Enantioselective synthesis of α-amino phosphonic acids by an application of stereoselective opening of homochiral dioxane acetals with triethyl phosphite
Tetrahedron AsymmetryPublished 1 January 1992
Tsutomu Yokomatsu, Shiroshi Shibuya
Citations96
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Abstract
Stereoselective opening of homochiral acetals (2a–c) with triethyl phosphite was applied to the enantioselective synthesis of phosphono alcohols (1a–c), which were succssefully converted to the α-amino phosphonic acid diethyl esters (6a–c).
Keywords
Chemistry
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