3-(N-苄基氨基)-L-丙氨酸合成路线 (共 5 条)
反应条件
1: C28H25Cl2N3NiO4 With acetic anhydride; sodium carbonate in acetonitrile T=25 - 70°C; 2: benzylamine With sodium hydroxide in acetonitrile T=50°C; Michael condensation; 3 h; 3: With hydrogenchloride; water in ethanol
参考文献
Tetrahedron Asymmetry, , vol. 21, # 21-22 p. 2638 - 2645
反应条件
1: C30H31N3NiO4 With acetic anhydride; sodium carbonate in acetonitrile T=25 - 70°C; 2: benzylamine With sodium hydroxide in acetonitrile T=50°C; Michael condensation; 2.5 h; 3: With hydrogenchloride; water in ethanol
参考文献
Tetrahedron Asymmetry, , vol. 21, # 21-22 p. 2638 - 2645
反应条件
1: C28H26ClN3NiO4 With acetic anhydride; sodium carbonate in acetonitrile T=25 - 70°C; 2: benzylamine With sodium hydroxide in acetonitrile T=50°C; Michael condensation; 0.25 h; 3: With hydrogenchloride; water in ethanol
参考文献
Tetrahedron Asymmetry, , vol. 21, # 21-22 p. 2638 - 2645
反应条件
1: C28H26FN3NiO4 With acetic anhydride; sodium carbonate in acetonitrile T=25 - 70°C; 2: benzylamine With sodium hydroxide in acetonitrile T=50°C; Michael condensation; 1.66667 h; 3: With hydrogenchloride; water in ethanol
参考文献
Tetrahedron Asymmetry, , vol. 21, # 21-22 p. 2638 - 2645
反应条件
Yield given. Multistep reaction;
参考文献
Tetrahedron, , vol. 44, # 17 p. 5507 - 5514