Abstract
A series of acylated α-aminophosphine oxides were synthesized by the microwave-assisted Kabachnik–Fields reaction of a series of carboxylic acid amides, formaldehyde and secondary phosphine oxides. To compensate the lower reactivity of the –NH2 reagents, they had to be used in an excess. The solvolytic condensations furnished the α-aminophosphine oxides in yields of 58–93% after purification by chromatography.
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Tripolszky, A., Zoboki, L., Bálint, E., Kóti, J., & Keglevich, G. (2019). Microwave-assisted synthesis of α-aminophosphine oxides by the Kabachnik–Fields reaction applying amides as the starting materials. Synthetic Communications, 49(8), 1047–1054. https://doi.org/10.1080/00397911.2019.1584675
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