Extended knowledge of (S)-4-Isobutyloxazolidine-2,5-dione

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 3190-70-3

Electric Literature of 3190-70-3, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.3190-70-3, Name is (S)-4-Isobutyloxazolidine-2,5-dione, molecular formula is C7H11NO3. In a article£¬once mentioned of 3190-70-3

SYNTHESIS OF N-TRIPEPTIDYL-D-GLUCOSAMINE BY THE STEPWISE REACTION OF N-CARBOXY alpha -AMINO ACID ANHYDRIDE.

N-Peptidyl-D-glucosamines were synthesized by the stepwise reaction of N-carboxy alpha -amino acid anhydrides (4-alkyl-2,5-oxazolidinediones) with D-glucosamine hydrochloride in the presence of equimolar sodium methoxide in a mixture of acetonitrile and methanol, or in methanol, at a low temperature. Polymerization reaction of N-carboxy alpha -amino acid anhydrides (NCAs) did not occur at minus 50 degree C. The mechanism of the reaction was then studied.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 3190-70-3

Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H1521NO – PubChem