Technology Process of 1,3-O-benzylidene-2.5-O-methylene-D-glycero-D-manno-heptitol
There total 8 articles about 1,3-O-benzylidene-2.5-O-methylene-D-glycero-D-manno-heptitol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
hydrogen;
palladium 10% on activated carbon;
In
methanol;
for 12h;
under 4137.29 Torr;
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: 1H-imidazole / N,N-dimethyl-formamide / 2 h / 0 °C / Inert atmosphere
2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0 °C
2.2: 0 - 20 °C
3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 h / 20 °C
4.1: sodium hydrogencarbonate; Dess-Martin periodane / 0.25 h / 20 °C
5.1: n-butyllithium / tetrahydrofuran; hexane / 1 h / -78 °C
5.2: -78 - 20 °C
6.1: AD-mix-β / water; tert-butyl alcohol / 168 h / 0 °C
7.1: hydrogen / palladium 10% on activated carbon / methanol / 12 h / 4137.29 Torr
With
1H-imidazole; n-butyllithium; AD-mix-β; tetrabutyl ammonium fluoride; hydrogen; sodium hydride; sodium hydrogencarbonate; Dess-Martin periodane;
palladium 10% on activated carbon;
In
tetrahydrofuran; methanol; hexane; water; N,N-dimethyl-formamide; mineral oil; tert-butyl alcohol;
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: n-butyllithium / tetrahydrofuran; hexane / 1 h / -78 °C
1.2: -78 - 20 °C
2.1: AD-mix-β / water; tert-butyl alcohol / 168 h / 0 °C
3.1: hydrogen / palladium 10% on activated carbon / methanol / 12 h / 4137.29 Torr
With
n-butyllithium; AD-mix-β; hydrogen;
palladium 10% on activated carbon;
In
tetrahydrofuran; methanol; hexane; water; tert-butyl alcohol;