Enantioselective Allylboration of Acetylene: A Versatile Tool for the Stereodivergent Synthesis of Natural Products

Efficient catalytic methods that allow the use of simple and abundant chemical feedstocks for the preparation of synthetically versatile compounds are central to modern synthetic chemistry. Acetylene is a basic feedstock with a remarkable production over one million tons per year, although it is underutilized in the stereoselective synthesis of fine chemicals. Here we report a facile catalytic multicomponent reaction that allows for the enantio‐ and diastereoselective allylboration of acetylene gas. This process is catalyzed by a chiral copper catalyst, operates without specialized equipment or pressurization, and provides chiral skipped dienes bearing stereodefined and orthogonally functionalized olefins with excellent levels of chemo‐, regio‐, enantio‐ and diastereoselectivity. The combined stereochemical features and orthogonal functionalization make the products privileged structural scaffolds to access the complete set of stereoisomers of the chiral skipped diene core through simple enantio‐ and diastereodivergent pathways. The utility of the method is demonstrated with the enantioselective synthesis of three bioactive natural skipped diene products, namely (+)‐Nyasol, (+)‐Hinokiresinol and Phorbasin C, and other related synthetically relevant chiral molecules. A method for the enantioselective conversion of acetylene gas under ambient temperature and pressure into a chiral orthogonally functionalized skipped diene is reported. The product represents a privileged scaffold to access the full set of stereoisomers of the chiral skipped diene core through simple stereodivergent pathways, thus serving as a versatile intermediate for the enantioselective total synthesis of natural skipped diene products.