Synthesis of diversely functionalised 2,2-disubstituted oxetanes: fragment motifs in new chemical space

Chem Commun (Camb). 2015 Oct 28;51(84):15446-9. doi: 10.1039/c5cc05740j.

Abstract

Di-, tri- and tetra-substituted oxetane derivatives with combinations of ester, amide, nitrile, aryl, sulfone and phosphonate substituents are prepared as fragments or building blocks for drug discovery. The synthesis of these novel oxetane functional groups, in new chemical space, is achieved via rhodium-catalysed O-H insertion and C-C bond forming cyclisation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclization
  • Drug Discovery
  • Ethers, Cyclic / chemical synthesis*
  • Ethers, Cyclic / chemistry
  • Molecular Structure

Substances

  • Ethers, Cyclic
  • oxetane