Mechanochemical borylation of aryldiazonium salts; merging light and ball milling

• José G. Hernández

Beilstein J. Org. Chem. 2017, 13, 1463–1469, doi:10.3762/bjoc.13.144

• . Simultaneous neat grinding/irradiation of the reactants and the photocatalyst led to the formation of boronates in a molten state. On the other hand, the catalyst-free liquid-assisted grinding/irradiation reaction also led to product formation, featuring a direct photolysis pathway facilitated by substrate

• spectroscopy revealed just the presence of both reactants, both in the presence or absence of the organic photocatalyst eosin Y (5.0 mol %). Ruling out a sole mechanochemical activation pathway (Table 1, entries 1 and 2). Repeating the reaction in the presence of the PC in the transparent PPMA milling jar

• reaction mixture reached 6:94 (entry 12 in Table 1). Alternatively, longer reaction times allowed reducing the amount of the organic photocatalyst to 1.0 mol % and 0.5 mol % (entry 13 in Table 1; for more details, see Table S1 in Supporting Information File 1). Then, using the green LEDs an experiment in

Photocatalyzed synthesis of isochromanones and isobenzofuranones under batch and flow conditions

• Manuel Anselmo,
• Lisa Moni,
• Hossny Ismail,
• Davide Comoretto,
• Renata Riva and
• Andrea Basso

Beilstein J. Org. Chem. 2017, 13, 1456–1462, doi:10.3762/bjoc.13.143

• loading of photocatalyst (0.5% vs 2%) and excess of alkene (2 equiv vs 3 equiv) employed; moreover, the use of an inert atmosphere did not lead to significant improvements. No differences were observed when the 440 nm laser was replaced by blue LEDs (maximum wavelength 455 nm). Diazonium salts were

Chemoselective synthesis of diaryl disulfides via a visible light-mediated coupling of arenediazonium tetrafluoroborates and CS₂

• Jing Leng,
• Shi-Meng Wang and
• Hua-Li Qin

Beilstein J. Org. Chem. 2017, 13, 903–909, doi:10.3762/bjoc.13.91

• tetrafluoroborates; carbon disulfide; chemoselectivity; diaryl disulfides; photocatalyst; Findings The development of methods for the functionalization of peptides and proteins under mild conditions is a current frontier in the fields of chemistry, biology and drug discovery [1][2][3][4]. Most of the

• reactions [15][22]. Based on the above research results, we envisioned that a radical pathway may facilitate the formation of diaryl disulfides. Therefore the photocatalyst Ru(bpy)3(PF6)2 (bpy = 2,2’-bipyridine) [23] and a 20 W blue-light LED were chosen as catalyst and the source of visible light

Stabilization of nanosized titanium dioxide by cyclodextrin polymers and its photocatalytic effect on the degradation of wastewater pollutants

• Tamás Zoltán Agócs,
• István Puskás,
• Erzsébet Varga,
• Mónika Molnár and
• Éva Fenyvesi

Beilstein J. Org. Chem. 2016, 12, 2873–2882, doi:10.3762/bjoc.12.286

• nanosized titanium dioxide (nanoTiO2) applied in photodegradation-based procedures can be stabilized with cyclodextrins in order to obtain a new, more efficient photocatalyst for the purification of waters polluted by xenobiotics applying UV irradiation. During our work, on the one hand, we studied the

Solvent-free, visible-light photocatalytic alcohol oxidations applying an organic photocatalyst

• Martin Obst and
• Burkhard König

Beilstein J. Org. Chem. 2016, 12, 2358–2363, doi:10.3762/bjoc.12.229

• . In this setup, thin liquid films are realized which is crucial for an effective photocatalytic conversion due to the low penetration depth of light in heterogeneous systems. Several benzylic alcohols were oxidized with riboflavin tetraacetate as photocatalyst under blue light irradiation of the

• , is a rather new field of great academic interest. Namely, visible-light photocatalysis applying an organic, redox-active catalyst allows mild and efficient transformations. By exciting the photocatalyst, which then exchanges electrons with the substrate, light energy is converted into chemical energy

• photocatalyst has been reported yet. In this work, we present a novel milling apparatus, which we developed especially for the conversion of solid substrates. Applying this apparatus, the solvent-free oxidation of various benzylic alcohols to their corresponding carbonyl compounds using riboflavin tetraacetate

Photocatalytic nucleophilic addition of alcohols to styrenes in Markovnikov and anti-Markovnikov orientation

• Martin Weiser,
• Sergej Hermann,
• Alexander Penner and
• Hans-Achim Wagenknecht

Beilstein J. Org. Chem. 2015, 11, 568–575, doi:10.3762/bjoc.11.62

• ) and styrene (6) into the Markovnikov- and anti-Markovnikov-type products was selectively achieved with 1-(N,N-dimethylamino)pyrene (Py) and 1,7-dicyanoperylene-3,4:9,10-tetracarboxylic acid bisimide (PDI) as photoredox catalysts. The regioselectivity was controlled by the photocatalyst. For the

• reductive mode towards the Markovnikov-type regioselectivity, Py was applied as photocatalyst and triethylamine as electron shuttle. This approach was also used for intramolecular additions. For the oxidative mode towards the anti-Markovnikov-type regioselectivety, PDI was applied together with Ph–SH as

• -Markovnikov-type addition of cyanide to styrene [18]. Recently, we showed by a library of different chromophores that 1-(N,N-dimethylamino)pyrene (Py) can be applied as photocatalyst for the nucleophilic addition of methanol to styrene derivatives into the Markovnikov orientation [19]. Most recently, Nicewicz

Eosin Y-catalyzed visible-light-mediated aerobic oxidative cyclization of N,N-dimethylanilines with maleimides

• Zhongwei Liang,
• Song Xu,
• Wenyan Tian and
• Ronghua Zhang

Beilstein J. Org. Chem. 2015, 11, 425–430, doi:10.3762/bjoc.11.48

• as a photocatalyst has been developed. The metal-free protocol involves aerobic oxidative cyclization via sp3 C–H bond functionalization process to afford good yields in a one-pot procedure under mild conditions. Keywords: aerobic oxidative cyclization; C–H functionalization; Eosin Y; photoredox

• significantly green because it utilizes visible light and atmospheric oxygen as the greenest reagents, and metal-free, cheap Eosin Y with a relatively low loading as the photocatalyst to deliver the product at room temperature in a simple one-pot procedure. This methodology expands the range of substrates in

An improved procedure for the preparation of Ru(bpz)₃(PF₆)₂ via a high-yielding synthesis of 2,2’-bipyrazine

• Danielle M. Schultz,
• James W. Sawicki and
• Tehshik P. Yoon

Beilstein J. Org. Chem. 2015, 11, 61–65, doi:10.3762/bjoc.11.9

• is an effective photocatalyst in oxidatively induced photoredox transformations where less strongly oxidizing complexes (e.g., 1) are not successful. For instance, we have reported that 2 is uniquely capable of promoting radical cation mediated Diels–Alder cycloadditions [12], radical thiol–ene

• couplings [13][14], and photooxygenation reactions [15][16]. Similarly, Zheng has reported oxidatively initiated indole synthesis [17] and [3 + 2] cycloaddition [18][19] reactions using photocatalyst 2. Finally, a variety of transition metal complexes bearing bipyrazyl ligands have been prepared and

• equiv of isopropanol, and 1.5 equiv of K2CO3 in DMF (0.4 M) at 100 °C; under these conditions, the reaction was complete in 2 h and afforded the desired homocoupling product in 81% isolated yield (Table 1, entry 9). Although our investigations were motivated by our specific need to access photocatalyst

Visible-light-induced bromoetherification of alkenols for the synthesis of β-bromotetrahydrofurans and -tetrahydropyrans

• Run Lin,
• Hongnan Sun,
• Chao Yang,
• Youdong Yang,
• Xinxin Zhao and
• Wujiong Xia

Beilstein J. Org. Chem. 2015, 11, 31–36, doi:10.3762/bjoc.11.5

• loading was reduced to even 1 mol %, the reaction also gave a comparable result (Table 1, entry 8). It should be pointed out that no reaction was observed in the absence of light or photocatalyst. With the optimized reaction conditions in hand, various substituted butenols were subsequently investigated

One-pot functionalisation of N-substituted tetrahydroisoquinolines by photooxidation and tunable organometallic trapping of iminium intermediates

• Joshua P. Barham,
• Matthew P. John and
• John A. Murphy

Beilstein J. Org. Chem. 2014, 10, 2981–2988, doi:10.3762/bjoc.10.316

• accessing the excited state [18][34][36]. The ability to adjust oxidising power through photocatalyst choice renders the transformation substrate-tunable. Thus, we selected photoredox catalysis as an oxidative functionalisation whose substrate scope might be extended (by catalyst selection) in future

• and were able to collect half (by mass) of the crude iminium salt 5a by filtration. Precipitation acts to stall reactions by shielding the photocatalyst from the light. Addition of vinylmagnesium bromide directly to the reaction mixture led to a complex mixture of products by HPLC. We found that

• -polar solvents, yet low photocatalyst solubility in these solvents precluded photoactivation of 4a. Thus, a solvent switch was used to capitalise on the beneficial properties of both solvents. At this stage, we employed an MeCN/H2O (4:1) solvent system and Ru(bpy)3Cl2 in photoactivations which

Come-back of phenanthridine and phenanthridinium derivatives in the 21st century

• Lidija-Marija Tumir,
• Marijana Radić Stojković and
• Ivo Piantanida

Beilstein J. Org. Chem. 2014, 10, 2930–2954, doi:10.3762/bjoc.10.312

• intriguing is the double role of the photocatalyst [fac-Ir(ppy)3], consisting of photo-induced generation of alkyl radical II and oxidation of radical IV to cationic intermediate V, the latter process also regenerated the catalyst. Finally, the deprotonation assisted by base resulted in various 6-alkylated

• -halobenzyl)arylamines, oxime carbonates, isocyanobiphenyls, etc.). Phenanthridines are usually obtained within 2–3 reaction steps, by application of different radical initiators. An intriguing alternative is the radical generation by UV irradiation with or even without a photocatalyst. The major advantage of

An integrated photocatalytic/enzymatic system for the reduction of CO₂ to methanol in bioglycerol–water

• Michele Aresta,
• Angela Dibenedetto,
• Tomasz Baran,
• Antonella Angelini,
• Przemysław Łabuz and
• Wojciech Macyk

Beilstein J. Org. Chem. 2014, 10, 2556–2565, doi:10.3762/bjoc.10.267

• from NAD+ would be of great interest due to their low cost, moderate (ambient) operational conditions and acceptable environmental impact. The most extensively applied photochemical processes are based on the use of TiO2 as a photocatalyst in oxidation reactions [14][15][16]. While pure TiO2 has a band

• most likely affects the enzyme activity by inducing structural modifications. In [7] a photocatalyst was used that operates on the border of the UV–vis spectrum. As described above, the goal of this research is to work in the visible-light range, possibly using direct irradiation with solar light

• reduction of NAD+ using bioglycerol as a H-donor and a Rh(III)-complex as an e−–H+ transfer agent were found. It was shown that the photocatalyst, the electron mediator and the H-donor have suitable energy levels that can be combined together for an effective recycling of NAD+. The cofactor can be used

Visible light photoredox-catalyzed deoxygenation of alcohols

• Daniel Rackl,
• Viktor Kais,
• Peter Kreitmeier and
• Oliver Reiser

Beilstein J. Org. Chem. 2014, 10, 2157–2165, doi:10.3762/bjoc.10.223

• light in the presence of [Ir(ppy)2(dtb-bpy)](PF6) as visible light photocatalyst and Hünig’s base as sacrificial electron donor in an acetonitrile/water mixture generally gave good to excellent yields of the desired defunctionalized compounds. Functional group tolerance is high but the protocol

• reduction potential (E0 = −1.51 V vs E0 = −1.31 V) [11]. Having identified a promising activation group for deoxygenation in combination with an iridium-based photocatalyst, different solvents and reaction temperatures were examined for the conversion of 3 (Table 2). Gratifyingly, toxic DMF could be

• after 16 h of irradiation (Table 2, entry 5). Control experiments suggest that the deoxygenation reaction of 3,5-bis(trifluoromethyl)benzoate 3 is indeed a photochemically mediated process (Table 2, entries 6 and 7): when either the photocatalyst (Table 2, entry 6) or the light source (Table 2, entry 7

Visible-light photoredox catalyzed synthesis of pyrroloisoquinolines via organocatalytic oxidation/[3 + 2] cycloaddition/oxidative aromatization reaction cascade with Rose Bengal

• Carlos Vila,
• Jonathan Lau and
• Magnus Rueping

Beilstein J. Org. Chem. 2014, 10, 1233–1238, doi:10.3762/bjoc.10.122

• /oxidative aromatization cascade using Rose Bengal as an organo-photocatalyst. A variety of pyrroloisoquinolines have been obtained in good yields under mild and metal-free reaction conditions. Keywords: alkaloids; [3 + 2] cycloaddition; organocatalysis; oxidation; photochemistry; photoredox catalysis; Rose

Homogeneous and heterogeneous photoredox-catalyzed hydroxymethylation of ketones and keto esters: catalyst screening, chemoselectivity and dilution effects

• Axel G. Griesbeck and
• Melissa Reckenthäler

Beilstein J. Org. Chem. 2014, 10, 1143–1150, doi:10.3762/bjoc.10.114

• -catalyzed photohydroxymethylation of ketones by methanol were investigated in order to evaluate the most active photocatalyst system. Dialkoxytitanium dichlorides are the most efficient species for chemoselective hydroxymethylation of acetophenone as well as other aromatic and aliphatic ketones. Pinacol

Direct C–H trifluoromethylation of di- and trisubstituted alkenes by photoredox catalysis

• Ren Tomita,
• Yusuke Yasu,
• Takashi Koike and
• Munetaka Akita

Beilstein J. Org. Chem. 2014, 10, 1099–1106, doi:10.3762/bjoc.10.108

• trifluoromethylation of alkenes by electrophilic CF3 reagents (+CF3) [65][66][67][68][69]. In addition, Cho et al. reported that the reaction of unactivated alkenes with gaseous CF3I in the presence of a Ru photocatalyst, [Ru(bpy)3]2+, and a base, DBU (diazabicyclo[5,4,0]undec-7-ene) produced CF3-alkenes through

• present reaction (Table 1, entries 4–6). Other solvent systems gave substantial amounts of the hydroxytrifluoromethylated byproduct, which we reported previously [37]. In addition, the present C–H trifluoromethylation proceeds even in the absence of a base (Table 1, entry 7). Another photocatalyst, [Ru

• (bpy)3](PF6)2, also promoted the present reaction, providing the product 3a in an 85% NMR yield (Table 1, entry 8). The Ru catalyst is less expensive than the Ir catalyst; thus, we chose the Ru photocatalyst for the experiments onward. Notably, product 3a was obtained neither in the dark nor in the

On the mechanism of photocatalytic reactions with eosin Y

• Michal Majek,
• Fabiana Filace and
• Axel Jacobi von Wangelin

Beilstein J. Org. Chem. 2014, 10, 981–989, doi:10.3762/bjoc.10.97

• have a profound effect on the outcome of a photocatalytic reaction. We have therefore examined if direct absorption of the arenediazonium ions can trigger a productive pathway under irradiation with broad-band light sources even in the absence of the photocatalyst. As representative examples we chose

• addition of the photocatalyst eosin Y, 54% yield of the borylation product were obtained by direct photolysis (Scheme 4). These observations are in full accord with a report of direct reaction of thermally generated aryl cations (from arenediazonium salts) with bispinacolato diboron to give the

• heterolysis of the substrate and subsequent ionic Ritter reaction. This notion was supported by our experiments performed in DMSO where a higher portion of the photocatalyst resides in the active EY3 and EY4 states. Following an otherwise identical protocol, irradiation at 535 nm resulted in the formation of

Visible light mediated intermolecular [3 + 2] annulation of cyclopropylanilines with alkynes

• Theresa H. Nguyen,
• Soumitra Maity and
• Nan Zheng

Beilstein J. Org. Chem. 2014, 10, 975–980, doi:10.3762/bjoc.10.96

• (Table 1). Similar to the annulation with alkenes [29], several reactivity patterns were observed. CH3NO2 was far superior to DMF and CH3CN as the solvent (Table 1; entries 1–3). Ru(bpz)3(PF6)2 was a more effective photocatalyst than Ru(bpy)3(PF6)2 (Table 1, entry 4). Air was detrimental to the

• lamps (CFLs). 13 W CFLs were used as the light source to mediate the annulation with alkenes [29]. White 18 W LEDs were found to be more effective for the annulation with alkynes, resulting in a higher yield (Table 1, entry 6). Control studies showed that both the photocatalyst and light were required

Metal and metal-free photocatalysts: mechanistic approach and application as photoinitiators of photopolymerization

• Jacques Lalevée,
• Sofia Telitel,
• Pu Xiao,
• Marc Lepeltier,
• Frédéric Dumur,
• Fabrice Morlet-Savary,
• Didier Gigmes and
• Jean-Pierre Fouassier

Beilstein J. Org. Chem. 2014, 10, 863–876, doi:10.3762/bjoc.10.83

• photocatalyst Ir(piq)2(tmd) (also known as bis(1-phenylisoquinolinato-N,C2’)iridium(2,2,6,6-tetramethyl-3,5-heptanedionate) is also proposed as an example of green light photocatalyst (toward the long wavelength irradiation). The chemical mechanisms associated with Ir(piq)2(tmd) are investigated by ESR spin

Visible-light photoredox catalysis enabled bromination of phenols and alkenes

• Yating Zhao,
• Zhe Li,
• Chao Yang,
• Run Lin and
• Wujiong Xia

Beilstein J. Org. Chem. 2014, 10, 622–627, doi:10.3762/bjoc.10.53

• photocatalyst or the light source did not afford the desired product 2a. Therefore, the reaction conditions of CBr4 (1 equiv) in dried CH3CN in the presence of Ru(bpy)3Cl2 (5.0 mol %) with visible light irradiation (blue LEDs, λmax = 435 nm) and open to air were utilized to test the scope of the reaction. With

Synthesis of five- and six-membered cyclic organic peroxides: Key transformations into peroxide ring-retaining products

• Alexander O. Terent'ev,
• Dmitry A. Borisov,
• Vera A. Vil’ and
• Valery M. Dembitsky

Beilstein J. Org. Chem. 2014, 10, 34–114, doi:10.3762/bjoc.10.6

• % yields. 2,4,6-Triphenylpyrylium tetrafluoroborate was used as the sensitizer for singlet oxygen generation (Scheme 54) [301]. It was found that tris(bipyrazyl)ruthenium(II) [(Ru(bpz)3(PF6)2] is an excellent photocatalyst for the synthesis of 1,2-dioxanes by aerobic photooxygenation of α,ω-dienes [302

New developments in gold-catalyzed manipulation of inactivated alkenes

• Michel Chiarucci and
• Marco Bandini

Beilstein J. Org. Chem. 2013, 9, 2586–2614, doi:10.3762/bjoc.9.294

• the [Au(I)]/[Au(III)] redox couple during the intramolecular oxy- and aminoarylation of alkenes (Scheme 40) [86]. Optimal conditions for the reaction involved the use of Ph3PAuNTf2 in presence of [Ru(bpy)3]2+ as redox photocatalyst and aryl diazonium salts 157. In the proposed tandem catalytic cycle

• )] intermediate 161 and regenerating the [Ru(II)(bpy)3]2+ photocatalyst. Finally, arylated tetrahydrofuran 158 was obtained by reductive elimination with concomitant regeneration of the [Au(I)] catalyst. Conclusion Metal catalyzed electrophilic activation of isolated alkenes is by far considered among the most

Recent advances in transition metal-catalyzed Csp²-monofluoro-, difluoro-, perfluoromethylation and trifluoromethylthiolation

• Grégory Landelle,
• Armen Panossian,
• Sergiy Pazenok,
• Jean-Pierre Vors and
• Frédéric R. Leroux

Beilstein J. Org. Chem. 2013, 9, 2476–2536, doi:10.3762/bjoc.9.287

• iodide and generate the corresponding radical (Scheme 13). Titanium dioxide was used as heterogeneous photocatalyst in the perfluoroalkylation of α-methylstyrene with perfluorohexyl iodide by M. Yoshida et al. [120]. While the main product arose from the formal perfluoroalkylation of a methyl sp3-C–H

The chemistry of amine radical cations produced by visible light photoredox catalysis

• Jie Hu,
• Jiang Wang,
• Theresa H. Nguyen and
• Nan Zheng

Beilstein J. Org. Chem. 2013, 9, 1977–2001, doi:10.3762/bjoc.9.234

• ). Therefore, a photocatalyst is often required to initialize electron-transfer reactions with amines. Some of the frequently used photocatalysts include ruthenium [24][25][26] and iridium [27][28] polypyridyl complexes as well as organic dyes [29][30] that are absorbed in the visible-light region. They all

• approach to exploit synthetic utility of photogenically produced amine radical cations. Reductive quenching of the photoexcited state of a photocatalyst (M) by amine 1 is governed by the reduction potentials of the photoexcited state and the amine (Scheme 1). The amine’s reduction potential, which can be

• 5 W blue LED as the light source. N-arylglycine derivatives 65, including esters and ketones, were successfully converted to the products 67. Rueping used Ir(ppy)2(bpy)PF6 as the photocatalyst, air, and an 11 W fluorescent bulb as the light source. Additionally, Zn(OAc)2 was employed as a Lewis acid

Metal-free aerobic oxidations mediated by N-hydroxyphthalimide. A concise review

• Lucio Melone and
• Carlo Punta

Beilstein J. Org. Chem. 2013, 9, 1296–1310, doi:10.3762/bjoc.9.146

• medium-band-gap semiconductor and has proved to be an efficient photocatalyst for synthetic purposes [66][67]. It has been demonstrated that the excited state of g-C3N4, obtained by irradiation with visible light, is able to activate O2 to the corresponding superoxide radical. The latter could undergo