Chemical Research Letters, May 2021. The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. Name: Argininine monohydrochloride,1119-34-2, Name is Argininine monohydrochloride, SMILES is O=C(O)[C@@H](N)CCCNC(N)=N.[H]Cl, belongs to pyrrolines compound. In a document, author is Hunter, R, introduce the new discover.
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.
The prevalence of solvent effects in heterogeneous catalysis in condensed media has motivated developing quantitative kinetic, their interactions with reaction intermediates. Interested yet? Read on for other articles about 1119-34-2. Name: Argininine monohydrochloride.
Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem