Technology Process of C53H53F6N3PtS2
There total 5 articles about C53H53F6N3PtS2 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: diethyl ether / 12 h / 0 - 20 °C / Schlenk technique; Inert atmosphere
1.2: 4 h / 20 °C / Schlenk technique; Inert atmosphere
2.1: acetonitrile; water / 18 h / Schlenk technique; Inert atmosphere; Reflux
3.1: triethylamine; copper(l) iodide / dichloromethane / 15 h / 30 °C / Schlenk technique; Inert atmosphere; Darkness
4.1: chloroform-d1 / 3 h / Schlenk technique; Inert atmosphere; UV-irradiation
With
copper(l) iodide; triethylamine;
In
diethyl ether; chloroform-d1; dichloromethane; water; acetonitrile;
DOI:10.1021/ja4131615
- Guidance literature:
-
Multi-step reaction with 2 steps
1: triethylamine; copper(l) iodide / dichloromethane / 15 h / 30 °C / Schlenk technique; Inert atmosphere; Darkness
2: chloroform-d1 / 3 h / Schlenk technique; Inert atmosphere; UV-irradiation
With
copper(l) iodide; triethylamine;
In
chloroform-d1; dichloromethane;
DOI:10.1021/ja4131615
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: diethyl ether / 12 h / 0 - 20 °C / Schlenk technique; Inert atmosphere
1.2: 4 h / 20 °C / Schlenk technique; Inert atmosphere
2.1: acetonitrile; water / 18 h / Schlenk technique; Inert atmosphere; Reflux
3.1: triethylamine; copper(l) iodide / dichloromethane / 15 h / 30 °C / Schlenk technique; Inert atmosphere; Darkness
4.1: chloroform-d1 / 3 h / Schlenk technique; Inert atmosphere; UV-irradiation
With
copper(l) iodide; triethylamine;
In
diethyl ether; chloroform-d1; dichloromethane; water; acetonitrile;
DOI:10.1021/ja4131615