Stereocontrolled Radical Thiophosphorylation
Molhm Nassir, Michał Ociepa, Hai‐Jun Zhang, Lauren N. Grant, Bryan J. Simmons, Martins S. Oderinde, Yu Kawamata, Anthony N. Cauley, Michael A. Schmidt, Martin D. Eastgate, Phil S. Baran
Abstract
The first practical, fully stereoselective P(V)-radical hydrophosphorylation is presented herein by using simple, limonene-derived reagent systems. A set of reagents have been developed that upon radical initiation react smoothly with olefins and other radical acceptors to generate P -chiral products, which can be further diversified (with conventional 2e – chemistry) to a range of underexplored bioisosteric building blocks. The reactions have a wide scope with excellent chemoselectivity, and the unexpected stereochemical outcome has been supported computationally and experimentally. Initial ADME studies are suggestive of the promising properties of this rarely explored chemical space.