Technology Process of C46H80NO15PSi
There total 12 articles about C46H80NO15PSi which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 7 steps
1: 93 percent / 2,6-lutidine / CH2Cl2 / 0.25 h / -78 - 20 °C
2: 60.4 percent / dihydroquinidine acetate, OsO4 / toluene / 5 h
3: 96 percent / H2 / 10percent Pd(OH)2/C / ethyl acetate / 2 h
4: 80 percent / 4A molecular sieves, camphorsulfonic acid / benzene; tetrahydrofuran / 2 h / Ambient temperature
5: 95 percent / dicyclohexylcarbodiimide (DCC) / CH2Cl2 / 0.33 h
6: 90.8 percent / aq. LiOH / tetrahydrofuran; methanol / 2 h / -15 - -10 °C
7: (benzotriazolyl-1-oxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP)
With
2,6-dimethylpyridine; lithium hydroxide; osmium(VIII) oxide; hydroquinidine acetate; 4 A molecular sieve; camphor-10-sulfonic acid; hydrogen; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; dicyclohexyl-carbodiimide;
palladium dihydroxide;
In
tetrahydrofuran; methanol; dichloromethane; ethyl acetate; toluene; benzene;
- Guidance literature:
-
Multi-step reaction with 8 steps
1: 73.5 percent / acetonitrile / 72 h / Heating
2: 93 percent / 2,6-lutidine / CH2Cl2 / 0.25 h / -78 - 20 °C
3: 60.4 percent / dihydroquinidine acetate, OsO4 / toluene / 5 h
4: 96 percent / H2 / 10percent Pd(OH)2/C / ethyl acetate / 2 h
5: 80 percent / 4A molecular sieves, camphorsulfonic acid / benzene; tetrahydrofuran / 2 h / Ambient temperature
6: 95 percent / dicyclohexylcarbodiimide (DCC) / CH2Cl2 / 0.33 h
7: 90.8 percent / aq. LiOH / tetrahydrofuran; methanol / 2 h / -15 - -10 °C
8: (benzotriazolyl-1-oxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP)
With
2,6-dimethylpyridine; lithium hydroxide; osmium(VIII) oxide; hydroquinidine acetate; 4 A molecular sieve; camphor-10-sulfonic acid; hydrogen; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; dicyclohexyl-carbodiimide;
palladium dihydroxide;
In
tetrahydrofuran; methanol; dichloromethane; ethyl acetate; toluene; acetonitrile; benzene;
- Guidance literature:
-
Multi-step reaction with 7 steps
1: 93 percent / 2,6-lutidine / CH2Cl2 / 0.25 h / -78 - 20 °C
2: 60.4 percent / dihydroquinidine acetate, OsO4 / toluene / 5 h
3: 96 percent / H2 / 10percent Pd(OH)2/C / ethyl acetate / 2 h
4: 80 percent / 4A molecular sieves, camphorsulfonic acid / benzene; tetrahydrofuran / 2 h / Ambient temperature
5: 95 percent / dicyclohexylcarbodiimide (DCC) / CH2Cl2 / 0.33 h
6: 90.8 percent / aq. LiOH / tetrahydrofuran; methanol / 2 h / -15 - -10 °C
7: (benzotriazolyl-1-oxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP)
With
2,6-dimethylpyridine; lithium hydroxide; osmium(VIII) oxide; hydroquinidine acetate; 4 A molecular sieve; camphor-10-sulfonic acid; hydrogen; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; dicyclohexyl-carbodiimide;
palladium dihydroxide;
In
tetrahydrofuran; methanol; dichloromethane; ethyl acetate; toluene; benzene;