Makaluvamine A合成路线 (共 32 条)
反应条件
ammonium chloride in methanol
Ambient temperature;
参考文献
Roberts, David; Joule, John A.; Antonieta Bros; Alvarez, Mercedes
Journal of Organic Chemistry, 1997 , vol. 62, # 3 p. 568 - 577
反应条件
hydrogen; palladium on activated charcoal in methanol
P=1551.4 Torr; Ambient temperature;
参考文献
Sun; Sakemi; Burres; McCarthy
Journal of Organic Chemistry, 1990 , vol. 55, # 16 p. 4964 - 4966
反应条件
hydrogen; palladium on activated charcoal in methanol
P=1551.4 Torr; Ambient temperature;
参考文献
Sun; Sakemi; Burres; McCarthy
Journal of Organic Chemistry, 1990 , vol. 55, # 16 p. 4964 - 4966
反应条件
1: H2 / 10percent Pd/C / 3800 Torr
2: pyridine
3: 1.) NaH
4: 100 percent / aq. NaOH
5: pyridine
6: 77 percent / Fremy's salt
7: 41 percent / benzylamine hydrochloride, NaHCO3 / acetonitrile; methanol
8: 1.) H2, 2.) O2 / 1.) 10percent Pd/C
View Scheme
参考文献
Yamada, Fumio; Hamabuchi, Shin; Shimizu, Aya; Somei, Masanori
Heterocycles, 1995 , vol. 41, # 9 p. 1905 - 1908
反应条件
1: 99 percent / pyridine / 4 h / 60 °C
2: 1.) NaH
3: 95 percent / aq. NaOH
4: 77 percent / Fremy's salt
5: 41 percent / benzylamine hydrochloride, NaHCO3 / acetonitrile; methanol
6: 1.) H2, 2.) O2 / 1.) 10percent Pd/C
View Scheme
参考文献
Yamada, Fumio; Hamabuchi, Shin; Shimizu, Aya; Somei, Masanori
Heterocycles, 1995 , vol. 41, # 9 p. 1905 - 1908
反应条件
1: 77 percent / Fremy's salt
2: 41 percent / benzylamine hydrochloride, NaHCO3 / acetonitrile; methanol
3: 1.) H2, 2.) O2 / 1.) 10percent Pd/C
View Scheme
参考文献
Yamada, Fumio; Hamabuchi, Shin; Shimizu, Aya; Somei, Masanori
Heterocycles, 1995 , vol. 41, # 9 p. 1905 - 1908
反应条件
1: 1.) NaH
2: 95 percent / aq. NaOH
3: 77 percent / Fremy's salt
4: 41 percent / benzylamine hydrochloride, NaHCO3 / acetonitrile; methanol
5: 1.) H2, 2.) O2 / 1.) 10percent Pd/C
View Scheme
参考文献
Yamada, Fumio; Hamabuchi, Shin; Shimizu, Aya; Somei, Masanori
Heterocycles, 1995 , vol. 41, # 9 p. 1905 - 1908
反应条件
1: 95 percent / aq. NaOH
2: 77 percent / Fremy's salt
3: 41 percent / benzylamine hydrochloride, NaHCO3 / acetonitrile; methanol
4: 1.) H2, 2.) O2 / 1.) 10percent Pd/C
View Scheme
参考文献
Yamada, Fumio; Hamabuchi, Shin; Shimizu, Aya; Somei, Masanori
Heterocycles, 1995 , vol. 41, # 9 p. 1905 - 1908
反应条件
1: O2, salcomine / dimethylformamide / 2 h / Ambient temperature
2: NH4Cl / methanol / 13 h / Ambient temperature
View Scheme
参考文献
Iwao, Masatomo; Motoi, Osamu; Fukuda, Tsutomu; Ishibashi, Fumito
Tetrahedron, 1998 , vol. 54, # 31 p. 8999 - 9010
反应条件
1: 63 percent / HNO3 / 1.) -50-(-40) deg C, 1 h, 2.) -30 deg C, 25 min
2: 73 percent / TFA, t-BuI, I2, FeCl2 / dimethylsulfoxide / 5 h / 80 - 85 °C
3: 93 percent / HCl / diethyl ether / 65 h / Heating
4: 86 percent / NiCl2, BaBH4 / methanol / 0.08 h / 50 °C
5: 64 percent / aq. HCl / tetrahydrofuran / 1 h / 40 °C
6: CH2Cl2 / 15 h / Ambient temperature
7: 1.) NaH / 1.) THF, room temperature 45 min, reflux - 15 min, 2.) THF, 14 h
8: 80 percent / TFA / CH2Cl2 / 1.5 h / Ambient temperature
9: 60 percent / ceric ammonium nitrate
10: 98 percent / NH4Cl
View Scheme
参考文献
Roberts, David; Joule, John A.; Antonieta Bros; Alvarez, Mercedes
Journal of Organic Chemistry, 1997 , vol. 62, # 3 p. 568 - 577