Technology Process of (1R,2R)-(m-tolylprop)-2,3-glycidol
There total 4 articles about (1R,2R)-(m-tolylprop)-2,3-glycidol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
styrene monooxygenase;
In
aq. phosphate buffer;
at 30 ℃;
for 15h;
pH=7;
enantioselective reaction;
DOI:10.1039/c4ob02186j
- Guidance literature:
-
Multi-step reaction with 2 steps
1: tetrahydrofuran / Cooling
2: Escherichia coli BL21 harboring the plasmid pET28a(+) encoding the styAB gene from Pseudomonas sp. LQ26 / 16 h / pH 6.5 / aq. phosphate buffer; Enzymatic reaction
With
Escherichia coli BL21 harboring the plasmid pET28a(+) encoding the styAB gene from Pseudomonas sp. LQ26;
In
tetrahydrofuran;
DOI:10.1039/c0cc04360e
- Guidance literature:
-
Multi-step reaction with 2 steps
1: D-glucose; nicotinamide adenine dinucleotide phosphate; glucose dehydrogenase; ChKRED03 DNA from Chryseo bacterium / aq. phosphate buffer / 5 h / 30 °C / pH 7
2: styrene monooxygenase / aq. phosphate buffer / 15 h / 30 °C / pH 7
With
glucose dehydrogenase; D-glucose; styrene monooxygenase; ChKRED03 DNA from Chryseo bacterium; nicotinamide adenine dinucleotide phosphate;
In
aq. phosphate buffer;
DOI:10.1039/c4ob02186j
