Transformation of the cyclohexane ring to the cyclopentane fragment of biologically active compounds

• Natalya Akhmetdinova,
• Ilgiz Biktagirov and
• Liliya Kh. Faizullina

Beilstein J. Org. Chem. 2025, 21, 2416–2446, doi:10.3762/bjoc.21.185

• trimethylamine N-oxide and Dess–Martin periodinane, α-selenylation, and hydrogen peroxide-induced selenoxide elimination led to unsaturated ketone 183, from which artalbic acid (180) was obtained through a series of chemical transformations. The synthetic versatility of the photoinduced carboborative ring

C2 to C6 biobased carbonyl platforms for fine chemistry

• Jingjing Jiang,
• Muhammad Noman Haider Tariq,
• Florence Popowycz,
• Yanlong Gu and
• Yves Queneau

Beilstein J. Org. Chem. 2025, 21, 2103–2172, doi:10.3762/bjoc.21.165

•  15) [74][75][76]. Tang et al. recently reported the environmentally friendly production of glyceraldehyde and dihydroxyacetone from using glycerol through photocatalytic oxidation under visible light using a Cuδ+-decorated WO3 photocatalyst in the presence of hydrogen peroxide (H2O2) [77]. The

[3 + 2] Cycloaddition of thioformylium methylide with various arylidene-azolones in the synthesis of 7-thia-3-azaspiro[4.4]nonan-4-ones

• Daniil I. Rudik,
• Irina V. Tiushina,
• Anatoly I. Sokolov,
• Alexander Yu. Smirnov,
• Alexander R. Romanenko,
• Alexander A. Korlyukov,
• Andrey A. Mikhaylov and
• Mikhail S. Baranov

Beilstein J. Org. Chem. 2025, 21, 1791–1798, doi:10.3762/bjoc.21.141

• , proved to be a more promising derivatization approach (Scheme 4). Thus, the short-term action of hydrogen peroxide successfully converted compounds 7e, 7c, and 9e to their corresponding sulfoxides 11e, 11c, and 13e. However, prolonged oxidation led not only to sulfone formation but also to deeper

Research progress on calixarene/pillararene-based controlled drug release systems

• Liu-Huan Yi,
• Jian Qin,
• Si-Ran Lu,
• Liu-Pan Yang,
• Li-Li Wang and
• Huan Yao

Beilstein J. Org. Chem. 2025, 21, 1757–1785, doi:10.3762/bjoc.21.139

Advances in the use of metal-free tetrapyrrolic macrocycles as catalysts

• Mandeep K. Chahal

Beilstein J. Org. Chem. 2024, 20, 3085–3112, doi:10.3762/bjoc.20.257

• to the vacant axial site of the metal centers. This binding is followed by reduction to either hydrogen peroxide (H2O2) via a two-electron (2e−) pathway, water (H2O) through a four-electron (4e−) pathway, or a combination of both products through a concerted transfer of electrons and protons [126

Efficient modification of peroxydisulfate oxidation reactions of nitrogen-containing heterocycles 6-methyluracil and pyridine

• Alfiya R. Gimadieva,
• Yuliya Z. Khazimullina,
• Aigiza A. Gilimkhanova and
• Akhat G. Mustafin

Beilstein J. Org. Chem. 2024, 20, 2599–2607, doi:10.3762/bjoc.20.219

• in two different ways: with metallophthalocyanine catalysts present and by including hydrogen peroxide as a co-oxidant (Scheme 1). Metal–phthalocyanine complexes (PcM) are recognized as catalysts for gentle, particular oxidation reactions under aerobic [14] and H2O2-based conditions [15][16][17][18

• peroxydisulfate ion, leading to the production of oxygen [39]: Oxygen accumulation is additionally achieved by hydrogen peroxide self-decay, which is known to be increased in alkaline conditions [40]: Additionally, it has been reported [41] that hydroxyl radicals, produced from the decomposition of H2O2, can

• oxidation of nitrogen-containing heterocyclic compounds can be enhanced by the introduction of phthalocyanine catalysts or hydrogen peroxide into the reaction mixture. This approach has the potential to significantly increase the yield of the target compounds. Conclusion In conclusion, it is noted that we

Multicomponent syntheses of pyrazoles via (3 + 2)-cyclocondensation and (3 + 2)-cycloaddition key steps

• Ignaz Betcke,
• Alissa C. Götzinger,
• Maryna M. Kornet and
• Thomas J. J. Müller

Beilstein J. Org. Chem. 2024, 20, 2024–2077, doi:10.3762/bjoc.20.178

Syntheses and medicinal chemistry of spiro heterocyclic steroids

• Laura L. Romero-Hernández,
• Ana Isabel Ahuja-Casarín,
• Penélope Merino-Montiel,
• Sara Montiel-Smith,
• José Luis Vega-Báez and
• Jesús Sandoval-Ramírez

Beilstein J. Org. Chem. 2024, 20, 1713–1745, doi:10.3762/bjoc.20.152

• straightforward method to synthesize a series of steroidal spiro 1,2,4-triazolidin-3-ones 96 [52][53][54]. The spiro derivatives were selectively obtained as the unique isomers by reacting semicarbazones 95 with hydrogen peroxide at 0 °C. The reactions were conducted in chloroform, yielding all products in good

• yields (82–85%) (Scheme 28). The authors proposed a free radical mechanism facilitated by hydrogen peroxide, generating a primary radical at the terminal nitrogen atom -CO-HN• which then adds to the carbon atom of the imino group. The reaction mechanism was substantiated by theoretical calculations

• ester under basic conditions was carried out, followed by the transformation of the carboxyl group to the amides 165 and 166 by treatment with thionyl chloride and the corresponding amine. Tetraoxanes were obtained from ketones 163, 165, and 166 by a peroxyacylation reaction using an acidic hydrogen

Light on the sustainable preparation of aryl-cored dibromides

• Fabrizio Roncaglia,
• Alberto Ughetti,
• Nicola Porcelli,
• Biagio Anderlini,
• Andrea Severini and
• Luca Rigamonti

Beilstein J. Org. Chem. 2024, 20, 1076–1087, doi:10.3762/bjoc.20.95

• redox couple NaBr–NaBrO3 in acidic media [40][41]. Other variations include the system KBr–Oxone® [42]. However, based on a literature review, we concluded that unparalleled efficiency and sustainability can be achieved through the well-established redox equilibria between hydrogen peroxide and halide

• process, the residual halogen (if any) can decompose hydrogen peroxide into molecular oxygen (Equation 4) [45]. Over the years, various peroxide-bromide processes have been developed based on this chemistry. In particular, significant attention has been given to the preparation of benzyl (mono)bromides

• as the activator, and hydrogen peroxide was slowly added, by means of a syringe pump. As the bromine colour generated after each H2O2 drop disappeared quickly, the reaction time was reduced from 24 h to 8 h. In these conditions, the process exhibited complete conversion, but strong selectivity in

Methodology for awakening the potential secondary metabolic capacity in actinomycetes

• Shun Saito and
• Midori A. Arai

Beilstein J. Org. Chem. 2024, 20, 753–766, doi:10.3762/bjoc.20.69

• ), which upon sensing ROS, release their repression and activate the expression of various genes [93][94][95]. Wei et al. reported that the production of validamycin A (25) by Streptomyces hygroscopicus 5008 could be activated at the transcriptional level by simply adding hydrogen peroxide (H2O2; which

Optimizations of lipid II synthesis: an essential glycolipid precursor in bacterial cell wall synthesis and a validated antibiotic target

• Milandip Karak,
• Cian R. Cloonan,
• Brad R. Baker,
• Rachel V. K. Cochrane and
• Stephen A. Cochrane

Beilstein J. Org. Chem. 2024, 20, 220–227, doi:10.3762/bjoc.20.22

• -phosphite intermediate was then oxidized with hydrogen peroxide to yield dibenzyl α-phosphate 6, achieving an overall yield of 89% for these two steps. Removal of the 2-(phenylsulfonyl)ethanol protecting group in compound 6 was successfully achieved through treatment with 1,8-diazabicyclo[5.4.0]undec-7-ene

Aromatic systems with two and three pyridine-2,6-dicarbazolyl-3,5-dicarbonitrile fragments as electron-transporting organic semiconductors exhibiting long-lived emissions

• Karolis Leitonas,
• Brigita Vigante,
• Dmytro Volyniuk,
• Audrius Bucinskas,
• Pavels Dimitrijevs,
• Sindija Lapcinska,
• Pavel Arsenyan and
• Juozas Vidas Grazulevicius

Beilstein J. Org. Chem. 2023, 19, 1867–1880, doi:10.3762/bjoc.19.139

• the photocatalytic production of H2 while the nanospheres produced hydrogen peroxide (H2O2). The introduction of the additional carbazolylphenyl moiety in the CPC molecule [4] allowed us to improve the EQEmax of an OLED to 25% [7]. In continuation of our studies in the field of the development of new

Radical chemistry in polymer science: an overview and recent advances

• Zixiao Wang,
• Feichen Cui,
• Yang Sui and
• Jiajun Yan

Beilstein J. Org. Chem. 2023, 19, 1580–1603, doi:10.3762/bjoc.19.116

• , such as organic peroxides, hydrogen peroxide, persulfates undergo homolysis of O–O bonds generating radicals that can break C–H bonds followed by a hydrogen abstraction reaction. Phenolic compounds can be oxidized by molecular oxygen in the presence of laccase, and the resulting phenolic radical reacts

Cyclodextrins permeabilize DPPC liposome membranes: a focus on cholesterol content, cyclodextrin type, and concentration

• Ghenwa Nasr,
• Hélène Greige-Gerges,
• Sophie Fourmentin,
• Abdelhamid Elaissari and
• Nathalie Khreich

Beilstein J. Org. Chem. 2023, 19, 1570–1579, doi:10.3762/bjoc.19.115

• . Triton X-100, sodium chloride (NaCl), and Sephadex G25 gel were purchased from Sigma-Aldrich, Belgium. Ammonium molybdate, hydrogen peroxide, potassium dihydrogen phosphate, sodium sulfite, sodium bisulfite, chloroform, and methanol were purchased from Sigma-Aldrich, Germany. Cholesterol and

Synthesis of ether lipids: natural compounds and analogues

• Marco Antônio G. B. Gomes,
• Alicia Bauduin,
• Chloé Le Roux,
• Romain Fouinneteau,
• Wilfried Berthe,
• Mathieu Berchel,
• Hélène Couthon and
• Paul-Alain Jaffrès

Beilstein J. Org. Chem. 2023, 19, 1299–1369, doi:10.3762/bjoc.19.96

Selective and scalable oxygenation of heteroatoms using the elements of nature: air, water, and light

• Damiano Diprima,
• Hannes Gemoets,
• Stefano Bonciolini and
• Koen Van Aken

Beilstein J. Org. Chem. 2023, 19, 1146–1154, doi:10.3762/bjoc.19.82

• selectivity and safety. Traditional oxidants, such as Oxone, CrO3, NaIO4, or KMnO4, produce significant amounts of toxic waste, exacerbating these issues (Scheme 1A) [1]. As environmental concerns and economic factors increasingly affect chemical processes, hydrogen peroxide and oxygen (or air) are becoming

• more popular as oxidants due to their low cost and minimal side products. However, these reagents have practical limitations. Hydrogen peroxide is typically produced off-site and requires transportation and storage, and is commonly obtained through the non-sustainable anthraquinone process (Scheme 1B

• ) [2][3][4]. Additionally, practical implementation of hydrogen peroxide can be challenging due to requirements for precise dosing to avoid issues such as dismutation, overoxidation, and catalyst degradation [5]. In this respect, oxygen, or preferably air, represents a better alternative to traditional

An efficient metal-free and catalyst-free C–S/C–O bond-formation strategy: synthesis of pyrazole-conjugated thioamides and amides

• Shubham Sharma,
• Dharmender Singh,
• Sunit Kumar,
• Vaishali,
• Rahul Jamra,
• Naveen Banyal,
• Deepika,
• Chandi C. Malakar and
• Virender Singh

Beilstein J. Org. Chem. 2023, 19, 231–244, doi:10.3762/bjoc.19.22

• , metal-free and easy to perform reaction conditions. Moreover, the pyrazole C-3/5-linked amide conjugates were also synthesized via an oxidative amination of pyrazole carbaldehydes and 2-aminopyridines using hydrogen peroxide as an oxidant. Keywords: C–S/O bond formation; metal-free; oxidative amidation

• (entry 16, Table 2). From the above screening experiments, it was concluded that 10.0 equiv of hydrogen peroxide in THF at 70 °C proved to be the optimal conditions for the construction of the pyrazole-pyridine conjugate with an amide linkage (entry 16, Table 2). Having the optimized conditions in hand

• available substituted 2-aminopyridines and hydrogen peroxide as an oxidant. The biological evaluation of the thioamide and amide conjugates is underway in our laboratory. Experimental General information All chemicals and reagents were purchased from Sigma-Aldrich, Acros, Avera Synthesis, Spectrochem Pvt

Redox-active molecules as organocatalysts for selective oxidative transformations – an unperceived organocatalysis field

• Elena R. Lopat’eva,
• Igor B. Krylov,
• Dmitry A. Lapshin and
• Alexander O. Terent’ev

Beilstein J. Org. Chem. 2022, 18, 1672–1695, doi:10.3762/bjoc.18.179

• , the acidic and basic sites of the catalyst are suggested to be involved in the activation of only hydrogen peroxide within a well-defined and deep chiral cavity. The enantioselective approach of sulfide to H2O2 is ensured by the sterically demanding structure of the catalyst. It should also be noted

Design, synthesis, and evaluation of chiral thiophosphorus acids as organocatalysts

• Karen R. Winters and
• Jean-Luc Montchamp

Beilstein J. Org. Chem. 2022, 18, 1471–1478, doi:10.3762/bjoc.18.154

• synthesized from 2-aminobiphenyl according to the literature [47]. Subsequent reaction with phosphorus trichloride and electrophilic aromatic substitution gave a chlorophosphine intermediate, which was directly reacted with (S)-1-phenylethylamine, then hydrogen peroxide. Phosphonamide diastereoisomers 17 were

Synthetic strategies for the preparation of γ-phostams: 1,2-azaphospholidine 2-oxides and 1,2-azaphospholine 2-oxides

• Jiaxi Xu

Beilstein J. Org. Chem. 2022, 18, 889–915, doi:10.3762/bjoc.18.90

• derivatives 83 followed by an intramolecular cyclization via the intramolecular Arbuzov reaction under heating generated 1,2-azaphospholidine 2-oxides 89. Compounds 89 were further transformed into N-phosphoryl- and N-thiophosphoryl-1,2-azaphospholidine 2-oxides 90/2-sulfides 91 via oxidation with hydrogen

• peroxide and sulfurization with sulfur, respectively (Scheme 16) [37][38]. Synthesis via formation of the C–C bond neighboring at the ring phosphorus atom In 1984, Collins and co-workers attempted the synthesis of benzo-γ-phosphonolactams 56a and 93 from (chloromethyl)(phenyl)-N-methyl-N

Synthesis of odorants in flow and their applications in perfumery

• Merlin Kleoff,
• Paul Kiler and
• Philipp Heretsch

Beilstein J. Org. Chem. 2022, 18, 754–768, doi:10.3762/bjoc.18.76

• flowers of orchids among with the structurally related and better known Ambrettolide [(Z)-7-hexadecen-16-olide], having a sweet odor with “great tenacity and fixative power” [9][48]. Notably, and already in 1970, Story and co-workers described that cyclic ketones can be reacted with hydrogen peroxide

• safe two-step synthesis of 56 from cyclohexanone. In the first step, a solution of cyclohexanone in dodecane is mixed in a Q-piece with hydrogen peroxide, nitric acid, and formic acid and subsequently pumped at room temperature through a PTFE tube reactor with a residence time of 93 min. The resulting

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

• •−), hydrogen peroxide (H2O2), hydroxyl radical (•OH), and hydroperoxyl radical (•OOH) (Figure 3) [35]. Additionally, the menadione semiquinone radical can participate in another redox cycle, such as, the Fenton reaction, also resulting in the production of hydroxyl and hydroperoxyl radicals (Figure 3) [39][40

• menadione (10), as was demonstrated by Minisci and co-workers [66]. In this work, the oxidation of 17 with 60% aqueous hydrogen peroxide, using bromine and sulfuric acid as catalysts, provided menadione in 90% yield (Table 2, entry 1) [66]. According to the proposed mechanism, the first step involves the

• different benzylamines (1:1:2.2) (Table 2, entry 7). The reaction was carried out in tert-amyl alcohol (TAA), which led to product 10 in 55% yield and 99% conversion of 17 [55]. In addition to hydrogen peroxide, other oxidizing agents can be used in the synthesis of menadione (10) from 17 and include

Recent advances and perspectives in ruthenium-catalyzed cyanation reactions

• Thaipparambil Aneeja,
• Cheriya Mukkolakkal Abdulla Afsina,
• Padinjare Veetil Saranya and
• Gopinathan Anilkumar

Beilstein J. Org. Chem. 2022, 18, 37–52, doi:10.3762/bjoc.18.4

• the cyanation reaction. This strategy utilized eco-friendly hydrogen peroxide and molecular oxygen as the oxidant system. This method was found highly favorable to tertiary amines with electron-donating substituents. The first report on an MCM-41-immobilized N-alkylethylenediamine Ru(III) complex (MCM

• to furnish the desired products in good yields. In 2008, they described the scope and mechanism of the oxidative cyanation of tertiary amines using H2O2 and O2 [34]. They pointed out the fact that the hydrogen peroxide system was found to be more efficient in catalyzing the cyanation reaction of

• cyclic amines than the aerobic oxidation system. The catalytic cycle for the hydrogen peroxide system involves the formation of the oxoruthenium species (A) and the low-valent ruthenium species (B), whereas the aerobic oxidation system includes C–H activation and a subsequent reaction with molecular

Efficient N-arylation of 4-chloroquinazolines en route to novel 4-anilinoquinazolines as potential anticancer agents

• Rodolfo H. V. Nishimura,
• Thiago dos Santos,
• Valter E. Murie,
• Luciana C. Furtado,
• Leticia V. Costa-Lotufo and
• Giuliano C. Clososki

Beilstein J. Org. Chem. 2021, 17, 2968–2975, doi:10.3762/bjoc.17.206

• . While anthranilamide (5) bromination with N-bromosuccinimide in acetonitrile at room temperature [29] furnished 2-amino-5-bromobenzamide (6a) in 78% yield, iodination of 5 with iodine in the presence of hydrogen peroxide in water [30] at 50 °C provided 2-amino-5-iodobenzamide (6b) in 89% yield. After

Highly stereocontrolled total synthesis of racemic codonopsinol B through isoxazolidine-4,5-diol vinylation

• Lukáš Ďurina,
• Anna Ďurinová,
• František Trejtnar,
• Ľuboš Janotka,
• Lucia Messingerová,
• Jana Doháňošová,
• Ján Moncol and
• Róbert Fischer

Beilstein J. Org. Chem. 2021, 17, 2781–2786, doi:10.3762/bjoc.17.188

• hydrogen peroxide catalyzed by phosphotungstic heteropoly acid. Each of the key reactions proceeded with an excellent diastereoselectivity (dr > 95:5). (±)-Codonopsinol B was prepared in 10 steps with overall 8.4% yield. The antiproliferative effect of (±)-codonopsinol B and its N-nor-methyl analogue was

•  1, page S25). Although the syn selectivity was further improved (80:20) by using the in situ-generated trifluoroperoxyacetic acid [28], the reaction suffered from formation of a high level of impurities. Gratifyingly, this issue has been overcome by the use of hydrogen peroxide in the presence of

• formation. Since the aqueous tungstic acid-catalyzed hydrogen peroxide epoxidations of monosubstituted allylic alcohols usually proceed in anti (erythro) stereoselective fashion [32], we propose that the high syn selectivity can be attributed to the presence of the unprotected hydroxy group in the