Search results

Search for "phosphite" in Full Text gives 120 result(s) in Beilstein Journal of Organic Chemistry.

Synthesis of oligonucleotides on a soluble support

  • Harri Lönnberg

Beilstein J. Org. Chem. 2017, 13, 1368–1387, doi:10.3762/bjoc.13.134

Graphical Abstract
  • with acyl chlorides or chlorophosphates [11][12][13]. On applying the phosphoramidite chemistry, the phosphite triesters obtained are oxidized to phosphate triesters in each coupling cycle, whereas the H-phosphonate diesters may be stable enough to become oxidized only at the end of chain assembly
  • , capping and oxidation (Scheme 4). The building blocks were base-moiety protected 5´-O-DMTr-nucleoside 3´-(2-cyanoethyl-N,N-diisopropylphosphoramidites), i.e., the ones used in standard solid-supported synthesis. Phosphite triesters were oxidized to phosphate triesters after each coupling with tert-butyl
  • -dicyanoimidazole (DCI, 1.5 equiv) as an activator. The resulting phosphite triesters were converted to phosphate esters by conventional aq iodine oxidation. Precipitation by dilution with MeOH removed all traces of reagents and monomeric nucleoside derivatives. As a proof of concept, a pentamer, d(5´-AGCCT-3
PDF
Album
Review
Published 12 Jul 2017

The reductive decyanation reaction: an overview and recent developments

  • Jean-Marc R. Mattalia

Beilstein J. Org. Chem. 2017, 13, 267–284, doi:10.3762/bjoc.13.30

Graphical Abstract
  • the phosphite ligands (39b, 43). Interestingly, an ester group in the α-position increases the reactivity (43). The reaction works well with simple primary and secondary alkyl cyanides but requires a higher reaction temperature. Aliphatic nitriles containing β-hydrogen atoms are successfully reduced
PDF
Album
Review
Published 13 Feb 2017

The synthesis of α-aryl-α-aminophosphonates and α-aryl-α-aminophosphine oxides by the microwave-assisted Pudovik reaction

  • Erika Bálint,
  • Ádám Tajti,
  • Anna Ádám,
  • István Csontos,
  • Konstantin Karaghiosoff,
  • Mátyás Czugler,
  • Péter Ábrányi-Balogh and
  • György Keglevich

Beilstein J. Org. Chem. 2017, 13, 76–86, doi:10.3762/bjoc.13.10

Graphical Abstract
  • -aminophosphonate derivatives embrace the Kabachnik–Fields (phospha-Mannich) three-component condensation, where an amine, an aldehyde or ketone and a >P(O)H reagent, such as a dialkyl phosphite or a secondary phosphine oxide react in a one-pot manner [6][7][8][9][10], and the Pudovik (aza-Pudovik) reaction, in
  • the dialkyl phosphite were applied [43][44][45][46][47][48][49][50][51][52]. The synthesis of α-aryl-α-aminophosphine oxides by the addition of secondary phosphine oxides to imines is much less studied. Only a few publications were found and the reported reactions were performed in solvent (in DEE
  • (Table 1). The products were α-aminophosphonates 2a–d and α-aminophosphine oxide 2e. The addition of 1 equivalent of dimethyl phosphite (DMP) to imine 1a at 80 °C was almost complete after 30 min, and dimethyl ((butylamino)(phenyl)methyl)phosphonate (2a) could be isolated in a yield of 73% (Table 1
PDF
Album
Supp Info
Full Research Paper
Published 12 Jan 2017

First DMAP-mediated direct conversion of Morita–Baylis–Hillman alcohols into γ-ketoallylphosphonates: Synthesis of γ-aminoallylphosphonates

  • Marwa Ayadi,
  • Haitham Elleuch,
  • Emmanuel Vrancken and
  • Farhat Rezgui

Beilstein J. Org. Chem. 2016, 12, 2906–2915, doi:10.3762/bjoc.12.290

Graphical Abstract
  • , followed by thermal Arbuzov rearrangement of the intermediate allyl phosphites (Scheme 1, reaction 1). Recently, an efficient protocol for the conversion of common allyl and benzyl alcohols into the corresponding phosphonates through their treatment with triethyl phosphite and ZnI2, was described [16
  • ]. Similarly, Das and co-workers [17] have directly converted acyclic Morita–Baylis–Hillman (MBH) alcohols into the corresponding allylphosphonates upon their treatment with trialkyl phosphite in the presence of FeCl3 (Scheme 1, reaction 2). On the other hand, treatment of MBH acetates with triethyl phosphite
  • , without any additive, provided, after thermal Arbuzov rearrangement, a variety of diethyl allylphosphonates (Scheme 1, reaction 3) [18]. Moreover, the asymmetric allylic substitution of MBH carbonates with diphenyl phosphonate using chiral thiourea phosphite as catalyst, afforded the related
PDF
Album
Supp Info
Full Research Paper
Published 30 Dec 2016

Microwave-assisted synthesis of (aminomethylene)bisphosphine oxides and (aminomethylene)bisphosphonates by a three-component condensation

  • Erika Bálint,
  • Ádám Tajti,
  • Anna Dzielak,
  • Gerhard Hägele and
  • György Keglevich

Beilstein J. Org. Chem. 2016, 12, 1493–1502, doi:10.3762/bjoc.12.146

Graphical Abstract
  • antibacterial, antiparasitic, anticancer and herbicidal activities [5]. (Aminomethylene)bisphosphonates may be prepared in different ways [5]. One of the most convenient and widespread methods is the three-component condensation involving an amine, an orthoformate and a dialkyl phosphite. Usually, primary or
  • secondary amines were reacted with an equivalent, or a small excess of triethyl orthoformate and 2–7 equivalents of diethyl phosphite [6][7][8][9][10][11][12][13][14][15][16][17][18][19][20][21]. In most cases, the corresponding acids were the target molecules that were obtained by hydrolysis of the esters
  • step is the nucleophilic addition of diethyl phosphite to the C=N bond of the imines resulting in phosphonates III or IV, respectively. Then, the elimination of an amine or ethanol and the addition of another unit of diethyl phosphite may lead to (aminomethylene)bisphosphonates (VI). If the amine is in
PDF
Album
Supp Info
Full Research Paper
Published 19 Jul 2016

Towards potential nanoparticle contrast agents: Synthesis of new functionalized PEG bisphosphonates

  • Souad Kachbi-Khelfallah,
  • Maelle Monteil,
  • Margery Cortes-Clerget,
  • Evelyne Migianu-Griffoni,
  • Jean-Luc Pirat,
  • Olivier Gager,
  • Julia Deschamp and
  • Marc Lecouvey

Beilstein J. Org. Chem. 2016, 12, 1366–1371, doi:10.3762/bjoc.12.130

Graphical Abstract
  • is a procedure developed in our laboratory to introduce the bisphosphonate from acyl chloride and tris(trimethylsilyl)phosphite in one step. Keywords: bisphosphonate; Fe2O3 nanoparticle; polyethylene glycol derivatives; surface ligand synthesis; Introduction Numerous researchers are interested in
  • functionalized substrates. In contrast, our lab has developed a new synthetic strategy starting from an acid chloride and tris(trimethylsilyl) phosphite, followed by a methanolysis step [15]. This one-pot procedure allows the synthesis of various aliphatic and aromatic bisphosphonic acids under mild conditions
  • (trimethylsilyl) phosphite to the acyl chloride derivatives 8 and 9a,b yielded the corresponding silylated PEG-HMBP. The formation of silylated bisphosphonate was monitored by 31P NMR. After evaporation of volatile compounds under vacuum the silylated PEG-HMBP was hydrolyzed with methanol at room temperature for
PDF
Album
Supp Info
Full Research Paper
Published 04 Jul 2016

Multicomponent reactions: A simple and efficient route to heterocyclic phosphonates

  • Mohammad Haji

Beilstein J. Org. Chem. 2016, 12, 1269–1301, doi:10.3762/bjoc.12.121

Graphical Abstract
  • -aminophosphonate 26 in 99% yield (Scheme 7) [34]. The reaction of isatin (27) with diethyl phosphite and benzylamine under similar conditions gave the corresponding α-aminophosphonate 28 in 90% yield together with small amounts of α-hydroxyphosphonate 29 as a side product (Scheme 8). The one-pot reaction of
  • substituted isatins 30 with aniline (32) and dimethyl- or diethyl phosphite under solvent-free conditions in the presence of magnetic Fe3O4 nanoparticle-supported phosphotungstic acid as a recyclable catalyst at 80 °C furnished α-aminophosphonates 33 in yields from 80% to 98% depending on the reaction time
  • and the structure of the dialkyl phosphite and isatin (Scheme 9) [35]. In this way a one-pot three-component reaction between 1-tosylpiperidine-4-one (34), aromatic amines 35 and diethyl phosphonate in the presence of magnesium perchlorate as a catalyst, under neat conditions at 80 °C afforded α
PDF
Album
Review
Published 21 Jun 2016

Synthesis, fluorescence properties and the promising cytotoxicity of pyrene–derived aminophosphonates

  • Jarosław Lewkowski,
  • Maria Rodriguez Moya,
  • Anna Wrona-Piotrowicz,
  • Janusz Zakrzewski,
  • Renata Kontek and
  • Gabriela Gajek

Beilstein J. Org. Chem. 2016, 12, 1229–1235, doi:10.3762/bjoc.12.117

Graphical Abstract
  • further reaction without purification. Aminophosphonates 3Aa–h, 3Ba–e and 3Ca–d, 3Cg have been synthesized via an aza-Pudovik reaction [22], i.e., the addition of the appropriate phosphite 2A–C to the azomethine bond of the Schiff bases 1a–h. Nevertheless, the important modifications had to be introduced
  • dichloromethane solutions with a saturated aqueous sodium bicarbonate solution, which allowed to remove dimethyl phosphite. This procedure was followed by column chromatography, and, in a case of N-benzyl derivative 3Aa, triturating the product with diethyl ether until the precipitation of a solid was
  • . Aminophosphonates 3Ba–e were purified by column chromatography. The most complex procedure was used to isolate and to purify the dibenzyl aminophosphonates 3Ca–d and 3Cg. The crude reaction mixtures were dissolved in small amounts of pyridine and then, treated with elemental iodine to decompose dibenzyl phosphite
PDF
Album
Supp Info
Full Research Paper
Published 16 Jun 2016

Modular synthesis of the pyrimidine core of the manzacidins by divergent Tsuji–Trost coupling

  • Sebastian Bretzke,
  • Stephan Scheeff,
  • Felicitas Vollmeyer,
  • Friederike Eberhagen,
  • Frank Rominger and
  • Dirk Menche

Beilstein J. Org. Chem. 2016, 12, 1111–1121, doi:10.3762/bjoc.12.107

Graphical Abstract
  • on a report of Garcia for a related system we first evaluated Pd2(dba)3 with different phosphite ligands [39]. However, the best results were obtained with the stable catalyst Pd(PPh3)4 and depending on the solvent used, either the syn-isomer 23 or the anti-isomer 24 could be selectively obtained
PDF
Album
Supp Info
Full Research Paper
Published 02 Jun 2016

Nucleic acids through condensation of nucleosides and phosphorous acid in the presence of sulfur

  • Tuomas Lönnberg

Beilstein J. Org. Chem. 2016, 12, 670–673, doi:10.3762/bjoc.12.67

Graphical Abstract
  • Tuomas Lonnberg Department of Chemistry, University of Turku, Vatselankatu 2, FIN-20014 Turku, Finland 10.3762/bjoc.12.67 Abstract Short phosphorothioate oligonucleotides have been prepared by refluxing an equimolar mixture of thymidine and triethylammonium phosphite in toluene in the presence of
  • elemental sulfur. Desulfurization and subsequent digestion of the products by P1 nuclease revealed that nearly 80% of the internucleosidic linkages thus formed were of the canonical 3´,5´-type. Keywords: H-phosphonate; nucleic acid; polymerization; phosphite; sulfurization; Introduction Arguably the most
  • acid [5]. Furthermore, phosphite salts are up to 1000-fold more soluble in water than phosphate salts [6]. For these reasons, compounds of reduced phosphorus (i.e., phosphorus at oxidation state lower than +5) were first proposed to have played a role in prebiotic phosphorylation reactions as early as
PDF
Album
Supp Info
Full Research Paper
Published 11 Apr 2016

Olefin metathesis in air

  • Lorenzo Piola,
  • Fady Nahra and
  • Steven P. Nolan

Beilstein J. Org. Chem. 2015, 11, 2038–2056, doi:10.3762/bjoc.11.221

Graphical Abstract
  • complexes in DCM and toluene in comparison with 85; catalyst loadings were between 1 and 2 mol % and reaction times, with the synthesised complexes, were shorter than with 85. Phosphite-based catalysts In 2010, the Cazin group reported a study on the synthesis and activity of a new family of complexes (98a
  • phosphite-based catalysts. Schiff base–ruthenium complexes synthesized by Verpoort. Synthesis of mixed Schiff base–NHC complexes. RCM in water and MeOH under air.a Metathesis reaction in water under air. Metathesis reactions catalysed by Scorpio-type complexes in air.a RCM with commercially available
PDF
Album
Review
Published 30 Oct 2015

[2.2]Paracyclophane derivatives containing tetrathiafulvalene moieties

  • Laura G. Sarbu,
  • Lucian G. Bahrin,
  • Peter G. Jones,
  • Lucian M. Birsa and
  • Henning Hopf

Beilstein J. Org. Chem. 2015, 11, 1917–1921, doi:10.3762/bjoc.11.207

Graphical Abstract
  • The Cambridge Crystallographic Data Center via http://www.ccdc.cam.ac.uk/data_request/cif. The desulfurative dimerization of 1,3-dithiol-2-thione 6 was effected by heating it with trimethyl phosphite at 100 °C (Scheme 2). Purification of the crude reaction mixture by column chromatography resulted in
PDF
Album
Supp Info
Letter
Published 15 Oct 2015

Nitro-Grela-type complexes containing iodides – robust and selective catalysts for olefin metathesis under challenging conditions

  • Andrzej Tracz,
  • Mateusz Matczak,
  • Katarzyna Urbaniak and
  • Krzysztof Skowerski

Beilstein J. Org. Chem. 2015, 11, 1823–1832, doi:10.3762/bjoc.11.198

Graphical Abstract
  • the first Z-selective catalysts [18][19][20][21]. Their efficiency, however, is noticeably lower than that observed for classical complexes. The second generation indenylidene catalysts with phosphite ligand (frequently reported as “Cazin-type catalysts”) bearing mixed chloride–fluoride or difluoride
PDF
Album
Supp Info
Full Research Paper
Published 06 Oct 2015

Synthesis of racemic and chiral BEDT-TTF derivatives possessing hydroxy groups and their achiral and chiral charge transfer complexes

  • Sara J. Krivickas,
  • Chiho Hashimoto,
  • Junya Yoshida,
  • Akira Ueda,
  • Kazuyuki Takahashi,
  • John D. Wallis and
  • Hatsumi Mori

Beilstein J. Org. Chem. 2015, 11, 1561–1569, doi:10.3762/bjoc.11.172

Graphical Abstract
  • and acetic acid in chloroform. Oxo compound 11 was then cross-coupled with 1.2 equivalents of thione 12 in triethyl phosphite to afford the racemic protected donor 13 in reasonable yield (37%). Basic hydrolysis of the acetyl protecting group afforded the racemic donor 1 in an 81% yield. The syntheses
  • equiv) and the oxo-compound 11 (480 mg, 1.63 mmol, 1 equiv) in triethyl phosphite (10 mL) was stirred overnight at 90 °C. After cooling, hexane was added and the precipitate collected by vacuum filtration and purified by column chromatography (silica gel, 4:1 hexane/ethyl acetate) to afford the cross
  • mmol, 2 equiv) and oxo compound (S,S)-16 (50 mg, 0.14 mmol, 1 equiv) in triethyl phosphite (2 mL) was stirred at 90 °C for 5 hours. After cooling hexane was added, the precipitate collected and purified by column chromatography (silica gel, hexane/ethyl actetate) to afford the enantiopure cross coupled
PDF
Album
Supp Info
Full Research Paper
Published 08 Sep 2015

Ruthenium indenylidene “1st generation” olefin metathesis catalysts containing triisopropyl phosphite

  • Stefano Guidone,
  • Fady Nahra,
  • Alexandra M. Z. Slawin and
  • Catherine S. J. Cazin

Beilstein J. Org. Chem. 2015, 11, 1520–1527, doi:10.3762/bjoc.11.166

Graphical Abstract
  • Stefano Guidone Fady Nahra Alexandra M. Z. Slawin Catherine S. J. Cazin EaStCHEM School of Chemistry, University of St Andrews, St Andrews, UK, KY16 9ST, UK 10.3762/bjoc.11.166 Abstract The reaction of triisopropyl phosphite with phosphine-based indenylidene pre-catalysts affords “1st generation
  • -type ligands. Keywords: 1st generation; indenylidene; metathesis; phosphite; ruthenium; Introduction The olefin metathesis reaction is a powerful tool for C–C bond formation in the synthesis of highly valuable organic compounds [1][2][3][4]. Protocols involving W-, Mo- and Ru-based pre-catalysts can
  • [10][11][12][13][24]. In order to reduce the cost of the Ru-based pre-catalyst, our group has investigated the use of phosphites as an economical alternative to phosphines. The reaction of triisopropyl phosphite with the pyridine-containing indenylidene complex [RuCl2(Ind)(SIMes)(py)] (SIMes = N,N
PDF
Album
Supp Info
Full Research Paper
Published 01 Sep 2015

A new method for the synthesis of α-aminoalkylidenebisphosphonates and their asymmetric phosphonyl-phosphinyl and phosphonyl-phosphinoyl analogues

  • Anna Kuźnik,
  • Roman Mazurkiewicz,
  • Mirosława Grymel,
  • Katarzyna Zielińska,
  • Jakub Adamek,
  • Ewa Chmielewska,
  • Marta Bochno and
  • Sonia Kubica

Beilstein J. Org. Chem. 2015, 11, 1418–1424, doi:10.3762/bjoc.11.153

Graphical Abstract
  • orthoformate, diethyl phosphite and monoethyl methylphosphonite, followed by chromatographic separation of the three possible condensation products and the final hydrolysis, gave the expected phosphinylalkylphosphonic acid in only 17% yield [20]. The stepwise method consisted in the condensation of diethyl
  • -picoline [20]. In 1989, Schrader and Steglich described an example of synthesis of diethyl 1-(N-acylamino)-1-[ethoxy(methylphosphinyl)]methylphosphonate using a Michaelis–Arbuzov-like condensation of the corresponding ethyl [1-(N-acylamino)-1-bromomethyl]methylphosphinate with triethyl phosphite in 79
  • -(dimethylamino)methyl]dipropylphosphine oxide [(Pr)2POCH(NMe2)OEt] with diethyl phosphite in 74% yield [35]. In the present paper we report a novel method for α-phosphonylation, α-phosphinylation or α-phosphinoylation of 1-(N-acetylamino)alkylphosphonates that enables effective transformation of the starting
PDF
Album
Supp Info
Full Research Paper
Published 13 Aug 2015

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

Graphical Abstract
  • constructing a half-unit functionalised with a 1,3-dithiol-2-one, that can undergo a triethyl phosphite-mediated homocoupling to synthesise the central dithienoTTF in the final step. Herein, we present an alternative divergent route to dithienoTTFs, by utilising 4,6,4’,6’-tetrabromo-[2,2’]bis(thieno[3,4-d][1,3
  • ]dithiolylidene) [15] as a core and appending heterocyclic arms through microwave assisted Stille couplings. It is worth noting that the tetrabromo-dithienoTTF core is still prepared via a triethyl phosphite-mediated homocoupling, but in this divergent route valuable heterocyclic groups can be introduced at the
  • the synthesis of a half-unit and a final triethyl phosphite mediated homo-coupling. The resultant compounds, 1 and 2, were fully characterised and their optical and electrochemical properties elucidated via UV–vis spectroscopy and cyclic voltammetry, and explained in conjunction with DFT level
PDF
Album
Supp Info
Full Research Paper
Published 10 Jul 2015

Advances in the synthesis of functionalised pyrrolotetrathiafulvalenes

  • Luke J. O’Driscoll,
  • Sissel S. Andersen,
  • Marta V. Solano,
  • Dan Bendixen,
  • Morten Jensen,
  • Troels Duedal,
  • Jess Lycoops,
  • Cornelia van der Pol,
  • Rebecca E. Sørensen,
  • Karina R. Larsen,
  • Kenneth Myntman,
  • Christian Henriksen,
  • Stinne W. Hansen and
  • Jan O. Jeppesen

Beilstein J. Org. Chem. 2015, 11, 1112–1122, doi:10.3762/bjoc.11.125

Graphical Abstract
  • derivatives can be prepared from 6 and 7 by means of coupling reactions in triethyl phosphite (Scheme 3). The known homocoupling reaction of 6 affords the bis-tosylated BPTTF 5a in high yield with minimal purification [25]. We have obtained a comparable yield (76% vs 84%) working at twice the previously
PDF
Album
Supp Info
Full Research Paper
Published 03 Jul 2015

Regioselective synthesis of chiral dimethyl-bis(ethylenedithio)tetrathiafulvalene sulfones

  • Flavia Pop and
  • Narcis Avarvari

Beilstein J. Org. Chem. 2015, 11, 1105–1111, doi:10.3762/bjoc.11.124

Graphical Abstract
  • -BEDT-TTF precursor. Compounds (S,S)-1 and (R,R)-1 were synthesized in two steps from the corresponding enantiopure dithiole-thiones (S,S)-5 and (R,R)-5 and the dithiolone-dithiopropionitrile 4 (Scheme 2). In the first step the phosphite-mediated heterocoupling between the two units provides the
PDF
Album
Supp Info
Full Research Paper
Published 02 Jul 2015

A hybrid electron donor comprising cyclopentadithiophene and dithiafulvenyl for dye-sensitized solar cells

  • Gleb Sorohhov,
  • Chenyi Yi,
  • Michael Grätzel,
  • Silvio Decurtins and
  • Shi-Xia Liu

Beilstein J. Org. Chem. 2015, 11, 1052–1059, doi:10.3762/bjoc.11.118

Graphical Abstract
  • (0.160 g, 0.5 mmol) in toluene (50 mL) was added dropwise into a hot solution of 3 (0.212, 0.5 mmol) and triethyl phosphite (10 mL) in toluene (50 mL) under nitrogen protection. The resulting mixture was stirred at reflux overnight. After removing the solvent under reduced pressure, the residue was
  • (hexylthio)-1,3-dithiole-2-thione (0.090 g, 0.2 mmol) in toluene (50 mL) was added dropwise into a hot solution of 5 (0.101 g, 0.2 mmol) and triethyl phosphite (5 mL) in toluene (100 mL) under nitrogen protection. The resulting mixture was stirred at reflux overnight. After removing the solvent under reduced
PDF
Album
Full Research Paper
Published 22 Jun 2015

Synthesis and characterization of the cyanobenzene-ethylenedithio-TTF donor

  • Sandrina Oliveira,
  • Dulce Belo,
  • Isabel C. Santos,
  • Sandra Rabaça and
  • Manuel Almeida

Beilstein J. Org. Chem. 2015, 11, 951–956, doi:10.3762/bjoc.11.106

Graphical Abstract
  • -tetrathiafulvalene (CNB-EDT-TTF), was obtained in high yield, by a cross-coupling reaction with triethyl phosphite between 2-thioxobenzo[d][1,3]dithiole-5-carbonitrile and 5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-one. This new donor was characterized namely by single crystal X-ray diffraction, cyclic
  • pure triethyl phosphite during 4 hours at 130 °C leading to the formation of 3 in relatively high yield (63%) (Scheme 1). This coupling reaction also gives rise to smaller amounts of BEDT-TTF (14% yield) and dicyanodibenzene tetrathiafulvalene (dcdb-TTF) [13] as byproducts resulting from homocoupling
  • anisotropic thermal parameters whereas H-atoms were placed in idealised positions and allowed to refine riding on the parent C atom. Molecular graphics were prepared using MERCURY 1.4.2 [29]. General procedure for the synthesis of 3 In freshly destilled triethyl phosphite (10 mL), 2-thioxobenzo[d][1,3
PDF
Album
Supp Info
Letter
Published 03 Jun 2015

Tuning of tetrathiafulvalene properties: versatile synthesis of N-arylated monopyrrolotetrathiafulvalenes via Ullmann-type coupling reactions

  • Vladimir A. Azov,
  • Diana Janott,
  • Dirk Schlüter and
  • Matthias Zeller

Beilstein J. Org. Chem. 2015, 11, 860–868, doi:10.3762/bjoc.11.96

Graphical Abstract
  • in hot triethyl or trimethyl phosphite. Using the second approach [17][18][19], the aryl group is attached to the MPTTF moiety using a direct copper-mediated Ullmann-type N-arylation reaction [20][21]; this method was also used for the preparation of arylated bis-pyrrolotetrathiafulvalenes 2
PDF
Album
Supp Info
Full Research Paper
Published 21 May 2015

Trifluoromethyl-substituted tetrathiafulvalenes

  • Olivier Jeannin,
  • Frédéric Barrière and
  • Marc Fourmigué

Beilstein J. Org. Chem. 2015, 11, 647–658, doi:10.3762/bjoc.11.73

Graphical Abstract
  • -withdrawing groups (EWG) is obtained by phosphite coupling involving CF3-substituted 1,3-dithiole-2-one derivatives. The relative effects of the EWG such as CF3, CO2Me and CN on the TTF core were investigated from a combination of structural, electrochemical, spectrochemical and theoretical investigations
  • MeOH gives the corresponding primary amide 7 in 63% yield. Its dehydration with POCl3 in sulfolane gives 2ac in 60% yield. A similar phosphite-based cross-coupling reaction between the bis(trifluoromethyl)-1,3-dithiole-2-one derivative 9cc and the diester derivative 10bb gave the TTF 3bc in 15% yield
PDF
Album
Supp Info
Full Research Paper
Published 06 May 2015

TTFs nonsymmetrically fused with alkylthiophenic moieties

  • Rafaela A. L. Silva,
  • Bruno J. C. Vieira,
  • Marta M. Andrade,
  • Isabel C. Santos,
  • Sandra Rabaça,
  • Dulce Belo and
  • Manuel Almeida

Beilstein J. Org. Chem. 2015, 11, 628–637, doi:10.3762/bjoc.11.71

Graphical Abstract
  • analogous transition metals complexes, enabling their processing from solutions. Results and Discussion Synthesis The TTF donors fused non-symetrically with substituted thiophene moieties 1 and 2 were obtained by the cross coupling, in the presence of trimethyl phosphite, between compounds I and II and
PDF
Album
Supp Info
Full Research Paper
Published 05 May 2015

Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams

  • Katherine M. Byrd

Beilstein J. Org. Chem. 2015, 11, 530–562, doi:10.3762/bjoc.11.60

Graphical Abstract
  • -acylpyrroles [265] (Scheme 39). In their work, diethylzinc and 147 acts as a bifunctional catalyst system where the α,β-unsaturated system is activated through Lewis acid coordination and the catalyst acts as a directing group for the phosphite. Overall the reaction proceeds in both high yield and
PDF
Album
Review
Published 23 Apr 2015
Other Beilstein-Institut Open Science Activities