Article ID Journal Published Year Pages File Type
5267649 Tetrahedron Letters 2012 4 Pages PDF
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.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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