Syntheses of spliceostatins and thailanstatins: a review

• William A. Donaldson

Beilstein J. Org. Chem. 2020, 16, 1991–2006, doi:10.3762/bjoc.16.166

• oxidation stereoselectively generated the spirocyclic epoxide 76. A second-protecting group shuffle afforded the primary alcohol 77. A Mitsunobu substitution of 77 with 2-mercaptobenzothiazole, followed by an oxidation with a large excess of mCPBA afforded the sulfone 78. While not producing the identical

• afforded the fragment 125. The cross-metathesis of 125 with an excess of methacrolein in the presence of the Ru catalyst 122 gave the aldehyde 126. This coupling is analogous to Koide’s cross-metathesis of 121 (cf. Scheme 20). A modified Julia olefination of 126 with the anion generated from the sulfone 78

• , followed by the cleavage of the 4’-TBS protecting group gave 127 in an acceptable yield (52%). A protecting-group adjustment finalized the synthesis of 124. Notably, these authors found that switching the sulfone and aldehyde functionalities, i.e., an olefination of the aldehyde generated by the oxidation

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

• investigations on their more stable analogs resulted in the synthesis of stable 1-O-phoshono-β-ᴅ-psicofuranosyl sulfone, which was prepared by a simultaneous phosphorylation and oxidation of ethyl 2-thio-β-ᴅ-psicofuranoside with dibenzyl N,N-dimethylphosphoramidite catalyzed by 1H-tetrazole and followed by

• thiol from exo-face of the bicyclic skeleton. Subsequent simultaneous phosphorylation and oxidation of ethyl 2-thio-ᴅ-tagatofuranoside 13 under identical conditions as used for the fructofuranose pathway provided 1-O-dibenzyloxyphosphoryl-ᴅ-tagatofuranosyl sulfone 14 (Scheme 3). Removal of the pivaloyl

Pauson–Khand reaction of fluorinated compounds

• Jorge Escorihuela,
• Daniel M. Sedgwick,
• Alberto Llobat,
• Mercedes Medio-Simón,
• Pablo Barrio and
• Santos Fustero

Beilstein J. Org. Chem. 2020, 16, 1662–1682, doi:10.3762/bjoc.16.138

• testing a variety of reaction conditions. More complex biorelevant examples such as isatin derivatives were also suitable substrates, affording the corresponding spirocyclic derivatives, albeit in low yields (Scheme 21) [59]. Unfortunately, thioether and sulfone-based linkers were unsuitable in this

Heterogeneous photocatalysis in flow chemical reactors

• Christopher G. Thomson,
• Ai-Lan Lee and
• Filipe Vilela

Beilstein J. Org. Chem. 2020, 16, 1495–1549, doi:10.3762/bjoc.16.125

• (Figure 11) [129]. Four conjugated polymers containing dibenzothiophene sulfone (FSO) monomers, linked by either biphenyl (FSO-BP), fluorene (FSO-F), 2,8-dibenzothiophene (FSO-FSz), or 3,7-dibenzothiophene (FSO-FS) monomers were synthesised and applied in the photocatalytic hydrogen evolution reaction

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

Asymmetric synthesis of CF₂-functionalized aziridines by combined strong Brønsted acid catalysis

• Xing-Fa Tan,
• Fa-Guang Zhang and
• Jun-An Ma

Beilstein J. Org. Chem. 2020, 16, 638–644, doi:10.3762/bjoc.16.60

• Tianjin University, Fuzhou 350207, China 10.3762/bjoc.16.60 Abstract A diastereo- and enantioselective approach to access chiral CF2-functionalized aziridines from difluorodiazoethyl phenyl sulfone (PhSO2CF2CHN2) and in situ-formed aldimines is described. This multicomponent reaction is enabled by a

• phosphoric acid (Scheme 1a) [26]. In comparison, there is a significant dearth of available synthetic approaches to CF2-functionalized aziridines, particularly in a stereocontrolled manner. Indeed, a handful of reported methods document the employment of difluoromethylimines, difluoromethyl phenyl sulfone

• phenyl sulfone under mild conditions by a combined strong Brønsted acid system consisting of chiral disulfonimide and 2-carboxyphenylboronic acid. The optical purity of the obtained CF2-substituted aziridines could be further improved by a practical dissolution–filtration procedure. Substrate expansion

Recent advances in photocatalyzed reactions using well-defined copper(I) complexes

• Mingbing Zhong,
• Xavier Pannecoucke,
• Philippe Jubault and
• Thomas Poisson

Beilstein J. Org. Chem. 2020, 16, 451–481, doi:10.3762/bjoc.16.42

• isolated in moderate to good yields. Using the more reactive allyl sulfone, a panel of symmetrical diaryliodonium salts was reacted, giving the products in good yields. The authors conducted some mechanistic studies and suggested a plausible catalytic cycle involving [Cu(I)]/[Cu(I)]*/[Cu(II)] species. The

Copper-promoted/copper-catalyzed trifluoromethylselenolation reactions

• Clément Ghiazza and
• Anis Tlili

Beilstein J. Org. Chem. 2020, 16, 305–316, doi:10.3762/bjoc.16.30

• arylcopper(I) species was the key intermediate. Terminal alkynes were also investigated under similar reaction conditions (Scheme 13) [37]. Aromatic and π-activated aliphatic substrates led to the desired products in moderate to very good yields. Moreover, vinyl sulfone derivatives were formed when the

Iodine-mediated hydration of alkynes on keto-functionalized scaffolds: mechanistic insight and the regiospecific hydration of internal alkynes

• Zachary Lee,
• Brandon R. Jones,
• Nyochembeng Nkengbeza,
• Michael Phillips,
• Kayla Valentine,
• Alexis Stewart,
• Brandon Sellers,
• Nicholas Shuber and
• Karelle S. Aiken

Beilstein J. Org. Chem. 2019, 15, 2747–2752, doi:10.3762/bjoc.15.265

• were used to probe the existence of an α-iodo intermediate 9, and methodology work was used to investigate the outcome of the reaction using alkyl-capped, asymmetric, internal alkynes 11. The NMR investigations utilized different electrophilic iodine sources and the β-keto sulfone 8, which allowed for

• intermediate 9, we turned our attention to investigating the reaction of internal alkynes 11 to examine the regioselectivity of the hydration process. Ester, sulfone, and phosphonate substrates were employed and, in all cases, the internal alkyne unit was capped by an ethyl group (Scheme 2). In general

• recovered. In contrast, the phosphonate 11d and the sulfone 11e smoothly converted to 15d and 15e in yields of 68% and 71%, respectively. The hydration of the phosphonate required 22 h, while the reaction of the sulfone was complete in 3.5 h. Overall, successful outcomes were obtained for the phosphonate

Fluorine-containing substituents: metabolism of the α,α-difluoroethyl thioether motif

• Andrea Rodil,
• Alexandra M. Z. Slawin,
• Nawaf Al-Maharik,
• Ren Tomita and
• David O’Hagan

Beilstein J. Org. Chem. 2019, 15, 1441–1447, doi:10.3762/bjoc.15.144

• significantly more slowly to the sulfone. When the substrate was (p-OMe)PhSCF2CH3, then the resultant (demethylated) phenol sulfoxide had an enantiomeric excess of 60%, and when the substrate was the β-substituted-SCF2CH3 naphthalene, then the enantiomeric excess of the resultant sulfoxide was 54%. There was no

• 19F NMR spectrum consistent with non-equivalence of the fluorines, immediately indicative of sulfoxide formation. Isolation and subsequent 1H and 19F NMR analyses as well as high-resolution mass spectrometry secured the identity of these metabolites as sulfoxides 6 and 7 and sulfone 8. The structure

• . Sulfone 8 was a relatively minor metabolite, at only 10% of sulfoxide 6. A chiral HPLC (IC column, solvent: 5% isopropanol in hexane; 1 mL/min) enantiomeric assay was conducted for sulfoxide 6 and the outcome compared with a racemic sample of 6, prepared by chemical oxidation of thioether 4 [22]. Although

Synthesis of non-racemic 4-nitro-2-sulfonylbutan-1-ones via Ni(II)-catalyzed asymmetric Michael reaction of β-ketosulfones

• Alexander N. Reznikov,
• Anastasiya E. Sibiryakova,
• Marat R. Baimuratov,
• Eugene V. Golovin,
• Victor B. Rybakov and
• Yuri N. Klimochkin

Beilstein J. Org. Chem. 2019, 15, 1289–1297, doi:10.3762/bjoc.15.127

• 5-HT1 receptor agonist for the treatment of migraine) [7], and apremilast (3, Otezla®, inhibitor of the PDE4 for the treatment of certain types of psoriasis and psoriatic arthritis) [8] (Figure 1). Recently we have shown that racemic sulfone 4 exhibits high antiviral activity against BVDV with low

• 8a or 9a. Оne of the stereoisomers can be formed directly during the reaction. To test this hypothesis, we decided to study the evolution of dr on the course of reaction by 1H NMR spectroscopy (Figure 3). The reaction of sulfone 5a with ω-nitrostyrene (6a) was chosen as the model reaction. Conversion

• was determined by decrease of the integral intensity of the sulfone 5a methylene group signal at 4.75 ppm. The diastereomers 8a:9a ratio was determined by the ratio of the integral intensities of signals of the methine groups of 8a and 9a at 4.62–4.57 and 4.53–4.47 ppm, respectively. As the studies

An anomalous addition of chlorosulfonyl isocyanate to a carbonyl group: the synthesis of ((3aS,7aR,E)-2-ethyl-3-oxo-2,3,3a,4,7,7a-hexahydro-1H-isoindol-1-ylidene)sulfamoyl chloride

• Aytekin Köse,
• Aslı Ünal,
• Ertan Şahin,
• Uğur Bozkaya and
• Yunus Kara

Beilstein J. Org. Chem. 2019, 15, 931–936, doi:10.3762/bjoc.15.89

• material was 2-ethyl-3a,4,7,7a-tetrahydro-1H-isoindole-1,3(2H)-dione (9), which we have synthesized in previous studies [16][17]. Imide 9 was synthesized via the cycloaddition of 3-sulfone to maleic anhydride. The reaction of ethylamine with anhydride 8 in the presence of a toluene/triethylamine mixture (3

An efficient and concise access to 2-amino-4H-benzothiopyran-4-one derivatives

• Peng Li,
• Yongqi Wu,
• Tingting Zhang,
• Chen Ma,
• Ziyun Lin,
• Gang Li and
• Haihong Huang

Beilstein J. Org. Chem. 2019, 15, 703–709, doi:10.3762/bjoc.15.65

• and ethyl sulfone 3, respectively (Scheme 2). With the substrates including sulfide, sulfoxide and sulfone in hand, we screened various solvents with compounds 1a, 2a, 3a and 1-benzylpiperazine as the model substrates and the results are summarized in Table 1. No target compound 4a was obtained at

• , thereby providing opportunities for discovering more active compounds for medicinal chemistry research. Representative strategies for the synthesis of N-substituted 2-aminobenzothiopyranones. The synthesis of sulfide 1, sulfoxide 2, and sulfone 3. Scope of the synthesis of versatile 2

Thiol-free chemoenzymatic synthesis of β-ketosulfides

• Adrián A. Heredia,
• Martín G. López-Vidal,
• Marcela Kurina-Sanz,
• Fabricio R. Bisogno and
• Alicia B. Peñéñory

Beilstein J. Org. Chem. 2019, 15, 378–387, doi:10.3762/bjoc.15.34

• generate the corresponding chiral sulfoxides or sulfone derivatives [32]. Multicomponent reactions (MCRs), in which three or more reagents react giving rise to generally complex molecules in one-pot, have arisen as a powerful tool to connect fragments in a simple manner, avoiding cost and time-consuming

• chromatography (petroleum ether/EtOAc 9:1) a 68% isolated yield was obtained for the S-allyl-β-ketosulfide 2h. The obtained β-ketosulfides can be chemoselectively converted into the corresponding sulfoxide/sulfone derivative [47][48]. It is well known that β-ketosulfoxides and β-ketosulfones are valuable

Synthesis of mono-functionalized S-diazocines via intramolecular Baeyer–Mills reactions

• Miriam Schehr,
• Daniel Hugenbusch,
• Tobias Moje,
• Christian Näther and
• Rainer Herges

Beilstein J. Org. Chem. 2018, 14, 2799–2804, doi:10.3762/bjoc.14.257

• sulfur bridge is oxidized to the sulfoxide or sulfone. Hence, neither reductive nor oxidative conditions are compatible with the –CH2-S– bridge. An alternative strategy, that applies weakly acidic conditions is the condensation of aryl nitroso compounds with anilines. This Baeyer–Mills reaction was

Unprecedented nucleophile-promoted 1,7-S or Se shift reactions under Pummerer reaction conditions of 4-alkenyl-3-sulfinylmethylpyrroles

• Takashi Go,
• Akane Morimatsu,
• Hiroaki Wasada,
• Genzoh Tanabe,
• Osamu Muraoka,
• Yoshiharu Sawada and
• Mitsuhiro Yoshimatsu

Beilstein J. Org. Chem. 2018, 14, 2722–2729, doi:10.3762/bjoc.14.250

• determined by analysing the single-crystal X-ray diffraction spectrum of the corresponding sulfone of 4a; the structure was a pyrrole bearing both 3-sulfanylmethyl and 4-allylaminomethyl groups (see Supporting Information File 1). To develop a useful Pummerer reaction procedure, we selected allylamine

• Information For crystallographic data see also CCDC 1824587 and 1824588. Supporting Information File 226: Schemes S1 and S2 on the syntheses of compounds 1, 2, and 3a–g; the NMR study for the structure determinations, further DFT calculations, the ORTEP drawing of both sulfone of 5a, 11d and the 1H and 13C

• NMR charts. Supporting Information File 227: Crystallographic information of compound 11d. Supporting Information File 228: Crystallographic information of the sulfone of compound 5a.

Learning from B₁₂ enzymes: biomimetic and bioinspired catalysts for eco-friendly organic synthesis

• Keishiro Tahara,
• Ling Pan,
• Toshikazu Ono and
• Yoshio Hisaeda

Beilstein J. Org. Chem. 2018, 14, 2553–2567, doi:10.3762/bjoc.14.232

• (III) form of 1 has recently been found to catalyze atom transfer radical addition of alkyl halides to olefins (phenyl vinyl sulfone and acrylates) in the presence of NaBH4 [115]. In addition, a new light-driven method for generating acyl radicals from 2-S-pyridyl thioesters was developed through the

Visible light-mediated difluoroalkylation of electron-deficient alkenes

• Vyacheslav I. Supranovich,
• Vitalij V. Levin,
• Marina I. Struchkova,
• Jinbo Hu and
• Alexander D. Dilman

Beilstein J. Org. Chem. 2018, 14, 1637–1641, doi:10.3762/bjoc.14.139

• were coupled with alkenes 2 (Figure 1). Esters and amides of acrylic acid, acrylonitrile, and vinyl phosphonate used in a small excess (1.2 equiv) were successfully fluoroalkylated. For vinyl(phenyl)sulfone, significant amounts of hydrodeiodination product RfH was formed, likely because of the

• decreased reactivity of the sulfone double bond toward fluorinated radicals. In this case, two equivalents of the alkene have to be used to achieve good yields of products 3t,u. It should also be pointed out that the reaction tolerates aromatic bromide substituents (products 3b,c,n,o), a boryl fragment

Oligonucleotide analogues with cationic backbone linkages

• Melissa Meng and
• Christian Ducho

Beilstein J. Org. Chem. 2018, 14, 1293–1308, doi:10.3762/bjoc.14.111

• motifs. Such artificial neutral linkages include, among others, sulfone [14], amide [15][16][17][18][19][20][21][22], triazole [23][24][25][26][27], phosphoramidate [28] and phosphate triester [29] moieties. Using a different approach, positive charges have been introduced into nucleic acid structures

Recent advances on organic blue thermally activated delayed fluorescence (TADF) emitters for organic light-emitting diodes (OLEDs)

• Thanh-Tuân Bui,
• Fabrice Goubard,
• Malika Ibrahim-Ouali,
• Didier Gigmes and
• Frédéric Dumur

Beilstein J. Org. Chem. 2018, 14, 282–308, doi:10.3762/bjoc.14.18

• , theoretical calculations also showed the higher electron-accepting ability of the phenoxathiin dioxide moiety compared to that of the phenoxaphosphine oxide group owing to the stronger electron-withdrawing properties of the sulfone group, with a theoretical LUMO level at −1.52 and −1.24 eV for P2 and P1

Transition-metal-free [3 + 3] annulation of indol-2-ylmethyl carbanions to nitroarenes. A novel synthesis of indolo[3,2-b]quinolines (quindolines)

• Michał Nowacki and
• Krzysztof Wojciechowski

Beilstein J. Org. Chem. 2018, 14, 194–202, doi:10.3762/bjoc.14.14

• when the σH-adducts, obtained from an allyl sulfone carbanion, were treated with a silylating agent or a Lewis acid [24]. In a similar reaction σH-adducts of benzyl carbanions of arylacetonitriles upon treatment with trialkylchlorosilanes yielded 9-cyanoacridines [25]. This [3 + 3] annulation leading

• carbanions and nitroarenes, to indolo[3,2-b]quinoline derivatives. As starting nucleophile precursors, we have chosen derivatives of indole-2-ylmethyl phenyl sulfone (1a), tert-butyl indol-2-ylacetate (1b,c) and indol-2-ylacetonitrile (1d). As a model compound for screening of the reaction conditions, we

• used sulfone 1a. We found that no reaction occurred when the sulfone and 4-chloronitrobenzene were treated with DBU and trimethylchlorosilane. Even when we kept these reagents for a prolonged time (up to six days) no product was observed and the starting materials were recovered. When we treated these

Photocatalytic formation of carbon–sulfur bonds

• Alexander Wimmer and
• Burkhard König

Beilstein J. Org. Chem. 2018, 14, 54–83, doi:10.3762/bjoc.14.4

• order to close the catalytic cycle, the aryl sulfinate salt is oxidized to the respective sulfur-centred radical, which adds regioselectively to the alkene moiety. Further oxidation and deprotonation leads to the respective vinyl sulfone. One year later, we successfully expanded the scope of the Eosin Y

• styrenes. Even aliphatic methane sulfinic acid could be converted to the respective allyl sulfone in moderate yield. The authors propose a reductive photocatalytic cycle, where the aryl sulfinic acid anion is photooxidized by the excited state of Eosin Y. The sulfur-centred radical adds to the alkene to

• Eosin Y as photoredox catalyst generates both, the sulfur-centred radical of the sulfinic acid as well as the α-vinyl carbon-centred radical. Radical/radical cross-coupling leads to the desired vinyl sulfone in Markovnikov orientation. The reaction is applicable to diverse functionalized terminal

CF₃SO₂X (X = Na, Cl) as reagents for trifluoromethylation, trifluoromethylsulfenyl-, -sulfinyl- and -sulfonylation. Part 1: Use of CF₃SO₂Na

• Hélène Guyon,
• Hélène Chachignon and
• Dominique Cahard

Beilstein J. Org. Chem. 2017, 13, 2764–2799, doi:10.3762/bjoc.13.272

• -Markovnikov selectivity. Notably, styrene failed to react under these conditions. A selection of α,β-unsaturated electron-withdrawing motifs that included a sulfone, esters, an amide, and a ketone were investigated for the first time and the β-addition products were obtained regioselectively in moderate to

Recent progress in the racemic and enantioselective synthesis of monofluoroalkene-based dipeptide isosteres

• Myriam Drouin and
• Jean-François Paquin

Beilstein J. Org. Chem. 2017, 13, 2637–2658, doi:10.3762/bjoc.13.262

• [CF=CH]-Gly 9, from benzothiazolyl fluoroaminosulfones (Scheme 2) [24][25]. The Julia–Kocienski olefination of 3-alkoxypropanal 7 with phthalimido sulfone 6 afforded the corresponding monofluoroalkene 8 as a (Z):(E) mixture (54:46). Removal of the benzyl group using titanium tetrachloride gave the

Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective

• Yaroslav D. Boyko,
• Valentin S. Dorokhov,
• Alexey Yu. Sukhorukov and
• Sema L. Ioffe

Beilstein J. Org. Chem. 2017, 13, 2214–2234, doi:10.3762/bjoc.13.220

• proceeds only at elevated temperatures (50 °C), that may account for relatively low yields of products 62. Furthermore, the reaction of sulfone 63 with lithium (trimethylsilyl)acetylide furnished only enoxime 64. Apparently, the application of more convenient and selective nitrosoalkene sources (e.g., TBS