A convenient synthesis of 2-alkoxy-2-oxo-1,4,2-oxazaphosphinanes

Heteroatom Chemistry

Volumn 18, Issue 1, 2007, Pages 65-69

  Wang, Bin ^a   Miao, Zhiwei ^a   Huang, You ^a   Chen, Ruyu ^a  

^a NANKAI UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ORGANIC COMPOUNDS; PROTONS; STEREOCHEMISTRY; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL); X RAY DIFFRACTION ANALYSIS;

CHEMICAL SHIFTS; DICHLOROPHOSPHINITES; GEOMETRIC STEREOISOMERS; ORGANOPHOSPHORUS HETEROCYCLES;

PHOSPHORUS COMPOUNDS;

EID: 33846869049     PISSN: 10427163     EISSN: 10981071     Source Type: Journal    
DOI: 10.1002/hc.20258     Document Type: Article

References (18)

1. Allen, M. C.; Fuhrer, W.; Tuck, B.; Wade, R. J Med Chem 1998, 32, 1652-1661.
2. Baylis, E. K.; Campbell, C. D.; Dingwall, J. G. J Chem Soc, Perkin Trans 1 1984, 2845-2853.
3. Kafarski, P.; Lejczak, B. Phosphorus, Sulfur, Sillion 1991, 63, 193-215.
4. Hirschmann, R.; Smith, A. B.; Taylor, C. M.; Benkovic, P. A.; Taylor, S. D.; Yager, K. M.; Sprengler, P. A.; Venkovic, S. J. Science 1994, 265, 234-237.
5. Nishizuka, Y. Nature 1984, 308, 693-698.
6. Boyd, V. L.; Summers, M. F.; Ludeman, S. M.; Egan, W.; Zon, G.; Regan, J. B. J Med Chem 1987, 30, 366-374.
7. Wu, S. Y.; Casida, J. E. Phosphorus, Sulfur, Silicon 1995, 102, 177-184.
8. Reddy, C. D.; Reddy, M. S.; Berlin, K. D. Phosphorus, Sulfur, Silicon 1995, 102, 103-109.
9. Dimukhametov, M. N.; Bajandina, E. V.; Davydova, E. Y.; Dobrynin, A. B.; Guvaidullin, A. T.; Litvinov, I. A.; Alfonsov, V. A. Mendeleev Commun 2001, 1-2.
10. Dimukhametov, M. N.; Bajandina, E. V.; Davydova, E. Y.; Litvinov, I. A.; Gubaidullin, A. T.; Dobrynin, A. B.; Zyablikova, T. A.; Alfonsov, V. A. Heteroatom Chem 2003, 14, 56-61.
11. Maury, C.; Gharbaoui, T.; Royer, J.; Husson, H. P. J Org Chem 1996, 61, 3687-3693.
12. Linzaga, I.; Escalante, J.; Munoz, M.; Juaristi, E. Tetrahedron 2002, 58, 8973-8978.
13. Cristau, H. J.; Monbran, J.; Tilland, M.; Pirat, J. L. Tetrahedron 2003, 44, 3183-3187.
14. Pirat, J. L.; Monbrun, J.; Virieux, D.; Volle, J. N.; Tillard, M.; Cristau, H. J. J Org Chem 2005, 70, 7035-7041.
15. Cristau, H. J.; Pirat, J. L.; Virieux, D.; Monbrun, J.; Ciptadi, C.; Bekro, Y. A. J Organomet Chem 2005, 690, 2472-2481.
16. Zhou, J.; Qiu, Y. G.; Feng, K. S.; Chen, R. Y. Synthesis 1999, 1, 40-42.
17. Crystallographic data were deposited at Cambridge Crystallographic Data Center, 12 Union Road, Cambridge CB2 1EZ, UK, and are available from there under the deposition number CCDC 286963 for 4k and CCDC 286964 for one isomer of 4r.
18. Martin, D. R.; Pizzolato, P. J. J Am Chem Soc 1950, 72, 4584-4586.