Abstract
The synthesis of some new α-aminophosphonates (4a-l) was accomplished by one pot reaction of equimolar quantities of 2-amino-4-chlorophenol (1), various aromatic aldehydes (2a-l) and diethylphosphite (3) in dry toluene at reflux temperature. Products 4a-l were characterized by IR, 1H, 13C, 31P NMR and in the case of 4g by X-ray crystal diffraction data. ©ARKAT USA, Inc.
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Prasad, G. S., Krishna, J. R., Manjunath, M., Reddy, O. V. S., Krishnaiah, M., Reddy, C. S., & Puranik, V. G. (2007). Synthesis, NMR, X-ray crystallography and bioactivity of some α-aminophosphonates. Arkivoc, 2007(13), 133–141. https://doi.org/10.3998/ark.5550190.0008.d16
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