Extracurricular laboratory: Synthetic route of 1214711-48-4

Here is a brief introduction to this compound(1214711-48-4)Category: quinuclidine, if you want to know about other compounds related to this compound(1214711-48-4), you can read my other articles.

Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Tetrahedron called N-Heterocyclic carbene catalyzed aza-benzoin reaction for access to α-aminoketone molecules containing benzothiazole fragments, Author is Li, Wei; Lv, Jie; Chi, Yonggui Robin, which mentions a compound: 1214711-48-4, SMILESS is ClC1=C(N2N=C3[N+]([C@@]4([H])[C@@](CC5=C4C=CC=C5)([H])OC3)=C2)C(Cl)=CC(Cl)=C1.F[B-](F)(F)F, Molecular C18H13BCl3F4N3O, Category: quinuclidine.

An N-Heterocyclic carbene (NHC) catalyzed aza-benzoin reaction of benzothiazole-2-carboxaldehydes and N-sulfonylimines is reported for the first time. The target benzothiazole-containing aminoketone products bearing different substituents and substitution patterns can be obtained in good to excellent yields under mild conditions.

Here is a brief introduction to this compound(1214711-48-4)Category: quinuclidine, if you want to know about other compounds related to this compound(1214711-48-4), you can read my other articles.

Reference:
Quinuclidine – Wikipedia,
Quinuclidine | C7H13N | ChemSpider