Interesting scientific research on 56353-15-2

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New Advances in Chemical Research in 2021. Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage , causing turnover rates to depend strongly on interfacial structure. 56353-15-2, Name is (S)-2-(3-Acetamidopropanamido)-3-(1H-imidazol-4-yl)propanoic acid, molecular formula is , belongs to pyrrolines compound. In a document, author is Sato, Kazuto, Quality Control of (S)-2-(3-Acetamidopropanamido)-3-(1H-imidazol-4-yl)propanoic acid.

Synthetic Studies on Cyclocitrinol: Construction of the ABC Ring System Based on Epoxy-Nitrile Cyclization

The stereoselective synthesis of a model compound containing the ABC ring system of cyclocitrinol was accomplished. After connecting a C ring allyltitanium segment with an A ring bi-cyclo[4.1.0]heptanone segment, the seven-membered B ring moiety was constructed by an intramolecular cyclization reaction of an epoxy nitrile. The enone moiety was introduced through an oxidative decyanation reaction, and the bicyclo[4.4.1]undecane skeleton with the highly strained olefin moiety was formed through a ring-opening reaction of the bicyclo[4.1.0]heptane substructure.

If you are hungry for even more, make sure to check my other article 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