Highly Efficient Approach to Orthogonally Protected (2<i>S</i>,4<i>R</i>)- and (2<i>S</i>,4<i>S</i>)-4-Hydroxyornithine

Abstract

[reaction: see text] A concise stereoselective approach to both orthogonally protected (2S,4R)- and (2S,4S)-4-hydroxyornithine, key constituents of the biphenomycin- and clavalanine-type antibiotics, respectively, has been developed. The approach is based on bis(oxazoline) copper(II)-complex-catalyzed diastereoselective Henry reactions of nitromethane with the homoserine-derived aldehyde 6. The synthesis of this versatile chiral building block has been markedly improved.