5-(Diarylimino)- and 5-(sulfoximido)dibenzothiophenium triflates: syntheses and applications as electrophilic aminating reagents. Issue 13 (16th March 2021)

• Record Type: Journal Article
• Authors: Li, Zhen; Vijaykumar, Gonela; Li, Xiangdong; Golz, Christopher; Alcarazo, Manuel
• Is Part Of: Organic & biomolecular chemistry. Volume 19:Issue 13(2021)
• Page Start: 2941
• Page End: 2948
• Publication Date: 2021-03-16
• Subjects: Chemistry, Organic -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1039/d1ob00285f
• Languages: English
• ISSNs: 1477-0520

Abstract

Abstract : A new method has been developed for the synthesis of dibenzothiophenium salts containing diarylimino and sulfoximido substituents. The reactivity of these compounds under photochemical conditions is presented. Abstract : The one-pot synthesis of well-defined 5-(diarylimino) and 5-(sulfoximido)dibenzothiophenium triflates, respectively from diarylimines or sulfoximines, is reported and the structures of a series of these compounds are elucidated by X-ray crystallography. In analogy to their hypervalent I(iii ) analogues, the iminoyl and sulfoximidoyl groups of these compounds can be selectively transferred to organic substrates. Specifically, the uncatalyzed imination of thiols or sulfinates proceeds with good yields, while under the mild reaction conditions offered by visible light photoredox catalysis, the radical amination of hydrazones or the sulfoximidation of benzylic, allylic and propargylic C–H bonds takes place satisfactorily.