Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 616-43-3, is researched, SMILESS is CC1=CNC=C1, Molecular C5H7NJournal, Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999) called Acid-catalyzed proton exchange on pyrrole and alkylpyrroles, Author is Bean, Gerritt P.; Wilkinson, Timothy J., the main research direction is kinetics proton exchange pyrrole.Recommanded Product: 3-Methyl-1H-pyrrole.
The rates of D-H exchange in D2O-dioxane solution of pyrrole at the α- and β-positions were equal in F3CCO2D and D3O+; in DOAC the α-position was selectively protonated. Alkyl substituents activated adjacent position(s) toward H-D exchange, the influence of N-alkyl being less than that of 2-, 3-, 4-, and 5-alkyl.
The article 《Acid-catalyzed proton exchange on pyrrole and alkylpyrroles》 also mentions many details about this compound(616-43-3)Recommanded Product: 3-Methyl-1H-pyrrole, you can pay attention to it, because details determine success or failure
Reference:
Synthesis and Crystal Structure of a Chiral C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur–nitrogen–oxygen ligand derived from aminothiourea and sodium D-camphor-β-sulfonate