Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5267649 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
Addition of dialkyl phosphites to (S)-N-tert-butanesulfinyl imine derived from fluoral afforded, under mild conditions, the corresponding N-tert-butanesulfinyl α-aminophosphonates in moderate to high yields and diastereoselectivity. The major diastereomers of N-tert-butanesulfinyl α-aminophosphonates of (SS,S) configuration were isolated, and after partial or complete deprotection, converted into enantiomerically pure phosphonotrifluoroalanine and its dialkyl esters.
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Authors
Gerd-Volker Röschenthaler, Valery P. Kukhar, Irine B. Kulik, Michael Yu. Belik, Alexander E. Sorochinsky, Eduard B. Rusanov, Vadim A. Soloshonok,