Quality Control of (S)-2-(3-Acetamidopropanamido)-3-(1H-imidazol-4-yl)propanoic acid, New research progress on 56353-15-2 in 2021.The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. 56353-15-2, Name is (S)-2-(3-Acetamidopropanamido)-3-(1H-imidazol-4-yl)propanoic acid, SMILES is O=C(O)[C@@H](NC(CCNC(C)=O)=O)CC1=CNC=N1, belongs to pyrrolines compound. In a article, author is Hunter, R, introduce new discover of the category.
Synthesis of the tricyclic core of the marine alkaloid Lepadiformine
A stereoselective synthesis of the tricyclic core in racemic form of the marine alkaloid Lepadiformine is described from 4-methoxy-3-pyrrolin-2-one (methyl tetramate). Key steps involve 5,5-dialkylation of the tetramate, metathesis closure to an A/C 1-azaspirocycle and stereoselective hydrogenation for the trans A/B 1-azadecalin system.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 56353-15-2. Quality Control of (S)-2-(3-Acetamidopropanamido)-3-(1H-imidazol-4-yl)propanoic acid.
Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem