Technology Process of C30H31NO9
There total 23 articles about C30H31NO9 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
C25H25NO7; di-tert-butyl dicarbonate;
With
ytterbium(III) triflate;
In
dichloromethane;
at 0 ℃;
for 48h;
With
ortho-iodoxybenzoic acid;
In
dimethyl sulfoxide;
at 25 ℃;
for 20h;
DOI:10.1021/ja063304f
- Guidance literature:
-
With
1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione;
In
dimethyl sulfoxide;
at 25 ℃;
for 20h;
Inert atmosphere;
DOI:10.1002/chem.200701998
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: 75 percent / Cs2CO3 / acetonitrile / 20 h / 25 °C
2.1: AgOTf / CH2Cl2 / 1 h / 25 °C
2.2: 77 percent / TBAT / CH2Cl2 / 20 h / -45 - 25 °C
3.1: 74 percent / samarium diiodide; HMPA / 2-methyl-propan-2-ol / 3 h / -78 - -45 °C
4.1: 99 percent / Schwartz's reagent / tetrahydrofuran / 16 h / Heating
5.1: 86 percent / KHMDS / tetrahydrofuran / 1 h / 0 °C
6.1: 99 percent / HCl; methanol / 16 h / 25 °C
7.1: Yb(OTf)3*xH2O / CH2Cl2 / 48 h / 0 °C
7.2: 50 percent / ortho-iodoxybenzoic acid / dimethylsulfoxide / 20 h / 25 °C
With
hydrogenchloride; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; samarium diiodide; Schwartz's reagent; silver trifluoromethanesulfonate; potassium hexamethylsilazane; caesium carbonate; ytterbium(III) triflate;
In
tetrahydrofuran; dichloromethane; acetonitrile; tert-butyl alcohol;
DOI:10.1021/ja063304f