Search results

Search for "organophosphorus compounds" in Full Text gives 27 result(s) in Beilstein Journal of Organic Chemistry.

Valence isomerization of cyclohepta-1,3,5-triene and its heteroelement analogues

  • Helen Jansen,
  • J. Chris Slootweg and
  • Koop Lammertsma

Beilstein J. Org. Chem. 2011, 7, 1713–1721, doi:10.3762/bjoc.7.201

Graphical Abstract
  • +G(d,p) level [7]. Also for the phosphepine system [108], benzannulation leads to interesting targets. Namely, the thermal lability of the transition-metal-complexed 3H-benzophosphepine 33 was explored by Lammertsma et al. for the synthesis of a variety of organophosphorus compounds by means of [1
PDF
Album
Review
Published 21 Dec 2011

Synthesis of phosphorothioates using thiophosphate salts

  • Babak Kaboudin and
  • Fatemeh Farjadian

Beilstein J. Org. Chem. 2006, 2, No. 4, doi:10.1186/1860-5397-2-4

Graphical Abstract
  • alumina under solvent-free conditions using microwave irradiation. Introduction Organophosphorus compounds have found a wide range of application in the areas of industrial, agricultural, and medicinal chemistry owing to their biological and physical properties as well as their utility as synthetic
  • the utility of surface-mediated reactions for the synthesis of organophosphorus compounds, [37][38][39][40][41][42][43][44][45][46][47][48] we report a new method for the preparation of phosphorothioates by reaction of diethyl phosphite with alkyl halides in the presence of a mixture of ammonium
  • group (hard electrophilic center) gives the O-acylation product. As a part of our efforts to explore the utility of surface-mediated reactions for the synthesis of organophosphorus compounds, [16][17][18] herein we report a new method for the preparation of phosphorothioates by reaction of diethyl
PDF
Album
Supp Info
Full Research Paper
Published 16 Mar 2006
Other Beilstein-Institut Open Science Activities