Heteroleptic metallosupramolecular aggregates/complexation for supramolecular catalysis

• Prodip Howlader and
• Michael Schmittel

Beilstein J. Org. Chem. 2022, 18, 597–630, doi:10.3762/bjoc.18.62

• reaction of ligand 111, deck 82, DABCO (60), and [Cu(CH3CN)4](PF6) (4:2:3:2) furnished the supramolecular cage [(82)2(60)3] with 60 = DABCO acting as pillars whereas biped [Cu(111)2]+ remained uncoordinated [112]. In an analogous self-assembly with 83 instead of [Cu(111)2]+, ligand 83 was left

Sesquiterpenes from the soil-derived fungus Trichoderma citrinoviride PSU-SPSF346

• Wiriya Yaosanit,
• Vatcharin Rukachaisirikul,
• Souwalak Phongpaichit,
• Sita Preedanon and
• Jariya Sakayaroj

Beilstein J. Org. Chem. 2022, 18, 479–485, doi:10.3762/bjoc.18.50

• silica gel using a mixture of MeOH/H2O 3:2 to yield six subfractions (A4G1–A4G6). Subfraction A4G2 (18.2 mg) was separated by CC over silica gel using a mixture of CH2Cl2/hexane/MeOH 17:2:1 followed by CC over Sephadex LH-20 using MeOH to obtain compound 2 (2.6 mg). The mycelial EtOAc extract (2.6 g) was

Tosylhydrazine-promoted self-conjugate reduction–Michael/aldol reaction of 3-phenacylideneoxindoles towards dispirocyclopentanebisoxindole derivatives

• Sayan Pramanik and
• Chhanda Mukhopadhyay

Beilstein J. Org. Chem. 2022, 18, 469–478, doi:10.3762/bjoc.18.49

• heterocyclic frameworks [31][32]. During our preliminary investigations as shown in Table 1, we commenced our study by reacting two equivalents of (E)-3-(2-(4-chlorophenyl)-2-oxoethylidene)indolin-2-one (1a) under reflux conditions with one equivalent of tosylhydrazine (2) as hydrogen source in ethanolic

• proposed mechanism at first we performed an HRMS analysis of the crude reaction mixture before completion of the reaction, starting with (E)-1-methyl-3-(2-oxo-2-phenylethylidene)indolin-2-one (1j) and tosylhydrazine under the optimized reaction conditions. To our delight, the HRMS spectrum clearly shows

• the peaks of the corresponding intermediate A at 266.1195 [M + H] and final product 3j at 529.2141 [M + H] (Figure 4). Further we attempted a study to isolate the corresponding intermediate A. We carried out a reaction by taking an 1:1 equivalent mixture of tosylhydrazine and (E)-1-methyl-3-(2-oxo-2

Synthesis of 3,4,5-trisubstituted isoxazoles in water via a [3 + 2]-cycloaddition of nitrile oxides and 1,3-diketones, β-ketoesters, or β-ketoamides

• Md Imran Hossain,
• Md Imdadul H. Khan,
• Seong Jong Kim and
• Hoang V. Le

Beilstein J. Org. Chem. 2022, 18, 446–458, doi:10.3762/bjoc.18.47

• Agriculture, Agricultural Research Service, University of Mississippi, Mississippi 38677, USA 10.3762/bjoc.18.47 Abstract Herein we report a method for the synthesis of 3,4,5-trisubstituted isoxazoles in water under mild basic conditions at room temperature via a [3 + 2]-cycloaddition of nitrile oxides and

• 1,3-diketones, β-ketoesters, or β-ketoamides. We optimized the reaction conditions to control the selectivity of the production of isoxazoles and circumvent other competing reactions, such as O-imidoylation or hetero [3 + 2]-cycloaddition. The reaction happens fast in water and completes within 1–2

• prevalent scaffold in biomedical research and drug discovery programs. We also proposed a plausible mechanism for the selectivity of the [3 + 2]-cycloaddition reaction to produce 3,4,5-trisubstituted isoxazoles. Not to be overlooked are our optimized reaction conditions for the dimerization of hydroximoyl

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

• ]. Chang’s group reported the use of 3D crystalline polyoxometalate-based coordination polymers (POMCPs) as heterogeneous catalysts, with H2O2, to synthesize 10 and the best result was obtained using H[CuII(ttb)(H2O)3]2[CuII(ttb)Cl]2[PW12O40]·4H2O (Httb = 1-(tetrazol-5-yl)-4-(triazol-1-yl)benzene) as the

New advances in asymmetric organocatalysis

• Radovan Šebesta

Beilstein J. Org. Chem. 2022, 18, 240–242, doi:10.3762/bjoc.18.28

• nitromethane to β-silyl α,β-unsaturated carbonyl compounds catalyzed by bifunctional squaramide catalysts are effective under solvent-free conditions [26]. Zhai and Du demonstrated that asymmetric [3 + 2] annulation reactions of 2-isothiocyanato-1-indanones with barbiturate-based olefins are efficiently

Glycosylated coumarins, flavonoids, lignans and phenylpropanoids from Wikstroemia nutans and their biological activities

• Meifang Wu,
• Xiangdong Su,
• Yichuang Wu,
• Yuanjing Luo,
• Ying Guo and
• Yongbo Xue

Beilstein J. Org. Chem. 2022, 18, 200–207, doi:10.3762/bjoc.18.23

• compounds were isolated and their structures were determined as 7-(β-ᴅ-glucopyranosyloxy)-7'-hydroxy-3-[(2-oxo-2H-1-benzopyran-7-yl)oxy]-[8,8'-bis(2H-1-benzopyran)]-2,2'-dione (2) [11], 6-(β-ᴅ-glucopyranosyloxy)-7-[(2-oxo-2H-1-benzopyran-7-yl)oxy]-2H-1-benzopyran-2-one (3) [9], rutarensin (4) [12

Ready access to 7,8-dihydroindolo[2,3-d][1]benzazepine-6(5H)-one scaffold and analogues via early-stage Fischer ring-closure reaction

• Irina Kuznetcova,
• Felix Bacher,
• Daniel Vegh,
• Hsiang-Yu Chuang and
• Vladimir B. Arion

Beilstein J. Org. Chem. 2022, 18, 143–151, doi:10.3762/bjoc.18.15

• -phenylhydrazine in acetic acid that delivers methyl 2-(1-benzyl-3-(2-nitrophenyl)-1H-indol-2-yl)acetate in 55% yield. Keywords: anticancer; Fischer indole synthesis; Heck reaction; heterocyclic compounds; indolobenzazepines; latonduines; paullones; Introduction Indolobenzazepines are fused heterocyclic

• ]. The N-protected 3-(2-nitrophenyl)indole was considered an important intermediate in this synthetic route (Scheme 1). The second retrosynthetic pathway (b) involved cyclization at position 3 of the indole ring, with a halo-aryl precursor [24]. In this case N-protected indole-2-acetic acid was regarded

• -oxobutanoate (Scheme 1). To construct scaffold C by route (a) we first tried to synthesize 3-(2-nitrophenyl)indole by Heck reaction of indole and o-iodo-nitrobenzene [25]. However, in this case we obtained an isomeric mixture of 3- and 2-(2-nitrophenyl)indole in a 3:1 molar ratio, quite difficult to separate

Bifunctional thiourea-catalyzed asymmetric [3 + 2] annulation reactions of 2-isothiocyanato-1-indanones with barbiturate-based olefins

• Jiang-Song Zhai and
• Da-Ming Du

Beilstein J. Org. Chem. 2022, 18, 25–36, doi:10.3762/bjoc.18.3

• Jiang-Song Zhai Da-Ming Du School of Chemistry and Chemical Engineering, Beijing Institute of Technology, No.5 Zhongguancun South Street, Beijing 100081, People’s Republic of China 10.3762/bjoc.18.3 Abstract Bifunctional thiourea-catalyzed asymmetric [3 + 2] annulation reactions of 2

• construction of bispirobarbiturates [30][31]. In 2019, for example, An and co-workers reported an asymmetric Michael/Mannich [3 + 2] cycloaddition reaction between N-(2,2,2-trifluoroethyl)isatin ketimines and barbiturate-based olefins (Scheme 1a) [32]. Based on the current knowledge, the construction of

• % ee) could still be maintained (Scheme 6b). This one-pot three-component reaction would be more convenient for potential industrial applications. Finally, in order to understand the enantioselective formation process of product 3, we proposed the possible mechanisms for the [3 + 2] cyclization

Stepwise PEG synthesis featuring deprotection and coupling in one pot

• Logan Mikesell,
• Dhananjani N. A. M. Eriyagama,
• Yipeng Yin,
• Bao-Yuan Lu and
• Shiyue Fang

Beilstein J. Org. Chem. 2021, 17, 2976–2982, doi:10.3762/bjoc.17.207

• extensive chromatography. Thus, this method had been put aside. In our lab, we can produce 1 in large quantities without any chromatography [25], and therefore, we decided to use a route for the synthesis of 2 using 1 as the starting material. As shown in Scheme 3, 2-phenylethan-1-ol was reacted with 1

Total synthesis of the O-antigen repeating unit of Providencia stuartii O49 serotype through linear and one-pot assemblies

• Tanmoy Halder and
• Somnath Yadav

Beilstein J. Org. Chem. 2021, 17, 2915–2921, doi:10.3762/bjoc.17.199

• on the hydroxy groups. First, the concomitant removal of the Troc group and the N-acetylation was achieved using Zn/AcOH/Ac2O 3:2:1 as reagent in one pot (Scheme 6) [52]. Then, O-deacetylation was accomplished by using a catalytic amount of NaOMe in MeOH at room temperature. Finally, the benzylidene

Host–guest interaction and properties of cucurbit[8]uril with chloramphenicol

• Lin Zhang,
• Jun Zheng,
• Guangyan Luo,
• Xiaoyue Li,
• Yunqian Zhang,
• Zhu Tao and
• Qianjun Zhang

Beilstein J. Org. Chem. 2021, 17, 2832–2839, doi:10.3762/bjoc.17.194

• hydrochloric acid solution (VD2O/VDCl = 3:2) was used as the NMR solvent. Consequently, the interaction between Q[8] and CPE in hydrochloric acid solution was studied (Figure 3C and D). The results show that the molar ratio of CPE and Q[8] was 1:1 under acidic conditions, which was the same as that observed

• (CPE) = 30 μmol/L, (c(Q[8])/c(CPE)) = 0, 0.2, 0.4, 0.6, 0.8, 1.0; ··· 2.8), insets in (A, C) are the plot of absorbances at 278 nm of CPE. ITC data obtained for the binding of Q[8] with CPE in an aqueous solution at 25 °C. 1H NMR spectra of CPE, CPE@Q[8] and Q[8] (VD2O/VDCl = 3:2). IR spectra recorded

• , pH 6.8). Thermodynamic parameters related to the CPE@Q[8] system at 25 °C. Changes in1H NMR chemical shift of CPE after the addition of Q[8] (VD2O/VDCl = 3:2). The minimum effective concentration (MIC) of CPE, CPE@Q[8] against E. coli and S. aureus. Supporting Information Supporting Information File

The PIFA-initiated oxidative cyclization of 2-(3-butenyl)quinazolin-4(3H)-ones – an efficient approach to 1-(hydroxymethyl)-2,3-dihydropyrrolo[1,2-a]quinazolin-5(1H)-ones

• Alla I. Vaskevych,
• Nataliia O. Savinchuk,
• Ruslan I. Vaskevych,
• Eduard B. Rusanov,
• Oleksandr O. Grygorenko and
• Mykhailo V. Vovk

Beilstein J. Org. Chem. 2021, 17, 2787–2794, doi:10.3762/bjoc.17.189

• well as by Sm(OTf)3-catalyzed stereoselective [3 + 2] cycloaddition of bis-silyldienediolate and imines, in turn synthesized from anthranylamides and benzaldehydes [32]. A promising approach to the synthesis of 2,3-dihydropyrrolo[1,2-a]quinazolin-5(1H)-one derivatives substituted at the pyrrolidine

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

• rt, 16 h, 68%; (c) oxone, NaHCO3, acetone/H2O 3:2, 0 °C to rt, 80 min, 99%; (d) HCl (37 wt % in H2O), acetone/H2O 4:1, 0 °C, 30 min, 93%. Synthesis of final pyrrolidines (±)-1 and (±)-2. Reagents and conditions: (a) vinyl-MgBr, CeCl3, THF, 0 °C to rt, 16 h, 73%; (b) Zn dust, AcOH, 40 °C, 24 h, 85

Recent advances in the asymmetric phosphoric acid-catalyzed synthesis of axially chiral compounds

• Alemayehu Gashaw Woldegiorgis and
• Xufeng Lin

Beilstein J. Org. Chem. 2021, 17, 2729–2764, doi:10.3762/bjoc.17.185

• ]. Zhou and co-workers published an excellent paper in 2019 on the conversion of central to axial chirality in an enantioselective [3 + 2] annulation of 1-styrylnaphthols 32 with azonaphthalenes 33. Under defined conditions, the cycloaddition product 34 was prepared in high yield (99%) with exclusive

• diastereoselectivity and 99% ee in the presence of the chiral phosphoric acid CPA 2. Subsequently, using the chiral phosphoric acid-catalyzed [3 + 2] formal cycloaddition and a moderate DDQ oxidation method over 34, enantiomerically enriched 2,3-diarylbenzoindoles 35 were successfully prepared by performing a central

• atroposelective C–H allylation. Enantioselective synthesis of axially chiral (a) aryl indoles and (b) biaryldiols. Asymmetric arylation of indoles enabled by azo groups. Proposed mechanism for the asymmetric arylation of indoles. Enantioselective synthesis of axially chiral N-arylindoles [38]. Enantioselective [3

N-Sulfinylpyrrolidine-containing ureas and thioureas as bifunctional organocatalysts

• Viera Poláčková,
• Dominika Krištofíková,
• Boglárka Némethová,
• Renata Górová,
• Mária Mečiarová and
• Radovan Šebesta

Beilstein J. Org. Chem. 2021, 17, 2629–2641, doi:10.3762/bjoc.17.176

• compounds with heterocyclic substituents are of high biological and medicinal relevance [34][35]. Therefore, we have decided to evaluate sulfinylurea and thiourea catalysts C1 and C2 also with (E)-2-(2-nitrovinyl)furan (9) and (E)-3-(2-nitrovinyl)pyridine (11) as Michael acceptors. As Michael donor, we

• ). The aliphatic aldehydes propanal (6d) and hexanal (6b) provided medium yields and diastereoselectivity and enantioselectivity. The Michael addition of 3-phenylpropanal (6c) to (E)-3-(2-nitrovinyl)pyridine (11) required long reaction times (120 h) in solution, similar to those for the reaction with (E

α-Ketol and α-iminol rearrangements in synthetic organic and biosynthetic reactions

• Scott Benz and
• Andrew S. Murkin

Beilstein J. Org. Chem. 2021, 17, 2570–2584, doi:10.3762/bjoc.17.172

• episilvestrol (35), natural products with potent anticancer properties. The step prior to the rearrangement involved a photoinduced [3 + 2] cycloaddition between hydroxyflavone 36 and methyl cinnamate (37), resulting in the bicyclic α-ketol 38 as a mixture of diastereomers (Ph and CO2Me groups trans) (Figure 9

• the mixture of 38 and 39 induced a second α-ketol rearrangement to 40 as a tautomeric mixture. The same research group later utilized the same [3 + 2] cycloaddition and α-ketol rearrangement approach to prepare the 2′′′-epimer of 35, which bears an inverted methyl acetal in the dioxane ring, but this

Visible-light-mediated copper photocatalysis for organic syntheses

• Yajing Zhang,
• Qian Wang,
• Zongsheng Yan,
• Donglai Ma and
• Yuguang Zheng

Beilstein J. Org. Chem. 2021, 17, 2520–2542, doi:10.3762/bjoc.17.169

• functionalization, organic halides functionalization, and alkyl C–H functionalization, are highlighted. Review 1. Special features of photoredox-catalyzed processes by copper complexes To understand photoredox-catalyzed processes, a discussion of the general mechanism of [Ru(bpy)3]2+ is needed [25][26][27]. When

• Cu-based complexes could replace ruthenium- or iridium-based photocatalysts in the future. Photoredox catalysis mechanism of [Ru(bpy)3]2+. Photoredox catalysis mechanism of CuI. Ligands and CuI complexes. Mechanism of CuI-based photocatalysis. Mechanisms of CuI–substrate complexes. Mechanism of CuII

Facile and innovative catalytic protocol for intramolecular Friedel–Crafts cyclization of Morita–Baylis–Hillman adducts: Synergistic combination of chiral (salen)chromium(III)/BF₃·OEt₂ catalysis

• Karthikeyan Soundararajan,
• Helen Ratna Monica Jeyarajan,
• Raju Subimol Kamarajapurathu and
• Karthik Krishna Kumar Ayyanoth

Beilstein J. Org. Chem. 2021, 17, 2186–2193, doi:10.3762/bjoc.17.140

• -ium-2-ide (7a) was synthesised at room temperature by treating methyl acrylate, hydrazine hydrate and benzaldehyde in a yield of 67%. On treating the synthesised azomethine imine 7a (1.2 mM) and 2-substituted-1H-indenes 6b and 6c (1 mM) in toluene at 70 °C affords 8a and 8b via [3 + 2] cycloaddition

• purified by column chromatography to afford the corresponding [3 + 2] cycloaddition product 8a in 61% yield. Compound (8a): Yield: 192 mg (61%); yellowish oil; IR (cm−1): 2972, 2254, 1954, 1562, 1671, 1455, 1245; 1H NMR (CDCl3, 400 MHz) δH 7.80–7.06 (m, 9H, Aro-H), 5.90 (s, 1H, HC-N-CO), 4.36–4.21 (m, 2H

Towards new NIR dyes for free radical photopolymerization processes

• Haifaa Mokbel,
• Guillaume Noirbent,
• Didier Gigmes,
• Frédéric Dumur and
• Jacques Lalevée

Beilstein J. Org. Chem. 2021, 17, 2067–2076, doi:10.3762/bjoc.17.133

• (10) CI10. Photopolymerization profiles of PETIA monomer under air (acrylate functions conversion vs irradiation time) in the presence of a NIR dye/iod/NPG 0.1:3:2. %w/w/w system. A) NIR dyes with BPh4− and Na+ as counter anion and counter cation: (1) Ca, (2) Cb, (3) CBPh1, (4) CBPh4, (5) CNa, and (6

• vs irradiation time) in the presence of a NIR dye/iod/DABA 0.1:3:2, %w/w/w system. A) NIR dyes with BPh4− and Na+ as counter anion and counter cation: (1) Cb, (2) CBPh1, (3) CBPh3, (4) CBPh4, (5) CNa, and (6) IR 813. B) NIR dyes with I− as counter anion: (1) CI1, (2) CI3, (3) CI5, (4) CI9, (5) CI10

• reaction enabling the formation of “soft” salts CBPh1-CBPh4. Pictures of polymers obtained for a thickness of 1.4 mm, using a NIR dye/iod/amine 0.1:3:2, %w/w/w system. A) amine = NPG and B) amine = DABA; upon exposure to a 785 nm laser diode (0.9 W/cm2) for 120 seconds under air. Proposed mechanism for the

Progress and challenges in the synthesis of sequence controlled polysaccharides

• Giulio Fittolani,
• Theodore Tyrikos-Ergas,
• Denisa Vargová,
• Manishkumar A. Chaube and
• Martina Delbianco

Beilstein J. Org. Chem. 2021, 17, 1981–2025, doi:10.3762/bjoc.17.129

• trichloroacetimidate donor 75 was controlled by SN2 displacement of the α-trichloroacetimidate LG upon activation with BF3·OEt2 in CH2Cl2/n-hexane (3:2) (Scheme 11B). The orthogonal N-trichloroacetyl (N-TCA) and N-benzyloxycarbonyl (N-Cbz) PGs permitted the synthesis of chitobioses with different PA. N-TCA groups

Asymmetric organocatalyzed synthesis of coumarin derivatives

• Natália M. Moreira,
• Lorena S. R. Martelli and
• Arlene G. Corrêa

Beilstein J. Org. Chem. 2021, 17, 1952–1980, doi:10.3762/bjoc.17.128

• and colleagues proposed an asymmetric [3 + 2] cycloaddition employing a coumarin dipolarophile 43 with azomethine ylides 60 organocatalyzed by quinidine (62) for the formation of fused pyrrolidine compounds through activation of the coumarin substrate by hydrogen bonding [53]. The methodology enabled

• addition in the least hindered Re face, consequently resulting in products of (R)-configurations, which were determined via X-ray crystallography. A stereoselective [3 + 2] cycloaddition with indandione alkylidenes 103 and 3-homoacylcoumarin 70 as the 1,3-dipole precursor, to generate a series of coumarin

• hydroxylated malonate 53 catalyzed by NHC 55. Oxidative [4 + 2] cycloaddition of enals 57 to coumarins 56 catalyzed by NHC 59. Asymmetric [3 + 2] cycloaddition of coumarins 43 to azomethine ylides 60 organocatalyzed by quinidine 62. Synthesis of α-benzylaminocoumarins 64 through Mannich reaction between 4

On the application of 3d metals for C–H activation toward bioactive compounds: The key step for the synthesis of silver bullets

• Renato L. Carvalho,
• Amanda S. de Miranda,
• Mateus P. Nunes,
• Roberto S. Gomes,
• Guilherme A. M. Jardim and
• Eufrânio N. da Silva Júnior

Beilstein J. Org. Chem. 2021, 17, 1849–1938, doi:10.3762/bjoc.17.126

• similar catalyst, [Sc-2], which bears a more electron-rich cyclopentadienyl ligand, in a scandium-catalyzed C–H [3 + 2] cyclization (Scheme 5B) [40]. In this transformation, several aminoindane derivatives were obtained from benzylimines in the presence of the catalyst [Sc-2], alkenes and [Ph3C][B(C6F5)4

• benzylic, allylic, 3°, 2°, and 1° aliphatic, using unsubstituted linear sulfamate esters (Scheme 17A and B) [130]. This method is also compatible with substrates containing adjacent substituents like protected amines and tolerates the presence of electron-withdrawing groups as well as α-substituted alkynes

Sustainable manganese catalysis for late-stage C–H functionalization of bioactive structural motifs

• Jongwoo Son

Beilstein J. Org. Chem. 2021, 17, 1733–1751, doi:10.3762/bjoc.17.122

• conjugative transformations, such as azide–alkyne [3 + 2]-cycloaddition [30][31][32][33][34][35][36][37]. Based on their previous late-stage fluorination studies [22][25], Groves et al. further showcased a manganese(III)–salen-catalyzed azidation process using an aqueous azide solution as a convenient azide

Electron-rich triarylphosphines as nucleophilic catalysts for oxa-Michael reactions

• Susanne M. Fischer,
• Simon Renner,
• A. Daniel Boese and
• Christian Slugovc

Beilstein J. Org. Chem. 2021, 17, 1689–1697, doi:10.3762/bjoc.17.117

• reactions [17], or in umpolung [3 + 2] annulations [18]. In all these cases, the reactions were performed without protective gas indicating that electronically modified arylphosphines tolerate the presence of oxygen. Herein we wish to report the scope of three different triarylphosphine catalysts in the oxa