The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 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, in an article , author is Hunter, R, once mentioned of 56353-15-2, Recommanded Product: (S)-2-(3-Acetamidopropanamido)-3-(1H-imidazol-4-yl)propanoic acid.
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.
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Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem