(E,Z)-1,1,1,4,4,4-Hexafluorobut-2-enes: hydrofluoroolefins halogenation/dehydrohalogenation cascade to reach new fluorinated allene

• Nataliia V. Kirij,
• Andrey A. Filatov,
• Yurii L. Yagupolskii,
• Sheng Peng and
• Lee Sprague

Beilstein J. Org. Chem. 2024, 20, 452–459, doi:10.3762/bjoc.20.40

• oxirane [14]. A related study has demonstrated that (E)-butene 1a reacts with potassium persulfate to form 4,5-bistrifluoromethyl)-1,3,2-dioxathiolane 2,2-dioxide [15]. In 2021 Petrov published an article on the interaction of fluorinated olefins with fluorinated thioketones. In this publication it was

Pyridine C(sp²)–H bond functionalization under transition-metal and rare earth metal catalysis

• Haritha Sindhe,
• Malladi Mounika Reddy,
• Karthikeyan Rajkumar,
• Akshay Kamble,
• Amardeep Singh,
• Anand Kumar and
• Satyasheel Sharma

Beilstein J. Org. Chem. 2023, 19, 820–863, doi:10.3762/bjoc.19.62

• intact under the reaction conditions without any further oxidation. Different oxidants resulted in different products such as the monoarylated product 118 formed in the presence of TBHP as oxidant and the benzylated product 119 was obtained when potassium persulfate was used. Interestingly, aza-fluorene

Sulfate radical anion-induced benzylic oxidation of N-(arylsulfonyl)benzylamines to N-arylsulfonylimines

• Joydev K. Laha,
• Pankaj Gupta and
• Amitava Hazra

Beilstein J. Org. Chem. 2023, 19, 771–777, doi:10.3762/bjoc.19.57

• deliver N-arylsulfonylimines under mild reaction conditions is highly desirable. Previously, we reported a tandem oxidative intramolecular cyclization of N-aryl(benzyl)amines, having an internal nucleophile substituted at the ortho-position in the aniline ring, to nitrogen heterocycles using potassium

• persulfate (K2S2O8) as the exclusive reagent [14]. The mechanistic study revealed that an initial oxidation to an iminium ion could be the key intermediate in the intramolecular cyclization step. In sharp contrast, when N-aryl(benzyl)amines that do not have an ortho-substituted nucleophile in aniline ring

Menadione: a platform and a target to valuable compounds synthesis

• Acácio S. de Souza,
• Ruan Carlos B. Ribeiro,
• Dora C. S. Costa,
• Fernanda P. Pauli,
• David R. Pinho,
• Matheus G. de Moraes,
• Fernando de C. da Silva,
• Luana da S. M. Forezi and
• Vitor F. Ferreira

Beilstein J. Org. Chem. 2022, 18, 381–419, doi:10.3762/bjoc.18.43

• in Scheme 17 below the optimized reaction conditions are shown for the synthesis of compounds 62 and 64 (Scheme 17) [110]. In 2019, Sultan and co-workers described a methodology for the synthesis of quinone derivatives using a combination of potassium persulfate, trifluoroacetic acid (TFA), and blue

Synthesis of highly substituted fluorenones via metal-free TBHP-promoted oxidative cyclization of 2-(aminomethyl)biphenyls. Application to the total synthesis of nobilone

• Ilya A. P. Jourjine,
• Lukas Zeisel,
• Jürgen Krauß and
• Franz Bracher

Beilstein J. Org. Chem. 2021, 17, 2668–2679, doi:10.3762/bjoc.17.181

• published for fluorenone syntheses starting from other functionalized biphenyls with a key oxidative cyclization step. Starting from biphenyl-2-carbaldehyde (2l), Shi and Glorius [34] reported a fluorenone yield of 68%, utilizing potassium persulfate/tetraethylammonium bromide, the Singh group [35] reported

Access to highly substituted oxazoles by the reaction of α-azidochalcone with potassium thiocyanate

• Mysore Bhyrappa Harisha,
• Pandi Dhanalakshmi,
• Rajendran Suresh,
• Raju Ranjith Kumar and
• Shanmugam Muthusubramanian

Beilstein J. Org. Chem. 2020, 16, 2108–2118, doi:10.3762/bjoc.16.178

• azidochalcones, when treated with potassium thiocyanate in the presence of potassium persulfate, lead to 2,4,5-trisubstituted oxazoles in good yields. Incidentally, 2-aminothiazoles are the products when ferric nitrate is employed instead of persulfate in the above reaction. Keywords: aminothiazole; oxazole

• ; potassium persulfate; thiazole; vinyl azide; Introduction Vinyl azide is one of the most versatile and potent building blocks explored in the synthesis of several heterocycles [1][2][3][4][5]. It can undergo photolysis or thermolysis to afford highly strained three-membered 2H-azirine, which can act as the

• thiocyanate 2 in the presence of several oxidants and metal salts (Table 1). The initial attempts employing iodine, CAN and ZnCl2 upon refluxing in acetonitrile for 6 hours did not yield any product (Table 1, entries 1, 2 and 4). When potassium persulfate (K2S2O8) is employed, highly substituted oxazole 3i

Metal-free synthesis of phosphinoylchroman-4-ones via a radical phosphinoylation–cyclization cascade mediated by K₂S₂O₈

• Qiang Liu,
• Weibang Lu,
• Guanqun Xie and
• Xiaoxia Wang

Beilstein J. Org. Chem. 2020, 16, 1974–1982, doi:10.3762/bjoc.16.164

• afforded the title compounds in moderate yields. Keywords: chroman-4-ones; diphenylphosphine oxide; metal-free; potassium persulfate; radical cyclization; Introduction The chroman-4-one framework is a privileged structural motif found in numerous natural products and pharmaceuticals with extraordinary

• potassium persulfate [42][43][44]. Based on literature precedent [29][30][42][43][44][45][46] and preliminary mechanistic experiments, a plausible mechanism was proposed in Scheme 5 which was different from the predominant mechanism observed in the Ag-catalyzed radical cascade for the preparation of

When metal-catalyzed C–H functionalization meets visible-light photocatalysis

• Lucas Guillemard and
• Joanna Wencel-Delord

Beilstein J. Org. Chem. 2020, 16, 1754–1804, doi:10.3762/bjoc.16.147

• single electron-transfer process (Figure 36). In the first place, a bidentate chelated species is formed by the coordination of 1-naphthylamine derivatives with copper salt. The subsequent oxidation of this intermediate with potassium persulfate produces a Cu(III) species, furnishing a radical cation on

Photocatalysis with organic dyes: facile access to reactive intermediates for synthesis

• Stephanie G. E. Amos,
• Marion Garreau,
• Luca Buzzetti and
• Jerome Waser

Beilstein J. Org. Chem. 2020, 16, 1163–1187, doi:10.3762/bjoc.16.103

• salt 6.1 was promoted by the acridinium photocatalyst OD2. The resulting alkyl radical can be intercepted by a protonated heteroarene 6.2. The addition of potassium persulfate leads to the regeneration of the photocatalyst and the rearomatization of the intermediate, delivering the desired alkylated

Oxidative radical ring-opening/cyclization of cyclopropane derivatives

• Yu Liu,
• Qiao-Lin Wang,
• Zan Chen,
• Cong-Shan Zhou,
• Bi-Quan Xiong,
• Pan-Liang Zhang,
• Chang-An Yang and
• Quan Zhou

Beilstein J. Org. Chem. 2019, 15, 256–278, doi:10.3762/bjoc.15.23

• 2016, the silver-promoted oxidative ring-opening/alkynylation of cyclopropanols 91 with ethynylbenziodoxolones (EBX) 116 had been presented by Li and co-workers (Scheme 29) [109]. Both silver(I) nitrate and potassium persulfate played an important role in this transformation. In 2016, Hu and co-workers

An overview on recent advances in the synthesis of sulfonated organic materials, sulfonated silica materials, and sulfonated carbon materials and their catalytic applications in chemical processes

• Hashem Sharghi,
• Pezhman Shiri and
• Mahdi Aberi

Beilstein J. Org. Chem. 2018, 14, 2745–2770, doi:10.3762/bjoc.14.253

• graphite powder (141), potassium persulfate, phosphorus pentoxide, and sulfuric acid was heated at 80 °C for 2 h. The resulted solid was filtered and washed with water, methanol, and ether. Then, the obtained black paste was dried. After mixing the resulting material with sulfuric acid at 0 °C, potassium

CF₃SO₂X (X = Na, Cl) as reagents for trifluoromethylation, trifluoromethylsulfenyl-, -sulfinyl- and -sulfonylation. Part 1: Use of CF₃SO₂Na

• Hélène Guyon,
• Hélène Chachignon and
• Dominique Cahard

Beilstein J. Org. Chem. 2017, 13, 2764–2799, doi:10.3762/bjoc.13.272

• CF3SO2Na by means of an oxidative system comprising catalytic amounts of silver(I) nitrate and potassium persulfate K2S2O8. Both atmospheric oxygen and K2S2O8 can be the source of the oxygen atom of the ketone moiety. A series of experiments that include the formation of TEMPO–CF3 (TEMPO: 2,2,6,6

• with a catalytic amount of potassium persulfate to activate CF3SO2Na (Scheme 7) [26]. The heteroatom must be a good leaving group or part of it (X = Br, Cl, NHCOMe, N3, OP(O)(OEt)2). A mechanistic investigation demonstrated the role of oxygen: 93% isotopic purity of the ketone product was obtained when

• . Simultaneously, Shen, Zhang and co-workers reported a milder regioselective trifluoromethylation of 8-aminoquinolines using the supported catalyst CS@Cu(OAc)2 (CS = chitosan), potassium persulfate as the oxidant and CF3SO2Na as the CF3• source (Scheme 45) [68]. After optimisation of the reaction conditions, the

Rearrangements of organic peroxides and related processes

• Ivan A. Yaremenko,
• Vera A. Vil’,
• Dmitry V. Demchuk and
• Alexander O. Terent’ev

Beilstein J. Org. Chem. 2016, 12, 1647–1748, doi:10.3762/bjoc.12.162

Cross-dehydrogenative coupling for the intermolecular C–O bond formation

• Igor B. Krylov,
• Vera A. Vil’ and
• Alexander O. Terent’ev

Beilstein J. Org. Chem. 2015, 11, 92–146, doi:10.3762/bjoc.11.13

• lower temperature (50 °C instead of 100 °C, as in the case of CH-reagents 22 and 23) [53]. The ortho-acetoxylation and methoxylation of O-methyl aryl oximes 31 with Pd(OAc)2 combined with such oxidants as oxone, potassium persulfate, and (diacetoxyiodo)benzene (Scheme 7, coupling products 32 and 33

• , (diacetoxyiodo)benzene, or potassium persulfate served as oxidants. The former three reactions are applicable to a broad range of substrates and alcohols. The drawback is that a large excess of alcohols is required. Unlike the alkoxylation of 84–86, the trifluoroacetoxylation of 87 was performed with

Bioactive selaginellins from Selaginella tamariscina (Beauv.) Spring

• Chao Yang,
• Yutian Shao,
• Kang Li and
• Wujiong Xia

Beilstein J. Org. Chem. 2012, 8, 1884–1889, doi:10.3762/bjoc.8.217

• ABTS solution with 2.45 mM potassium persulfate solution (final concentration) followed by incubation in the dark at room temperature for 16 h. The resultant ABTS•+ solution was diluted with ethanol to give an absorbance of 0.70 ± 0.02 at 734 nm and equilibrated at 30 °C. After the addition of 2.85 mL