Technology Process of diallyl (2-benzoyloxyethyl 2-acetamido-3-O-benzoyl-2,4-dideoxy-β-L-threo-hex-4-enopyranoside-6-yl)-phosphonate
There total 8 articles about diallyl (2-benzoyloxyethyl 2-acetamido-3-O-benzoyl-2,4-dideoxy-β-L-threo-hex-4-enopyranoside-6-yl)-phosphonate which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: 68 percent / trimethylsilyl triflate / CH2Cl2 / 1 h / 0 °C
2.1: 96 percent / zinc; acetic acid / tetrahydrofuran / 2 h / 20 °C / sonification
3.1: 68 percent / sodium methylate / methanol / 0 °C
4.1: 92 percent / triethylamine; DMAP / dimethylformamide / 3 h / 0 °C
5.1: 98 percent / pyridine / 3 h / -15 °C
6.1: 81 percent / acetyl chloride / methanol; diethyl ether / 2 h / 0 °C
7.1: phosphoric acid; pyridine; DCC / toluene; dimethylsulfoxide / 72 h / 20 °C
7.2: oxalic acid monohydrate / toluene; methanol / 0.5 h / 20 °C
7.3: 48 percent / triethylamine / CH2Cl2 / 2 h
8.1: 87 percent / triethylamine / CH2Cl2 / 1.5 h / 20 °C
With
pyridine; dmap; trimethylsilyl trifluoromethanesulfonate; phosphoric acid; sodium methylate; acetic acid; triethylamine; acetyl chloride; dicyclohexyl-carbodiimide; zinc;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene;
7.1: Pfitzner-Morffatt oxidation;
DOI:10.1021/ja017370n
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: 68 percent / trimethylsilyl triflate / CH2Cl2 / 1 h / 0 °C
2.1: 96 percent / zinc; acetic acid / tetrahydrofuran / 2 h / 20 °C / sonification
3.1: 68 percent / sodium methylate / methanol / 0 °C
4.1: 92 percent / triethylamine; DMAP / dimethylformamide / 3 h / 0 °C
5.1: 98 percent / pyridine / 3 h / -15 °C
6.1: 81 percent / acetyl chloride / methanol; diethyl ether / 2 h / 0 °C
7.1: phosphoric acid; pyridine; DCC / toluene; dimethylsulfoxide / 72 h / 20 °C
7.2: oxalic acid monohydrate / toluene; methanol / 0.5 h / 20 °C
7.3: 48 percent / triethylamine / CH2Cl2 / 2 h
8.1: 87 percent / triethylamine / CH2Cl2 / 1.5 h / 20 °C
With
pyridine; dmap; trimethylsilyl trifluoromethanesulfonate; phosphoric acid; sodium methylate; acetic acid; triethylamine; acetyl chloride; dicyclohexyl-carbodiimide; zinc;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene;
7.1: Pfitzner-Morffatt oxidation;
DOI:10.1021/ja017370n
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: 92 percent / triethylamine; DMAP / dimethylformamide / 3 h / 0 °C
2.1: 98 percent / pyridine / 3 h / -15 °C
3.1: 81 percent / acetyl chloride / methanol; diethyl ether / 2 h / 0 °C
4.1: phosphoric acid; pyridine; DCC / toluene; dimethylsulfoxide / 72 h / 20 °C
4.2: oxalic acid monohydrate / toluene; methanol / 0.5 h / 20 °C
4.3: 48 percent / triethylamine / CH2Cl2 / 2 h
5.1: 87 percent / triethylamine / CH2Cl2 / 1.5 h / 20 °C
With
pyridine; dmap; phosphoric acid; triethylamine; acetyl chloride; dicyclohexyl-carbodiimide;
In
methanol; diethyl ether; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene;
4.1: Pfitzner-Morffatt oxidation;
DOI:10.1021/ja017370n