A recent overview on the synthesis of 1,4,5-trisubstituted 1,2,3-triazoles

• Pezhman Shiri,
• Ali Mohammad Amani and
• Thomas Mayer-Gall

Beilstein J. Org. Chem. 2021, 17, 1600–1628, doi:10.3762/bjoc.17.114

• -triazole-based phenol or alcohol coordinates to the Pd center to form complex 158. Then, the electrophilic palladation of the 1,2,3-triazole ring occurs to achieve Pd(II) intermediate 159. Isocyanide migrates to 159 to obtain the seven‐ or eight‐membered palladium cycle 160. The reductive elimination of

Breaking paracyclophane: the unexpected formation of non-symmetric disubstituted nitro[2.2]metaparacyclophanes

• Suraj Patel,
• Tyson N. Dais,
• Paul G. Plieger and
• Gareth J. Rowlands

Beilstein J. Org. Chem. 2021, 17, 1518–1526, doi:10.3762/bjoc.17.109

• pathway involves electrophilic addition para to the phenol to form the ipso-substituted nitro 12 compound. Subsequent rearrangement of the nitro species 12 to the nitrito dienone 13, by homolysis and recombination of the radical pair, is followed by hydrolysis to furnish alcohol 6 [70]. Addition of the

Co-crystallization of an organic solid and a tetraaryladamantane at room temperature

• Fabian Rami,
• Jan Nowak,
• Felix Krupp,
• Wolfgang Frey and
• Clemens Richert

Beilstein J. Org. Chem. 2021, 17, 1476–1480, doi:10.3762/bjoc.17.103

• as guest molecules. Here we report the co-crystal structures of phenol, which is solid at room temperature, with both 1,3,5,7-tetrakis(2,4-dimethoxyphenyl)adamantane (TDA) and 1,3,5,7-tetrakis(2,4-diethoxyphenyl)adamantane (TEO). The co-crystals were obtained from solutions in dichloromethane by slow

• configuration [18]. One limitation of the EnOC method was that the guest compound to be encapsulated had to be a liquid, so that it could act as solvent for the TAA, which would rapidly crystallize upon cooling of a hot, saturated solution. Here we report two co-crystal structures of TAAs with phenol, obtained

• by crystallization at room temperature, using dichloromethane as solvent. Results We opted for a benzene derivative for our first foray into organic solids to be encapsulated in TAA crystals, because a number of benzene derivatives have been found in EnOCs in the past [13][14][15]. Phenol was

Icilio Guareschi and his amazing “1897 reaction”

• Gian Cesare Tron,
• Alberto Minassi,
• Giovanni Sorba,
• Mara Fausone and
• Giovanni Appendino

Beilstein J. Org. Chem. 2021, 17, 1335–1351, doi:10.3762/bjoc.17.93

• hue dependent on the structure of the phenol. The mechanism of many color reactions popular in the 19th century is rather complex, and the one involved in the Schiff test of aldehyde is still not completely clear, despite the relevance in medical histology [22]. The report by Schiff on the Guareschi

• chloroform–phenol reaction attracted the attention of Karl Reimer (1845–1883) and Ferdinand Tiemann (1848–1899), who set out to investigate the chemistry involved in the color formation, eventually discovering the phenol formylation that bears their name [6]. The Guareschi reaction, then extensively applied

• to the identification of pharmaceutical phenols by Sigmund Lustgarten, is carried out under anhydrous conditions, either on an alkaline salt of the phenol or by adding solid KOH or NaOH to a chloroform solution of the phenol [5][21]. Reimer and Tiemann discovered that, in the presence of water, the

Recent advances in palladium-catalysed asymmetric 1,4–additions of arylboronic acids to conjugated enones and chromones

• Jan Bartáček,
• Jan Svoboda,
• Martin Kocúrik,
• Jaroslav Pochobradský,
• Alexander Čegan,
• Miloš Sedlák and
• Jiří Váňa

Beilstein J. Org. Chem. 2021, 17, 1048–1085, doi:10.3762/bjoc.17.84

• was chosen DMF, although the use of polar aprotic solvents usually leads to products of the oxidative Heck reaction. The authors noticed a significant reduction of Pd(II) to Pd(0) (by secondary processes such as oxidative homocoupling or oxidation of boronic acid to the corresponding phenol). The Pd(0

Application of the Meerwein reaction of 1,4-benzoquinone to a metal-free synthesis of benzofuropyridine analogues

• Rashmi Singh,
• Tomas Horsten,
• Rashmi Prakash,
• Swapan Dey and
• Wim Dehaen

Beilstein J. Org. Chem. 2021, 17, 977–982, doi:10.3762/bjoc.17.79

• spectrum of 15 showed two apparent singlets separately at δH 7.86 and δH 8.35, which confirmed that the hydrogen atoms of the phenol ring had a para-relationship. The 1H NMR spectrum of compound 14 was similar to that of compound 15 concerning the pyridine part. However, two separate doublet signals

Metal-free glycosylation with glycosyl fluorides in liquid SO₂

• Krista Gulbe,
• Jevgeņija Lugiņina,
• Edijs Jansons,
• Artis Kinens and
• Māris Turks

Beilstein J. Org. Chem. 2021, 17, 964–976, doi:10.3762/bjoc.17.78

• -glycosides to demonstrate the scope of acceptors compatible with our glycosylation conditions (Scheme 1). Most of the primary alcohols (2a, 2d–3f) were glycosylated in high yields (up to 91%). In the case of less reactive secondary alcohols (2b, 2h, 2j, 2k) and phenol (2l) better yields were obtained when

• 3.0 equiv of nucleophile were used. For example, the yield of mannoside 3l was increased from 34% to 79% when the amount of phenol (2l) was changed from 1.0 to 3.0 equiv. Similar reactivity relationships were observed in a series of thiols (2c, 2m–p), but the glycosylation yields comparing to the

Prins cyclization-mediated stereoselective synthesis of tetrahydropyrans and dihydropyrans: an inspection of twenty years

• Asha Budakoti,
• Pradip Kumar Mondal,
• Prachi Verma and
• Jagadish Khamrai

Beilstein J. Org. Chem. 2021, 17, 932–963, doi:10.3762/bjoc.17.77

• phenol-tethered alkenyl alcohol 310 and o-aminobenzaldehyde 311 using chiral phosphoric acids (Scheme 72) [114]. Diverse functionalized trans-fused pyranotetrahydroquinoline derivatives 312 were synthesized in excellent yield and selectivity (up to 99% yield and 99% ee). List et al. reported a chiral

Enhanced target cell specificity and uptake of lipid nanoparticles using RNA aptamers and peptides

• Roslyn M. Ray,
• Anders Højgaard Hansen,
• Maria Taskova,
• Bernhard Jandl,
• Jonas Hansen,
• Citra Soemardy,
• Kevin V. Morris and
• Kira Astakhova

Beilstein J. Org. Chem. 2021, 17, 891–907, doi:10.3762/bjoc.17.75

• removal of the side-chain protecting groups was achieved by using trifluoroacetic acid (TFA)/phenol/water/triisopropylsilane (TIPS) 88:5:5:2 (3 × 60 min). After cleavage, the remaining resin was extracted with DCM (2 × 10 min). All DCM extracts and TFA cleavages were combined, and the resulting mixture

Synthesis of bis(aryloxy)fluoromethanes using a heterodihalocarbene strategy

• Carl Recsei and
• Yaniv Barda

Beilstein J. Org. Chem. 2021, 17, 813–818, doi:10.3762/bjoc.17.70

• (difluoromethoxy)arenes, while the reaction with dichlorocarbene gives salicylaldehydes via hydrolysis of an ortho-dichloromethylphenol: the Reimer–Tiemann reaction. The literature, other than this single reference with pentafluorophenol [6], is bereft of references to the capture of heterodihalocarbenes by phenol

• limitations that we had encountered in terms of yield and regioselectivity were presumably specific to the ambident nucleophile 6. We considered that a different ambident nucleophile, a phenol, might also give unusual selectivity for production of a bis(aryloxy)fluoromethane over a Reimer–Tiemann formylation

• aldehydes were present, and that unreacted phenol comprised a further 26% of the mass balance. Thus, the reactivity of fluorobromocarbene in this case mirrored the tendency of difluorocarbene to react with phenoxides to form dihalomethyl phenyl ethers, rather than forming aldehydes as with dichlorocarbene

Synthetic reactions driven by electron-donor–acceptor (EDA) complexes

• Zhonglie Yang,
• Yutong Liu,
• Kun Cao,
• Xiaobin Zhang,
• Hezhong Jiang and
• Jiahong Li

Beilstein J. Org. Chem. 2021, 17, 771–799, doi:10.3762/bjoc.17.67

• them in view of their great significance in organic synthesis. In 2018, Miyake and colleagues [50] found a protocol for the preparation of (Z)-2-iodovinyl phenyl ether 168 by utilizing ethynylbenziodoxol(on)e (EBX) 167 and phenol derivative 166 (Scheme 59). Due to the lack of significant electronic

• effects of phenol, a variety of phenols, including electron-donor and electron-withdrawing groups, were been converted into corresponding 2-iodovinyl phenyl ethers in moderate to excellent yield with high regio- and stereoselectivities. According to the analysis of the mechanism (Scheme 60), a molecule of

• phenol anion is first added to the alkyne group of an EBX, forming electron acceptor 169, which causes the destabilization of the C–I bond. Then, electron acceptor 169 forms an EDA complex with phenol anion, along with light-promoted electron transfer occurring. Thereby, the C–I bond and the I–O bond

Synthesis of dibenzosuberenone-based novel polycyclic π-conjugated dihydropyridazines, pyridazines and pyrroles

• Ramazan Koçak and
• Arif Daştan

Beilstein J. Org. Chem. 2021, 17, 719–729, doi:10.3762/bjoc.17.61

• and the p-quinone methides part was reduced to phenol. After the phenolic part of 13a,b was oxidized to p-quinone methides with PIFA, 14a and 14b were synthesized in 87% and 91% yields, respectively. Moreover, by submitting 13a,b to reductive conditions in presence of Zn, the pyridazine part of 13a,b

Valorisation of plastic waste via metal-catalysed depolymerisation

• Francesca Liguori,
• Carmen Moreno-Marrodán and
• Pierluigi Barbaro

Beilstein J. Org. Chem. 2021, 17, 589–621, doi:10.3762/bjoc.17.53

• developed, using a solvent or molecular hydrogen as cleaving agents [81]. The main solvolytic process include: hydrolysis (water) alcoholysis (methanol, ethanol, 1-butanol, 2-ethyl-1-hexanol, phenol) glycolysis (ethylene glycol (EG), 1,2-propanediol (PD), 1,3- and 1,4-butanediol (BD)), diethylene glycol

Synthetic strategies of phosphonodepsipeptides

• Jiaxi Xu

Beilstein J. Org. Chem. 2021, 17, 461–484, doi:10.3762/bjoc.17.41

• sequential alcoholysis with phenol and benzyl (4-hydroxybutanoyl)glycinate (93), respectively, to give the protected phosphonodepsitripeptide 94. After hydrogenolysis, the free γ-phosphonodepsitripeptide 95 was obtained (Scheme 15) [30]. Seven years later, various enantiopure 2-hydroxyalkanoic acids 96 were

• -aminophosphonodichloride 92 with phenol and methyl (S)-2-hydroxypentanoate (18). All synthetic phosphonodepsipeptides 99, 102, and 104 were considered as glutathione-analogue phosphonopeptides as mechanism-based inhibitors of γ-glutamyl transpeptidase for probing the cysteinyl-glycine binding site (Scheme 16) [31

Regioselective chemoenzymatic syntheses of ferulate conjugates as chromogenic substrates for feruloyl esterases

• Olga Gherbovet,
• Fernando Ferreira,
• Apolline Clément,
• Mélanie Ragon,
• Julien Durand,
• Sophie Bozonnet,
• Michael J. O'Donohue and
• Régis Fauré

Beilstein J. Org. Chem. 2021, 17, 325–333, doi:10.3762/bjoc.17.30

• polyhydroxylated molecules of interest (e.g., antioxidants) [4][26] and of novel chromogenic feruloylated substrates with various physicochemical features for screening applications. Accordingly, we observed that transesterifications only occurred when using primary benzylic alcohols; no phenol acylation was

• detected with hydroxynitrobenzylic alcohol (Table 1, no side product of 4 and 9 with transfer on an aromatic secondary alcohol; i.e., phenol), 2-chloro-4-nitrophenol, or 4NTC (data not shown). Additionally, the exact position of the benzyl alcohol affected the transfer, with ortho-substitutions (R1

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

Total synthesis of decarboxyaltenusin

• Lucas Warmuth,
• Aaron Weiß,
• Marco Reinhardt,
• Anna Meschkov,
• Ute Schepers and
• Joachim Podlech

Beilstein J. Org. Chem. 2021, 17, 224–228, doi:10.3762/bjoc.17.22

• -tetramethyl-1,3,2-dioxaborolane [23]. The electrophilic compound suitable for the projected cross coupling was obtained by mono-demethylation of commercially available 1-bromo-3,5-dimethoxybenzene (7) with boron tribromide (Scheme 3). A satisfactory yield of phenol 8 was observed with 0.9 equivalents of the

• the product with 55% yield. The O-benzylation of phenol 8 furnishing the bromide 9b was accomplished with virtually quantitative yield. Suzuki coupling of the benzyl-protected compounds 6b and 9b led to biaryl 10b with 89% yield; it was deprotected with palladium on charcoal under eight bar hydrogen

Insight into functionalized-macrocycles-guided supramolecular photocatalysis

• Minzan Zuo,
• Krishnasamy Velmurugan,
• Kaiya Wang,
• Xueqi Tian and
• Xiao-Yu Hu

Beilstein J. Org. Chem. 2021, 17, 139–155, doi:10.3762/bjoc.17.15

• edge is hydrophobic, while the narrower lower edge is hydrophilic due to the presence of phenolic oxygen atoms. Depending on the number of phenol units, calixarenes have a variable cavity size, and thus are able to combine with different guests. Therefore, calixarenes can be used as effective

Synthesis of aryl 2-bromo-2-chloro-1,1-difluoroethyl ethers through the base-mediated reaction between phenols and halothane

• Yukiko Karuo,
• Ayaka Kametani,
• Atsushi Tarui,
• Kazuyuki Sato,
• Kentaro Kawai and
• Masaaki Omote

Beilstein J. Org. Chem. 2021, 17, 89–96, doi:10.3762/bjoc.17.9

• utility of halothane for the synthesis of aryl gem-difluoroalkyl ethers containing the bromochloromethyl group. Keywords: aryl 1,1-difluoroethyl ether; 1,1-difluoroethene; fluorine compound; halothane; phenol; Introduction Molecules containing fluoroalkyl groups are of interest in pharmaceutical and

• ether was the reaction of phenol with 2-chloro-1,1,1-trifluoroethane, also known as HCFC-133a, in the presence of potassium hydroxide (KOH) to give the gem-difluoromethyl ethers along with the formation of 1-fluoro-2-chlorovinyl ether (route (d), Scheme 1) [41]. On the basis of our previous reports, we

• functionalized aryl 2-bromo-2-chloro-1,1-difluoroethyl ethers as well as several considerations of the reaction mechanism. Results and Discussion We began our study to optimize the reaction conditions (Table 1). When two equivalents of halothane and sodium hydride (NaH) were treated with phenol (1a) at room

Progress in the total synthesis of inthomycins

• Bidyut Kumar Senapati

Beilstein J. Org. Chem. 2021, 17, 58–82, doi:10.3762/bjoc.17.7

• oxidation of (Z)-15a followed by immediate aldol condensation afforded racemic phenol ester (rac)-17 via aldehyde 16. However, several attempts to form enantioenriched aldol fragment 18 using both a chiral auxiliary [25][26][27][28] and catalytic asymmetric [29][30] procedures proceeded without success

A novel and robust heterogeneous Cu catalyst using modified lignosulfonate as support for the synthesis of nitrogen-containing heterocycles

• Bingbing Lai,
• Meng Ye,
• Ping Liu,
• Minghao Li,
• Rongxian Bai and
• Yanlong Gu

Beilstein J. Org. Chem. 2020, 16, 2888–2902, doi:10.3762/bjoc.16.238

• needed. In this work, we present a novel heterogeneous Cu catalyst using modified LS as support by a consecutive process involving the phenol–aldehyde condensation of LS with 2-formylbenzenesulfonic acid sodium (FAS), ion exchange and acidification. Special interest is given in the application of the

• , the support was prepared through phenol–formaldehyde condensation reaction of LS and FAS. The FAS was chosen to embellish LS in consideration of the following reason: FAS skeleton consists of both aldehyde and sulfonic groups, so the grafting of FAS and LS can be easily realized via phenol

Dawn of a new era in industrial photochemistry: the scale-up of micro- and mesostructured photoreactors

• Emine Kayahan,
• Mathias Jacobs,
• Leen Braeken,
• Leen C.J. Thomassen,
• Simon Kuhn,
• Tom van Gerven and
• M. Enis Leblebici

Beilstein J. Org. Chem. 2020, 16, 2484–2504, doi:10.3762/bjoc.16.202

• conditions and the kinetics of the selected reaction can lead to drastic changes in the PSTY. de Sá et al. combined external and internal numbering up in meso- and microchemical reactors of various sizes (Figure 3e). Photocatalytic degradations of methylene blue, rhodamine B, and phenol with TiO2 were

• reactants, the light distribution throughout the catalyst layer, and the reaction rate. Leblebici et al. [49] showed that increasing the flow rate of the reactants did not increase the apparent reaction rate for phenol degradation in an immobilized photoreactor. Increasing the flow rate would result in a

Styryl-based new organic chromophores bearing free amino and azomethine groups: synthesis, photophysical, NLO, and thermal properties

• Anka Utama Putra,
• Deniz Çakmaz,
• Nurgül Seferoğlu,
• Alberto Barsella and
• Zeynel Seferoğlu

Beilstein J. Org. Chem. 2020, 16, 2282–2296, doi:10.3762/bjoc.16.189

• donor than the phenol group [52][53]. Furthermore, trifluoroacetic acid (TFA) was added to a solution containing the deprotonated forms of dyes 8–12 in DMSO, so as to investigate the reversible protonation of the dyes. As can be seen in Figure 5, the addition of 5 equiv of TFA to a basic solution of 12

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

• 74 into the stable derivatives 75 having a strong C–C bond through the nucleophilic substitution reaction with phenol and anisole in the presence of trifluoromethanesulfonic acid (TfOH) with total stereoinversion. This suggests that the nucleophile attacks occur from the concave face of the π-bowl

• [48]. Although, for the nucleophilic substitution reaction with phenol derivatives, they have tried several reaction conditions including the amount of acid as well as phenols. After several experimentations, they found that 30 equivalents of phenol and 1 equivalent of TfOH at 0 °C provided the best

• formation was observed. Therefore, they used a Pd-catalyzed carbonylative esterification in the presence of phenyl formate which in situ generated CO and phenol to provide the required product 97 in 73% yield (Scheme 24). In an independent work reported in 2017, Fukushima and co-workers detailed the

pH- and concentration-dependent supramolecular self-assembly of a naturally occurring octapeptide

• Goutam Ghosh and
• Gustavo Fernández

Beilstein J. Org. Chem. 2020, 16, 2017–2025, doi:10.3762/bjoc.16.168

• temperature, and this was stirred for 2 hours following the same procedure as before. At the final stage, we cleaved the peptide from the resin by using a proper cleavage cocktail: TFA/phenol/water/TIPS 88:5:5:2. DTT was included, as this peptide contains cysteine. After adding the cleavage cocktail to the

• different concentrations at pH 7.4. Detailed synthetic scheme for PEP-1. (i) 20% piperidine in DMF, (ii) HBTU, (iii) NMM, (iv) Ac2O/Py/DMF 1:2:3 and (v) TFA/phenol/water/TIPS 88:5:5:2. Supporting Information Supporting Information File 374: Materials and methods as well as additional figures. Funding G. G