Synthesis, structural characterization, and optical properties of benzo[f]naphtho[2,3-b]phosphoindoles

• Mio Matsumura,
• Takahiro Teramoto,
• Masato Kawakubo,
• Masatoshi Kawahata,
• Yuki Murata,
• Kentaro Yamaguchi,
• Masanobu Uchiyama and
• Shuji Yasuike

Beilstein J. Org. Chem. 2021, 17, 671–677, doi:10.3762/bjoc.17.56

• phosphorus atom of 2 was carried out; the results are shown in Scheme 1. The reaction of 2 with hydrogen peroxide or elemental sulfur afforded the corresponding phosphine oxide 3 and sulfide 4 in 92% and 88% yield, respectively. Treatment of 2 with methyl triflate afforded phospholium triflate 5 in 81% yield

Breakdown of 3-(allylsulfonio)propanoates in bacteria from the Roseobacter group yields garlic oil constituents

• Anuj Kumar Chhalodia and
• Jeroen S. Dickschat

Beilstein J. Org. Chem. 2021, 17, 569–580, doi:10.3762/bjoc.17.51

• minutes, 30% hydrogen peroxide solution (0.52 mL, 0.57 g, 5.0 mmol, 2.0 equiv) was added dropwise. The color of the reaction mixture changed from colorless to yellow. The reaction mixture was stirred for 30 minutes at room temperature. After completion of the reaction, EtOAc (10 mL) was added, causing

A new and efficient methodology for olefin epoxidation catalyzed by supported cobalt nanoparticles

• Lucía Rossi-Fernández,
• Viviana Dorn and
• Gabriel Radivoy

Beilstein J. Org. Chem. 2021, 17, 519–526, doi:10.3762/bjoc.17.46

• greener oxidizing agents as molecular oxygen, hydrogen peroxide or tert-butyl hydroperoxide (TBHP) [14][15][16][17]. However, using any of these oxidants alone results in considerable low reactivity and selectivity in olefin epoxidation reactions. Thus, several transition-metal-based catalytic methods

¹⁹F NMR as a tool in chemical biology

• Diana Gimenez,
• Aoife Phelan,
• Cormac D. Murphy and
• Steven L. Cobb

Beilstein J. Org. Chem. 2021, 17, 293–318, doi:10.3762/bjoc.17.28

Recent progress in the synthesis of homotropane alkaloids adaline, euphococcinine and N-methyleuphococcinine

• Dimas J. P. Lima,
• Antonio E. G. Santana,
• Michael A. Birkett and
• Ricardo S. Porto

Beilstein J. Org. Chem. 2021, 17, 28–41, doi:10.3762/bjoc.17.4

• piperidine (17). The synthetic sequence performed by the authors is described in Scheme 3. Oxidation of 17 in the presence of hydrogen peroxide, catalyzed by selenium dioxide provided tetrahydropyridine N-oxide 18 in 88% yield. 18 was treated with (R)-p-tolylsulfinylmethyllithium 25 in THF at −78 °C to

• provide β-sulfinyl hydroxylamine 19 in a diastereoisomeric ratio of 67:33 in 52% yield. Oxidation of 19 to nitrone 20 occurred chemoselectivelly through treatment with a solution of hydrogen peroxide in 3 mol % of 5-ethyluminiflavin perchlorate (FIEt+.ClO4) as a catalyst in 55% yield. The reaction of β

Synthetic approaches to bowl-shaped π-conjugated sumanene and its congeners

• Shakeel Alvi and
• Rashid Ali

Beilstein J. Org. Chem. 2020, 16, 2212–2259, doi:10.3762/bjoc.16.186

• sumanene-based trisulfone derivative 156 in the presence of hydrogen peroxide in AcOH as detailed in the Scheme 40. Liu et al. has revealed the functionalization of a sulfur-doped sumanene by means of perbromination followed by nucleophilic substitution as depicted in Scheme 41 [78]. They first performed

Synthesis of new dihydroberberine and tetrahydroberberine analogues and evaluation of their antiproliferative activity on NCI-H1975 cells

• Giacomo Mari,
• Lucia De Crescentini,
• Serena Benedetti,
• Francesco Palma,
• Stefania Santeusanio and
• Fabio Mantellini

Beilstein J. Org. Chem. 2020, 16, 1606–1616, doi:10.3762/bjoc.16.133

• , namely pyrrolino-tetrahydroberberines, synthesized by some of us [68], exhibited enhanced antioxidant properties in comparison to THBER against a wide variety of pathophysiologically relevant oxidants such as peroxyl radicals, ferrous ion, and hydrogen peroxide [65]. In continuation of our ongoing

Synthesis of 3-substituted isoxazolidin-4-ols using hydroboration–oxidation reactions of 4,5-unsubstituted 2,3-dihydroisoxazoles

• Lívia Dikošová,
• Júlia Laceková,
• Ondrej Záborský and
• Róbert Fischer

Beilstein J. Org. Chem. 2020, 16, 1313–1319, doi:10.3762/bjoc.16.112

• isoxazolidin-4-ols. The strategy relies on a highly regio- and trans-stereoselective hydroboration–oxidation reaction of the 4,5-unsubstituted 2,3-dihydroisoxazoles with basic hydrogen peroxide. The consecutive oxidation/reduction route, sequentially employing Dess–Martin periodinane and ʟ-selectride, is used

• -hydroxyisoxazolidines by the treatment of boronic ester-substituted isoxazolidines with basic hydrogen peroxide has previously been described [30][31]. To start with, the phenyl-substituted 2,3-dihydroisoxazole 5a was chosen as the starting substrate. After optimizing Kang's reaction conditions in terms of the borane

• -substituted isoxazolidin-4-ols employing the hydroboration–oxidation reaction of 4,5-unsubstituted 2,3-dihydroisoxazoles with basic hydrogen peroxide. A patient addition of both NaOH (aq) and H2O2 (aq) accompanied by intense cooling was a crucial part of the procedure in terms of product yield. All

Activated carbon as catalyst support: precursors, preparation, modification and characterization

• Melanie Iwanow,
• Tobias Gärtner,
• Volker Sieber and
• Burkhard König

Beilstein J. Org. Chem. 2020, 16, 1188–1202, doi:10.3762/bjoc.16.104

• the surface of the treated carbons in form of carboxyl groups, ketones, ether groups and carboxyl-carbonate structures is higher using nitric acid compared to hydrogen peroxide [116]. Nitrogen adsorption–desorption isotherms: The surface area and pore size distribution of solid catalyst materials can

Recent applications of porphyrins as photocatalysts in organic synthesis: batch and continuous flow approaches

• Rodrigo Costa e Silva,
• Luely Oliveira da Silva,
• Aloisio de Andrade Bartolomeu,
• Timothy John Brocksom and
• Kleber Thiago de Oliveira

Beilstein J. Org. Chem. 2020, 16, 917–955, doi:10.3762/bjoc.16.83

• UNLPF-12 afforded the Mannich products in 87–98% yields (Scheme 63) [40]. As previously shown (Scheme 50), the oxidation of amines to imines by singlet oxygen furnishes hydrogen peroxide as a byproduct. In 2014, Seeberger and co-workers used this byproduct, in a continuous-flow approach, as an

Architecture and synthesis of P,N-heterocyclic phosphine ligands

• Wisdom A. Munzeiwa,
• Bernard Omondi and
• Vincent O. Nyamori

Beilstein J. Org. Chem. 2020, 16, 362–383, doi:10.3762/bjoc.16.35

• carbon dioxide and phenyllithium gives the phosphine ferrocene carboxylic acid 152 as the major reagent. Oxidation of the phosphine using hydrogen peroxide generated the phosphine oxide 153. In situ chlorination of the carboxylic acid followed by addition of the chiral amino alcohols gave the phosphoryl

Chiral terpene auxiliaries V: Synthesis of new chiral γ-hydroxyphosphine oxides derived from α-pinene

• Anna Kmieciak and
• Marek P. Krzemiński

Beilstein J. Org. Chem. 2019, 15, 2493–2499, doi:10.3762/bjoc.15.242

• % yield) allowed to upgrade the enantiomeric purity of dIpc2BH [25]. Oxidation of the resulting dialkylborane with hydrogen peroxide provided enantiomerically pure (−)-isopinocampheol (7) in 78% yield. The Brown–Garg protocol [26] was employed to oxidize 7 with an aqueous solution of sodium dichromate and

• selenium dioxide in methanol [28]. The obtained phenyl selenide 14 was oxidized with hydrogen peroxide in the presence of pyridine to selenoxide, which readily undergoes intramolecular syn-elimination to produce α,β-unsaturated (+)-apoverbenone (15) [28][29]. In the next step, Luche reduction of 15

• sodium hydroxide (2.7 mL, 8.1 mmol) were carefully added. After cooling to 0 °C, a 30% solution of hydrogen peroxide (1.2 mL, 12 mmol) was added dropwise to the reaction mixture. The solution was stirred for 30 minutes at rt and 1 h at 50 °C. After this time, potassium carbonate was added to saturate the

A review of the total syntheses of triptolide

• Xiang Zhang,
• Zaozao Xiao and
• Hongtao Xu

Beilstein J. Org. Chem. 2019, 15, 1984–1995, doi:10.3762/bjoc.15.194

• the desired stereochemistry of the C-7 benzylic hydroxy group. Compound 46 was converted to triptonide 2 by Alder periodate reaction (NaIO4, 74%), and a sequencing m-CPBA epoxidation and basic hydrogen peroxide oxidation (H2O2/OH−) procedure (two steps, 28%). Finally, sodium borohydride reduction of 2

Stereo- and regioselective hydroboration of 1-exo-methylene pyranoses: discovery of aryltriazolylmethyl C-galactopyranosides as selective galectin-1 inhibitors

• Alexander Dahlqvist,
• Axel Furevi,
• Niklas Warlin,
• Hakon Leffler and
• Ulf J. Nilsson

Beilstein J. Org. Chem. 2019, 15, 1046–1060, doi:10.3762/bjoc.15.102

• route to 2-deoxyhepuloses 3, 5 and 7 [27][28][29][30]. The hydroboration of enol ethers 2, 4, and 6 with borane dimethyl sulfide in THF, followed by oxidation using hydrogen peroxide and sodium hydroxide gave 2-deoxygalactoheptulose 3 and 2-deoxymannoheptulose 5 in good yields (89% and 78%) and with

• , 14.00 mmol, 1 M) and hydrogen peroxide (33%, 2 mL, 20.5 mmol) were added, and the reaction mixture left for 2 h. Upon completion of the reaction, 1 M hydrochloric acid was added to the reaction mixture until the pH was approximately 7. The reaction mixture was poured into brine (150 mL), extracted with

• observed. After completion of the gas evolution, sodium hydroxide (131 µL, 0.131 mmol, 1 M) and hydrogen peroxide (33%, 13 µL, 0.131 mmol) were added, and the reaction mixture left for 2 h. Upon completion of the reaction, 1 M hydrochloric acid was added to the reaction mixture until the pH was

Towards the preparation of synthetic outer membrane vesicle models with micromolar affinity to wheat germ agglutinin using a dialkyl thioglycoside

• Dimitri Fayolle,
• Nathalie Berthet,
• Bastien Doumeche,
• Olivier Renaudet,
• Peter Strazewski and
• Michele Fiore

Beilstein J. Org. Chem. 2019, 15, 937–946, doi:10.3762/bjoc.15.90

• color was developed using OPD (100 μL per well, 0.4 mg mL−1 in 0.05 M phosphate-citrate buffer) and urea hydrogen peroxide (0.4 mg mL−1). The reaction was stopped after 10 min by adding H2SO4 (30% v/v, 50 μL per well) and the absorbance was measured at 490 nm. The percentage of inhibition was determined

Azologization of serotonin 5-HT₃ receptor antagonists

• Karin Rustler,
• Galyna Maleeva,
• Piotr Bregestovski and
• Burkhard König

Beilstein J. Org. Chem. 2019, 15, 780–788, doi:10.3762/bjoc.15.74

• reacted with the 2-chloroacetylacetone ester derivative 7 providing hydrazine 8 [66]. Upon reaction of the chloro-ester 8 with phenylenediamine (9) in the presence of triethylamine the quinoxaline moiety was formed [67]. Oxidation of the hydrazine derivative 10 using hydrogen peroxide under an oxygen

Syntheses and chemical properties of β-nicotinamide riboside and its analogues and derivatives

• Mikhail V. Makarov and
• Marie E. Migaud

Beilstein J. Org. Chem. 2019, 15, 401–430, doi:10.3762/bjoc.15.36

• hexachloroacetone [28][71] or cobalt(II) acetate in the presence of hydrogen peroxide followed by removal of the cobalt cations with QuadraSil AP resin [60]. The nature of the counter anion vary as a function of the conditions applied. Reduction of N1-substituted 3-nicotinamide salts to the corresponding 1,4

• cobalt acetate in the presence of hydrogen peroxide. This approach required the subsequent removal of metal ions by Quadrasil resin. The oxidized acetonides 45 were subsequently deprotected using

Catalysis of linear alkene metathesis by Grubbs-type ruthenium alkylidene complexes containing hemilabile α,α-diphenyl-(monosubstituted-pyridin-2-yl)methanolato ligands

• Tegene T. Tole,
• Johan H. L. Jordaan and
• Hermanus C. M. Vosloo

Beilstein J. Org. Chem. 2019, 15, 194–209, doi:10.3762/bjoc.15.19

• %), 1-octene (99% GC), nonane (reagent plus 99%) and toluene (99%) were purchased from Sigma-Aldrich. Toluene-d8 (99.5%) was purchased from MERCK and tert-butyl hydrogen peroxide (80%) from Riedel-de Haen. Diethyl ether and THF were dried over Na in the presence of benzophenone. Pentane was distilled

• min with a gastight syringe (1 mL), transferred to a GC vial (1 mL), quenched with toluene (0.3 mL) and tert-butyl hydrogen peroxide (2 drops), and then injected into a GC/FID by auto sampler. The metathesis reaction was terminated after 1440 minutes and analysed by GC/FID. Some samples were also

Repurposing the anticancer drug cisplatin with the aim of developing novel Pseudomonas aeruginosa infection control agents

• Mingjun Yuan,
• Song Lin Chua,
• Yang Liu,
• Daniela I. Drautz-Moses,
• Joey Kuok Hoong Yam,
• Thet Tun Aung,
• Roger W. Beuerman,
• May Margarette Santillan Salido,
• Stephan C. Schuster,
• Choon-Hong Tan,
• Michael Givskov,
• Liang Yang and
• Thomas E. Nielsen

Beilstein J. Org. Chem. 2018, 14, 3059–3069, doi:10.3762/bjoc.14.284

• ] and hydrogen peroxide treatments [32]. In addition, cisplatin treatment induced the expression of a series of genes involved in energy metabolism, which corroborated with previous proteomics work showing that cisplatin could interfere with stress response and energy metabolism in E. coli [33]. To

Copper(I)-catalyzed tandem reaction: synthesis of 1,4-disubstituted 1,2,3-triazoles from alkyl diacyl peroxides, azidotrimethylsilane, and alkynes

• Muhammad Israr,
• Changqing Ye,
• Munira Taj Muhammad,
• Yajun Li and
• Hongli Bao

Beilstein J. Org. Chem. 2018, 14, 2916–2922, doi:10.3762/bjoc.14.270

• . Furthermore, the scope of the alkyl diacyl peroxides was then studied (Scheme 3). The alkyl diacyl peroxides 2 were synthesized from the corresponding aliphatic carboxylic acids in a single step by DCC-mediated dehydrative condensation with hydrogen peroxide, and were used directly after simple filtration

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

• permanganate was added and stirred at 35 °C for 2 h. In the next step, the reaction mixture was cooled to 0 °C. Hydrogen peroxide (30%) in deionized water was added to the reaction mixture. The solid was gathered by centrifugation, washed with deionized water, methanol, and ether, and then dried at 40 °C under

Bioinspired cobalt cubanes with tunable redox potentials for photocatalytic water oxidation and CO₂ reduction

• Zhishan Luo,
• Yidong Hou,
• Jinshui Zhang,
• Sibo Wang and
• Xinchen Wang

Beilstein J. Org. Chem. 2018, 14, 2331–2339, doi:10.3762/bjoc.14.208

• g, 10 mmol) and CH3CO2Na·3H2O (2.7 g, 20 mmol) in methanol (30 mL) heated to refluxing temperature, is added pyridine (0.8 mL, 10 mmol) while stirring. Then a portion of 30% hydrogen peroxide (v/v, 5 mL, 50 mmol) is slowly added to the reaction mixture, and stirring under refluxing conditions is

The enzymes of microbial nicotine metabolism

• Paul F. Fitzpatrick

Beilstein J. Org. Chem. 2018, 14, 2295–2307, doi:10.3762/bjoc.14.204

• it contains covalently-bound FAD and produces hydrogen peroxide as a product in addition to 4-aminobutryate [5][38]. Mabo also catalyzes the oxidative demethylation of sarcosine. Based on these results, the mechanism of the enzyme is similar to that of sarcosine oxidase, direct oxidation of the C–N

Recent advances in hypervalent iodine(III)-catalyzed functionalization of alkenes

• Xiang Li,
• Pinhong Chen and
• Guosheng Liu

Beilstein J. Org. Chem. 2018, 14, 1813–1825, doi:10.3762/bjoc.14.154

• was used as a stoichiometric oxidant [45]. In contrast to the intramolecular cyclization, the intermolecular reaction is much more attractive. Li and co-workers reported a syn-diacetoxylation of alkenes, using iodoarenes as catalyst which was oxidized to hypervalent iodine(III) by hydrogen peroxide in

An amine protecting group deprotectable under nearly neutral oxidative conditions

• Shahien Shahsavari,
• Chase McNamara,
• Mark Sylvester,
• Emily Bromley,
• Savannah Joslin,
• Bao-Yuan Lu and
• Shiyue Fang

Beilstein J. Org. Chem. 2018, 14, 1750–1757, doi:10.3762/bjoc.14.149

• conditions [13][14][15][16][17]. This group was deprotected under oxidative conditions under which the commonly used Boc, Fmoc, benzyl and Teoc groups could potentially survive. Oxidation was achieved by hydrogen peroxide in the presence of an ammonium molybdate catalyst. Recently, we reported the use of the