Technology Process of Coenzyme A,esters,S-(2Z)-2-butenoate
There total 8 articles about Coenzyme A,esters,S-(2Z)-2-butenoate 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
CoaA, CoaD and CoaE enzymes were amplified from a colony of E. coli BL21(DE3);
In
dimethyl sulfoxide;
at 30 ℃;
for 3h;
pH=6.5 - 7.5;
Enzymatic reaction;
DOI:10.1021/acs.orglett.5b02113
- Guidance literature:
-
With
sodium hydroxide; 4-hydroxybutyryl-CoA dehydratase;
at 37 ℃;
for 0.333333h;
DOI:10.1002/anie.200705473
- Guidance literature:
-
Multi-step reaction with 3 steps
1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h
2: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 18 h
3: CoaA, CoaD and CoaE enzymes were amplified from a colony of E. coli BL21(DE3) / dimethyl sulfoxide / 3 h / 30 °C / pH 6.5 - 7.5 / Enzymatic reaction
With
CoaA, CoaD and CoaE enzymes were amplified from a colony of E. coli BL21(DE3); benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine;
In
dichloromethane; dimethyl sulfoxide;
DOI:10.1021/acs.orglett.5b02113
