Studies directed toward the exploitation of vicinal diols in the synthesis of (+)-nebivolol intermediates

• Runjun Devi and
• Sajal Kumar Das

Beilstein J. Org. Chem. 2017, 13, 571–578, doi:10.3762/bjoc.13.56

• have demonstrated that the synthesis of 1a could be achieved using the 2-substituted chroman derivatives (R)-1-((R)-6-fluorochroman-2-yl)ethane-1,2-diol (2) and (R)-1-((S)-6-fluorochroman-2-yl)ethane-1,2-diol (3) or the corresponding chroman epoxides 4 and 5 as late-stage intermediates. Although the

• consensus synthetic strategy for 1a involves the convergent assembly of chroman-based key subunits, the question of how best to access them remains open. The intramolecular ring-opening of enantiomerically pure epoxides by the phenolic hydroxy group is one of the most popular methods to construct 3 (Scheme

• . However, it has been reviewed that not only benzylic epoxides but also non-benzylic epoxides are sensitive to the standard hydrogenation/debenzylation conditions [35]. Whereas benzylic epoxides are highly sensitive to hydrogenation conditions, non-benzylic epoxides, depending on the reaction conditions

Synthesis of 1-indanones with a broad range of biological activity

• Marika Turek,
• Dorota Szczęsna,
• Marek Koprowski and
• Piotr Bałczewski

Beilstein J. Org. Chem. 2017, 13, 451–494, doi:10.3762/bjoc.13.48

• rhodium(II) complex 220 followed by the carboxylic methyl ester hydrolysis/decarboxylation in DMSO/H2O at 120 °C with up to 72% enantiomeric excess (Scheme 60) [89]. 1.7 From epoxides and cyclopropanes The chalcone epoxides 221 ring opening catalyzed by indium(III) chloride, followed by a intramolecular

• Friedel–Crafts alkylation has been used by Ahmed et al. for the synthesis of 2-hydroxyindan-1-one derivatives 222 in good yields (Scheme 61) [90]. The same research group used the THP (tetrahydropyranyl) and MOM (methoxymethyl) protected chalcone epoxides and tin(IV) chloride under mild conditions to

Solid-phase enrichment and analysis of electrophilic natural products

• Frank Wesche,
• Yue He and
• Helge B. Bode

Beilstein J. Org. Chem. 2017, 13, 405–409, doi:10.3762/bjoc.13.43

• extracts via their reactivity against azide as a nucleophile followed by their subsequent enrichment using a cleavable azide-reactive resin (CARR). Using this approach, natural products carrying epoxides and α,β-unsaturated enones as well as several unknown compounds were identified in crude extracts from

• entomopathogenic Photorhabdus bacteria. Keywords: azides; click chemistry; enrichment; electrophilic natural products; epoxides; glidobactin; Photorhabdus; stilbenes; Introduction Microorganisms are a major source for novel natural products and the subsequent development of new drugs for all kinds of

• dehydroalanine [6][7], ketones, aldehydes [8][9], carboxylic acids [8][9], amines [8][9][10], thiols [8][9], alcohols [11], epoxides [12], terminal alkynes [13][14] and azides [15] can be targeted to introduce a label. Such labels might increase the visibility in UV or MS detection in liquid chromatography

New approaches to organocatalysis based on C–H and C–X bonding for electrophilic substrate activation

• Pavel Nagorny and
• Zhankui Sun

Beilstein J. Org. Chem. 2016, 12, 2834–2848, doi:10.3762/bjoc.12.283

• activation is accomplished through a C–H hydrogen bond with cyclic ester carbonyls. The following study by the Bibal group described the use of catalysts L11 as hydrogen bond donors for the activation of epoxides toward ring-opening aminolysis with amines (Scheme 6) [54]. Significant rate enhancement was

cis-Diastereoselective synthesis of chroman-fused tetralins as B-ring-modified analogues of brazilin

• Dimpee Gogoi,
• Runjun Devi,
• Pallab Pahari,
• Bipul Sarma and
• Sajal Kumar Das

Beilstein J. Org. Chem. 2016, 12, 2816–2822, doi:10.3762/bjoc.12.280

• using 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) as reaction medium as well as the reaction promoter. The first choice of HFIP was based on its recently found ability to promote high-yielding IFCEA cyclization of benzylic epoxides [29]. Unfortunately, however, refluxing a solution of (±)-6a in HFIP for 4

• epoxides are compatible under IFCEA cyclization (as demonstarted previously by us [22][23] and others [29][33]), this methodology should also be applicable with the enantioenriched substrates. Further work is in progress aimed at synthesizing such type of fused hybrid molecules with different ring sizes

Sydnone C-4 heteroarylation with an indolizine ring via Chichibabin indolizine synthesis

• Florin Albota,
• Mino R. Caira,
• Constantin Draghici,
• Florea Dumitrascu and
• Denisa E. Dumitrescu

Beilstein J. Org. Chem. 2016, 12, 2503–2510, doi:10.3762/bjoc.12.245

• transformation of N-heteroaromatic salts into the corresponding N-ylides with epoxides was reported recently [5][17][18]. The next step represents a 1,3-dipolar cycloaddition of the bis(1,3-dipoles) 10 with formation of dihydro-indolizines 11 which, under the reaction conditions, are dehydrogenated to the final

Rearrangements of organic peroxides and related processes

• Ivan A. Yaremenko,
• Vera A. Vil’,
• Dmitry V. Demchuk and
• Alexander O. Terent’ev

Beilstein J. Org. Chem. 2016, 12, 1647–1748, doi:10.3762/bjoc.12.162

• related to the application and preparation of unsaturated compounds, such as epoxides, aldehydes, ketones, carboxylic acids, and their derivatives [72][73][74][75][76][77][78][79][80][81][82][83][84][85][86][87][88][89][90][91][92][93][94][95][96][97][98][99][100][101][102][103][104][105][106][107][108

Cp₂TiCl/D₂O/Mn, a formidable reagent for the deuteration of organic compounds

• Antonio Rosales and
• Ignacio Rodríguez-García

Beilstein J. Org. Chem. 2016, 12, 1585–1589, doi:10.3762/bjoc.12.154

• (Scheme 1). This SET is capable of promoting and/or catalyzing several transformations in organic chemistry [17][18][19][20][21][22][23][24][25]. One of the most relevant transformations is the H/D-atom transfer from H2O/D2O to carbon radicals (pathway A) (obtained from epoxides [26][27][28], ozonides [29

• epoxides [2][27][37], ozonides [29], ketones [31][32], activated halides [30][31][32], alkenes and alkynes [33]. Several examples are presented in Scheme 3. The results show that the combination Cp2TiCl/D2O/Mn is able to promote and/or catalyze deuteration of organic compounds by reduction or radical

• summary, we presented an overview of the Cp2TiCl/D2O/Mn combination as an efficient, cheap, selective, and sustainable reagent compatible with different functional groups that mediates the deuteration of organic compounds from epoxides, ozonides, carbonyl compounds, activated halides, alkenes and alkynes

Biosynthesis of oxygen and nitrogen-containing heterocycles in polyketides

• Franziska Hemmerling and
• Frank Hahn

Beilstein J. Org. Chem. 2016, 12, 1512–1550, doi:10.3762/bjoc.12.148

• are biosynthesised in seven principal ways (Scheme 2). Those comprise nucleophilic addition of a hydroxy group to electrophiles like epoxides 4, carbonyl groups 6 or Michael acceptors 9, potentially followed by further processing (a–c in Scheme 2). Lactones 12 are formed by transacylation of a

• building block [34][35][36]. 1.1.3 Epoxide opening: The nucleophilic opening of epoxides is probably the most abundant type of reaction leading to furans and pyrans. It, for example, plays an important role in the biosynthesis of ionophoric terrestrial and marine polyethers (see chapter 1.3). In this

• experiments. The process starts by oxidoreductase domain MmpE-catalysed epoxidation of the double bond between C10 and C11. Olefin 53 is thus a branching point from which two series of analogous C10–C11 epoxides (53–61) and C10–C11 (not shown) olefins arise (Scheme 9). The fact that the wild-type titers of

Selective bromochlorination of a homoallylic alcohol for the total synthesis of (−)-anverene

• Frederick J. Seidl and
• Noah Z. Burns

Beilstein J. Org. Chem. 2016, 12, 1361–1365, doi:10.3762/bjoc.12.129

• limitation has inspired the development of several remote epoxidation methods for homoallylic and bishomoallylic alcohols [4][5], now allowing chemists to directly access a greater variety of enantioenriched epoxides. Several years ago our laboratory developed the first catalytic enantioselective

Efficient syntheses of climate relevant isoprene nitrates and (1R,5S)-(−)-myrtenol nitrate

• Sean P. Bew,
• Glyn D. Hiatt-Gipson,
• Graham P. Mills and
• Claire E. Reeves

Beilstein J. Org. Chem. 2016, 12, 1081–1095, doi:10.3762/bjoc.12.103

• convenient and cheap Brønsted acid, transformed a range of epoxides [20] into the corresponding nitrato alcohols. Shepson substituted ethylene oxide for commercially available isoprene epoxide and generated eight stereo- and structurally isomeric IPNs. Within this mixture 3° nitrate rac-7, 1° nitrate rac-8

Synthesis and in vitro cytotoxicity of acetylated 3-fluoro, 4-fluoro and 3,4-difluoro analogs of D-glucosamine and D-galactosamine

• Štěpán Horník,
• Lucie Červenková Šťastná,
• Petra Cuřínová,
• Jan Sýkora,
• Kateřina Káňová,
• Roman Hrstka,
• Ivana Císařová,
• Martin Dračínský and
• Jindřich Karban

Beilstein J. Org. Chem. 2016, 12, 750–759, doi:10.3762/bjoc.12.75

• :2,3-dianhydro-4-O-benzyl-β-D-mannopyranose (10, one of the Černý epoxides available from D-glucal [31][32][33] or levoglucosan [34]). Regioselective azidolysis [21][35][36] of 10 yielded 2-azido alcohol 11 which was converted to 12 by benzoylation at O-3 and debenzylation at O-4. To prevent azide

Photoinduced 1,2,3,4-tetrahydropyridine ring conversions

• Baiba Turovska,
• Henning Lund,
• Viesturs Lūsis,
• Anna Lielpētere,
• Edvards Liepiņš,
• Sergejs Beljakovs,
• Inguna Goba and
• Jānis Stradiņš

Beilstein J. Org. Chem. 2015, 11, 2166–2170, doi:10.3762/bjoc.11.234

• –carbon double bond in enamines to give the corresponding epoxides, however, in most cases they have not been isolated [36]. The hydroperoxide 2 reacts in the same way. Fission of the epoxide ring may be induced by the base itself producing 3. Attack of a second molecule of hydroperoxide 2 on the imine

Stereoselective synthesis of hernandulcin, peroxylippidulcine A, lippidulcines A, B and C and taste evaluation

• Marco G. Rigamonti and
• Francesco G. Gatti

Beilstein J. Org. Chem. 2015, 11, 2117–2124, doi:10.3762/bjoc.11.228

• double bonds of (+)-limonene or (−)-isopulegol with m-chloroperbenzoic acid (MCPBA) to introduce the stereogenic center at the C(2’) position. Unfortunately both methods were only modestly stereoselective and resulted in mixtures of the respective epoxides. These results implied a not simple column

Cross metathesis of unsaturated epoxides for the synthesis of polyfunctional building blocks

• Meriem K. Abderrezak,
• Kristýna Šichová,
• Nancy Dominguez-Boblett,
• Antoine Dupé,
• Zahia Kabouche,
• Christian Bruneau and
• Cédric Fischmeister

Beilstein J. Org. Chem. 2015, 11, 1876–1880, doi:10.3762/bjoc.11.201

Robust bifunctional aluminium–salen catalysts for the preparation of cyclic carbonates from carbon dioxide and epoxides

• Yuri A. Rulev,
• Zalina Gugkaeva,
• Victor I. Maleev,
• Michael North and
• Yuri N. Belokon

Beilstein J. Org. Chem. 2015, 11, 1614–1623, doi:10.3762/bjoc.11.176

• one-component aluminium-based catalysts for the reaction between epoxides and carbon dioxide have been prepared. The catalysts are composed of aluminium–salen chloride complexes with trialkylammonium groups directly attached to the aromatic rings of the salen ligand. With terminal epoxides, the

• achieving this goal is to produce cyclic carbonates or polycarbonates from carbon dioxide and the corresponding epoxides (Scheme 1). Cyclic carbonates are an important class of solvents [2] and starting materials in organic synthesis [3][4][5][6]. Although a significant array of catalysts have been

• developed for the production of cyclic carbonates [7][8][9] and polycarbonates [10][11] from carbon dioxide and epoxides, the most developed and privileged set of catalysts are based on Lewis acidic metal–salen complexes. In particular, cobalt(III) and chromium(III) complexes were found to be highly

Dicarboxylic esters: Useful tools for the biocatalyzed synthesis of hybrid compounds and polymers

• Ivan Bassanini,
• Karl Hult and
• Sergio Riva

Beilstein J. Org. Chem. 2015, 11, 1583–1595, doi:10.3762/bjoc.11.174

• . Telechelics with allyl-ether ends. Telechelics with ends functionalized as epoxides. Activated derivatives of dicarboxylic acids. Biocatalyzed synthesis of paclitaxel derivatives. Biocatalyzed synthesis of hybrid diesters 17 and 18. Hybrid derivatives of sylibin. Acknowledgements The authors acknowledge

Surprisingly facile CO₂ insertion into cobalt alkoxide bonds: A theoretical investigation

• Willem K. Offermans,
• Claudia Bizzarri,
• Walter Leitner and
• Thomas E. Müller

Beilstein J. Org. Chem. 2015, 11, 1340–1351, doi:10.3762/bjoc.11.144

• Abstract Exploiting carbon dioxide as co-monomer with epoxides in the production of polycarbonates is economically highly attractive. More effective catalysts for this reaction are intensively being sought. To promote better understanding of the catalytic pathways, this study uses density functional theory

• such as ammonia, hydrogen, epoxides or lactones [8]. Nevertheless, the reactions frequently involve a substantial kinetic barrier or are accompanied by side reactions that, so far, have resulted in insufficient yields and/or selectivities. Even though there are numerous compounds that might react with

• CO2, active and selective catalysts for these reactions are scarce [9]. The reaction of CO2 with epoxides yields alternating polycarbonates, polyethercarbonates or cyclic carbonates (Scheme 1). The production of CO2-based polymers is considerably more challenging compared to the formation of cyclic

CO₂ Chemistry

• Thomas E. Müller and
• Walter Leitner

Beilstein J. Org. Chem. 2015, 11, 675–677, doi:10.3762/bjoc.11.76

• ]. Activation of carbon dioxide by inserting it into metal-alkoxide bonds allows for subsequent applications in polymer synthesis such as the copolymerisation of carbon dioxide with epoxides and other co-monomers [11]. Here, the catalysis with cobalt complexes still presents surprising effects [12]. More

Switching the reaction pathways of electrochemically generated β-haloalkoxysulfonium ions – synthesis of halohydrins and epoxides

• Akihiro Shimizu,
• Ryutaro Hayashi,
• Yosuke Ashikari,
• Toshiki Nokami and
• Jun-ichi Yoshida

Beilstein J. Org. Chem. 2015, 11, 242–248, doi:10.3762/bjoc.11.27

• ions generated by the reaction of electrogenerated Br+ and I+ ions stabilized by dimethyl sulfoxide (DMSO) reacted with sodium hydroxide and sodium methoxide to give the corresponding halohydrins and epoxides, respectively, whereas the treatment with triethylamine gave α-halocarbonyl compounds

• . Keywords: DMSO; electrosynthesis; epoxides; halohydrins; halogen cations; Introduction Alkene difunctionalization through three-membered ring halonium ion intermediates [1] is an important transformation in organic synthesis. Usually the halonium ions such as bromonium or iodonium ions are generated by

• expanding the utility of the present method. The treatment of β-haloalkoxysulfonium ions 3-X with sodium hydroxide gave the corresponding halohydrins 5-X, while the treatment with sodium methoxide gave epoxides 6 (Scheme 1). Results and Discussion Reactions of β-bromoalkoxysulfonium ions generated from (Z

Anion effect controlling the selectivity in the zinc-catalysed copolymerisation of CO₂ and cyclohexene oxide

• Sait Elmas,
• Muhammad Afzal Subhani,
• Walter Leitner and
• Thomas E. Müller

Beilstein J. Org. Chem. 2015, 11, 42–49, doi:10.3762/bjoc.11.7

• with epoxides (Scheme 1) is a prime example of a particularly attractive transformation of CO2 [8][9] and is at the verge of commercialisation [8]. In this transformation, the low energy level of the CO2 molecule is overcome by reacting CO2 with an epoxide as energy-rich comonomer [10]. Homogeneous and

• of the transition metal cations (Co, Cr) often employed in Type II catalysts, albeit zinc catalysts have lower activity in the copolymerisation of CO2 and epoxides [16]. The use of catalysts of Types I and II in the copolymerisation of CO2 and epoxides leads commonly to fully alternating

• ]. To keep the catalyst loading during the synthesis of such polyols low, chain transfer between the growing polymer chain and free alcohol groups needs to be realised. In this study, we have addressed such immortal copolymerisation of CO2 and epoxides with zinc catalysts. In the Type I lead catalyst

Thermal and oxidative stability of the Ocimum basilicum L. essential oil/β-cyclodextrin supramolecular system

• Daniel I. Hădărugă,
• Nicoleta G. Hădărugă,
• Corina I. Costescu,
• Ioan David and
• Alexandra T. Gruia

Beilstein J. Org. Chem. 2014, 10, 2809–2820, doi:10.3762/bjoc.10.298

• of 4.1% to 3.3%. In the recovered oil, reduced concentrations of 1.55% to 1.3%, and 2.1% to 1.75% were observed (see Table 1). Furthermore, all terpene epoxides (even those found in lower relative concentrations) were encapsulated in very low concentrations in the β-CD complexes in comparison with

• ) corresponds to a lower relative concentration of the degradation compound in the β-CD complex. Significant protection against oxidation at higher temperatures was observed in the case of alloaromadendrene and in unidentified sesquiterpenes. Their epoxides were encapsulated in β-CD in lower relative

• in β-CD as compared to some of the sesquiterpenes and especially with respect to sesquiterpene epoxides (some of them are reactive and possibly harmful compounds), which indicates the enhanced quality and stability of the O. basilicum L./β-CD complex. Experimental Materials The Ocimum basilicum L

Regio- and stereoselective synthesis of new diaminocyclopentanols

• Evgeni A. Larin,
• Valeri S. Kochubei and
• Yuri M. Atroshchenko

Beilstein J. Org. Chem. 2014, 10, 2513–2520, doi:10.3762/bjoc.10.262

• aminolysis of epoxides 6a,b afforded mainly C1 adducts 13a,b arising from trans-diaxal opening of the epoxide ring. Using a Lewis acid catalyst, epoxides 6a,b were transformed into diaminocyclopentanols 14a,b via an alternative pathway involving the formation of aziridinium intermediate 17. Keywords

• : diaminocyclopentanols; epoxides; regioselectivity; ring opening; stereoselectivity; Introduction In recent years mimicry of aminoglycosides [1][2][3][4][5][6][7] and nucleosides [8][9][10] has become an important field in pharmaceutical research. Regio- and stereochemical diversities within a sugar-like moiety in

• - and stereoisomeric aminocyclitol derivatives remains in demand. One of the optimal routes involves the stereoselective ring opening of epoxides by different nucleophiles in the presence of a variety of activators [15][16][17][18][19]. In this context, epoxidation of cyclic allylic amines and

Electrocarboxylation: towards sustainable and efficient synthesis of valuable carboxylic acids

• Roman Matthessen,
• Jan Fransaer,
• Koen Binnemans and
• Dirk E. De Vos

Beilstein J. Org. Chem. 2014, 10, 2484–2500, doi:10.3762/bjoc.10.260

• temperatures and pressures to activate CO2 [2][3]. Efficient chemical incorporation of CO2 is limited to rather reactive substrates, like epoxides [4][5][6] and amines [7][8][9] to produce cyclic carbonates and carbamates, respectively, and even then, elevated reaction temperatures and/or complex catalyst

Indium-mediated allylation in carbohydrate synthesis: A short and efficient approach towards higher 2-acetamido-2-deoxy sugars

• Christopher Albler,
• Ralph Hollaus,
• Hanspeter Kählig and
• Walther Schmid

Beilstein J. Org. Chem. 2014, 10, 2230–2234, doi:10.3762/bjoc.10.231

• obtained allylic epoxides were regio- and stereoselectively opened with trimethylsilyl azide under palladium catalysis. Finally, a suitable deprotection protocol, starting with acidic acetate cleavage and ozonolysis was established. Peracetylation of the products simplifies purification and subsequent

• (CHCO2Me)) generated allylic epoxides 4a–c, which in turn permitted the application of reliable palladium chemistry for the epoxide opening [27][28][29]. Thus, compounds 4a–c were regio- and stereoselectively opened with trimethylsilyl azide and Pd(PPh3)4 as a catalyst [30], furnishing syn-azido alcohols

• the use of a chiral L-proline derived epoxidation catalyst. The introduction of nitrogen was achieved via a Tsuji–Trost-like azide opening of allylic epoxides. Although global deprotection proved to be cumbersome, we were able to develop a versatile reaction sequence to overcome this problem. The