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Sulfurization of Trivalent Phosphorus Compounds with 1,2-Dithiole-3-thione

  • Drabowicz, Jozef (Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of Heteroorganic Chemistry) ;
  • Luczak, Jerzy (Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of Heteroorganic Chemistry) ;
  • Lyzwa, Piotr (Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of Heteroorganic Chemistry) ;
  • Mikolajczyk, Marian (Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of Heteroorganic Chemistry) ;
  • Pedersen, Carl Th. (Department of Chemistry, Odense University)
  • Published : 2004.11.20
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References

  1. Heydt, H.; Regitz, M. In Methoden der Organischen Chemie(Houben-Weyl); Ed. Regitz, M., Ed.; Georg Thieme verlag: Stuttart-New York, 1982; Vol. E-2, pp 77-92.
  2. Screttas, C.; Isbell, A. F. J. Org. Chem. 1963, 27, 2573. https://doi.org/10.1021/jo01054a064
  3. Harwood, H. J.; Pollart, K. A. J. Org. Chem. 1963, 28, 3430. https://doi.org/10.1021/jo01047a035
  4. Maier, L. Hel. Chim. Acta, Chem. Ber. 1961, 94, 3043.
  5. Maier, L. Hel. Chim. Acta, Chem. Ber. 1964, 47, 120. https://doi.org/10.1002/hlca.19640470115
  6. Olah, G. A.; Hehemann, D. J. Org. Chem. 1977, 42, 2190. https://doi.org/10.1021/jo00432a046
  7. Maier, L. In Topics in Phosphorus Chemistry; Gayson, M., Griffith, E. J., Eds.; Intrascience: New York, 1965; Vol. 2, p 43.
  8. Miranda, R.; Salas, I.; Mondragon, J.; Valasco, L. Synthetic Commun. 1992, 22, 1077. https://doi.org/10.1080/00397919208019299
  9. Young, D. P.; McEwen, W. E.; Valez, D. C.; Johnson, J. W.; Vander Werf, C. A. Tetrahedron Lett. 1964, 359.
  10. Pedersen, C. Th. Sulfur Lett. 1997, 20, 179.
  11. Miles, M. M.; Wager, J. S.; Wilson, J. D.; Siedle, A. R. J. Org. Chem. 1975, 40, 2577. https://doi.org/10.1021/jo00906a001
  12. Ogata, Y.; Yamashita, M.; Mizutani, M. Bull. Chem. Soc. Jpn. 1976, 49, 1721. https://doi.org/10.1246/bcsj.49.1721
  13. Horner, L.; Balzer, W. D. Tetrahedron Lett. 1965, 1175.
  14. Zon, G.; De Bruin, K. E.; Naumann, K.; Mislow, K. J. Am. Chem. Soc. 1969, 91, 7023. https://doi.org/10.1021/ja01053a022
  15. Horner, L. Pure Appl. Chem. 1964, 9, 225. https://doi.org/10.1351/pac196409020225
  16. Zon, G.; Mislow, K. Top. Curr. Chem. 1971, 19, 61.
  17. Drabowicz, J.;Lyzwa, P.; Omelanczuk, J.; Pietrusiewicz, K. M.; Mikolajczyk, M. Tetrahedron: Asymmetry 1999, 10, 2757. https://doi.org/10.1016/S0957-4166(99)00264-5
  18. Wang, F.; Polavarapu, P. L.; Drabowicz, J.; Mikolajczyk, M. J. Org. Chem. 200, 65, 7561. https://doi.org/10.1021/jo000923c
  19. Michalski, J.; Skrzypczynski, Z. J. Organomet. Chem. 1975, 97, C31. https://doi.org/10.1016/S0022-328X(00)89481-4
  20. Wang, F.; Polavarapu, P. L.; Drabowicz, J.; Mikolajczyk, M. J. Org. Chem. 2001, 66, 9015. https://doi.org/10.1021/jo0107406
  21. Trippett, S. Phosphorus Sulfur 1976, 1, 89. https://doi.org/10.1080/03086647608070718
  22. Meinetsberger, E.; Schoffer, A.; Behringer, H. Synthesis 1961, 802.
  23. Sherry, A. D.; Purcell, K. F. J. Am. Chem. Soc. 1972, 94, 1848. https://doi.org/10.1021/ja00761a010
  24. Ballah, V.; Subbarayan, P. J. Org. Chem. 1960, 25, 1833. https://doi.org/10.1021/jo01080a618
  25. Schimenz, G. P. Chem. Ber. 1966, 99, 504. https://doi.org/10.1002/cber.19660990218
  26. Schindlbauer, H. Chem. Ber. 1967, 100, 3432. https://doi.org/10.1002/cber.19671001035

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  2. Sulfurization of Trivalent Phosphorus Compounds with 1,2-Dithiole-3-thione. vol.36, pp.13, 2005, https://doi.org/10.1002/chin.200513188
  3. Optically Active T-Butylphenylphosphinothioic Acid: Synthesis, Selected Structural Studies and Applications as a Chiral Solvating Agent vol.189, pp.7, 2004, https://doi.org/10.1080/10426507.2014.905567
  4. Synthesis and Reactivity of 3H-1,2-dithiole-3-thiones vol.26, pp.12, 2004, https://doi.org/10.3390/molecules26123595