Methyltransferases from RiPP pathways: shaping the landscape of natural product chemistry

• Maria-Paula Schröder,
• Isabel P.-M. Pfeiffer and
• Silja Mordhorst

Beilstein J. Org. Chem. 2024, 20, 1652–1670, doi:10.3762/bjoc.20.147

• intermediate is then reduced with H2 [37]. When synthesising via a reductive ring opening, typically, an N-Fmoc-protected amino acid is condensed with formaldehyde in the presence of p-toluic acid in refluxing toluene to yield the 5-oxazolidinone. Reductive ring opening can be achieved by using an excess of

Supramolecular assemblies of amphiphilic donor–acceptor Stenhouse adducts as macroscopic soft scaffolds

• Ka-Lung Hung,
• Leong-Hung Cheung,
• Yikun Ren,
• Ming-Hin Chau,
• Yan-Yi Lam,
• Takashi Kajitani and
• Franco King-Chi Leung

Beilstein J. Org. Chem. 2024, 20, 1590–1603, doi:10.3762/bjoc.20.142

• fluorescent particles pointed at by orange arrows in (c) and (d) are the clustered hBM-MSCs. Illustration of the reversible visible-light-controlled ring closure and thermal-driven ring-opening-processes of DAn and supramolecular assemblies on different length scales. Synthetic pathway to DAn. Supporting

Towards an asymmetric β-selective addition of azlactones to allenoates

• Behzad Nasiri,
• Ghaffar Pasdar,
• Paul Zebrowski,
• Katharina Röser,
• David Naderer and
• Mario Waser

Beilstein J. Org. Chem. 2024, 20, 1504–1509, doi:10.3762/bjoc.20.134

• -selective manner with moderate levels of enantioselectivities (up to 83:17 er). Furthermore, the obtained products can be successfully engaged in nucleophilic ring opening reactions, thus giving highly functionalized α-amino acid derivatives. Keywords: allenoates; amino acids; azlactones; organocatalysis

• steric bulk (5p) leads to a somewhat lower enantioselectivity, while the methoxy-substituent does not have a strong impact on the yield. It should, however, be stated that some of the methoxy-containing products, i.e., the α-alkyl-substituted 5j and 5k tend to undergo partial nucleophilic ring opening by

• using Maruoka’s spirocyclic binaphthyl-based quaternary ammonium salts B as catalysts this transformation can be achieved with enantioselectivities up to 83:17 er. Furthermore, the herein accessed cyclic products 5 could be successfully engaged in ring-opening reactions with different amines, thus

Electrophotochemical metal-catalyzed synthesis of alkylnitriles from simple aliphatic carboxylic acids

• Yukang Wang,
• Yan Yao and
• Niankai Fu

Beilstein J. Org. Chem. 2024, 20, 1497–1503, doi:10.3762/bjoc.20.133

• system [48]. To probe the radical intermediate in the reaction, a radical rearrangement experiment with cyclopropane-derived acid 31 was subjected to the standard conditions, leading to the expected ring opening, alkene-containing nitrile product 32 in 62% isolated yield (Figure 3A). Moreover

Transition-metal-catalyst-free electroreductive alkene hydroarylation with aryl halides under visible-light irradiation

• Kosuke Yamamoto,
• Kazuhisa Arita,
• Masami Kuriyama and
• Osamu Onomura

Beilstein J. Org. Chem. 2024, 20, 1327–1333, doi:10.3762/bjoc.20.116

• , providing the corresponding product 3aa in 74% yield. Several control experiments were conducted to gain insight into the reaction mechanism of the electroreductive process. The hydroarylation of cyclopropane-substituted styrene 2l resulted in the formation of ring-opening product 3al’, and the simple

Cofactor-independent C–C bond cleavage reactions catalyzed by the AlpJ family of oxygenases in atypical angucycline biosynthesis

• Jinmin Gao,
• Liyuan Li,
• Shijie Shen,
• Guomin Ai,
• Bin Wang,
• Fang Guo,
• Tongjian Yang,
• Hui Han,
• Zhengren Xu,
• Guohui Pan and
• Keqiang Fan

Beilstein J. Org. Chem. 2024, 20, 1198–1206, doi:10.3762/bjoc.20.102

• plausible that the corresponding biosynthesis involves analogous oxidative ring opening and rearrangement steps. On the other side, in JadG-catalyzed reactions, compound 3 reacts with ʟ-isoleucine or other amino acids, leading to the formation of jadomycin A (6) or analogues, respectively [10]. In the

• bond cleavage, ring opening, and rearrangement reactions, yielding the respective products. Furthermore, the reactions of 8 catalyzed by JadG and AlpJ could be quenched by superoxide dismutase (SOD), supporting a catalytic mechanism involving the generation of a substrate radical and the superoxide

• biosynthesis of fluostatins involves analogous B-ring cleavage and contraction steps as observed in kinamycin biosynthesis [2][13][19][26]. A sequence analysis of a reported fluostatin biosynthetic gene cluster in reassembled environmental DNA identified Flu17 as the putative ring opening oxygenase [8]. The N

Mild and efficient synthesis and base-promoted rearrangement of novel isoxazolo[4,5-b]pyridines

• Vladislav V. Nikol’skiy,
• Mikhail E. Minyaev,
• Maxim A. Bastrakov and
• Alexey M. Starosotnikov

Beilstein J. Org. Chem. 2024, 20, 1069–1075, doi:10.3762/bjoc.20.94

• -b]pyridine took place, followed by a base-promoted decarbonylation/isoxazole ring opening. Such transformations have been previously reported for benzo[d]isoxazoles with a carbonyl or carboxyl group in position 3 or 3-unsubstituted benzo[d]isoxazoles [25][26][27][28][29]. This means that the formyl

Novel analogues of a nonnucleoside SARS-CoV-2 RdRp inhibitor as potential antivirotics

• Luca Julianna Tóth,
• Kateřina Krejčová,
• Milan Dejmek,
• Eva Žilecká,
• Blanka Klepetářová,
• Lenka Poštová Slavětínská,
• Evžen Bouřa and
• Radim Nencka

Beilstein J. Org. Chem. 2024, 20, 1029–1036, doi:10.3762/bjoc.20.91

• the benzoxazole ring-opening reaction, namely 16. Simplification of the hit molecule: synthesis of pyridone derivatives We decided to simplify the relatively large structure of HeE1-2Tyr (1) in order to obtain smaller, more accessible inhibitors with similar or better properties. The employed novel

(Bio)isosteres of ortho- and meta-substituted benzenes

• H. Erik Diepers and
• Johannes C. L. Walker

Beilstein J. Org. Chem. 2024, 20, 859–890, doi:10.3762/bjoc.20.78

• itself accessible in good yields from allyl chloride 1 using a route based on that reported by Schlüter [28]. Bifunctional 1,2-BCP (±)-4 bearing orthogonally protected alcohol functionalities was obtained from 3a through a three-step sequence of strain-release radical ring-opening with iodochloromethane

• 1,5-BCHeps is slightly smaller than in meta-benzene but the substituent and dihedral angles are remarkably similar. 1,5-BCHeps 126 and 127 were first reported by Gassman and Proehl [61] and by Wada [62]. The most common synthetic approach today is via the strain-release ring-opening of [3.1.1

Enhanced reactivity of Li⁺@C₆₀ toward thermal [2 + 2] cycloaddition by encapsulated Li⁺ Lewis acid

• Hiroshi Ueno,
• Yu Yamazaki,
• Hiroshi Okada,
• Fuminori Misaizu,
• Ken Kokubo and
• Hidehiro Sakurai

Beilstein J. Org. Chem. 2024, 20, 653–660, doi:10.3762/bjoc.20.58

• reasons for the irreversible redox properties after the second reduction process have not been thoroughly investigated, the observed phenomena could potentially be attributed to ring opening or simple decomposition under the conditions. From these results, the LUMO levels of the compounds were estimated

Chemical and biosynthetic potential of Penicillium shentong XL-F41

• Ran Zou,
• Xin Li,
• Xiaochen Chen,
• Yue-Wei Guo and
• Baofu Xu

Beilstein J. Org. Chem. 2024, 20, 597–606, doi:10.3762/bjoc.20.52

• a ring-opening rearrangement. Alternatively, it is proposed that the ring-opening rearrangement precedes the methyl modification at the oxygen atom of the succinimide ring. We aim to confirm the initial step of this pathway, where tryptophan and DMAPP are catalyzed by the enzyme ShnA to form a

Switchable molecular tweezers: design and applications

• Pablo Msellem,
• Maksym Dekthiarenko,
• Nihal Hadj Seyd and
• Guillaume Vives

Beilstein J. Org. Chem. 2024, 20, 504–539, doi:10.3762/bjoc.20.45

• allosteric catalytic regulation (Figure 21). Mirkin and co-workers reported the symmetric tweezers 40 based on a Rh(I) complex with a phosphine and a labile thioether site and Cr(III)–salen arms as catalytic sites for the asymmetric ring opening of cyclohexene oxide by TMSN3 [80]. The closed tweezers showed

• protecting arms to move away from the salen complex thereby exposing the catalytic site. This triple-layer catalyst was applied in the control of a ring-opening polymerization reaction. The open state achieved full monomer conversion, while the closed state exhibited minimal activity (7% conversion after 100

Unveiling the regioselectivity of rhodium(I)-catalyzed [2 + 2 + 2] cycloaddition reactions for open-cage C₇₀ production

• Cristina Castanyer,
• Anna Pla-Quintana,
• Anna Roglans,
• Albert Artigas and
• Miquel Solà

Beilstein J. Org. Chem. 2024, 20, 272–279, doi:10.3762/bjoc.20.28

• in both cases. This preference was rationalized by means of DFT calculations. Moreover, the photooxidation of one of the C–C double bonds of the new bis(fulleroids) afford open-cage C70 derivatives having a 12-membered ring opening. It is noteworthy to mention that examples of open-cage C70

• (fulleroid) derivatives. The aim is to shed light on the regioselectivity of the process through both experimental and computational approaches. In addition, the photooxidation of one of the C–C double bonds in the synthesized bis(fulleroids) affords open-cage C70 derivatives having a 12-membered ring

• opening. Keywords: cycloadditions; DFT calculations; [70]fullerene; open-cage fullerenes; rhodium; Introduction The discovery of C60 (buckminsterfullerene) in 1985 [1] initiated the search for possible technological applications of fullerenes. Nowadays, applications for these carbon-based molecules have

Perspectives on push–pull chromophores derived from click-type [2 + 2] cycloaddition–retroelectrocyclization reactions of electron-rich alkynes and electron-deficient alkenes

• Michio Yamada

Beilstein J. Org. Chem. 2024, 20, 125–154, doi:10.3762/bjoc.20.13

• intermediate. Subsequently, following the production of an oxide ion through the ring-opening reaction of the 2,5-dihydrofuran ring, the oxide ion attacks another TCNEO molecule. This sequence culminates in the elimination of the tetracyanodioxetane moiety (either as dioxetane or carbonyl dicyanide molecules

• also performed theoretical calculations, unveiling that the ring-opening step presented a higher energy barrier compared with the ring-formation step, particularly when the DCV compounds lacked aryl substituents. Subsequently, they successfully isolated the corresponding cyclobutene intermediate 13

• pyrrolidine at 0 °C, the pentafulvene derivative 36 was obtained with 63% yield via an additional ring-opening process. Similar skeletal transformation reactions were observed for azulene derivatives bearing similar substructures. The reaction of 1 with TCNE in an aqueous medium containing a surfactant

Cycloaddition reactions of heterocyclic azides with 2-cyanoacetamidines as a new route to C,N-diheteroarylcarbamidines

• Pavel S. Silaichev,
• Tetyana V. Beryozkina,
• Vsevolod V. Melekhin,
• Valeriy O. Filimonov,
• Andrey N. Maslivets,
• Vladimir G. Ilkin,
• Wim Dehaen and
• Vasiliy A. Bakulev

Beilstein J. Org. Chem. 2024, 20, 17–24, doi:10.3762/bjoc.20.3

• experimentally observed. The base-catalyzed cycloaddition of 3,3-diaminoacrylonitriles 1 to azides 2, thus proceeds in a Cornforth-type fashion, which involves a triazole–triazole isomerization through ring opening, rotation of the amidine substituent around the single bond, and cyclization. Cytotoxic activity

• deprotonation of acrylonitriles 1 to form anion 1′. The subsequent formal cycloaddition of anion 1′ with azides 2 then affords triazolines 5, which aromatize through a 1,3-H-shift to afford the triazoles 6. Two pathways towards the isomeric triazoles 3 can be proposed: the first involving the electrocyclic ring

• opening of triazole 6 to form diazo compound anti-7, followed by rotation around the C‒C bond of the amidine group to furnish rotamer syn-7 which then undergoes 1,5-dipolar cyclization to products 3. The second path involves a Dimroth-type cyclization to form products 3′, which however, were not

Synthesis of N-acyl carbazoles, phenoxazines and acridines from cyclic diaryliodonium salts

• Nils Clamor,
• Mattis Damrath,
• Thomas J. Kuczmera,
• Daniel Duvinage and
• Boris J. Nachtsheim

Beilstein J. Org. Chem. 2024, 20, 12–16, doi:10.3762/bjoc.20.2

• efficient method to synthesize N-acyl carbazoles from readily available iodolium salt and amides via a ring-opening/intramolecular coupling cascade (Scheme 1c) [20][21][22][23][24][25][26][27][28][29][30]. Our group recently explored principle synthetic pathways of hetero- and carbocyclic 5- and 6-membered

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

• mechanism (cf. section 3.2) [86]. 2.3 Metal-free ring opening metathesis polymerization (MF-ROMP) ROMP is a powerful and broadly applicable technique for synthesizing polymers. Traditional ROMP systems are initiated by transition-metal complexes and Ru-based alkylidene complexes, which are also known as

• monomer to generate a cyclobutene radical cation intermediate. The thermodynamically instable intermediate subsequently forms the propagating radical cation species via a ring-opening process. The reduced PC•− terminates the catalytic loop by reducing the propagating species to provide a polymer chain

N-Sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations

• Fatemeh Doraghi,
• Seyedeh Pegah Aledavoud,
• Mehdi Ghanbarlou,
• Bagher Larijani and
• Mohammad Mahdavi

Beilstein J. Org. Chem. 2023, 19, 1471–1502, doi:10.3762/bjoc.19.106

• the best of our knowledge there are no review articles focusing on the application of N-(sulfenyl)succinimides/phthalimides in sulfenylation reactions. In this context, we describe various sulfenylation reactions, such as electrophilic aromatic substitution, ring-opening, dehydrogenative cross

• -(arylthio)succinimides 1 or N-(arylseleno)succinimides 1’’ was developed under a Lewis acid catalysis system. This reaction involves ring-opening of the substituted cyclopropane 49, amination at the C1-site, and thiolation at the C3-site. In the transformation, sulfonamide acted as a nucleophile

• bond of 51 to give the three-membered ring III. Afterwards, intermediate IV was formed by an intramolecular ring opening of III (path I) and presumably produced IV' by path II, which through deprotonation delivered products 53 and 53' respectively. In the meantime, another Lewis acid-promoted

Application of N-heterocyclic carbene–Cu(I) complexes as catalysts in organic synthesis: a review

• Nosheen Beig,
• Varsha Goyal and
• Raj K. Bansal

Beilstein J. Org. Chem. 2023, 19, 1408–1442, doi:10.3762/bjoc.19.102

• [(6-NHC)CuMes] with t-BuOH. It was found that the diaminocarbene derivative was more thermally stable whereas the diamido derivative underwent both thermal and hydrolytic ring-opening reactions (Scheme 13). Demir Atli and co-worker, in 2018, synthesized a cationic (NHC)2Cu(I) complex 39 in very good

Photoredox catalysis harvesting multiple photon or electrochemical energies

• Mattia Lepori,
• Simon Schmid and
• Joshua P. Barham

Beilstein J. Org. Chem. 2023, 19, 1055–1145, doi:10.3762/bjoc.19.81

The unique reactivity of 5,6-unsubstituted 1,4-dihydropyridine in the Huisgen 1,4-diploar cycloaddition and formal [2 + 2] cycloaddition

• Xiu-Yu Chen,
• Hui Zheng,
• Ying Han,
• Jing Sun and
• Chao-Guo Yan

Beilstein J. Org. Chem. 2023, 19, 982–990, doi:10.3762/bjoc.19.73

• intermediate E by a charge coupling process. At elevated temperature, the ring-opening of the unstable cyclobutenyl ring gives a 1,2-dihydroazocine intermediate F, which is transformed into a 1,4-dihydroazocine intermediate G by a 1,5-H shift process. At last, the tetrahydrocyclopenta[b]pyrrole 6 is formed by

Aromatic C–H bond functionalization through organocatalyzed asymmetric intermolecular aza-Friedel–Crafts reaction: a recent update

• Anup Biswas

Beilstein J. Org. Chem. 2023, 19, 956–981, doi:10.3762/bjoc.19.72

• using Nps-iminophosphonates as electrophiles. Aza-Friedel–Crafts reaction between indole and α-iminophosphonate. [2.2]-Paracyclophane-derived chiral phosphoric acids as catalyst. Aza-Friedel–Crafts reaction through ring opening of sulfamidates. Isoquinoline-1,3(2H,4H)-dione scaffolds as electrophiles

Clauson–Kaas pyrrole synthesis using diverse catalysts: a transition from conventional to greener approach

• Dileep Kumar Singh and
• Rajesh Kumar

Beilstein J. Org. Chem. 2023, 19, 928–955, doi:10.3762/bjoc.19.71

• proposed by Wang [55] (Scheme 2b), 2,5-dimethoxytetrahydrofuran (2) is first protonated with acetic acid, followed by ring opening to form carbocation B. In the following step, primary amine 1 nucleophilically attacks carbocation B to produce intermediate C, which, after proton rearrangement and the

Synthesis of aliphatic nitriles from cyclobutanone oxime mediated by sulfuryl fluoride (SO₂F₂)

• Xian-Lin Chen and
• Hua-Li Qin

Beilstein J. Org. Chem. 2023, 19, 901–908, doi:10.3762/bjoc.19.68

• Xian-Lin Chen Hua-Li Qin School of Chemistry, Chemical Engineering and Life Science, Wuhan University of Technology, 205 Luoshi Road, Wuhan, 430070, PR China 10.3762/bjoc.19.68 Abstract A SO2F2-mediated ring-opening cross-coupling of cyclobutanone oxime derivatives with alkenes was developed for

• the construction of a range of δ-olefin-containing aliphatic nitriles with (E)-configuration selectivity. This new method features wide substrate scope, mild conditions, and direct N–O activation. Keywords: direct N–O activation; E-selectivity; nitrile synthesis; ring-opening cross-coupling; sulfuryl

• completely inhibited when the amount of added TEMPO was increased to 2 equivalents. Based upon the preliminary results and previous reports of this class of transformation [26][30][36][37][42][60][61], a plausible mechanism for the base-promoted, SO2F2-mediated ring-opening cross-coupling of cyclobutanone

First synthesis of acylated nitrocyclopropanes

• Kento Iwai,
• Rikiya Kamidate,
• Khimiya Wada,
• Haruyasu Asahara and
• Nagatoshi Nishiwaki

Beilstein J. Org. Chem. 2023, 19, 892–900, doi:10.3762/bjoc.19.67

• bulkier. The obtained nitrocyclopropane was transformed into furan upon treatment with tin(II) chloride via a ring-opening/ring-closure process. Keywords: acetoxyiodine; conjugate addition; dihydrofuran; nitroalkene; nitrocyclopropane; Introduction 3-Arylated 2-nitrocyclopropane-1,1-dicarbonylic acid

• reaction with dinucleophiles such as 2-aminopyridines, which affords pyrido[1,2-a]pyrimidinones through ring opening (Scheme 1, reaction a) [1]. Chemical transformations that take advantage of polyfunctionality are also possible. A six-membered ring forms between the aryl group and ester functionality

• compounds to give diarylated (oxoalkyl)malonates [6]. In the reaction using tin(II) chloride as the Lewis acid, the ring opening and nucleophilic attack of the nitro group occur, to produce functionalized isoxazolines (reaction d) [7]. In contrast, denitration under basic conditions generates highly