Fragmentation of a phenylphosphonamidic acid as a new technique for the generation of phenyl dioxophosphorane

Phosphorus, Sulfur and Silicon and Related Elements

Volumn 115, Issue , 1996, Pages 93-98

  Quin, Gyöngyi Szakal ^a   Jankowski, Stefan ^a   Quin, Louis D ^a  

^a UNIVERSITY OF MASSACHUSETTS   (United States)

Author keywords

N (1 adamantyl) phenylphosphonamidic acid; Phenyl dioxophosphorane; Phosphonylation

Indexed keywords

EID: 0042358959     PISSN: 10426507     EISSN: None     Source Type: Journal    
DOI: 10.1080/10426509608037956     Document Type: Article

References (11)

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3. L. D. Quin, Coord. Chem. Rev., 137, 525 (1994).
4. L. D. Quin and B. G. Marsi, J. Am. Chem. Soc., 107, 3389 (1985).
5. L. D. Quin and X.-P. Wu, Heteroatom Chem., 2, 359 (1991).
6. R. Hirschmann, K. M. Yager, C. M. Taylor, W. Moore, P. A. Sprengeler, J. Witherington, B. W. Phillips and A. B. Smith, III, J. Am. Chem. Soc., 117, 6370 (1995).
7. M. de F. Fernandez, C. P. Vlaar, H. Fan, Y.-H. Liu, F. R. Franczek and R. P. Hammer, J. Org. Chem., 60, 7390 (1995).
8. W. P. Malachowski and J. K. Coward, J. Org. Chem., 59, 7625 (1994).
9. N. S. Chandrakumar, C. P. Carron, D. M. Meyer, P. M. Beardsley, S. A. Nash, L. L. Tam and M. Rafferty, Bioorg. Med. Chem. Lett., 3, 309 (1993).
10. L. D. Quin and S. Jankowski, unpublished results.
11. 2, δ 160.6. All solvents were carefully dried and distilled before use, and apparatus was generally flame-dried. Reactions were conducted under argon.