The chemistry of bisallenes

• Henning Hopf and
• Georgios Markopoulos

Beilstein J. Org. Chem. 2012, 8, 1936–1998, doi:10.3762/bjoc.8.225

Synthesis and characterization of low-molecular-weight π-conjugated polymers covered by persilylated β-cyclodextrin

• Aurica Farcas,
• Ana-Maria Resmerita,
• Andreea Stefanache,
• Mihaela Balan and
• Valeria Harabagiu

Beilstein J. Org. Chem. 2012, 8, 1505–1514, doi:10.3762/bjoc.8.170

• bulkier silylated groups, affecting the ability of the diborate groups from the DOF molecule to partially penetrate the PS-βCD cavity. Keywords: alternating fluorene-bithiophene copolymer; cyclodextrins; interlocked molecules; macrocycles; persilylated β-cyclodextrin; polyrotaxanes; Introduction Organic

• mixture of PS-βCD and BT in acetone was isolated, purified and characterized by 1H NMR, as can be seen in Figure 1. The average number of PS-βCD macrocycles per BT unit was calculated by using the ratio of the integrated area of the peak assigned to the H from –CH3 groups of PS-βCD (0.09–0.11 ppm, IH-CH3

• ) and the proton peaks of BT (6.85–7.97 ppm, IBT), Figure 1. The average number of PS-βCD macrocycles per BT unit was calculated as (IBT/4)/(IH-CH3/63) and found to be 0.95 (i.e., ca. 95% coverage). Not surprisingly, due to the presence of PS-βCD the rotaxane PDOF-BTc copolymer showed a marked contrast

Superstructures with cyclodextrins: Chemistry and applications

• Helmut Ritter

Beilstein J. Org. Chem. 2012, 8, 1303–1304, doi:10.3762/bjoc.8.148

• covalent attachment of CDs to macromolecules and threading of CD molecules onto suitable macromolecular chains could be demonstrated. Unlike other macrocycles such as crown ethers or calixarenes, the cavity of CDs is big enough to include more or less hydrophobic molecules completely. In contrast to

Similarity analysis, synthesis, and bioassay of antibacterial cyclic peptidomimetics

• Workalemahu M. Berhanu,
• Mohamed A. Ibrahim,
• Girinath G. Pillai,
• Alexander A. Oliferenko,
• Levan Khelashvili,
• Farukh Jabeen,
• Bushra Mirza,
• Farzana Latif Ansari,
• Ihsan ul-Haq,
• Said A. El-Feky and
• Alan R. Katritzky

Beilstein J. Org. Chem. 2012, 8, 1146–1160, doi:10.3762/bjoc.8.128

• studied in order to identify new promising cyclic scaffolds. A large descriptor space coupled with cluster analysis was employed to digitize known antibacterial structures and to gauge the potential of new peptidomimetic macrocycles, which were conveniently synthesized by acylbenzotriazole methodology

• direction of the two chains attached to the cysteine residue. For example, one of the early cysteine-containing macrocycles was designed to mimic the cation binding ability of valinomycin [24]. Numerous literature approaches to the synthesis of 17-, 18- and 24-membered rings utilize: (i) acyl chlorides, (ii

• and axis Y denotes linkage distance); the red oval, blue rectangle, and green oval represent cluster 1, cluster 2, and cluster 3, respectively. Preparation of dicarboxylic benzotriazole derivatives. Preparation of pyridine-based cysteine-containing macrocycles. Preparation of pyridine–cysteine

Synthesis and anion recognition properties of shape-persistent binaphthyl-containing chiral macrocyclic amides

• Marco Caricato,
• Nerea Jordana Leza,
• Claudia Gargiulli,
• Giuseppe Gattuso,
• Daniele Dondi and
• Dario Pasini

Beilstein J. Org. Chem. 2012, 8, 967–976, doi:10.3762/bjoc.8.109

• , Italy INSTM Research Unit, Department of Chemistry, University of Pavia, 27100 Pavia, Italy 10.3762/bjoc.8.109 Abstract We report on the synthesis and characterization of novel shape-persistent, optically active arylamide macrocycles, which can be obtained using a one-pot methodology. Resolved, axially

• differing shapes, to give homochiral tetraamidic macrocycles. The recognition properties of these supramolecular receptors have been analyzed, and the results indicate a modulation of binding affinities towards dicarboxylate anions, with a drastic change of binding mode depending on the steric and

• electronic features of the functional groups in the 2,2' positions. Keywords: amides; anion recognition; chirality; macrocycles; molecular switches; supramolecular chemistry; Introduction Macrocyclic molecules possessing a high degree of shape persistency act as molecular cages, and the scientific interest

Molecular switches and cages

• Dirk Trauner

Beilstein J. Org. Chem. 2012, 8, 870–871, doi:10.3762/bjoc.8.97

• , optically active macrocycles (Pasini). Molecular switches that respond to changes in pH are covered as well (Haberhauer and Aprahamian), reflecting their importance in biology and in materials science. Finally, switching is highlighted as a synthetic strategy for building advanced materials that are useful

Synthesis of functionalized macrocyclic derivatives of trioxabicyclo[3.3.0]nonadiene

• Sabine Leber,
• Gert Kollenz and
• Curt Wentrup

Beilstein J. Org. Chem. 2012, 8, 738–743, doi:10.3762/bjoc.8.83

• the bisdioxine-derived macrocycles. Okazaki and co-workers designed bowl-shaped [8] and lantern-shaped [9] molecules containing a functionalized aryl group, which allowed the preparation of, among other things, stable simple enols [8] and a variety of unusual sulfur [9], selenium [10][11] and

• germanium [12] species. Clearly, the bisdioxine macrocycles such as 4 and 5 will not be nearly as rigid, but they may nevertheless exert some steric protection. Herein we report the realisation of the first step toward this end, the preparation of functionalized macrocyclic bisdioxine derivatives. Results

• triethylamine to afford the 2:2 adducts 8 and 11, respectively (Scheme 2 and Scheme 3). These compounds were characterized by elemental analysis and their 1H- and 13C NMR spectra. All proton and carbon resonances could be assigned by comparison with data for other, related, macrocycles [1][2][3][4][5][6][7

Enantioselective supramolecular devices in the gas phase. Resorcin[4]arene as a model system

• Caterina Fraschetti,
• Matthias C. Letzel,
• Antonello Filippi,
• Maurizio Speranza and
• Jochen Mattay

Beilstein J. Org. Chem. 2012, 8, 539–550, doi:10.3762/bjoc.8.62

• of tunable macrocycles largely studied in the context of host–guest chemistry, as cavitands [5] and capsules [6]. The great ability of resorcin[4]arenes to trap several classes of compounds makes them very suitable for the subtle study of the chemicophysical properties of their host–guest systems

Self-assembly of Ru₄ and Ru₈ assemblies by coordination using organometallic Ru(II)₂ precursors: Synthesis, characterization and properties

• Sankarasekaran Shanmugaraju,
• Dipak Samanta and
• Partha Sarathi Mukherjee

Beilstein J. Org. Chem. 2012, 8, 313–322, doi:10.3762/bjoc.8.34

• . Conversely, the similar combination of L with 2,5-dihydroxy-1,4-benzoquinonato (dhbq) bridged binuclear complex [Ru2(μ-η4-C6H2O4)(MeOH)2(η6-p-cymene)2](O3SCF3)2 (1c) in 1:2 molar ratio resulted in an octanuclear macrocyclic cage 2c. All the self-assembled macrocycles 2a–2c were isolated as their triflate

• tetranuclear rectangular geometry with the dimensions of 5.53 Å × 12.39 Å. Furthermore, the photo- and electrochemical properties of these newly synthesized assemblies have been studied by using UV–vis absorption and cyclic voltammetry analysis. Keywords: cages; macrocycles; ruthenium(II); self-assembly; self

• , we and others have recently reported several shape-persistent discrete macrocycles/cages using half-sandwich octanuclear Ru(II) piano-stool complexes in combination with polypyridyl or polycarboxylate donors [6][7][8][9][10]. Ligands with an imidazole functionality are of considerable interest due to

A ferrocene redox-active triazolium macrocycle that binds and senses chloride

• Nicholas G. White and
• Paul D. Beer

Beilstein J. Org. Chem. 2012, 8, 246–252, doi:10.3762/bjoc.8.25

• Information File 18: X-ray data of macrocycles 3 and 4. Acknowledgements We thank the Clarendon Fund and Trinity College, Oxford for funding and Diamond Light Source for the award of beam time on Beamline I19. Ben Mullaney is thanked for assistance with electrochemistry experiments.

Synthesis of multivalent host and guest molecules for the construction of multithreaded diamide pseudorotaxanes

• Nora L. Löw,
• Egor V. Dzyuba,
• Boris Brusilowskij,
• Lena Kaufmann,
• Elisa Franzmann,
• Wolfgang Maison,
• Emily Brandt,
• Daniel Aicher,
• Arno Wiehe and
• Christoph A. Schalley

Beilstein J. Org. Chem. 2012, 8, 234–245, doi:10.3762/bjoc.8.24

• wheel precursors. Keywords: multivalency; pseudorotaxanes; Sonogashira coupling; supramolecular chemistry; tetralactam macrocycles; Introduction Synthetic supramolecular complexes have the great potential to put those concepts to the test that govern much of the noncovalent chemistry in nature. Among

• this case to acids and bases, which induce motion of the wheel and axle components relative to each other. Tetralactam macrocycles (TLMs) [65][66] have widely been used in the synthesis of amide catenanes and rotaxanes [85][86][87][88][89][90][91][92] and represent excellent hosts for dicarbonyl

• rise to divalent axle 22, which was isolated as a side product in 37% yield. This molecule may be useful for other divalent hosts, such as two macrocycles connected through a butadiyne spacer or a thiophene unit. Such hosts have been reported previously [103] and are not included here. Formation of

Fifty years of oxacalix[3]arenes: A review

• Kevin Cottet,
• Paula M. Marcos and
• Peter J. Cragg

Beilstein J. Org. Chem. 2012, 8, 201–226, doi:10.3762/bjoc.8.22

• has been expanded to include numerous derivatives and complexes. This review describes the syntheses of the parent compounds, their derivatives, and their complexation behaviour towards cations. Extraction data are presented, as are crystal structures of the macrocycles and their complexes with guest

• species. Applications in fields as diverse as ion selective electrode modifiers, fluorescence sensors, fullerene separations and biomimetic chemistry are described. Keywords: calixarenes; host–guest chemistry; macrocycles; oxacalixarenes; Introduction Calixarenes, macrocycles which are widely used in

• ]. When one or more CH2 bridges are replaced by CH2OCH2 groups the macrocycles are known as homooxacalixarenes, or simply oxacalixarenes. The presence of the heteroatom is reflected in the name of the compound, for example, p-tert-butylcalix[4]arene (1) with a CH2OCH2 group instead of a CH2 bridge is p

Binding of group 15 and group 16 oxides by a concave host containing an isophthalamide unit

• Jens Eckelmann,
• Vittorio Saggiomo,
• Svenja Fischmann and
• Ulrich Lüning

Beilstein J. Org. Chem. 2012, 8, 11–17, doi:10.3762/bjoc.8.2

• ; macrocycle; molecular recognition; Introduction In the last decade, isophthalamide derivatives have become attractive neutral hosts as anion receptors [1][2]. Some of these derivatives show a high selectivity for one anion over others [3]. Isophthalamide units have also been incorporated into macrocycles [4

• ][5] or bi-macrocycles for ion-pair and ion-triplet recognition [6][7][8][9]. During the last few years, it was also shown that the orientation of the amide bonds of the isophthalamides plays an important role in the effectiveness of anion binding and subsequently in applications such as transmembrane

The allylic chalcogen effect in olefin metathesis

• Yuya A. Lin and
• Benjamin G. Davis

Beilstein J. Org. Chem. 2010, 6, 1219–1228, doi:10.3762/bjoc.6.140

• dibenzylamine (24), but the allyl sulfide analogue 22 remained the most reactive substrate in aqueous media (Scheme 7b) [17]. We considered these observation in the light of the early work by Fürstner in the synthesis of macrocycles by RCM [33], in which a “carbonyl-relayed” mechanism was proposed as the

Calix[4]arene-click-cyclodextrin and supramolecular structures with watersoluble NIPAAM-copolymers bearing adamantyl units: “Rings on ring on chain”

• Bernd Garska,
• Monir Tabatabai and
• Helmut Ritter

Beilstein J. Org. Chem. 2010, 6, 784–788, doi:10.3762/bjoc.6.83

• supramolecular complex formation with poly(NIPAAM) bearing attached adamantyl units was investigated by dynamic light scattering (DLS) and turbidity measurements. Keywords: β-cyclodextrin; calix[4]arene; click chemistry; poly(NIPAAM); Introduction Supramolecular interactions of macrocycles with different types

• superstructures, CDs and calixarenes turned out to be very attractive not only as molecular receptors but also as building blocks for the construction of supramolecular architectures [5]. For that reason, we were encouraged to couple these two different types of macrocycles via click type reactions. Recent

Molecular recognition of organic ammonium ions in solution using synthetic receptors

• Andreas Späth and
• Burkhard König

Beilstein J. Org. Chem. 2010, 6, No. 32, doi:10.3762/bjoc.6.32

• solvent-ligand bonds to break – as well as entropic – macrocycles [33] or cavities [34] being less conformationally flexible so losing fewer degrees of freedom upon complexation as a result of the reorganization energy already paid in advance in the synthesis. In a few examples, guest molecules are

• ]. Important heterocrowns (Figure 6) are macrocycles such as cyclens (6) and cyclams (7), which show excellent complexation properties towards transition metal ions [110]. Special classes of crown ethers are pyridino crowns (9), with one or more oxygen atoms replaced by pyridino moieties in the polyether chain

• )propane and the corresponding heteroaromatic macrocycles containing pyridine units [129] (Figure 9). The cyclic receptor 13 is a most effective carrier of ammonium ions (ν = 57 μM h−1) and exhibits an excellent selectivity for NH4+ in relation to three metal cations investigated (NH4+/Na+ = 9.2, NH4+/K

(Pseudo)amide-linked oligosaccharide mimetics: molecular recognition and supramolecular properties

• José L. Jiménez Blanco,
• Fernando Ortega-Caballero,
• Carmen Ortiz Mellet and
• José M. García Fernández

Beilstein J. Org. Chem. 2010, 6, No. 20, doi:10.3762/bjoc.6.20

• acid. Following the same objective, Xie’s group prepared orthogonally protected cyclic homo-oligomers with two to four SAA units that can be selectively or fully deprotected to afford macrocycles that can undergo further functionalisation (Figure 11) [55]. Conformational analysis by molecular modelling

Templated versus non-templated synthesis of benzo-21-crown-7 and the influence of substituents on its complexing properties

• Wei Jiang and
• Christoph A. Schalley

Beilstein J. Org. Chem. 2010, 6, No. 14, doi:10.3762/bjoc.6.14

• complexes with several C7 crown ethers, this peak distribution can only be assigned to a series of macrocycles with different sizes ranging from dibenzo-42-crown-14 (2-(1)) up to heptabenzo-168-crown-56 (2-(7)). Although the peak intensity does not necessarily reflect the solution composition quantitatively

Synthesis and binding studies of two new macrocyclic receptors for the stereoselective recognition of dipeptides

• Ana Maria Castilla,
• M. Morgan Conn and
• Pablo Ballester

Beilstein J. Org. Chem. 2010, 6, No. 5, doi:10.3762/bjoc.6.5

• explained below. The exploration of the conformational space of both macrocycles, using molecular modeling, indicated the existence of a built-in cavity. These studies also suggested that the reduced conformational flexibility of the receptors avoids the complete collapse of the cavity through the formation

• skeleton of the receptor. The two designed macrocycles, 1 and 2, have been synthesized and fully characterized. One of the key synthetic steps, which is common to both synthetic routes, consists in the use of a Stille carbonylative cross-coupling reaction that affords orthogonally tetraprotected 4,4’-bis

An enantiomerically pure siderophore type ligand for the diastereoselective 1 : 1 complexation of lanthanide(III) ions

• Markus Albrecht,
• Olga Osetska,
• Thomas Abel,
• Gebhard Haberhauer and
• Eva Ziegler

Beilstein J. Org. Chem. 2009, 5, No. 78, doi:10.3762/bjoc.5.78

• should be prototypes for further lanthanide(III) complexes with an enterobactine analogue binding situation. Keywords: CD spectroscopy; enterobactin; lanthanide; macrocycles; molecular modeling; Introduction The availability of metal ions for biological systems is essential for growth and function

Ring strain and total syntheses of modified macrocycles of the isoplagiochin type

• Andreas Speicher,
• Timo Backes,
• Kerstin Hesidens and
• Jürgen Kolz

Beilstein J. Org. Chem. 2009, 5, No. 71, doi:10.3762/bjoc.5.71

• Andreas Speicher Timo Backes Kerstin Hesidens Jurgen Kolz Department 8.1 Chemistry – Organic Chemistry, Saarland University, 66041 Saarbrücken, Germany 10.3762/bjoc.5.71 Abstract Macrocycles of the bisbibenzyl-type are natural products that are found exclusively in bryophytes (liverworts). The

• macrocycles. Keywords: axially chiral biaryl; isoplagiochin; macrocycle; ring strain; total synthesis; Introduction The cyclic bisbibenzyls isoplagiochin C (1) and D (2) were isolated from the liverworts Plagiochila fruticosa [1], Plagiochila deflexa [2], Herbertus sakuraii [3] and Lepidozia fauriana [4

• separated. By 2D NMR experiments (COSY, HSQC, HMBC) at 100 °C four sharp signals could be assigned to the methoxy groups in rings a–d (Figure 3). To gain insight into possible ring strain limitations for the preparation and stability of modified macrocycles of the isoplagiochin type we performed molecular

Synthesis of dihydrophenanthridines by a sequence of Ugi-4CR and palladium- catalyzed intramolecular C-H functionalization

• Florence Bonnaterre,
• Michèle Bois-Choussy and
• Jieping Zhu

Beilstein J. Org. Chem. 2008, 4, No. 10, doi:10.3762/bjoc.4.10

• developed two-step syntheses of a number of macrocycles including cyclophanes and cyclodepsipeptides [7][8][9][10]. We have also reported the elaboration of Ugi-adduct containing two arylhalide functions for the synthesis of 1,4-benzodiazepine-2,5-diones [11] and their tetracyclic derivatives [12] featuring

Shape- persistent macrocycle with intraannular alkyl groups: some structural limits of discotic liquid crystals with an inverted structure

• Sigurd Höger,
• Jill Weber,
• Andreas Leppert and
• Volker Enkelmann

Beilstein J. Org. Chem. 2008, 4, No. 1, doi:10.1186/1860-5397-4-1

• -Planck-Institut für Polymerforschung, Ackermannweg 10, 55128 Mainz, Germany 10.1186/1860-5397-4-1 Abstract The synthesis and thermal properties of new shape-persistent macrocycles of different sizes decorated with intraannular alkyl chains are described. The alkyl chain length is in all cases sufficient

• than spheres. For the larger macrocycles it is shown that longer adaptable substituents decrease the phase transition temperatures compared to previously described structures. Background During the past several years, the interest in the design and study of shape-persistent macrocycles with an

• , the supramolecular chemistry of rigid rings is currently investigated with considerable effort. For example, shape-persistent macrocycles can act as host structures for appropriate guest molecules; they can form 1D aggregates (in solution or gas phase) or regular 2D lattices after deposition at

Molecular recognition. 1. Crystal structures of hexaazamacrocyclic amines containing p-xylylene spacers and their adducts with acids

• Teresa Borowiak,
• Grzegorz Dutkiewicz,
• Maciej Kubicki,
• Marek Pietraszkiewicz,
• Agnieszka Gil and
• Rainer Mattes

Beilstein J. Org. Chem. 2005, 1, No. 16, doi:10.1186/1860-5397-1-16

• +-H groups which come from two different macrocycles. Hereby the zigzag arrangement mentioned above is formed. A second bifurcated hydrogen bonding is formed to two different water molecules which fill up the empty space between two neighbouring tapes (Figure 2). Further, each of two C-O- bonds of the