Technology Process of (4R,7R)-4,7-Dibenzyl-[1,3,2]dioxathiepane 2,2-dioxide
There total 6 articles about (4R,7R)-4,7-Dibenzyl-[1,3,2]dioxathiepane 2,2-dioxide which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
(2R,5R)-1,6-diphenylhexane-2,5-diol;
With
thionyl chloride; triethylamine;
In
dichloromethane;
at 0 - 20 ℃;
for 1.66667h;
With
ruthenium trichloride; sodium periodate;
In
tetrachloromethane; water; acetonitrile;
at 20 ℃;
for 1h;
DOI:10.1021/ol034706k
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: PBr3 / diethyl ether / 0.42 h / 0 - 20 °C
2.1: 61.2 g / Zn; I2 / diethyl ether / -40 - -30 °C
3.1: 97 percent / (DHDQ)2PHAL; K2OsO4*2H2O; K2CO3 / methanesulfonamide; K3Fe(CN)6 / H2O; 2-methyl-propan-2-ol; hexane / 64 h
4.1: Et3N / CH2Cl2 / -50 - 20 °C
5.1: 17.68 g / H2 / Raney-Ni / ethanol; acetone / 760 Torr
6.1: SOCl2; Et3N / CH2Cl2 / 1.67 h / 0 - 20 °C
6.2: 84 percent / NaIO4; RuCl3 / acetonitrile; CCl4; H2O / 1 h / 20 °C
With
potassium osmate(VI); thionyl chloride; hydrogen; iodine; phosphorus tribromide; potassium carbonate; 1,4-bis(9-O-dihydroquinidine)phthalazine; triethylamine; zinc;
methanesulfonamide; nickel; potassium hexacyanoferrate(III);
In
diethyl ether; ethanol; hexane; dichloromethane; water; acetone; tert-butyl alcohol;
3.1: Sharpless asymmetric dihydroxylation;
DOI:10.1021/ol034706k
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: 97 percent / (DHDQ)2PHAL; K2OsO4*2H2O; K2CO3 / methanesulfonamide; K3Fe(CN)6 / H2O; 2-methyl-propan-2-ol; hexane / 64 h
2.1: Et3N / CH2Cl2 / -50 - 20 °C
3.1: 17.68 g / H2 / Raney-Ni / ethanol; acetone / 760 Torr
4.1: SOCl2; Et3N / CH2Cl2 / 1.67 h / 0 - 20 °C
4.2: 84 percent / NaIO4; RuCl3 / acetonitrile; CCl4; H2O / 1 h / 20 °C
With
potassium osmate(VI); thionyl chloride; hydrogen; potassium carbonate; 1,4-bis(9-O-dihydroquinidine)phthalazine; triethylamine;
methanesulfonamide; nickel; potassium hexacyanoferrate(III);
In
ethanol; hexane; dichloromethane; water; acetone; tert-butyl alcohol;
1.1: Sharpless asymmetric dihydroxylation;
DOI:10.1021/ol034706k