2-methylpropanoate

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A reaction mixture of 50 mM Tris-HCl (pH 7.0), 10 mM MgCl2, 10 mM dithiotheritol 10 mM uridine 5'-diphosphate glucose, 1 mM isobutyrate, 2 units of GTI activity is made up. Reaction is carried out for 2 hrs. at 37° C. 1-O-isobutyryl-β-D-glucose is formed. Reaction at 37° C

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A reaction mixture of 50 mM Tris-HCl (pH 7.0), 10 mM MgCl2, 10 mM dithiotheritol 10 mM uridine 5'-diphosphate glucose, 1 mM isobutyrate, 2 units of GTI activity is made up. Reaction is carried out for 2 hrs. at 37° C. 1-O-isobutyryl-β-D-glucose is formed. Reaction at 37° C

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of 388A (1.70 g, 7.35 mmol) and PPh3 (5.80 g, 22.1 mmol) in anhydrous THF (35 ml) was added t-butyl 2-hydroxyisobutyrate (3.83 ml, 22.1 mmol) followed by DEAD (3.47 ml, 22.1 mmol), the reaction mixture was stirred at rt for 19 h. More reagents PPh3 (1.16 g, 4.41 mmol), isobutyrate (0.77 ml, 4.41 mmol) and DEAD (0.69 ml, 4.41 mmol) were added, and the mixture was stirred for another 50 h, concentrated and purified by silica gel flash column chromatography to afford 388B (2.62 g, 96%) as a light pink crystalline solid (50%-80% CH2Cl2-hexanes). the mixture was stirred for another 50 h concentrated purified by silica gel flash column chromatography

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A reaction mixture of 50 mM Tris-HCl (pH 7.0), 10 mM MgCl2, 10 mM dithiotheritol 10 mM uridine 5'-diphosphate glucose, 1 mM isobutyrate, 2 units of GTI activity is made up. Reaction is carried out for 2 hrs. at 37° C. 1-O-isobutyryl-β-D-glucose is formed. Reaction at 37° C