Comparison of crystal structure and DFT calculations of triferrocenyl trithiophosphite’s conformance

• Ruslan P. Shekurov,
• Mikhail N. Khrizanforov,
• Ilya A. Bezkishko,
• Tatiana P. Gerasimova,
• Almaz A. Zagidullin,
• Daut R. Islamov and
• Vasili A. Miluykov

Beilstein J. Org. Chem. 2022, 18, 1499–1504, doi:10.3762/bjoc.18.157

• describe the London dispersion interactions as implemented in the Gaussian 16 program. Results and Discussion Previous electrochemical studies for triferrocenyl trithiophosphite revealed in their cyclovoltammograms three reversible one-electron peaks corresponding to stepwise oxidation of the three

Experimental and theoretical studies on the synthesis of 1,4,5-trisubstituted pyrrolidine-2,3-diones

• Nguyen Tran Nguyen,
• Vo Viet Dai,
• Nguyen Ngoc Tri,
• Luc Van Meervelt,
• Nguyen Tien Trung and
• Wim Dehaen

Beilstein J. Org. Chem. 2022, 18, 1140–1153, doi:10.3762/bjoc.18.118

• reaction coordinates (IRCs) were performed at the same level of theory to determine two local minima through transition states in each stepwise [50]. Besides, the rate constant of reaction based on the transitional state theory method and quantum tunneling effect was calculated by the following expression

New azodyrecins identified by a genome mining-directed reactivity-based screening

• Atina Rizkiya Choirunnisa,
• Kuga Arima,
• Yo Abe,
• Noritaka Kagaya,
• Kei Kudo,
• Hikaru Suenaga,
• Junko Hashimoto,
• Manabu Fujie,
• Noriyuki Satoh,
• Kazuo Shin-ya,
• Kenichi Matsuda and
• Toshiyuki Wakimoto

Beilstein J. Org. Chem. 2022, 18, 1017–1025, doi:10.3762/bjoc.18.102

• stepwise HMM-based search using models for “VlmA'' (PF09924: LPG_synthase_C) and the amino acid sequence of VlmH identified 179 pairs of VlmA/VlmH, indicating that approximately 5.7% of the actinobacteria present in the NCBI Refseq database are potential producers of aliphatic azoxy natural products. The

First series of N-alkylamino peptoid homooligomers: solution phase synthesis and conformational investigation

• Maxime Pypec,
• Laurent Jouffret,
• Claude Taillefumier and
• Olivier Roy

Beilstein J. Org. Chem. 2022, 18, 845–854, doi:10.3762/bjoc.18.85

• -(alkylamino)glycine units is investigated. We demonstrate that N-(methylamino)glycine homooligomers can be readily synthesized in solution using N-Boc-N-methylhydrazine as a peptoid submonomer and stepwise or segment coupling methodologies. Their structures were analyzed in solution by 1D and 2D NMR, in the

Continuous flow synthesis of azobenzenes via Baeyer–Mills reaction

• Jan H. Griwatz,
• Anne Kunz and
• Hermann A. Wegner

Beilstein J. Org. Chem. 2022, 18, 781–787, doi:10.3762/bjoc.18.78

• the temperature and the residence time were successively changed to achieve the highest conversion to AB. The residence time was increased from 5.0 to 50.0 min and the temperature was raised stepwise from 25 °C up to 90 °C (Figure 1). After the set residence time an aliquot was collected, diluted with

Bioinspired tetraamino-bisthiourea chiral macrocycles in catalyzing decarboxylative Mannich reactions

• Hao Guo,
• Yu-Fei Ao,
• De-Xian Wang and
• Qi-Qiang Wang

Beilstein J. Org. Chem. 2022, 18, 486–496, doi:10.3762/bjoc.18.51

• ][46][47][48][49][50][51][52]. Results and Discussion Synthesis of macrocycles The tetraamino-bisthiourea chiral macrocycles were synthesized by a stepwise strategy (Scheme 1). The easily available chiral diamines including 1,2-cyclohexanediamines and 1,2-diphenylethylenediamines were chosen as the

A Se···O bonding catalysis approach to the synthesis of calix[4]pyrroles

• Qingzhe Tong,
• Zhiguo Zhao and
• Yao Wang

Beilstein J. Org. Chem. 2022, 18, 325–330, doi:10.3762/bjoc.18.36

• , several synthetic methods to access these compounds have been reported [54][55]. The classical approaches to synthesis of calix[4]pyrrole derivatives mainly involved a stepwise synthesis and Lewis acid as well as Brønsted acid catalysis [54][55]. Notably, a noncovalent catalysis approach to accessing

Trichloroacetic acid fueled practical amine purifications

• Aleena Thomas,
• Baptiste Gasch,
• Enzo Olivieri and
• Adrien Quintard

Beilstein J. Org. Chem. 2022, 18, 225–231, doi:10.3762/bjoc.18.26

• Aleena Thomas Baptiste Gasch Enzo Olivieri Adrien Quintard Aix-Marseille Univ, CNRS, Centrale Marseille, iSm2, Marseille, France 10.3762/bjoc.18.26 Abstract Amine purification have for long been dominated by tedious stepwise processes involving the generation of large amounts of undesired waste

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

• Logan Mikesell Dhananjani N. A. M. Eriyagama Yipeng Yin Bao-Yuan Lu Shiyue Fang Department of Chemistry, Michigan Technological University, 1400 Townsend Drive, Houghton, MI 49931, USA ChampionX, 11177 South Stadium Drive, Sugar Land, TX 77478, USA 10.3762/bjoc.17.207 Abstract The stepwise

• one pot. The deprotonation step, and the isolation and purification of the intermediate product after deprotection using existing approaches are no longer needed when the one-pot approach is used. Because the stepwise PEG synthesis usually requires multiple PEG elongation cycles, the new PEG synthesis

• peptides, proteins and nucleic acids and to evade undesired immune responses, monodisperse PEGs are required or highly desired [12][13]. To meet the needs of monodisperse PEGs, significant efforts have been made to develop stepwise methods for their synthesis [14][15][16][17][18][19][20][21][22][23][24][25

Iron-catalyzed domino coupling reactions of π-systems

• Austin Pounder and
• William Tam

Beilstein J. Org. Chem. 2021, 17, 2848–2893, doi:10.3762/bjoc.17.196

• substantial improvements in efficient synthesis because of domino reactions. These protocols are more atom-economic, produce less waste, and demand less time compared to a classical stepwise reaction. Although iron-catalyzed domino reactions require a mindset that differs from the more routine noble-metal

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

• -xylulose-5-phosphate reductoisomerase (DXR), uses a different mechanism to accomplish the carbon-skeleton rearrangement of its substrate 63 [19]; kinetic isotope effect experiments have excluded an α-ketol rearrangement and instead support a stepwise retro-aldol/aldol sequence for formation of intermediate

Advances in mercury(II)-salt-mediated cyclization reactions of unsaturated bonds

• Sumana Mandal,
• Raju D. Chaudhari and
• Goutam Biswas

Beilstein J. Org. Chem. 2021, 17, 2348–2376, doi:10.3762/bjoc.17.153

• allyl alcohol. Stepwise synthesis of 2,6-distubstituted dioxane derivatives. Cyclization of carbohydrate alkene precursor. Hg(II)-mediated synthesis of C-glucopyranosyl derivatives. Synthesis of C-glycosyl amino acid derivative using Hg(TFA)2. Hg(OAc)2-mediated synthesis of α-ᴅ-ribose derivative

A study on selective transformation of norbornadiene into fluorinated cyclopentane-fused isoxazolines

• Zsanett Benke,
• Attila M. Remete and
• Loránd Kiss

Beilstein J. Org. Chem. 2021, 17, 2051–2066, doi:10.3762/bjoc.17.132

• oxide 1,3-dipolar cycloaddition/ROM/CM strategies was presented. The stepwise functionalization of norbornadiene across the ring olefin bonds generated fluorine-containing alkenylated cyclopentane-fused isoxazolines. The synthetic protocol was based on selective nitrile oxide cycloaddition to 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

• capping step [279] permitted to drastically improve overall yields and to simplify the purification (Figure 6). The 100mer 93 was obtained with a calculated average stepwise yield of 98.75% (Scheme 14). Long α-mannosides have the advantageous feature of being highly soluble due to the high flexibility of

Development of N-F fluorinating agents and their fluorinations: Historical perspective

• Teruo Umemoto,
• Yuhao Yang and
• Gerald B. Hammond

Beilstein J. Org. Chem. 2021, 17, 1752–1813, doi:10.3762/bjoc.17.123

• -fluoropyridinium salts 5-4 could be synthesized in four different ways using 10% F2/N2 [28][31][33] (Scheme 10): method A (stepwise method) involved the fluorination of a pyridine derivative with F2/N2, to form a pyridine·F2 complex 5-2, followed by treatment with a non-nucleophilic anion salt, acid, or silyl

Fritsch–Buttenberg–Wiechell rearrangement of magnesium alkylidene carbenoids leading to the formation of alkynes

• Tsutomu Kimura,
• Koto Sekiguchi,
• Akane Ando and
• Aki Imafuji

Beilstein J. Org. Chem. 2021, 17, 1352–1359, doi:10.3762/bjoc.17.94

• generated in situ from chloromethyl p-tolyl sulfoxide, diethyl chlorophosphate, and LDA, and the reaction of the HWE reagent with carbonyl compounds gave sulfoxides 2e–g. The 2,2-disubstituted sulfoxides 2b–d, which could not be prepared by the one-pot HWE reaction, were prepared through a stepwise method

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

• β-(2-hydroxyaryl)enones [34]. Synthesis of enantiomerically enriched 1-aryl-1H-indenes [36]. Stepwise addition of arylboronic acids to electron-rich chalcones and Bayer–Villiger oxidation [3]. Synthesis of 4-aryldihydrocoumarins by stepwise 1,4-addition and Bayer–Villiger oxidation [3]. First report

Synthetic accesses to biguanide compounds

• Oleksandr Grytsai,
• Cyril Ronco and
• Rachid Benhida

Beilstein J. Org. Chem. 2021, 17, 1001–1040, doi:10.3762/bjoc.17.82

Simulating the enzymes of ganglioside biosynthesis with Glycologue

• Andrew G. McDonald and
• Gavin P. Davey

Beilstein J. Org. Chem. 2021, 17, 739–748, doi:10.3762/bjoc.17.64

• negative charge. Figure 1 shows the structure of the monosialylated ganglioside GM1a. The biosynthesis of gangliosides occurs in the endoplasmic reticulum and Golgi, where specific glycosyltransferases act, in stepwise fashion, by adding monosaccharides from sugar nucleotide donors, first to ceramide, and

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

• to decrease in the order Zn > Mn > Co > Cu > Ni, consistent with previous reports [209]. The best catalyst afforded BHET in 84.1% yield (Table 2, entry 9), which was rather constant over eight catalyst reuses [210]. A stepwise depolymerisation mechanism was proposed, via intermediate oligomers, in

Synthesis and physicochemical evaluation of fluorinated lipopeptide precursors of ligands for microbubble targeting

• Masayori Hagimori,
• Estefanía E. Mendoza-Ortega and
• Marie Pierre Krafft

Beilstein J. Org. Chem. 2021, 17, 511–518, doi:10.3762/bjoc.17.45

• structure [30]. These lipopeptides have a discrete molecular weight and are produced by Fmoc (fluorenylmethoxycarbonyl protecting group) SPPS, a procedure in which the peptide chain is assembled stepwise while attached to an insoluble resin support, which allows the easy removal of the byproducts at each

• (SG)5KSS peptide chain is assembled stepwise using a Fmoc solid-phase peptide synthesis procedure. In a second step, the two perfluoroalkylated chains are grafted to the peptide chain through a lysine moiety. Next, the surface activity of the synthesized lipopeptides is investigated by assessing their

Deoxygenative C2-heteroarylation of quinoline N-oxides: facile access to α-triazolylquinolines

• Geetanjali S. Sontakke,
• Rahul K. Shukla and
• Chandra M. R. Volla

Beilstein J. Org. Chem. 2021, 17, 485–493, doi:10.3762/bjoc.17.42

• the stepwise pathway. The plausible mechanism for the C2-triazolylation of quinoline N-oxides is presented in Scheme 7 [64]. The reaction initiates by the nucleophilic attack of quinoline N-oxide, e.g., 1a, on the sulfonyl group of N-sulfonyl-1,2,3-triazole 2, leading to the formation of intermediate

Biochemistry of fluoroprolines: the prospect of making fluorine a bioelement

• Vladimir Kubyshkin,
• Rebecca Davis and
• Nediljko Budisa

Beilstein J. Org. Chem. 2021, 17, 439–460, doi:10.3762/bjoc.17.40

• occurrences), in contrast to most abundant CCG codons (31603 occurrences) [77]. The incorporation of proline into proteins is accomplished by the natural biosynthetic machinery via a complex stepwise process (see steps 3–5 in Figure 8). The initial recognition of any amino acid that participates in protein

CF₃-substituted carbocations: underexploited intermediates with great potential in modern synthetic chemistry

• Anthony J. Fernandes,
• Armen Panossian,
• Bastien Michelet,
• Agnès Martin-Mingot,
• Frédéric R. Leroux and
• Sébastien Thibaudeau

Beilstein J. Org. Chem. 2021, 17, 343–378, doi:10.3762/bjoc.17.32

• of 93%, the Pummerer rearrangement of sulfoxide 214 under harsh conditions turned out to be less efficient, affording 204f in only 42% yield. This reaction is thought to proceed stepwise via a first oxidative electron transfer, followed by deprotonation, a second oxidative electron transfer, and

Hydrazides in the reaction with hydroxypyrrolines: less nucleophilicity – more diversity

• Dmitrii A. Shabalin,
• Evgeniya E. Ivanova,
• Igor A. Ushakov,
• Elena Yu. Schmidt and
• Boris A. Trofimov

Beilstein J. Org. Chem. 2021, 17, 319–324, doi:10.3762/bjoc.17.29

• TFA (Table 1, entry 6) did not significantly promote the 3aa→4aa transformation, that was apparently caused by the deactivation of the acid catalyst by ammonia, released in the preceding step (vide infra for the mechanism discussion). To prevent this process, a stepwise addition of TFA was tested