Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5271352 | Tetrahedron Letters | 2014 | 5 Pages |
Abstract
Aminomethylenebisphosphonic acids display a number of interesting biological activities. Although the structural optimization of amine substituents has been widely studied, potential modifications of the phosphonate groups remain virtually unexplored. Thus, a two-stage procedure for the synthesis of aminomethylenebis-H-phosphinates is developed. The three-component condensation of an amine, triethyl orthoformate, and ethyl diethoxymethyl-H-phosphinate and the subsequent hydrolysis are crucial steps in this synthetic pathway.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Marta Bochno, Åukasz Berlicki,