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. Application In Synthesis of 10-Hydroxy-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxamide,29331-92-8, Name is 10-Hydroxy-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxamide, SMILES is O=C(N1C2=CC=CC=C2CC(O)C3=CC=CC=C31)N, belongs to pyrrolines compound. In a document, author is Mattern, RH, introduce the new discover.
Synthesis of microcolin analogs using trimethylsilylated lactams
The synthesis of microcolin analogs is described using an approach that could be of considerable practical interest for structure-activity studies on microcolin and related peptides. This synthetic pathway is more efficient than the methods reported to date, and allows the variation of the Xaa-pyrrolin-2-one unit of these molecules, which has been shown to be crucial for the biological activity. (C) 1997 Elsevier Science Ltd.
The potential utility of systematic synthetic strategy will be applicable to efficient generations of chemical libraries of compounds to find ‘hit’ molecules. In my other articles, you can also check out more blogs about 29331-92-8. Application In Synthesis of 10-Hydroxy-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxamide.
Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem