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, Article, Chemical Communications (Cambridge, United Kingdom) called Stereoselective [3+2] cycloaddition of N-tert-butanesulfinyl imines to arynes facilitated by a removable PhSO2CF2 group: synthesis and transformation of cyclic sulfoximines, Author is Ye, Wenchao; Zhang, Laijun; Ni, Chuanfa; Rong, Jian; Hu, Jinbo, which mentions a compound: 305798-02-1, SMILESS is BrCC1=CC2=CC=C(Br)C=C2C=C1, Molecular C11H8Br2, Electric Literature of C11H8Br2.
An unprecedented [3+2] cycloaddition between N-tert-butanesulfinyl imines and arynes provides a stereoselective method for the synthesis of cyclic sulfoximines. Not only does the difluoro(phenylsulfonyl)methyl group play an important role in facilitating the cycloaddition reaction, it can also be removed or substituted through the transformation of the difluorinated cyclic sulfoximines, e.g. I, to cyclic sulfinamides, e.g. II.
In some applications, this compound(305798-02-1)Electric Literature of C11H8Br2 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.
Reference:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem