Intramolecular monomer-on-monomer (MoM) Mitsunobu cyclization for the synthesis of benzofused thiadiazepine-dioxides

Chem Commun (Camb). 2011 Dec 14;47(46):12524-6. doi: 10.1039/c1cc14807a. Epub 2011 Oct 26.

Abstract

The utilization of a monomer-on-monomer (MoM) intramolecular Mitsunobu cyclization reaction employing norbornenyl-tagged (Nb-tagged) reagents is reported for the synthesis of benzofused thiadiazepine-dioxides. Facile purification was achieved via ring-opening metathesis (ROM) polymerization initiated by one of three metathesis catalyst methods: (i) free metathesis catalyst, (ii) surface-initiated catalyst-armed silica, or (iii) surface-initiated catalyst-armed Co/C magnetic nanoparticles.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Benzene / chemistry*
  • Chemistry Techniques, Synthetic / methods*
  • Cyclization
  • Nanoparticles / chemistry
  • Thiadiazines / chemical synthesis*
  • Thiadiazines / chemistry*

Substances

  • Thiadiazines
  • Benzene