The preparation and properties of 1,1-difluorocyclopropane derivatives

• Kymbat S. Adekenova,
• Peter B. Wyatt and
• Sergazy M. Adekenov

Beilstein J. Org. Chem. 2021, 17, 245–272, doi:10.3762/bjoc.17.25

• ]. The radical ring-opening polymerization (RROP) provides a synthetic route to fluoropolymers, which are useful materials [91]. The RROP of gem-difluorovinylcyclopropane (90) gave mainly the polymer with an unsymmetrical repeating unit, by the cleavage of the C2–C3 bond in the ring (Scheme 44, path a

A sustainable strategy for the straightforward preparation of 2H-azirines and highly functionalized NH-aziridines from vinyl azides using a single solvent flow-batch approach

• Michael Andresini,
• Leonardo Degannaro and
• Renzo Luisi

Beilstein J. Org. Chem. 2021, 17, 203–209, doi:10.3762/bjoc.17.20

• isolate 3-(perfluorophenyl)-2H-azirine (2k) due to its rapid polymerization in the crude mixture. Interestingly, aliphatic vinyl azides 1h–j were found less reactive, and the corresponding azirines 2h–j were obtained in just 74–77% yield, in mixtures with unreacted starting materials. However, when the

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

• ultrahigh molecular weight (≈106 g⋅mol−1) and a reasonably low dispersity (Đ ≥ 1.33) by using various monomers. Triethanolamine (TEOA) was used as an electron donor to initiate the photoinduced electron transfer to the PDI–CB[7] system, and thus to start the polymerization reaction. In addition, the rate of

• macrocycle has inherent chromophores that can function as photosensitizers, the efficiency of the energy transfer will be higher and the systems will be simplified. 3) Other kinds of macrocycle-based catalysis need to be explored, such as esterification, polymerization, redox reaction, etc. 4) Hyperbranched

• supramolecular PDI–CB[7] complex and structures of monomers and the chain transfer agent. Republished with permission of The Royal Society of Chemistry from [48] (“Visible light induced aqueous RAFT polymerization using a supramolecular perylene diimide/cucurbit[7]uril complex” by Y. Yang et al., Polym. Chem

Supramolecular polymers with reversed viscosity/temperature profile for application in motor oils

• Jan-Erik Ostwaldt,
• Christoph Hirschhäuser,
• Stefan K. Maier,
• Carsten Schmuck and
• Jochen Niemeyer

Beilstein J. Org. Chem. 2021, 17, 105–114, doi:10.3762/bjoc.17.11

• develop such novel VIIs, we envisaged the use of ditopic building blocks, which are able to reversibly form supramolecular polymers at higher temperatures. Supramolecular polymerization should increase the hydrodynamic radius and thus was expected to lead to increased viscosities [9]. There are different

• mechanisms for the formation of supramolecular polymers from molecular building blocks: The isodesmic, the cooperative and the ring–chain-mediated supramolecular polymerization [10]. For an application in viscosity improvement, a higher degree of polymerization is desired at elevated temperatures, which can

• be achieved by a ring–chain-based polymerization [11]. In this context, Sijbesma and Meijer reported an early example of a low-molecular weight VII using a ditopic monomer which undergoes supramolecular polymerization at elevated temperatures (Figure 1) [12][13]. The system consists of two self

Supramolecular polymerization of sulfated dendritic peptide amphiphiles into multivalent L-selectin binders

• David Straßburger,
• Svenja Herziger,
• Katharina Huth,
• Moritz Urschbach,
• Rainer Haag and
• Pol Besenius

Beilstein J. Org. Chem. 2021, 17, 97–104, doi:10.3762/bjoc.17.10

• ionic strength on the supramolecular polymerization was probed via circular dichroism spectroscopy and cryogenic transmission electron microscopy. Physiological salt concentrations efficiently screen the charges of the dendritic building block equipped with eight sulfate groups and trigger the formation

• , post-functionalization using a subsequent copper-catalyzed azide–alkyne cycloaddition reaction became accessible [35][36]. At the same time the other two unmodified side arms of the dendritic amphiphile make sure that the fidelity of the β-sheet motifs and directed supramolecular polymerization remains

• polymerization strongly relies on the formation of secondary structure elements, leading to ordered domains that lead to characteristic CD band spectra. By probing aqueous solutions of I at different concentrations in H2O, a strongly negative CD band at around λ ≈ 220 nm became apparent (Figure 1A). In the past

Synthesis, crystal structures and properties of carbazole-based [6]helicenes fused with an azine ring

• Daria I. Tonkoglazova,
• Anna V. Gulevskaya,
• Konstantin A. Chistyakov and
• Olga I. Askalepova

Beilstein J. Org. Chem. 2021, 17, 11–21, doi:10.3762/bjoc.17.2

• electroactive materials [52][53][54]. Carbazole-based [6]helicenes [42] and [7]helicenes [50] showed deep blue electroluminescence and have been investigated in OLED devices. Some carbazole-based [5]- and [6]helicenes have been used as visible light photoinitiators for cationic and radical polymerization [41

Amine–borane complex-initiated SF₅Cl radical addition on alkenes and alkynes

• Audrey Gilbert,
• Pauline Langowski,
• Marine Delgado,
• Laurent Chabaud,
• Mathieu Pucheault and
• Jean-François Paquin

Beilstein J. Org. Chem. 2020, 16, 3069–3077, doi:10.3762/bjoc.16.256

• recently, it has been shown that some of these common amine–borane complexes can also be used as radical initiators for atom transfer radical addition of alkyl halides to alkenes [48]. They were also used in the free-radical polymerization of alkene-containing monomers such as methyl methacrylate or

Selected peptide-based fluorescent probes for biological applications

• Debabrata Maity

Beilstein J. Org. Chem. 2020, 16, 2971–2982, doi:10.3762/bjoc.16.247

• polymerization reaction between polydiacetylene. PDA liposomes turn colorless to red upon formation of cross-linked liposomes. The fluorescence of the naphthimide is completely quenched due to the energy transfer from the fluorophore to the cross-linked polymer. However, addition of LPS restores the fluorescence

Ring-closing metathesis of prochiral oxaenediynes to racemic 4-alkenyl-2-alkynyl-3,6-dihydro-2H-pyrans

• Viola Kolaříková,
• Markéta Rybáčková,
• Martin Svoboda and
• Jaroslav Kvíčala

Beilstein J. Org. Chem. 2020, 16, 2757–2768, doi:10.3762/bjoc.16.226

• reactions of unsaturated compounds, e.g., alkene and enyne cross metathesis (CM [1] and EYCM [2][3][4]), alkene and enyne ring-closing metathesis (RCM and RCEYM) [5][6], ring-opening metathetic polymerization (ROMP) [7], etc., the CM and RCM are the most popular in organic synthesis [8]. Furthermore, the

• be too unstable and prone to polymerization. On the other hand, the reactivity of oxaenediyne 3 was too sluggish. Hence, 4-(allyloxy)hepta-1,6-diyne (2a) and its derivatives became the framework of choice. The key starting compound for the synthesis of oxaenediyne 2a and its derivatives was hepta-1,6

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

• 27 in a single step. They also pointed out that when ethylene gas was used as an alkene source for the ring-opening step, diluted reaction conditions were necessary to dissolve the ethylene in dichloromethane to avoid polymerization. Therefore, after several experimentations, they noticed that liquid

Reactions of 3-aryl-1-(trifluoromethyl)prop-2-yn-1-iminium salts with 1,3-dienes and styrenes

• Thomas Schneider,
• Michael Keim,
• Bianca Seitz and
• Gerhard Maas

Beilstein J. Org. Chem. 2020, 16, 2064–2072, doi:10.3762/bjoc.16.173

• sequence. On the other hand, the successful thermal iminium-ion induced SE(Ar) reactions shown in Scheme 2 were not applicable to the iminium-substituted norbornadiene 2, which suffered undefined polymerization on moderate heating in various solvents. In contrast to so far unknown 9‑amino-9

Three new O-isocrotonyl-3-hydroxybutyric acid congeners produced by a sea anemone-derived marine bacterium of the genus Vibrio

• Dandan Li,
• Enjuro Harunari,
• Tao Zhou,
• Naoya Oku and
• Yasuhiro Igarashi

Beilstein J. Org. Chem. 2020, 16, 1869–1874, doi:10.3762/bjoc.16.154

• )-configured 3-hydroxy fatty acids [13], and 3-hydroxybutyric acid in 3 and 4 and 3-hydroxyhexanoic acid in 2 are the most common two building blocks for PHAs [14]. However, degrees of polymerization as low as for 1–4 and the dehydrative modifications are unprecedented, besides for 5 [9]. Because PHAs are by

Synthesis, docking study and biological evaluation of ᴅ-fructofuranosyl and ᴅ-tagatofuranosyl sulfones as potential inhibitors of the mycobacterial galactan synthesis targeting the galactofuranosyltransferase GlfT2

• Marek Baráth,
• Jana Jakubčinová,
• Zuzana Konyariková,
• Stanislav Kozmon,
• Katarína Mikušová and
• Maroš Bella

Beilstein J. Org. Chem. 2020, 16, 1853–1862, doi:10.3762/bjoc.16.152

• decaprenyl-P-P-GlcNAc-Rha, (glycolipid 2, GL2), which serves as a lipid carrier for arabinogalactan polymerization [7][8]. The latter enzyme, GlfT2, extends the product of GlfT1-catalyzed reaction, decaprenyl-P-P-GlcNAc-Rha-Galf2 (glycolipid 4, GL4), producing the lipid-linked galactan polymer [8]. Both

• -up of lipid-linked galactan precursors. The crude enzymes used in the assay allow for in situ synthesis of the acceptor for galactan polymerization, decaprenyl-P-P-GlcNAc-Rha (GL2), from endogenous decaprenyl phosphate and sugar nucleotides UDP-GlcNAc and TDP-Rha supplied in the reaction mixture

One-pot synthesis of oxazolidinones and five-membered cyclic carbonates from epoxides and chlorosulfonyl isocyanate: theoretical evidence for an asynchronous concerted pathway

• Esra Demir,
• Ozlem Sari,
• Yasin Çetinkaya,
• Ufuk Atmaca,
• Safiye Sağ Erdem and
• Murat Çelik

Beilstein J. Org. Chem. 2020, 16, 1805–1819, doi:10.3762/bjoc.16.148

• polymerization of the compounds containing cyclic carbonates such as methyl 4,6-O-benzylidene-2,3-O-carbonyl-α-ᴅ-glucopyranoside (MBCG) (5) [19][20] and glycerol carbonate (6) [21] were also reported (Scheme 1). Therefore, numerous synthetic approaches have been developed to date for the preparation of

Mechanochemical green synthesis of hyper-crosslinked cyclodextrin polymers

• Alberto Rubin Pedrazzo,
• Fabrizio Caldera,
• Marco Zanetti,
• Silvia Lucia Appleton,
• Nilesh Kumar Dhakar and
• Francesco Trotta

Beilstein J. Org. Chem. 2020, 16, 1554–1563, doi:10.3762/bjoc.16.127

• catalyst, if necessary. The solvents of choice were usually organic polar aprotic liquids, for example, N,N-dimethylformamide or dimethyl sulfoxide (DMSO). An alternative synthetic route relied on interfacial polymerization, where two immiscible solutions, one consisting of CDs dissolved in an alkaline

Oxime radicals: generation, properties and application in organic synthesis

• Igor B. Krylov,
• Stanislav A. Paveliev,
• Alexander S. Budnikov and
• Alexander O. Terent’ev

Beilstein J. Org. Chem. 2020, 16, 1234–1276, doi:10.3762/bjoc.16.107

• used in the development of organic magnetic materials [1], organic batteries [2][3][4], in the preparation of polymers by living polymerization [5][6], in the studies of biomolecules and living systems by EPR [7] and NMR [8] techniques. Stable N-oxyl radicals occupy a central place in organic chemistry

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

• . Poly(propiolate) salts are formed by polymerization of the starting materials after heating. The different cations of the propiolates cause changes in the thermal behavior of the starting materials since different temperatures are required for the decomposition or different amounts of gases are

• structures in the carbon source [6]. Diamadopoulos and co-workers observed also the production of smaller surface areas by H3PO4 activation of bagasse and rice husk due to a reaction of the activating reagent with the carbon precursor. Thereby, phosphate esters or polymerization byproducts are formed, which

• conform to the LaMer model and starts with a polymerization step of the carbohydrate monomers and followed by a carbonization step when the nucleation is caused by the supersaturation of the solution. The resulting nuclei grow uniformly until the final size is obtained depending on the growth parameters

Photocatalysis with organic dyes: facile access to reactive intermediates for synthesis

• Stephanie G. E. Amos,
• Marion Garreau,
• Luca Buzzetti and
• Jerome Waser

Beilstein J. Org. Chem. 2020, 16, 1163–1187, doi:10.3762/bjoc.16.103

Synthesis of esters of diaminotruxillic bis-amino acids by Pd-mediated photocycloaddition of analogs of the Kaede protein chromophore

• Esteban P. Urriolabeitia,
• Pablo Sánchez,
• Alexandra Pop,
• Cristian Silvestru,
• Eduardo Laga,
• Ana I. Jiménez and
• Carlos Cativiela

Beilstein J. Org. Chem. 2020, 16, 1111–1123, doi:10.3762/bjoc.16.98

• applications as internal donors in Ziegler–Natta catalysts for polymerization [14] or as building blocks in polymer chemistry [15]. A very closely related group of cyclobutanes are the 1,3-diaminotruxillic ester derivatives (Figure 1b). This type of bis-amino esters also shows remarkable pharmacological

Aldehydes as powerful initiators for photochemical transformations

• Maria A. Theodoropoulou,
• Nikolaos F. Nikitas and
• Christoforos G. Kokotos

Beilstein J. Org. Chem. 2020, 16, 833–857, doi:10.3762/bjoc.16.76

• ) aldehydes have as photoinitiators. The photophysical properties and photoreactivity of benzaldehyde are initially provided, followed by applications of aldehydes as initiators for polymerization reactions. Finally, the applications to date regarding aldehydes as photoinitiators in organic synthesis are

• are useful photocatalysts, the corresponding aldehydes are not so widely utilized to promote chemical reactions. In this review, our goal was to summarize the photophysical properties of aromatic aldehydes, highlight the use of aldehydes as photoinitiators in polymerization reactions, and provide all

• carbonyl compounds, including aliphatic or aromatic ketones and aldehydes, have been employed as photoinitiators in polymerization reactions. The first studies reported in the literature where carbonyl compounds were used as initiators inspired researchers to study the use of aldehydes as well. In 1978

A systematic review on silica-, carbon-, and magnetic materials-supported copper species as efficient heterogeneous nanocatalysts in “click” reactions

• Pezhman Shiri and
• Jasem Aboonajmi

Beilstein J. Org. Chem. 2020, 16, 551–586, doi:10.3762/bjoc.16.52

• 10 cycles. A mixture of GO, 1-vinylimidazole (98), and cross-linker 99 in ethanol was sonicated for 20 min [85]. Afterwards, the mixture was deoxygenated in an Ar atmosphere for 20 min. In the next step, polymerization was generated by adding AIBN (3 wt %). This was then heated at 70 °C for 24 h

KOt-Bu-promoted selective ring-opening N-alkylation of 2-oxazolines to access 2-aminoethyl acetates and N-substituted thiazolidinones

• Qiao Lin,
• Shiling Zhang and
• Bin Li

Beilstein J. Org. Chem. 2020, 16, 492–501, doi:10.3762/bjoc.16.44

• proceeded well with heterocycle-containing chlorides such as 2-chloro-5-(chloromethyl)thiophene (4e), leading to 2-aminoethyl acetate product 3k in 66% yield which has potential as bifunctional monomer for polymerization. Furthermore, oxazole derivative 2,4,4-trimethyl-4,5-dihydrooxazole (2b) was also

Synthesis of 4-amino-5-fluoropyrimidines and 5-amino-4-fluoropyrazoles from a β-fluoroenolate salt

• Tobias Lucas,
• Jule-Philipp Dietz and
• Till Opatz

Beilstein J. Org. Chem. 2020, 16, 445–450, doi:10.3762/bjoc.16.41

• ) and electron-withdrawing groups (compound 10l) were formed in nearly quantitative yields (95–99%). Only the 4-hydroxyphenyl derivative 10j was obtained in a moderate yield (69%) presumably due to competing polymerization of the enolate. The 4-chloro and 4-bromo derivatives (10m and 10n) were also

•  2). In the first reactions, only traces of the desired compound 13a were observed. Changing the temperature did not increase the yield. Acidic conditions were tested next but phenylhydrazine hydrochloride and acetic acid again gave only traces of 13a and polymerization of the enolate took place. To

• investigate the use of non-nucleophilic bases, but with DBU, polymerization of the fluoroenolate took place. When using aqueous sodium hydroxide as the base, a 19% yield could be achieved. Switching the solvent to water led to an improvement of the yield to 36% (Table 2). In water, but without using a base

Photophysics and photochemistry of NIR absorbers derived from cyanines: key to new technologies based on chemistry 4.0

• Bernd Strehmel,
• Christian Schmitz,
• Ceren Kütahya,
• Yulian Pang,
• Anke Drewitz and
• Heinz Mustroph

Beilstein J. Org. Chem. 2020, 16, 415–444, doi:10.3762/bjoc.16.40

• in lower molecular weight products caused by cleavage of the methine chain and conjugate acid, see Equation 7 [5][63]. The latter can initiate ring opening polymerization of aziridines [5] and oxiranes [63]. We also prefer to use the term conjugate acid instead of proton. The use of the latter widely

• = −0.64 V [5][84]) or the triazine 89 (Ered = −0.77 V [5]) carrying no charge as acceptor (Scheme 5). Thus, the positive charge of the iodonium cation is likely not the reason because 89 exhibits no charge. Both possess similar reduction potentials but the efficiency to initiate radical polymerization was

• as an issue. Particularly 48 showed remarkable polymerization efficiency in combination with 88 [5][63]. Photoinduced electron transfer typically followed an exothermal reaction route resulting in the formation of the cation radical of the sensitizer and the iodyl radical (Ar2-I•) formed by reduction

Room-temperature Pd/Ag direct arylation enabled by a radical pathway

• Amy L. Mayhugh and
• Christine K. Luscombe

Beilstein J. Org. Chem. 2020, 16, 384–390, doi:10.3762/bjoc.16.36

• -conjugated materials, avoiding the prefunctionalization required for traditional cross-coupling methods. A major effort in organic electronic materials development is improving the environmental and economic impact of production; direct arylation polymerization (DArP) is an effective method to achieve these

• goals. Room-temperature polymerization would further improve the cost and energy efficiencies required to prepare these materials. Reported herein is new mechanistic work studying the underlying mechanism of room temperature direct arylation between iodobenzene and indole. Results indicate that room

• bond (M = SnR3, B(OH)2, etc.) and a C–X (X = I, Br, OTs) coupling partner. In contrast, direct arylation couples C–H and C–X bonds directly without the need to prepare the C–M substrate. As a polymerization method, direct arylation polymerization (DArP) is of great interest due to its potential to