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The addition of diethyl phosphite to cyclic imines bearing alkyl, aryl, or heteroaryl substituents at the α-position in diethyl ether at room temperature presents an efficient route to substituted cyclic α-aminophosphonates. The application of boron trifluoride-diethyl ether complex as a catalyst significantly accelerates the reaction.
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Odinets et al. (2009) studied this question.
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