A 1,3-Dipolar Cycloaddition Route to the 3(R)- and 3(S)-Hydroxy-(2S)-arginines

Article abstract of DOI:10.1021/jo00387a012

The 3(R)- and 3(S)-hydroxy-(2S)-arginines (4a and 4b) were prepared from the corresponding β-hydroxyornithines (3a and 3b) via methyl 2(S)-<2-benzyl-(5(R,S)-isoxazolidinyl>acetates (5a and 5b).The isoxazolidines 5 were prepar