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α-Amination of Phosphonates: A Direct Synthesis of α-Amino Phosphonic Acids and Their Derivatives

Publication ,  Journal Article
McDonald, SL; Wang, Q
Published in: Synlett
July 9, 2014

A direct approach to access important α-amino phosphonic acids and their derivatives through the formation of C-N bonds is described. Several α-amination reactions of phosphonates that involve electrophilic aminating agents are reviewed. A recent development is highlighted in which an acyclic or cyclic amine is introduced into the α-position of a phosphonate in one step through deprotonative formation of an α-zincate followed by copper-catalyzed amination with an O-acylhydroxylamine. © Georg Thieme Verlag.

Duke Scholars

Published In

Synlett

DOI

EISSN

1437-2096

ISSN

0936-5214

Publication Date

July 9, 2014

Related Subject Headings

  • Organic Chemistry
  • 3405 Organic chemistry
  • 3404 Medicinal and biomolecular chemistry
  • 0305 Organic Chemistry
  • 0304 Medicinal and Biomolecular Chemistry
 

Citation

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Chicago
ICMJE
MLA
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McDonald, S. L., & Wang, Q. (2014). α-Amination of Phosphonates: A Direct Synthesis of α-Amino Phosphonic Acids and Their Derivatives (Accepted). Synlett. https://doi.org/10.1055/s-0034-1378324
McDonald, S. L., and Q. Wang. “α-Amination of Phosphonates: A Direct Synthesis of α-Amino Phosphonic Acids and Their Derivatives (Accepted).” Synlett, July 9, 2014. https://doi.org/10.1055/s-0034-1378324.
McDonald, S. L., and Q. Wang. “α-Amination of Phosphonates: A Direct Synthesis of α-Amino Phosphonic Acids and Their Derivatives (Accepted).” Synlett, July 2014. Scopus, doi:10.1055/s-0034-1378324.
Journal cover image

Published In

Synlett

DOI

EISSN

1437-2096

ISSN

0936-5214

Publication Date

July 9, 2014

Related Subject Headings

  • Organic Chemistry
  • 3405 Organic chemistry
  • 3404 Medicinal and biomolecular chemistry
  • 0305 Organic Chemistry
  • 0304 Medicinal and Biomolecular Chemistry