Parallel and four-step synthesis of natural-product-inspired scaffolds through modular assembly and divergent cyclization

• Hiroki Oguri,
• Haruki Mizoguchi,
• Hideaki Oikawa,
• Aki Ishiyama,
• Masato Iwatsuki,
• Kazuhiko Otoguro and
• Satoshi Ōmura

Beilstein J. Org. Chem. 2012, 8, 930–940, doi:10.3762/bjoc.8.105

• cytotoxic activities. Incorporation of dimethyl substituents on the scaffold resulted in diminished activity (41b: IC50 = 5.89 μg/mL) (Table 1, entry 3). Removal of the nosyl group (39b→39c) also caused substantial loss of the activities, suggesting the critical role of the aromatic sulfone amide moiety

Synthesis and characterization of a novel carboxyl group containing (co)polyimide with sulfur in the polymer backbone

• Miroslav Mrsevic,
• David Düsselberg and
• Claudia Staudt

Beilstein J. Org. Chem. 2012, 8, 776–786, doi:10.3762/bjoc.8.88

• previous work of our group showed that the imidization degree of chemically converted PAAs is superior to thermally imidized PAAs [24]. Aromatic diamines as shown in Scheme 1, carrying either sulfone (3,3′-diaminodiphenyl sulfone, 3,3′-DDS), or (as partly described in a previous work from our group

• ). Similar results were found for the sulfone-containing 6FDA-3,3′-DDS/6FDA-DABA 4:1, which is shown in Figure 4. All synthesized (co)polyimides showed the expected vibrational bands. GPC measurements Gel permeation chromatography (GPC) measurements of the synthesized (co)polyimides were performed in order

• -mentioned behavior. Apparently, the sulfide-containing (co)polyimides exhibit higher Tg values than the sulfone-containing (co)polyimides. This is due to the differently substituted aromatic diamines. The para-substituted 4,4′-SDA induces a higher stiffness compared to the meta-substituted 3,3′-DDS, which

Derivatives of phenyl tribromomethyl sulfone as novel compounds with potential pesticidal activity

• Krzysztof M. Borys,
• Maciej D. Korzyński and
• Zbigniew Ochal

Beilstein J. Org. Chem. 2012, 8, 259–265, doi:10.3762/bjoc.8.27

• tribromomethyl phenyl sulfone derivatives as novel potential pesticides is reported. The title sulfone was obtained by following three different synthetic routes, starting from 4-chlorothiophenol or 4-halogenphenyl methyl sulfone. Products of its subsequent nitration were subjected to the SNAr reactions with

• . Keywords: 2-nitroaniline derivatives; phenylhydrazones; pesticides; SNAr reaction; tribromomethyl sulfone derivatives; Introduction The rapid growth of the world population results in a continous increase in the demand for food. At the same time, about 35% of the global crops around the world are being

• containing a tribromomethylsulfonyl group, including derivatives of nitroaniline, nitrophenylhydrazine, diphenyl ether and benzimidazole (Scheme 1). All the target molecules are derived from a common precursor, namely 4-halogenphenyl tribromomethyl sulfone, efficiently synthesized from inexpensive 4

Improved syntheses of high hole mobility phthalocyanines: A case of steric assistance in the cyclo-oligomerisation of phthalonitriles

• Daniel J. Tate,
• Rémi Anémian,
• Richard J. Bushby,
• Suwat Nanan,
• Stuart L. Warriner and
• and Benjamin J. Whitaker

Beilstein J. Org. Chem. 2012, 8, 120–128, doi:10.3762/bjoc.8.14

• bis-alkylation of thiophene (1), oxidation to the corresponding sulfone 3, and treatment with fumaronitrile (Scheme 1, top line). However, for most of the phthalonitriles we have made, we have found that a much better route is the nickel-catalysed reaction of an alkylzinc iodide with the bistriflate

Synthesis and oxidation of some azole-containing thioethers

• Andrei S. Potapov,
• Nina P. Chernova,
• Vladimir D. Ogorodnikov,
• Tatiana V. Petrenko and
• Andrei I. Khlebnikov

Beilstein J. Org. Chem. 2011, 7, 1526–1532, doi:10.3762/bjoc.7.179

• characterized. Oxidation of the pyrazole-containing thioether by hydrogen peroxide proceeds selectively to provide a sulfoxide or sulfone, depending on the amount of oxidant used. Oxidation of the benzotriazole derivative by hydrogen peroxide is not selective, and sulfoxide and sulfone form concurrently

• . Selenium dioxide-catalyzed oxidation of benzotriazole thioether by H2O2, however, proceeds selectively and yields sulfoxide only. Keywords: azole; oxidation; sulfone; sulfoxide; thioether; Introduction Compounds comprising two pyrazole moieties linked by an aliphatic spacer act as bidentate chelating

• through its conversion to sulfoxide or sulfone derivatives. In this report we present the synthesis of pyrazole and benzotriazole thioether ligands and their oxidation to the corresponding sulfoxides and sulfones. Results and Discussion 1-(2-Hydroxyethyl)-3,5-dimethylpyrazole (1), the starting compound

Rh(I)-catalyzed intramolecular [2 + 2 + 1] cycloaddition of allenenes: Construction of bicyclo[4.3.0]nonenones with an angular methyl group and tricyclo[6.4.0.0^1,5]dodecenone

• Fuyuhiko Inagaki,
• Naoya Itoh,
• Yujiro Hayashi,
• Yumi Matsui and
• Chisato Mukai

Beilstein J. Org. Chem. 2011, 7, 404–409, doi:10.3762/bjoc.7.52

• proximal double bond of the allene might be mandatory. Removal of the allylic sulfone group in 2a was achieved by tributyltin hydride in the presence of AIBN to give 9g in 91% yield [35][36][37][38][39][40][41]. Thus, the phenylsulfonyl group of 2a can be regarded as a hydrogen surrogate and this procedure

Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation

• Vladimir N. Boiko

Beilstein J. Org. Chem. 2010, 6, 880–921, doi:10.3762/bjoc.6.88

Synthesis, characterization and photoinduced curing of polysulfones with (meth)acrylate functionalities

• Cemil Dizman,
• Sahin Ates,
• Lokman Torun and
• Yusuf Yagci

Beilstein J. Org. Chem. 2010, 6, No. 56, doi:10.3762/bjoc.6.56

• bands for the polyether sulfone backbone. The new broad but weak peak around 3435 cm−1 indicates the presence of phenolic end groups. Attachment of polymerizable acrylate and methylacrylate functional groups through the esterification process was evidenced by the disappearance of this peak and the

• appears in all the spectra at 1.69 ppm. The shifts between 6.70 and 7.86 ppm correspond to the aromatic protons of the poly(ether sulfone) backbone. The phenolic protons were not observed, probably due to the relatively high molecular weight of the precursor polymers. Distinctively, the aromatic protons

• important components of UV curable formulations for obtaining networks that could have application in coatings and membranes. Experimental Materials Bisphenol A and bis(p-chlorophenyl) sulfone (Hallochem Pharma Co. Ltd, China), methanol (Merck), dimethylacetamide (DMA, 99%, Merck) were used without any

Mitomycins syntheses: a recent update

• Jean-Christophe Andrez

Beilstein J. Org. Chem. 2009, 5, No. 33, doi:10.3762/bjoc.5.33

Reduction of arenediazonium salts by tetrakis(dimethylamino)ethylene (TDAE): Efficient formation of products derived from aryl radicals

• Mohan Mahesh,
• John A. Murphy,
• Franck LeStrat and
• Hans Peter Wessel

Beilstein J. Org. Chem. 2009, 5, No. 1, doi:10.3762/bjoc.5.1

• like a sulfide, sulfoxide or sulfone is necessary for the self-termination of the 5-exo-trig radical cyclization reactions to avoid competing intermolecular radical side-reactions. The TDAE-mediated radical-based addition-elimination route for the construction of indole ring systems warranted anhydrous

Recent progress on the total synthesis of acetogenins from Annonaceae

• Nianguang Li,
• Zhihao Shi,
• Yuping Tang,
• Jianwei Chen and
• Xiang Li

Beilstein J. Org. Chem. 2008, 4, No. 48, doi:10.3762/bjoc.4.48

• intermediate 31; further manipulation and chain elongation at both ends of 31 produced an advanced intermediate 32. The anion of the phenyl sulfone 33, readily prepared from D-glutamic acid, was condensed directly with the ester function of 32 to give the α-keto sulfone 34, which was futher elaborated to ester

Radical cascades using enantioenriched 7-azabenzonorbornenes and their applications in synthesis

• David M. Hodgson and
• Leonard H. Winning

Beilstein J. Org. Chem. 2008, 4, No. 38, doi:10.3762/bjoc.4.38

• -observed trend that alkenes bearing less strongly electron-withdrawing substituents were less effective electrophiles in this reaction. Phenyl vinyl sulfone gave trapped rearranged azacycle 13 in 43% yield, with rearranged–reduced azacycle 8 also isolated in 38% yield, suggesting that the rate of

• electrophile trapping with the sulfone corresponds approximately to the rate of hydrogen atom transfer from (TMS)3SiH. Attempted reaction with methyl vinyl ketone, N,N-dimethylacrylamide and methyl propiolate gave rearranged-reduced azacycle 8 in modest yields, as well as small quantities of hydrosilylated

• electrophile (for details see Supporting Information File 1) [26]. Having probed the generality of the reaction, attempts were made to optimise the yields of the electrophile trapping. These studies were performed with phenyl vinyl sulfone, since this had undergone partial electrophile trapping and partial

The role of an aromatic group in remote chiral induction during conjugate addition of α-sulfonylallylic carbanions to ethyl crotonate

• Shlomo Levinger,
• Ranjeet Nair and
• Alfred Hassner

Beilstein J. Org. Chem. 2008, 4, No. 32, doi:10.3762/bjoc.4.32

• -substituted allyl sulfone 1, containing a stereogenic center, proceeded with diastereoselectivity of greater than 8:2 (ratio of 3 to 4), when the Ar substituent in 1 was phenyl or 1-naphthyl (Scheme 1). On the other hand, when this substituent (Ar in Scheme 1) was cyclohexyl, no selectivity at all was

• observed (dr 1:1). We had proposed that π–Li+ interaction may be responsible for this phenomenon. We had shown earlier [2] that conjugate addition of lithiated allyl sulfone 5 to unsaturated esters of type 2 takes place α-regioselectively and almost exclusively in an anti fashion (where the syn and anti

• by X-ray analysis) to have the 3R,4S absolute configuration [1]. It was important to examine the effect of other aromatic substituents Ar in amino-substituted sulfone 1 and their influence on this remote induction of chirality, in the hope of further improving the remote diastereoselectivity. We

Efficient 1,4-addition of α-substituted fluoro(phenylsulfonyl)methane derivatives to α,β-unsaturated compounds

• G. K. Surya Prakash,
• Xiaoming Zhao,
• Sujith Chacko,
• Fang Wang,
• Habiba Vaghoo and
• George A. Olah

Beilstein J. Org. Chem. 2008, 4, No. 17, doi:10.3762/bjoc.4.17

• -addition to α,β-unsaturated esters, ketones, sulfone, nitriles and propynoates. Supporting Information Supporting Information File 83: Experimental procedures, full spectroscopic data and spectra. Supporting Information File 84: Spectra. Acknowledgements Support of our work by the Loker Hydrocarbon

The enantiospecific synthesis of (+)-monomorine I using a 5-endo- trig cyclisation strategy

• Malcolm B. Berry,
• Donald Craig,
• Philip S. Jones and
• Gareth J. Rowlands

Beilstein J. Org. Chem. 2007, 3, No. 39, doi:10.1186/1860-5397-3-39

• University, Private Bag 11 222, Palmerston North, New Zealand 10.1186/1860-5397-3-39 Abstract We have developed a general strategy for the synthesis of 2,5-syn disubstituted pyrrolidines that is based on the multi-faceted reactivity of the sulfone moiety and a 5-endo-trig cyclisation. This methodology was

• , such as tetrahydrofurans and pyrrolidines, makes these motifs attractive targets for synthesis. Over the last decade we have developed a powerful general strategy for the preparation of such compounds based upon the multi-faceted reactivity of the sulfone group and the formally disfavoured 5-endo-trig

• mode of cyclisation. [1][2][3][4][5][6] The methodology allows the conversion of epoxides (X = O) or aziridines (X = N-PG) (2) into the desired trisubstituted tetrahydrofurans or pyrrolidines (5) via a series of sulfone-mediated transformations (Scheme 1). Ring-opening 2 with the sulfone-stabilised