Technology Process of C56H63N5O13
There total 13 articles about C56H63N5O13 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
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Multi-step reaction with 7 steps
1.1: 92 percent / tetra-n-butylammonium fluoride / tetrahydrofuran / 0.17 h / 0 °C
2.1: 93 percent / Et3N / CH2Cl2 / 0.33 h / 0 °C
3.1: 83 percent / Pd(diphenylphosphinoferrocene)Cl2*CH2Cl2; K2CO3 / 1,2-dimethoxy-ethane / 12 h / Heating
4.1: 93 percent / tetra-n-butylammonium fluoride / tetrahydrofuran / 0.33 h / 25 °C
5.1: 87 percent / Dess-Martin periodinane; NaHCO3 / CH2Cl2 / 1 h / 25 °C
6.1: 87 percent / dimethylsulfoxide / 0.17 h / 25 °C
7.1: SmI2; hexamethylphosphoramide / tetrahydrofuran / 0.75 h / 25 °C
7.2: 41 percent / 1-hydroxy-1H-benzotriazole hydrate; 3-(3-dimethylaminopropyl)-1-ethylcarbodiimide / dimethylformamide / 30 h / 25 °C
With
N,N,N,N,N,N-hexamethylphosphoric triamide; samarium diiodide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; tetrabutyl ammonium fluoride; sodium hydrogencarbonate; potassium carbonate; Dess-Martin periodane; triethylamine;
In
tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; dimethyl sulfoxide;
3.1: Suzuki coupling;
DOI:10.1021/ja040091q
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: 93 percent / Et3N / CH2Cl2 / 0.33 h / 0 °C
2.1: 83 percent / Pd(diphenylphosphinoferrocene)Cl2*CH2Cl2; K2CO3 / 1,2-dimethoxy-ethane / 12 h / Heating
3.1: 93 percent / tetra-n-butylammonium fluoride / tetrahydrofuran / 0.33 h / 25 °C
4.1: 87 percent / Dess-Martin periodinane; NaHCO3 / CH2Cl2 / 1 h / 25 °C
5.1: 87 percent / dimethylsulfoxide / 0.17 h / 25 °C
6.1: SmI2; hexamethylphosphoramide / tetrahydrofuran / 0.75 h / 25 °C
6.2: 41 percent / 1-hydroxy-1H-benzotriazole hydrate; 3-(3-dimethylaminopropyl)-1-ethylcarbodiimide / dimethylformamide / 30 h / 25 °C
With
N,N,N,N,N,N-hexamethylphosphoric triamide; samarium diiodide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; tetrabutyl ammonium fluoride; sodium hydrogencarbonate; potassium carbonate; Dess-Martin periodane; triethylamine;
In
tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; dimethyl sulfoxide;
2.1: Suzuki coupling;
DOI:10.1021/ja040091q
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: 83 percent / Pd(diphenylphosphinoferrocene)Cl2*CH2Cl2; K2CO3 / 1,2-dimethoxy-ethane / 12 h / Heating
2.1: 93 percent / tetra-n-butylammonium fluoride / tetrahydrofuran / 0.33 h / 25 °C
3.1: 87 percent / Dess-Martin periodinane; NaHCO3 / CH2Cl2 / 1 h / 25 °C
4.1: 87 percent / dimethylsulfoxide / 0.17 h / 25 °C
5.1: SmI2; hexamethylphosphoramide / tetrahydrofuran / 0.75 h / 25 °C
5.2: 41 percent / 1-hydroxy-1H-benzotriazole hydrate; 3-(3-dimethylaminopropyl)-1-ethylcarbodiimide / dimethylformamide / 30 h / 25 °C
With
N,N,N,N,N,N-hexamethylphosphoric triamide; samarium diiodide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; tetrabutyl ammonium fluoride; sodium hydrogencarbonate; potassium carbonate; Dess-Martin periodane;
In
tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; dimethyl sulfoxide;
1.1: Suzuki coupling;
DOI:10.1021/ja040091q