Name: 2-Methyl-4H-benzo[d][1,3]oxazin-4-one, New Advances in Chemical Research, May 2021. Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. 525-76-8, Name is 2-Methyl-4H-benzo[d][1,3]oxazin-4-one, SMILES is O=C1C2=CC=CC=C2N=C(C)O1, belongs to pyrrolines compound. In a article, author is Marquardt, U, introduce new discover of the category.
Racemic synthesis of the new antibiotic tetramic acid reutericyclin
The synthesis of the new bacteriocidal compound reutericyclin, 3-acetyl-1-(2-trans-decenoyl)-2-hydroxy-5-isobutyl-Delta(2)-pyrrolin-4-one, is performed by coupling of N-(2-trans-decenoyl)-L-leucine to Meldrum’s acid followed by cyclization. The resulting N-acylated tetramic acid is directly C-acetylated in position 3. HPLC-purification on RP-C-18 gave racemic reutericyclin in high purity. 2D-NMR and FT-ICR-MS data are identical with those of natural reutericyclin.
Name: 2-Methyl-4H-benzo[d][1,3]oxazin-4-one, I am very proud of our efforts over the past few months and hope to 525-76-8 help many people in the next few years.
Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem