Oxidative C–C bond cleavage of N-alkoxycarbonylated cyclic amines by sodium nitrite in trifluoroacetic acid
スポンサーリンク
概要
- 論文の詳細を見る
Oxidative carbon–carbon bond cleavage of N-alkoxycarbonylated cyclic amines was accomplished by NaNO2 in TFA to afford ω-amino carboxylic acid in high yield. Optically active 3-hydroxypiperidine derivatives and 3-pipecolinate were converted to enantiomerically pure (R)-4-amino-3-hydroxybutanoic acid (GABOB) and (S)-2-pyrrolidone-4-carboxylate, respectively.
- Elsevier Ltdの論文
- 2008-11-17
Elsevier Ltd | 論文
- Inelastic collision processes of low energy protons in liquid water
- Evolution of the maturation rate collapses competitive coexistence
- Experimental evidence of the one-third magnetization plateau in the diamond chain compound Cu3(CO3)2(OH)2
- Stabilization and modulation of the output power of submillimeter wave gyrotron
- High-field ESR study on anomalous magnetization in CsFeCl3