(alphaS,gammaS)-4-甲氧基-3-(3-甲氧基丙氧基)-gamma-(1-甲基乙基)-alpha-[[(苯基甲氧基)羰基]氨基]苯戊酸合成路线 (共 7 条)
反应条件
1.1: 94 percent / EDCI / CH2Cl2 / 3.5 h / 0 °C 2.1: 67 percent / t-BuOH; SmI2 / tetrahydrofuran / 144 h / -78 °C 3.1: 85 mg / (S)-Alpine Hydride / tetrahydrofuran / 24 h / -78 °C 4.1: LiHMDS / tetrahydrofuran; hexane / 2 h / -78 °C 4.2: 91 percent / tetrahydrofuran; hexane / 2 h / -78 °C 5.1: PCl5 / CH2Cl2 / 2.5 h / 0 °C 5.2: 39 mg / H2 / Pd/C / ethanol / 48 h 6.1: ethanol / 1.5 h / 0 °C 7.1: 24 mg / NaBH4 / ethanol / 0.67 h / 20 °C View Scheme
参考文献
Lindsay, Karl B.; Skrydstrup, Troels
Journal of Organic Chemistry, 2006 , vol. 71, # 13 p. 4766 - 4777
反应条件
sodium hydroxide in tetrahydrofuran; methanol
T=20°C; 3.5 h;
参考文献
Lindsay, Karl B.; Skrydstrup, Troels
Journal of Organic Chemistry, 2006 , vol. 71, # 13 p. 4766 - 4777
反应条件
1.1: n-BuLi / tetrahydrofuran / -75 °C
1.2: 90 percent / tetrahydrofuran / -75 - -18 °C
2.1: 99 percent / HCl / H2O; acetonitrile
3.1: 89 percent / pyridine / CH2Cl2 / 2 h / 20 °C
4.1: aq. NaOH / tetrahydrofuran; methanol / 3.5 h / 20 °C
View Scheme
参考文献
Lindsay, Karl B.; Skrydstrup, Troels
Journal of Organic Chemistry, 2006 , vol. 71, # 13 p. 4766 - 4777
反应条件
1: 89 percent / pyridine / CH2Cl2 / 2 h / 20 °C
2: aq. NaOH / tetrahydrofuran; methanol / 3.5 h / 20 °C
View Scheme
参考文献
Lindsay, Karl B.; Skrydstrup, Troels
Journal of Organic Chemistry, 2006 , vol. 71, # 13 p. 4766 - 4777
反应条件
1.1: 94 percent / EDCI / CH2Cl2 / 3.5 h / 0 °C
2.1: 67 percent / t-BuOH; SmI2 / tetrahydrofuran / 144 h / -78 °C
3.1: 85 mg / (S)-Alpine Hydride / tetrahydrofuran / 24 h / -78 °C
4.1: LiHMDS / tetrahydrofuran; hexane / 2 h / -78 °C
4.2: 91 percent / tetrahydrofuran; hexane / 2 h / -78 °C
5.1: PCl5 / CH2Cl2 / 2.5 h / 0 °C
5.2: 39 mg / H2 / Pd/C / ethanol / 48 h
6.1: 63 percent / Et3N / tetrahydrofuran / 18 h / 20 °C
View Scheme
参考文献
Lindsay, Karl B.; Skrydstrup, Troels
Journal of Organic Chemistry, 2006 , vol. 71, # 13 p. 4766 - 4777
反应条件
1: 94 percent / EDCI / CH2Cl2 / 3.5 h / 0 °C
2: 67 percent / t-BuOH; SmI2 / tetrahydrofuran / 144 h / -78 °C
3: 85 mg / (S)-Alpine Hydride / tetrahydrofuran / 24 h / -78 °C
View Scheme
参考文献
Lindsay, Karl B.; Skrydstrup, Troels
Journal of Organic Chemistry, 2006 , vol. 71, # 13 p. 4766 - 4777
反应条件
1.1: 94 percent / EDCI / CH2Cl2 / 3.5 h / 0 °C
2.1: 67 percent / t-BuOH; SmI2 / tetrahydrofuran / 144 h / -78 °C
3.1: 85 mg / (S)-Alpine Hydride / tetrahydrofuran / 24 h / -78 °C
4.1: LiHMDS / tetrahydrofuran; hexane / 2 h / -78 °C
4.2: 91 percent / tetrahydrofuran; hexane / 2 h / -78 °C
5.1: PCl5 / CH2Cl2 / 2.5 h / 0 °C
5.2: 39 mg / H2 / Pd/C / ethanol / 48 h
6.1: Et3N / tetrahydrofuran / 18 h / 20 °C
View Scheme
参考文献
Lindsay, Karl B.; Skrydstrup, Troels
Journal of Organic Chemistry, 2006 , vol. 71, # 13 p. 4766 - 4777