Ozonolysis of 2-(1,4-cyclohexadienyl)glycine

Add time:09/29/2019    Source:sciencedirect.com

Derivatives of 2-(1,4-cyclohexadienyl)glycine were subjected to total ozonolysis. The free esters as well as the N-protected esters tend to cyclize to yield 2-carbethoxy-3-hydroxy pyrrole derivatives. By treatment of the ozonolysis mixture with hydroxylamine or phenylhydrazine heterocyclic derivatives of glycine were obtained. The structure and formation of pyrazolyl and isoxazolyl glycine derivatives is discussed. The structure of N-acetyl-2-(1-phenylpyrazol-3-yl)glycine ethyl ester by X-ray single crystal analysis is reported.

We also recommend Trading Suppliers and Manufacturers of 2-(4-Methyl-2,4-cyclohexadienyl)-2-propanol (cas 1686-20-0). Pls Click Website Link as below: cas 1686-20-0 suppliers

Prev:Visible-light-mediated trifluoroethylation of 2-isocyanobiaryl with trifluoroethyl iodide: Synthesis of 6-trifluoroethyl-phenanthridines
Next:Gas phase synthesis and physico‐chemical properties of vanadium oxide nanoparticles)