Technology Process of a-L-ido-4-Octulopyranosonic acid,2,3-dideoxy-3-(4-hydroxyphenyl)-, g-lactone (9CI)
There total 5 articles about a-L-ido-4-Octulopyranosonic acid,2,3-dideoxy-3-(4-hydroxyphenyl)-, g-lactone (9CI) which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
C28H32O8;
With
palladium 10% on activated carbon; hydrogen;
In
methanol; ethyl acetate;
for 30h;
under 3040.2 Torr;
With
trifluoroacetic acid;
at 20 ℃;
for 18h;
diastereoselective reaction;
DOI:10.1016/j.tetlet.2021.153072
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: Dess-Martin periodane; sodium hydrogencarbonate / dichloromethane / 1 h / 0 - 20 °C
2.1: toluene / 110 h / 125 °C / Inert atmosphere
3.1: hydrogen; palladium 10% on activated carbon / methanol; ethyl acetate / 30 h / 3040.2 Torr
3.2: 18 h / 20 °C
With
palladium 10% on activated carbon; hydrogen; sodium hydrogencarbonate; Dess-Martin periodane;
In
methanol; dichloromethane; ethyl acetate; toluene;
2.1: |Wittig-Horner Reaction;
DOI:10.1016/j.tetlet.2021.153072
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: Dess-Martin periodane; sodium hydrogencarbonate / dichloromethane / 2.5 h / 0 - 20 °C
2.1: n-butyllithium / tetrahydrofuran; hexane / 0.25 h / -78 °C / Inert atmosphere
2.2: -78 - 20 °C / Inert atmosphere
3.1: Dess-Martin periodane; sodium hydrogencarbonate / dichloromethane / 1 h / 0 - 20 °C
4.1: toluene / 110 h / 125 °C / Inert atmosphere
5.1: hydrogen; palladium 10% on activated carbon / methanol; ethyl acetate / 30 h / 3040.2 Torr
5.2: 18 h / 20 °C
With
n-butyllithium; palladium 10% on activated carbon; hydrogen; sodium hydrogencarbonate; Dess-Martin periodane;
In
tetrahydrofuran; methanol; hexane; dichloromethane; ethyl acetate; toluene;
4.1: |Wittig-Horner Reaction;
DOI:10.1016/j.tetlet.2021.153072