144870-19-9Relevant articles and documents
Asymmetric Syntheses of α-Aminophosphonic Acids, V - Synthesis of Enantiomerically Pure Diethyl 2-Pyrrolidinyl- and 5-Oxo-2-pyrrolidinylphosphonates
Groth, Ulrich,Richter, Lutz,Schoellkopf, Ulrich
, p. 903 - 910 (2007/10/02)
Enantiomerically pure 3- and 4-substituted phosphonic acid derivatives 5 of pyroglutamic acid were prepared by a Michael addition of the lithiated (+)-camphor derivative 2 to α,β-unsaturated esters and subsequent hydrolysis.The reduction of the lactams 5 with LiBH4/BF3*OEt2 afforded substituted phosphonic acid analogues 7 of proline.Key Words: Phosphoglutamic acids / Phosphoprolines / Michael additions / Lactams