Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. , Safety of (R)-Methyl 3-hydroxybutanoate, 3976-69-0, Name is (R)-Methyl 3-hydroxybutanoate, molecular formula is C5H10O3, belongs to chiral-catalyst compound. In a document, author is Prasanna, R., introduce the new discover.
A simple and an efficient stereoslective synthesis of glycospiroheterocycles has been accomplished via 1, 3-dipolar cycloaddition (1,3-DC) reaction. The azomethine ylide generated by decarboxylative condensation of N-alkylated alpha-amino acids with various diketones was trapped by sugar derived dipolarophiles to give glycospiroheterocycles in good yield (72-94%). All the cycloadducts were well characterized by FTIR, NMR, HRMS and HPLC. The structures were established by 2D NMR. The regio- and stereochemical outcome of some of the cycloadducts were confirmed by a single crystal X-ray analysis. Effect of various solvents on 1, 3 DC reaction was also studied. (C) 2020 Elsevier Ltd. All rights reserved.
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 3976-69-0. Safety of (R)-Methyl 3-hydroxybutanoate.
Reference:
Chiral Catalysts,
,Chiral catalysts – SlideShare