Technology Process of (S)-1-phenethyl-3,4-dihydro-1H-isochromene
There total 12 articles about (S)-1-phenethyl-3,4-dihydro-1H-isochromene which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
palladium 10% on activated carbon; hydrogen;
In
methanol;
at 20 ℃;
for 2.5h;
under 760.051 Torr;
optical yield given as %ee;
Inert atmosphere;
DOI:10.1021/ja207585p
- Guidance literature:
-
With
methyldi-t-butylphosphine; potassium tert-butylate; palladium diacetate;
In
tert-Amyl alcohol;
at 20 ℃;
for 24h;
optical yield given as %ee;
Inert atmosphere;
DOI:10.1021/ja207585p
- Guidance literature:
-
Multi-step reaction with 6 steps
1: dimethylsulfide borane complex / tetrahydrofuran / 1 h / Inert atmosphere; Reflux
2: toluene-4-sulfonic acid; lithium bromide / 24 h / Inert atmosphere; Reflux
3: trimethylsilyl trifluoromethanesulfonate / acetonitrile / 0 - 20 °C / Inert atmosphere
4: 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane / 24 h / 20 °C / Inert atmosphere
5: copper(l) iodide; trimethylsilyl trifluoromethanesulfonate; triethylamine / 20 °C / Inert atmosphere
6: palladium 10% on activated carbon; hydrogen / methanol / 2.5 h / 20 °C / 760.05 Torr / Inert atmosphere
With
copper(l) iodide; trimethylsilyl trifluoromethanesulfonate; dimethylsulfide borane complex; palladium 10% on activated carbon; hydrogen; toluene-4-sulfonic acid; triethylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; lithium bromide;
In
tetrahydrofuran; methanol; dichloromethane; acetonitrile;
DOI:10.1021/ja207585p