High yield synthesis of tetraethyl alkylenediphosphonates via the Michaelis-Arbuzov reaction

Article abstract of DOI:10.1080/00397919808004465

A high-yield synthesis of tetraethyl alkylenediphosphonates was achieved via the Michaelis-Arbuzov reaction. Application of optimized reaction conditions for a series of homologous alkylenediphosphonates establishes the generality of the approach.

Full text of DOI:10.1080/00397919808004465

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High Yield Synthesis of
Tetraethyl Alkylene-
Diphosphonates via the
Michaelis-Arbuzov Reaction
Julie A. Griffith a , David J. McCauley a
,
Richard E. Barrans Jr. b & Albert W. Herlinger a
a Department of Chemistry, Loyola University
Chicago, Chicago, Illinois, 60626
b Chemistry Division, Argonne National
Laboratory, Argonne, Illinois, 60439
Published online: 23 Aug 2006.
To cite this article: Julie A. Griffith , David J. McCauley , Richard E. Barrans
Jr. & Albert W. Herlinger (1998) High Yield Synthesis of Tetraethyl Alkylene-
Diphosphonates via the Michaelis-Arbuzov Reaction, Synthetic Communications:
An International Journal for Rapid Communication of Synthetic Organic
Chemistry, 28:23, 4317-4323, DOI: 10.1080/00397919808004465
To link to this article: http://dx.doi.org/10.1080/00397919808004465
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