Asymmetric synthesis of α-aminophosphonates using the inexpensive chiral catalyst 1,1'-binaphthol phosphate

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Abstract

Asymmetric addition under mild conditions of dialkyl phosphites on aldimines derived from cinnamaldehyde catalyzed by the inexpensive chiral organocatalyst (R)-3,3'- [4-fluorophenyl]2-1,1'-binaphthol phosphate has been found effective to give new α- amino-phosphonates 9 in moderate yields (30-65%) and enantiomeric excess (8.4%-61.9%). © 2010 by the authors.

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Xu, W., Zhang, S., Yang, S., Jin, L. H., Bhadury, P. S., Hu, D. Y., & Zhang, Y. (2010). Asymmetric synthesis of α-aminophosphonates using the inexpensive chiral catalyst 1,1’-binaphthol phosphate. Molecules, 15(8), 5782–5796. https://doi.org/10.3390/molecules15085782

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