Technology Process of (1R)-1-(4-ETHYLPHENYL)ETHANOL
There total 9 articles about (1R)-1-(4-ETHYLPHENYL)ETHANOL 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
bis(1,5-cyclooctadiene)diiridium(I) dichloride; (SC,SC,RFC)-1-(diphenylphosphino)-2-[1-N-((4S)-4-tert-butyl-2-oxazolinyl-2-ylmethyl)ethyl]ferrocene; hydrogen; potassium carbonate;
In
isopropyl alcohol;
at 25 ℃;
for 2h;
under 15201 Torr;
enantioselective reaction;
Glovebox;
Autoclave;
DOI:10.1021/acs.orglett.6b01290
- Guidance literature:
-
1-ethyl-4-ethynylbenzene;
With
chloro(1,3-bis(2,6-di-i-propylphenyl)imidazol-2-ylidene)gold(I); water;
In
methanol;
at 110 ℃;
for 6h;
With
C26H26ClN2O2RhS; water; sodium formate;
In
methanol;
at 30 ℃;
for 24h;
- Guidance literature:
-
((1-(4-ethylphenyl)vinyl)oxy)trimethylsilane;
With
tri-tert-butyl phosphine; C52H54; hydrogen; bis(pentafluorophenyl)borohydride;
In
1,3,5-trimethyl-benzene; pentane;
at 50 ℃;
for 24h;
under 30003 Torr;
Inert atmosphere;
Sealed tube;
With
tetrabutyl ammonium fluoride;
In
tetrahydrofuran; 1,3,5-trimethyl-benzene; pentane;
at 20 ℃;
for 1h;
enantioselective reaction;
DOI:10.1021/acs.orglett.5b00085
