Synthesis of ferrocenyl-substituted 1,3-dithiolanes via [3 + 2]-cycloadditions of ferrocenyl hetaryl thioketones with thiocarbonyl S-methanides

• Grzegorz Mlostoń,
• Róża Hamera-Fałdyga,
• Anthony Linden and
• Heinz Heimgartner

Beilstein J. Org. Chem. 2016, 12, 1421–1427, doi:10.3762/bjoc.12.136

• described [1]. The latter substrates were prepared efficiently via acylation of ferrocene with in situ generated mixed anhydrides containing a trifluoroacetyl unit or, alternatively, by ferrocenylation of furan, thiophene or selenophene with mixed trifluoroacetyl anhydride. The obtained ferrocenyl

• polar axis, but achiral. Refinement of the absolute structure parameter [14][15] yielded a value of 0.13(1), which indicates that the crystal is a partial inversion twin with a major twin fraction of 0.87(1). In the cases of 5e and 5f, the thiophene and selenophene rings are disordered over two

Biradical vs singlet oxygen photogeneration in suprofen–cholesterol systems

• Fabrizio Palumbo,
• Francisco Bosca,
• Isabel M. Morera,
• Inmaculada Andreu and
• Miguel A. Miranda

Beilstein J. Org. Chem. 2016, 12, 1196–1202, doi:10.3762/bjoc.12.115

• relevant interaction was found between the allylic proton at C7 and the protons of the thiophene ring (Figure 4). More details are provided in the Supporting Information File 1. Having established the nature of the occurring photochemical reactions, it appeared interesting to explore the possible

The role of alkyl substituents in deazaadenine-based diarylethene photoswitches

• Christopher Sarter,
• Michael Heimes and
• Andres Jäschke

Beilstein J. Org. Chem. 2016, 12, 1103–1110, doi:10.3762/bjoc.12.106

• benzenesulfonyl chloride, resulting in a four-fold increased yield of 6 compared to the original route. The other part of the diarylethene, namely the cyclopentenyl bridge with the attached substituted thiophene ring was furnished as shown in Scheme 3 and activated as boronic acid pinacolate ester. Suzuki

Syntheses of dibenzo[d,d']benzo[2,1-b:3,4-b']difuran derivatives and their application to organic field-effect transistors

• Minh Anh Truong and
• Koji Nakano

Beilstein J. Org. Chem. 2016, 12, 805–812, doi:10.3762/bjoc.12.79

• far reported, thiophene-fused π-conjugated compounds have been widely studied as organic semiconducting materials and found to exhibit high semiconducting performances [5][13][14][15][16]. Furan-containing π-conjugated compounds have attracted less attention until recently [17][18][19][20][21][22][23

Iridium/N-heterocyclic carbene-catalyzed C–H borylation of arenes by diisopropylaminoborane

• Mamoru Tobisu,
• Takuya Igarashi and
• Naoto Chatani

Beilstein J. Org. Chem. 2016, 12, 654–661, doi:10.3762/bjoc.12.65

• instability of 11-B during isolation (Table 2, entry 8). Our protocol was able to borylate non-benzofused five-membered heteroarenes. Pyrrole 12 was much less reactive than indoles, and required neat conditions to obtain a modest yield of the borylated product 12-B (Table 2, entry 9). Thiophene (13) afforded

Copper-mediated arylation with arylboronic acids: Facile and modular synthesis of triarylmethanes

• H. Surya Prakash Rao and
• A. Veera Bhadra Rao

Beilstein J. Org. Chem. 2016, 12, 496–504, doi:10.3762/bjoc.12.49

• respective pyrene-containing unsymmetrical triarylmethanes 11q–r in good yields (Table 3). Next, the coupling reaction of phenyl(ferrocenyl)methanol (9d) with thiophen-3-ylboronic acid (10m) provided triarylmethane 11s, which has ferrocene, thiophene and phenyl rings installed on the central carbon. The

A quadruple cascade protocol for the one-pot synthesis of fully-substituted hexahydroisoindolinones from simple substrates

• Hong-Bo Zhang,
• Yong-Chun Luo,
• Xiu-Qin Hu,
• Yong-Min Liang and
• Peng-Fei Xu

Beilstein J. Org. Chem. 2016, 12, 253–259, doi:10.3762/bjoc.12.27

• , entry 11). A heteroaromatic substrate such as thiophene could also be successfully employed to afford rac-3 with medium yield and diastereoselectivity (Table 2, entry 13). 3,4-Dichloro-substituted and 3,5-dimethoxy-substituted substrates produced the desired products in 84% and 55% yield with 20:1 and

Hydroquinone–pyrrole dyads with varied linkers

• Hao Huang,
• Christoffer Karlsson,
• Maria Strømme,
• Martin Sjödin and
• Adolf Gogoll

Beilstein J. Org. Chem. 2016, 12, 89–96, doi:10.3762/bjoc.12.10

• utilized for C–C cross coupling of benzyl halides with heteroarylboronic acids. However, in contrast to its use for the synthesis of thiophene and furane derivatives, it has rarely been employed for the coupling of pyrrolylboronic acids with benzyl halides [13][14][15][16][17]. We applied the Suzuki

N-Methylphthalimide-substituted benzimidazolium salts and PEPPSI Pd–NHC complexes: synthesis, characterization and catalytic activity in carbon–carbon bond-forming reactions

• Senem Akkoç,
• Yetkin Gök,
• İlhan Özer İlhan and
• Veysel Kayser

Beilstein J. Org. Chem. 2016, 12, 81–88, doi:10.3762/bjoc.12.9

• entry 9. However, when we further increased the temperature by more than 30 degrees to 110 °C, a maximum yield of 98% was obtained (Table 1, entry 11). In the reaction catalyzed by 5, 2-butyl-5-(4-methoxyphenyl)thiophene was obtained in 79% yield (Table 1, entry 12). Catalytic activity of synthesized

• –NHC complex as catalyst resulted in low yields and conversions (Table 3, entries 9–12). The usage of the morpholinoethyl substituted benzimidazolium compound 4 with Pd(OAc)2 resulted in higher yields of 2-(4-nitrophenyl)benzo[b]thiophene compared to the usage of compounds 1–3. Generally, the PEPPSI Pd

Pyridylidene ligand facilitates gold-catalyzed oxidative C–H arylation of heterocycles

• Kazuhiro Hata,
• Hideto Ito,
• Yasutomo Segawa and
• Kenichiro Itami

Beilstein J. Org. Chem. 2015, 11, 2737–2746, doi:10.3762/bjoc.11.295

• reaction gave sterically congested heterobiaryl 3da in 17% yield (Table 2, entry 8). In the case of the reaction of indole 1e, 3-arylindole 3ea was exclusively obtained in 44% yield (Table 2, entry 9). On the other hand, arylation of benzo[b]thiophene (1f) mainly afforded 2-arylbenzothiophene 3fa along

Carbon–carbon bond cleavage for Cu-mediated aromatic trifluoromethylations and pentafluoroethylations

• Tsuyuka Sugiishi,
• Hideki Amii,
• Kohsuke Aikawa and
• Koichi Mikami

Beilstein J. Org. Chem. 2015, 11, 2661–2670, doi:10.3762/bjoc.11.286

• reaction conditions of copper-catalyzed nucleophilic trifluoromethylation. Electron-rich iodoarenes underwent the nucleophilic trifluoromethylation to afford the corresponding trifluoromethylated benzenes. Furthermore, the trifluoromethyl group was introduced into naphthalenes and thiophene with hemiaminal

Copper-catalyzed asymmetric conjugate addition of organometallic reagents to extended Michael acceptors

• Thibault E. Schmid,
• Sammy Drissi-Amraoui,
• Christophe Crévisy,
• Olivier Baslé and
• Marc Mauduit

Beilstein J. Org. Chem. 2015, 11, 2418–2434, doi:10.3762/bjoc.11.263

• were reported. In order to fully demonstrate the synthetic significance of such a methodology, compounds 27 were reconjugated in the presence of DBU and subsequently reacted in the 1,4-ACA (Scheme 5). The optimized conditions for the conversion of 28 to 29 involved copper(I) thiophene-2-carboxylate

• system, a combination of Josiphos L9 as chiral ligand and copper thiophene 2-carboxylate (CuTC) afforded the desired 1,6-adducts 43 with very good regioselectivity (up to 5/95) and enantioselectivities (up to 91% ee). Enantioselective 1,4-addition to extended Michael acceptors With dialkylzinc reagents

Molecular-oxygen-promoted Cu-catalyzed oxidative direct amidation of nonactivated carboxylic acids with azoles

• Wen Ding,
• Shaoyu Mai and
• Qiuling Song

Beilstein J. Org. Chem. 2015, 11, 2158–2165, doi:10.3762/bjoc.11.233

• conditions, providing the desired products 20 and 21 in 59% and 88% yield, respectively. Additionally, heterocyclic acids, such as thiophene- and furan-3-carboxylic acid were well tolerated, providing the amides 22 and 23 in acceptable yields. Gratifyingly, aliphatic carboxylic acids, such as

C–H bond halogenation catalyzed or mediated by copper: an overview

• Wenyan Hao and
• Yunyun Liu

Beilstein J. Org. Chem. 2015, 11, 2132–2144, doi:10.3762/bjoc.11.230

• , I) and a proper additive promoted smoothly the synthesis of various o-haloaryl-2-carboxamides 11. This synthetic protocol tolerated not only carbon aryls, but also various heteroaryls such as thiophene, furan and pyridine in the amide component. Interestingly, in an earlier example studying the

Efficient synthesis of π-conjugated molecules incorporating fluorinated phenylene units through palladium-catalyzed iterative C(sp²)–H bond arylations

• Fatiha Abdelmalek,
• Fazia Derridj,
• Safia Djebbar,
• Jean-François Soulé and
• Henri Doucet

Beilstein J. Org. Chem. 2015, 11, 2012–2020, doi:10.3762/bjoc.11.218

• -coupling reactions are one of the most powerful technologies for the efficient synthesis of π-conjugated oligomers. As example, a π-conjugated thiophene triad incorporating a difluorinated phenylene unit has been previously synthesized in 60% yield using the Stille reaction of trimethyl(thiophen-2-yl

• , respectively. Notably, the thiophene derivative was regioselectively arylated at the C4 position and the benzothiophene at the C3 position, which are challenging positions to functionalize using aryl bromides as the coupling partners [58]. Substrates 1–6 contain several reactive C–H bonds in palladium

• -bromopyridine as coupling partners, a C–H arylation on the trifluorobenzene moiety of 14 did not proceed. We surveyed next the reactivity of 3-(2,3,4-trifluorophenyl)thiophene derivatives 5 and 6 in palladium catalyzed direct arylation using the same reaction conditions (Scheme 4). As expected, with 2-pentyl-4

Polythiophene and oligothiophene systems modified by TTF electroactive units for organic electronics

• Alexander L. Kanibolotsky,
• Neil J. Findlay and
• Peter J. Skabara

Beilstein J. Org. Chem. 2015, 11, 1749–1766, doi:10.3762/bjoc.11.191

• Abstract The aim of this review is to give an update on current progress in the synthesis, properties and applications of thiophene-based conjugated systems bearing tetrathiafulvalene (TTF) units. We focus mostly on the synthesis of poly- and oligothiophenes with TTF moieties fused to the thiophene units

• PT conjugated systems with TTF units within the polymer backbone or as pendant units The most straightforward way to modify PT conjugated systems is to incorporate the TTF unit into the polymer backbone or attach it as a pendant unit, as only minor modifications to the synthesis of the TTF/thiophene

• potentiodynamic and potentiostatic electrodeposition. Nevertheless, the labile ester bond and its potential cleavage remain an issue due to formation of acid upon electropolymerisation. Roncali and co-workers used more reliable ether bonds to anchor a TTF moiety to a thiophene monomer via a long aliphatic spacer

An efficient synthesis of N-substituted 3-nitrothiophen-2-amines

• Sundaravel Vivek Kumar,
• Shanmugam Muthusubramanian,
• J. Carlos Menéndez and
• Subbu Perumal

Beilstein J. Org. Chem. 2015, 11, 1707–1712, doi:10.3762/bjoc.11.185

• . Regarding aryl substituents, the thiophene synthesis was compatible with the presence of unsubstituted phenyl rings (compound 3e) and phenyl substituents bearing moderately electron-withdrawing groups such as m- and p-halogens and m-trifluoroalkyl substituents (compounds 3a–d and 3l–n), although substrates

Pyridinoacridine alkaloids of marine origin: NMR and MS spectral data, synthesis, biosynthesis and biological activity

• Louis P. Sandjo,
• Victor Kuete and
• Maique W. Biavatti

Beilstein J. Org. Chem. 2015, 11, 1667–1699, doi:10.3762/bjoc.11.183

• the synthesis of derivatives 43–49, which imitate the ascididemin (42) structure. Compounds 43–45 have one pyridine ring less and do not contain the quinolinophenanthroline core as ascididemin. The pyridine ring missing in the structures of 43–45 has been replaced in 48 and 49, by a thiophene and a

Design and synthesis of hybrid cyclophanes containing thiophene and indole units via Grignard reaction, Fischer indolization and ring-closing metathesis as key steps

• Sambasivarao Kotha,
• Ajay Kumar Chinnam and
• Mukesh E. Shirbhate

Beilstein J. Org. Chem. 2015, 11, 1514–1519, doi:10.3762/bjoc.11.165

• Sambasivarao Kotha Ajay Kumar Chinnam Mukesh E. Shirbhate Department of Chemistry, Indian Institute of Technology-Bombay, Powai, Mumbai-400 076, India, Fax: 022-2572 7152 10.3762/bjoc.11.165 Abstract We demonstrate a new synthetic strategy to cyclophanes containing thiophene and indole moieties

• cyclophanes the development of powerful and general synthetic methods is highly desirable. Herein, we report a new approach to thiophene- and indole-containing hybrid cyclophane derivatives via Grignard addition, Fischer indolization and RCM as key steps. Strategy The retrosynthetic strategy to the target

• cyclophane 1 containing the thiophene and indole moieties is shown in Figure 1. Here, we conceived thiophene-containing diolefin 3 as a possible synthon to assemble the target molecule 1 via 2. Route A involves an RCM of 3 followed by Fischer indolization of 2 (Figure 1). Alternatively, Fischer indolization

Deproto-metallation of N-arylated pyrroles and indoles using a mixed lithium–zinc base and regioselectivity-computed CH acidity relationship

• Mohamed Yacine Ameur Messaoud,
• Ghenia Bentabed-Ababsa,
• Madani Hedidi,
• Aïcha Derdour,
• Floris Chevallier,
• Yury S. Halauko,
• Oleg A. Ivashkevich,
• Vadim E. Matulis,
• Laurent Picot,
• Valérie Thiéry,
• Thierry Roisnel,
• Vincent Dorcet and
• Florence Mongin

Beilstein J. Org. Chem. 2015, 11, 1475–1485, doi:10.3762/bjoc.11.160

• thiophene ring took place. After subsequent interception with iodine, N-(5-iodo-2-thienyl)pyrrole (3a) was isolated in nearly quantitative yield. Under the same reaction conditions, the corresponding indole substrate 2a was similarly converted into N-(5-iodo-2-thienyl)indole (4a) (Scheme 3). Starting from

• (it is delocalized within the aromatic π-electron ring system), a coordination by the sulfur atom of the thiophene substituent could take place with a possible decrease of neighbouring pKa values. As for 1a and 2a, deproto-metallation has not yet been reported for 1b and 2b (Scheme 4 and Figure 5). In

• in A2058 melanoma cells (Figure 6). The best result was obtained with 1f at 10−5 M, which induced 31.9 ± 0.1% growth inhibition in cells treated for 72 h. The linear N-arylated pyrroles 1b and 1e were poorly active. Arylation by a thiophene moiety (1a and 2a) moderately increased the

A new and efficient procedure for the synthesis of hexahydropyrimidine-fused 1,4-naphthoquinones

• Marcelo Isidoro P. Reis,
• Vinícius R. Campos,
• Jackson A. L. C. Resende,
• Fernando C. Silva and
• Vitor F. Ferreira

Beilstein J. Org. Chem. 2015, 11, 1235–1240, doi:10.3762/bjoc.11.137

• naphthoquinones (Figure 1) such as naphtho[2,3-b]furan [5][6][7][8][9][10][11][12][13][14], naphtho-pyran [15][16][17][18], benzo[f]indole [19][20][21][22][23][24], benzo[g]quinolone [25], benzo[b]carbazole [26], naphtho[2,3-b]thiophene [27][28][29][30][31][32][33] and naphtho[2,3-b]]oxazole [34] have been

• pyrrole-, furan- and thiophene-fused naphthoquinones [36]. For several years, our group has been interested in developing new synthetic methods for the preparation of heterocycle-fused 1,4-naphthoquinones or heterocycle-tethered 1,4-naphthoquinones. 1,3-Quinazolines are nitrogenated heterocycles that are

Thiazole-induced rigidification in substituted dithieno-tetrathiafulvalene: the effect of planarisation on charge transport properties

• Rupert G. D. Taylor,
• Joseph Cameron,
• Iain A. Wright,
• Neil Thomson,
• Olena Avramchenko,
• Alexander L. Kanibolotsky,
• Anto R. Inigo,
• Tell Tuttle and
• Peter J. Skabara

Beilstein J. Org. Chem. 2015, 11, 1148–1154, doi:10.3762/bjoc.11.129

• Physical-Organic Chemistry and Coal Chemistry, 02160 Kyiv, Ukraine 10.3762/bjoc.11.129 Abstract Two novel tetrathiafulvalene (TTF) containing compounds 1 and 2 have been synthesised via a four-fold Stille coupling between a tetrabromo-dithienoTTF 5 and stannylated thiophene 6 or thiazole 4. The optical

• demonstrated that the substitution of thiophene units for thiazoles was found to increase the observed charge transport, which is attributed to induced planarity through S–N interactions of adjacent thiazole nitrogen atoms and TTF sulfur atoms and better packing in the bulk. Keywords: non-covalent

• crystal devices. Similarly, oligothiophenes have demonstrated excellent properties for use in both light-emitting [12] and light-harvesting devices [11][13]. Previously, our group reported a series of molecules containing various oligothiophenes fused to a TTF moiety through the central thiophene [11][14

New tris- and pentakis-fused donors containing extended tetrathiafulvalenes: New positive electrode materials for rechargeable batteries

• Shintaro Iwamoto,
• Yuu Inatomi,
• Daisuke Ogi,
• Satoshi Shibayama,
• Yukiko Murakami,
• Minami Kato,
• Kazuyuki Takahashi,
• Kazuyoshi Tanaka,
• Nobuhiko Hojo and
• Yohji Misaki

Beilstein J. Org. Chem. 2015, 11, 1136–1147, doi:10.3762/bjoc.11.128

• Strategy Initiative for Catalysts and Batteries (ESICB), Kyoto University, Katsura, Kyoto 615-8520, Japan 10.3762/bjoc.11.128 Abstract Derivatives of tris-fused TTF extended with two ethanediylidenes (5), tris- and pentakis-fused TTFs extended with two thiophene-2,5-diylidenes (6–9) were successfully

• extended-TTF unit, (iii) increase of the number of (extended) TTF units. As for the modification (ii), insertion of a π-spacer is sometimes useful. A vinylogous TTF (3, Figure 1) [14][15][16] shows lower solubility in ordinary organic solvents than TTF, although the thiophene-containing analog (4, Figure 1

• ) [17][18][19] is more soluble than TTF. Increase of the TTF units might be the best way; however, the preparation of tetrakis- and/or pentakis-fused TTFs is not easy because of the low solubility of the precursor molecules. Insertion of thiophene spacers is a possible strategy for synthesizing fused

Single-molecule conductance of a chemically modified, π-extended tetrathiafulvalene and its charge-transfer complex with F₄TCNQ

• Raúl García,
• M. Ángeles Herranz,
• Edmund Leary,
• M. Teresa González,
• Gabino Rubio Bollinger,
• Marius Bürkle,
• Linda A. Zotti,
• Yoshihiro Asai,
• Fabian Pauly,
• Juan Carlos Cuevas,
• Nicolás Agraït and
• Nazario Martín

Beilstein J. Org. Chem. 2015, 11, 1068–1078, doi:10.3762/bjoc.11.120

• viologen [5][6], aniline [7][8], thiophene [9], anthraquinone [10] and ferrocene [11] have been previously studied. However, a particularly suitable redox-active molecule for molecular electronics is the well-known electron donor tetrathiafulvalene (TTF) molecule. Pristine TTF, as well as the

Thiazole formation through a modified Gewald reaction

• Carl J. Mallia,
• Lukas Englert,
• Gary C. Walter and
• Ian R. Baxendale

Beilstein J. Org. Chem. 2015, 11, 875–883, doi:10.3762/bjoc.11.98

• substitution of the α-carbon to the cyano group. Keywords: design of experiment (DOE); 1,4-dithiane-2,5-diol; Gewald reaction; thiazole; thiophene; Introduction Thiazoles are privileged motifs which are encountered in many naturally occurring bioactive compounds and pharmaceuticals with indications in a

• facile formation of 2-substituted thiazole compounds as core building blocks. Results and Discussion Screening for the bifurcation conditions Initially, the reaction of several nitriles was screened with aldehyde precursor 10 to determine the selectivity between thiophene and thiazole products. In

• original pathway for the thiophene formation (Scheme 1) follows the Gewald mechanism and has already been described [31]. However, the alternative mechanism for the thiazole formation as described herein has not previously been reported and initially presented some queries. We envisaged two putative