Technology Process of (2R,3S,5R)-3-methoxy-5-methyl-6-(5-nitro-2,3,6-trimethoxy-phenyl)-hexan-1,2-diol
There total 17 articles about (2R,3S,5R)-3-methoxy-5-methyl-6-(5-nitro-2,3,6-trimethoxy-phenyl)-hexan-1,2-diol 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
ammonium cerium(IV) nitrate;
In
water; acetonitrile;
at 0 ℃;
for 0.5h;
DOI:10.1021/ol0068997
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: 63 percent / triflic acid / CH2Cl2 / 24 h / -78 °C
2.1: BH3*Me2S / tetrahydrofuran / 8 h / 20 °C
2.2: aq. NaOH; aq. H2O2 / tetrahydrofuran / 1.5 h / 0 - 20 °C
3.1: 135.6 mg / proton sponge; molecular sieves 4 Angstroem / CH2Cl2 / 12 h / 20 °C
4.1: 97 percent / LiBH4 / diethyl ether; methanol / 0 - 20 °C
5.1: 84 percent / Et3SiH; Sc(OTf)3 / CH2Cl2 / 24 h / 25 °C
With
triethylsilane; lithium borohydride; Proton Sponge; trifluorormethanesulfonic acid; dimethylsulfide borane complex; 4 A molecular sieve; scandium tris(trifluoromethanesulfonate);
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane;
DOI:10.1021/ja067234o
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: BH3*Me2S / tetrahydrofuran / 8 h / 20 °C
1.2: aq. NaOH; aq. H2O2 / tetrahydrofuran / 1.5 h / 0 - 20 °C
2.1: 135.6 mg / proton sponge; molecular sieves 4 Angstroem / CH2Cl2 / 12 h / 20 °C
3.1: 97 percent / LiBH4 / diethyl ether; methanol / 0 - 20 °C
4.1: 84 percent / Et3SiH; Sc(OTf)3 / CH2Cl2 / 24 h / 25 °C
With
triethylsilane; lithium borohydride; Proton Sponge; dimethylsulfide borane complex; 4 A molecular sieve; scandium tris(trifluoromethanesulfonate);
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane;
DOI:10.1021/ja067234o