One pot synthesis of diastereomeric phosphonates

Article abstract of DOI:10.1080/10426500008082404

The reaction of diaryl methylphosphonate with sterically hindered alcohols in presence of sodium hydride provide arylalkyl methylphosphonate esters with high diastereoselectivity at the phosphorus center.

Full text of DOI:10.1080/10426500008082404

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Phosphorus, Sulfur, and
Silicon and the Related
Elements
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One Pot Synthesis
of Diastereomeric
Phosphonates
Shefali Saxena a , Mamta Sharma a & Purnanand
a
a Defence Research & Development
Establishment , Gwalior, 474002, India
Published online: 03 Jan 2007.
To cite this article: Shefali Saxena , Mamta Sharma & Purnanand (2000) One Pot
Synthesis of Diastereomeric Phosphonates, Phosphorus, Sulfur, and Silicon and the
Related Elements, 167:1, 259-266, DOI: 10.1080/10426500008082404
To link to this article: http://dx.doi.org/10.1080/10426500008082404
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