Technology Process of C60H73Cl6N2O18P
There total 18 articles about C60H73Cl6N2O18P 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:
-
With
formic acid; N-butylamine;
tetrakis(triphenylphosphine) palladium(0);
In
tetrahydrofuran;
at 20 ℃;
for 1h;
DOI:10.1016/S0040-4020(98)00133-1
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 70 percent / Sn(OTf)2 / diethyl ether / 2 h / -20 - 0 °C
2: BH3*Me2NH; BF3*Et2O / CH2Cl2 / 2 h / -40 - 0 °C
3: 325 mg / BF3*Et2O / CH2Cl2 / 1 h / 0 °C
4: 91 percent / molecular sieves 4A; trimethylsilyl triflate / 1,2-dichloro-ethane / 0.5 h / -20 °C
5: 98 percent / dicyclohexylcarbodiimide; 4-(dimethylamino)pyridine / 1,2-dichloro-ethane / 1 h / 20 °C
6: 85 percent / n-BuNH2; HCOOH / tetrakis(triphenylphosphine)palladium(0) / tetrahydrofuran / 1 h / 20 °C
With
dmap; tin(II) trifluoromethanesulfonate; formic acid; trimethylsilyl trifluoromethanesulfonate; dimethylamine borane; 4 A molecular sieve; boron trifluoride diethyl etherate; N-butylamine; dicyclohexyl-carbodiimide;
tetrakis(triphenylphosphine) palladium(0);
In
tetrahydrofuran; diethyl ether; dichloromethane; 1,2-dichloro-ethane;
1: Alkylation / 2: Ring cleavage / 3: dealkylation / 4: Condensation / 5: Acylation / 6: deprotection;
DOI:10.1016/S0040-4020(98)00133-1
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 87 percent / triethylamine / ethyl acetate / 0 - 20 °C
2: 91 percent / hexamethyldisiloxane; TMSOTf; triethylsilane / tetrahydrofuran / 2.2 h / 0 °C
3: 71 percent / AcOH; zinc-copper couple / 2 h / 20 °C
4: 98 percent / dicyclohexylcarbodiimide; 4-(dimethylamino)pyridine / 1,2-dichloro-ethane / 1 h / 20 °C
5: 85 percent / n-BuNH2; HCOOH / tetrakis(triphenylphosphine)palladium(0) / tetrahydrofuran / 1 h / 20 °C
With
triethylsilane; dmap; formic acid; zinc copper; Hexamethyldisiloxane; trimethylsilyl trifluoromethanesulfonate; acetic acid; N-butylamine; triethylamine; dicyclohexyl-carbodiimide;
tetrakis(triphenylphosphine) palladium(0);
In
tetrahydrofuran; ethyl acetate; 1,2-dichloro-ethane;
1: Esterification / 2: Alkylation / 3: Reduction / 4: Acylation / 5: deprotection;
DOI:10.1016/S0040-4020(98)00133-1