Build-up of double carbohelicenes using nitroarenes: dual role of the nitro functionality as an activating and leaving group. Issue 28 (6th July 2020)

• Record Type: Journal Article
• Authors: Zhou, Fulin; Zhou, Fujian; Su, Rongchuan; Yang, Yudong; You, Jingsong
• Is Part Of: Chemical science. Volume 11:Issue 28(2020)
• Page Start: 7424
• Page End: 7428
• Publication Date: 2020-07-06
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d0sc02058c
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : Disclosed herein is a concise route to double carbohelicenes starting from nitroarenes, in which the nitro group serves as an activating group for ortho -C–H arylation and a leaving group for the denitrative alkenylation. Abstract : The construction of double carbohelicenes is highly fascinating yet challenging work. Disclosed herein is a streamlined and simplified synthetic route to double carbohelicenes starting from nitroarenes through sequential nitro-activated ortho -C–H arylation, denitrative alkenylation and intramolecular cyclodehydrogenation. In this synthetic strategy, the nitro group plays a dual role namely as a leaving group for the denitrative alkenylation and as an activating group for ortho -C–H arylation, which is distinct from those of aryl halides in a conventional coupling reaction. In this work, the palladium-catalyzed Heck-type alkenylation of nitroarenes has been presented, in which the conventionally inert Ar–NO2 bond is cleaved. This work provides a novel synthetic strategy for polycyclic aromatic hydrocarbons (PAHs).