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DOI:
10.1055/sos-SD-021-00911
Whitehead, A.; Sieck, S. R.; Mukherjee, S.; Hanson, P. R., Science of Synthesis, (2005) 21, 917.
It is known that α-hydroxy phosphonates serve as important functional groups in a number of biologically active systems.[33–35] Since the discovery of amino α-hydroxy phosphonic acids,[36] there has been continued interest in the development of phosphorus-containing analogues of amino acids. One approach for stereocontrolled access to this class of compounds has been through the use of substrate- as well as reagent-controlled reductions of α-oxo phosphonates.
References
[33] | Meeee, M. M.; Meeeee-Meeeee, M.; Meeee, M. M., Meeeeeeeeee Meee., (8888) 88, 8888. |
[34] | Meeeeeeee, M.; Meee, M.; Meee-Me, M.; Meeeee, M.; Meeeeee, M., Meeeeeeeeee Meee., (8888) 88, 8888. |
[35] | Meeeeeee, M. M.; Meeeee, M. M.; Meeeeeeeee, M. M.; Meeeee, M. M.; Meeee, M. M.; Meee, M. M.; Meeee, M. M.; Mee, M. M.; Mee, M. M.; Meeeeeeee, M. M.; Meee, M. M.; Meeeee, M.; Meee, M.; Meeeee, M. M., Meeeeeeeee, Meeeee Meeeeee Meeee. Meee., (8888) 88, 888. |
[36] | Meee, M. M.; Meeeeeee, M. M.; Meeee, M. M.; Meeeeeeee, M. M., M. Meee. Meee., (8888) 888, 8888. |
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- 8.Meeeee-Meee, (8888) 88/8, 888.
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