Abstract
Three kinds of O,O-diethyl N-dehydroabietic aminoarylmethylphosphonates were synthesized from natural product derivatives by two steps of solvent-free reactions through imines intermediates and their structures were characterized by IR, 1H NMR and 31P NMR spectroscopy. The solvent-free reactions afforded good yields of N-dehydroabietic imines and α-aminophosphonates although the strong space block of dehydroabietylamine to amino group. The green approaches resulted negligible waste and the reactions were environment friendly without using noxious solvents.
Acknowledgement
We thank the Chinese government “The 10th 5-year programme to tackle key problems” foundation for the financial support.