derivatives using [1.1.1]-propellane as the starting material has been witnessed in the past few years. In this review, we highlight the most recent advances in this field. Accordingly, the reactivity of [1.1.1]-propellane can be divided into three pathways, including radical, anionic and transition metal-catalyzed pathways under appropriateconditions.