Flexible application of in synthetic route 616-43-3

Compound(616-43-3)Recommanded Product: 616-43-3 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(3-Methyl-1H-pyrrole), if you are interested, you can check out my other related articles.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Elucidation of the mechanism of pyrrole formation during thermal degradation of 13C-labeled L-serines, published in 2001-07-31, which mentions a compound: 616-43-3, mainly applied to serine Maillard reaction pyrrole pyrazine, Recommanded Product: 616-43-3.

Pyrolysis of [13C-1], [13C-2] and [13C-3]-labeled L-serines generated mono-substituted Me and Et derivatives of pyrroles and pyrazines among other compounds Analyses of label incorporation into the pyrroles have indicated their formation through aldol condensation of acetaldehyde with different α-aminocarbonyl compounds followed by cyclization and loss of water (Knorr pyrrole synthesis). Comparison of the label incorporation patterns of the α-aminocarbonyls involved in the formation of Me and ethyl-substituted pyrroles with that of similarly substituted pyrazines, revealed their common origin. In addition, α-aminocarbonyls involved in the formation of 2- and 3-substituted pyrroles had identical label distribution patterns, indicating their formation through the same carbonyl precursors. Furthermore, the major pathway (55%) leading to the formation of the α-aminocarbonyl precursors of methyl-substituted pyrroles involved aldol addition of formaldehyde to glycolaldehyde, whereas the only pathway leading to the formation of the α-aminocarbonyl precursors of ethyl-substituted pyrroles involved the interaction of alanine – formed in situ – with glycolaldehyde.

Compound(616-43-3)Recommanded Product: 616-43-3 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(3-Methyl-1H-pyrrole), if you are interested, you can check out my other related articles.

Reference:
Synthesis and Crystal Structure of a Chiral C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur–nitrogen–oxygen ligand derived from aminothiourea and sodium D-camphor-β-sulfonate