Reductive Dearomative Arylcarboxylation via Visible-Light Photoredox Catalysis

Reductive couplings of two electrophiles and one C=C bond have been well investigated via TM-mediated two electron transfer. Herein, we report a successive single electron transfer strategy for the reductive dearomative arylcarboxylation of indoles with CO2 via visible light photoredox catalysis.
Reductive Dearomative Arylcarboxylation via Visible-Light Photoredox Catalysis

The research group of Prof. Da-Gang Yu at Sichuan University has been focusing on developing new strategies for CO2 utilization and visible-light photoredox catalysis in the past 5 years. In the area of visible-light-driven CO2 utilization, we have developed the visible-light-driven difluoroalkylation and alkylation of allylamines to synthesize oxazolinones (OL 2017, 20, 190; OL 2018, 20, 3049), the thiocarboxylation of alkenes with unique regioselectivity (ACIE 201756, 15416), the reductive hydrocarboxylation of enamides/imines (ACIE 201857, 13897), umpolung carboxylation of C-N bonds in the tetraalkyl ammonium salts (JACS 2018, 140, 17338) as well as redox-neutral phosphonocarboxylation of alkenes with CO2 (Nat. Commun. 2019, 10, 3592). Very recently, we have developed a novel strategy for reductive dearomative arylcarboxylation of indoles with CO2 via visible-light photoredox catalysis, as shown below.

Tandem reductive cyclization/cross coupling of unsaturated bond has been an important tool in organic synthesis.1 Conventional transition metal (TM)-catalyzed reductive coupling is powerful protocol in tuning the reactivity and selectivity. However, air- and moisture-sensitive organometallic reagents and unavoidable side reaction remain unsolved challenge.2 On the other hand, dearomatization of indoles is an efficient method to provide 3D cyclic skeletons indolines, which exist widely in pharmaceuticals and bioactive natural products.3 Although many methods have been developed in this field,4-9 the dearomative reductive coupling of indoles with two electrophiles is still challenging due to the stability of carbon-carbon double bond within aromaticity and thus slow migratory insertion rate. With these challenges in mind, we envisioned and successfully realized such reductive dearomative difunctionalization via radical pathway with successive single electron transfer (SSET)  process. Notably, this reaction is highly chemoselective, as common side reactions in transition metal catalysis, including ipso-carboxylation of aryl halides and β-hydride elimination, are avoided. This method also shows high selectivity, low loading of photocatalyst, generally good yields, mild reaction conditions (room temperature, 1 atm), good functional group tolerance and broad substrate scope, providing great potential for the synthesis of valuable but difficultly accessible indoline-3-carboxylic acids. Mechanistic studies indicate that the benzylic radicals and anions might be generated as the key intermediates. In addition, gram-scale reaction and facile derivatizations have been demonstrated that the utility of this strategy.

In conclusion, the successive single electron transfer (SSET) strategy not only provides a direction for dearomative difunctionalization but also represents a strategy to realize selective tandem reductive cyclization/cross couplings, preventing the undesired two-component couplings and reductive Heck-type reactions via β-hydride elimination. More details of this work can be found here: “Reductive Dearomative Arylcarboxylation of Indoles with CO2 via Visible-Light Photoredox Catalysis” in Nature Communications.


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