Technology Process of 3,5-dimethylnorleucine
There total 9 articles about 3,5-dimethylnorleucine which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
With
pyridoxal 5'-phosphate; α-keto acidmethyltranferase from Streptomyces griseoviridis; branched chain L-aminoacids transaminase from Escherichia coli; halide methyltransferase from Burkholderiaxenovorans; sodium phosphate; S-(5'-adenosyl)-L-homocysteine;
In
aq. phosphate buffer;
at 20 ℃;
for 24h;
pH=8;
diastereoselective reaction;
Enzymatic reaction;
DOI:10.1002/anie.201916025
- Guidance literature:
-
With
pyridoxal 5'-phosphate; α-keto acidmethyltranferase from Streptomyces griseoviridis; halide methyltransferase from Burkholderiaxenovorans; PLP-dependent d-α-amino acid transaminases; sodium phosphate; S-(5'-adenosyl)-L-homocysteine;
In
aq. phosphate buffer;
at 20 ℃;
pH=8;
diastereoselective reaction;
Enzymatic reaction;
DOI:10.1002/anie.201916025
- Guidance literature:
-
With
pyridoxal 5'-phosphate; α-keto acidmethyltranferase from Streptomyces griseoviridis; halide methyltransferase from Burkholderiaxenovorans; PLP-dependent d-α-amino acid transaminases; sodium phosphate; S-(5'-adenosyl)-L-homocysteine;
In
aq. phosphate buffer;
at 20 ℃;
pH=8;
diastereoselective reaction;
Enzymatic reaction;
DOI:10.1002/anie.201916025