240408-64-4Relevant academic research and scientific papers
Highly diastereoselective radical addition to oxime ethers: Asymmetric synthesis of β-amino acids
Miyabe, Hideto,Fujii, Kayoko,Naito, Takeaki
, p. 569 - 572 (1999)
(Matrix presented) Highly diastereoselective alkyl radical addition to Oppolzer's camphorsultam derivatives of oxime ethers provided a convenient method for preparing the enantiomerically pure α,β-dialkyl-β-amino acids. The phase-transfer-catalyzed alkyla
Radical addition to oxime ethers for asymmetric synthesis of β-amino acid derivatives
Miyabe, Hideto,Fujii, Kayoko,Naito, Takeaki
, p. 381 - 390 (2007/10/03)
The diastereoselective alkyl radical addition to chiral oxime ethers was studied with a view to preparing enantiomerically pure α,β-dialkyl-β-amino acid derivatives. The phase transfer-catalyzed alkylation of Oppolzer's camphorsultam derivative of oxime e
