Journals in Catalysis, Organic and Inorganic Chemistry

Best of Journals in Catalysis, Organic and Inorganic Chemistry

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Chairman of the Editor: Editorial Board:

Joe P. Richmond Ryoji Noyori Heidelberg, Germany Nagoya University, Nagoya, Japan and RIKEN, Saitama, Japan Members of the Editorial Board: Highlights: • The leading primary journal in organic, organometallic, and applied chemistry • 2013 Impact Factor 5.542 • App available: bit.ly/CHEMAPPS

Stephen L. Buchwald Eric N. Jacobsen Shu Kobayashi Massachusetts Institute of Harvard University, University of Tokyo, Japan Technology, Cambridge, USA Cambridge, USA

Andreas Pfaltz Chris Senanayake Qi-Lin Zhou Universitt Basel, Switzerland Boehringer Ingelheim Nankai University, Tianjin, Pharmaceuticals, China Ridgefield, CT, USA International Advisory Board: Comprising 64 world-renowned scientists, from all around the globe, from industry and academia.

2 Increassing the Reactivity of Amides towards Organometallic Reagents: An Overview Vittorio Pace*, Wolfgang Holzer, Berit Olofsson*

Adv. Synth. Catal. DOI: 10.1002/adsc.201400630

Visible Light-Induced Aromatic Difluoroalkylation Jaehun Jung, Eunjin Kim, Youngmin You*, Eun Jin Cho*

Adv. Synth. Catal. DOI: 10.1002/adsc.201400542

Asymmetric Synthesis of α-Amino Acids under Operationally Convenient Conditions Manuel Jörres, Xia Chen, José Luis Aceña, Carina Merkens, Carsten Bolm*, Hong Liu*, Vadim A. Soloshonok*

Adv. Synth. Catal. DOI: 10.1002/adsc.201400405

Direct Oxidative Arylation of C(sp3)–H Bonds Adjacent to Oxygen of Ethers and Alcohols Rameshwar Prasad Pandit, Yong Rok Lee*

Adv. Synth. Catal. DOI: 10.1002/adsc.201400295

Cross-Coupling of Heteroarenes by C–H Functionalization: Recent Progress towards Direct Arylation and Heteroarylation Reactions Involving Heteroarenes Containing One Heteroatom Renzo Rossi*, Fabio Bellina*, Marco Lessi, Chiara Manzini

Adv. Synth. Catal. DOI: 10.1002/adsc.201300922

3 The essential forum A journal of for all catalysis www.chemcatchem.org Free Sample Copy

Editor-in-Chief:

Michael Rowan Editorial Board Chairs:

Uwe Bornscheuer Luis Oro Bert Weckhuysen Universität Greifswald, Universidad Universiteit Utrecht, Germany de Zaragoza, Spain The Netherlands Highlights: Editorial Board: • Short Publication Times Antonio Echavarren Institut Català d’Investigació Química, Spain Hermenegildo García Universitat Politècnica de València, Spain • Open Access Available George Huber University of Massachusetts-Amherst, USA • Free Color Marc Koper Universiteit Leiden, The Netherlands An-Hui Lu Dalian University of Technology, China • Expert Editors Per-Ola Norrby Göteborgs Universitet, Sweden • App available: bit.ly/CHEMAPPS Kyoko Nozaki The University of Tokyo, Japan Gianfranco Pacchioni Università degli Studi di Milano-Bicocca, Italy • Impact Factor 5.044 (2013) Robert Schlögl Fritz-Haber-Institut der Max-Planck-Gesellschaft, Berlin, Germany • A journal of ChemPubSoc Europe, Nick Turner University of Manchester, UK supported by GECATS Jin-Quan Yu The Scripps Research Institute, USA Jincai Zhao Institute of Chemistry, CAS, Beijing, China Honorary Board: Gerhard Ertl Fritz-Haber-Institut der Max-Planck-Gesellschaft, Berlin, Germany Robert H. Grubbs California Institute of Technology, Pasadena, USA Henri B. Kagan Université Paris-Sud, France Ryoji Noyori RIKEN and Nagoya Universty, Japan Richard R. Schrock Massachusetts Institute of Technology, Cambridge, UK K. Barry Sharpless Scripps Research Institute, USA Gabor A. Somorjai University of California, Berkeley, USA John M. Thomas University of Cambridge, UK Chi-Huey Wong Academia Sinica, Taiwan International Advisory Board: Comprising 71 world-renowned scientists from all around the globe. 4 Evidence of Intracrystalline Mesostructured Porosity in Zeolites by Advanced Gas Sorption, Electron Tomography and Rotation Electron Diffraction Javier Garcia-Martinez*, Changhong Xiao, Katie A. Cychosz, Kunhao Li, Wei Wan, Xiaodong Zou*, Matthias Thommes* Advanced characterization by electron tomography, three-dimensional rotation electron diffraction, and high resolution gas adsorption coupled with hysteresis scanning and density functional theory unambiguously revealed ChemCatChem the intracystalline nature and connectivity of the introduced mesopores in the DOI: 10.1002/cctc.201402499 surfactant-templated mesostructured zeolite Y.

Regioselective Biocatalytic Aromatic Hydroxylation in a Gas–Liquid Multiphase Tube-in-Tube Reactor Bartłomiej Tomaszewski, Richard C. Lloyd, Antony J. Warr, Katja Buehler, Andreas Schmid* Flow power: A tube-in-tube reactor is presented for a gas- dependent biocatalytic reaction, overcoming typical limitations such as mass transfer, product and substrate inhibition, and challenges ChemCatChem with gas delivery with productivities superior to standard batch DOI: 10.1002/cctc.201402354 reactors or conventional microreactors.

Asymmetric Intramolecular Hydroamination of Alkenes in Mild and Wet Conditions—Structure and Reactivity of Cationic Binuclear Gold(I) Catalysts Marc-Antoine Abadie, Xavier Trivelli, Florian Medina, Frédéric Capet, Pascal Roussel, Francine Agbossou-Niedercorn*, Christophe Michon* Hydroamination with golden conditions: Selected diphosphine binuclear gold(I) complex catalyzes efficiently the asymmetric intramolecular hydroamination of alkenes with high conversions and enantioselectivities for both enantiomers, in mild and wet conditions. The gold(I) cationic active species was characterized for the first time by X-ray analysis and DOSY 1 ChemCatChem H NMR experiments. No contribution of silver chloride was observed on the DOI: 10.1002/cctc.201402350 bonding mode of the catalyst.

Au/NiCo2O4 Arrays with High Activity for Water Oxidation Xijun Liu, Junfeng Liu*, Yaping Li, Yingjie Li, Xiaoming Sun* The man with the golden array: Electrodes made from a novel Au/

NiCo2O4 hybrid array exhibit high catalytic activity for the oxygen evolution reaction and outperform commercial Ir/C. The enhanced ChemCatChem performance can be attributed to the optimized chemical environment DOI: 10.1002/cctc.201402217 of the Co ions and the construction of well-aligned nanoarrays.

5 Free Applied Organometallic Sample Copy Chemistry wileyonlinelibrary.com/journal/aoc

Chair of the Editor-in-Chief: Editorial Board:

Cornelis J. Elsevier, Marcel Gielen, Amsterdam, Vrije Universiteit Brussel The Netherlands (V.U.B.), Brussel, Belgium

Associate Editors

Helmut Bönnemann, Ryan Richards, Edward R.T. Tiekink, Francis Verpoort, Max-Planck-Institut für Colorado School of Mines, University of Malaya, Ghent University, Kohlenforschung, Mühlheim, Golden, CO, USA Kuala Lumpur, Malaysia Gent, Belgium Germany Editorial Advisory Board

Didier Astruc, France Todd B. Marder, England Lies Bouwman, The Netherlands Scott McIndoe, Canada Pierre Braunstein, France Nils Metzler-Nolte, Germany Sukbok Chang, Korea Seik Weng Ng, Malaysia Bhanu Chauhan, USA Masamichi Ogasawara, Japan Chunming Cui, China Francois Ribot, France Paul J. Dyson, Switzerland Ed Rosenberg, USA Helena Grennberg, Sweden Masaichi Saito, Japan Narayan Hosmane, USA Ales Ruzicka, Czech Republic Juncheng Hu, China Claudiu T. Supuran, Italy Philippe Kalck, France Rudolph Willem, Belgium Kimoon Kim, South Korea Bernd Wrackmeyer, Germany Marc Knecht, USA Aleksander M. Wrobel, Poland Pavel Kocovsky, UK Zhenfeng Xi, China

6 Recent progress and current applications of Sonogashira coupling reaction in water Mohammad Bakherad* The use of aqueous media in palladium-catalyzed reactions has become popular because water-based synthetic processes are inherently safer as well as being inexpensive. Moreover, it does not require dry solvents, and the products may easily be isolated by extraction, which greatly facilitates the operation. Thus the use of water in palladium-catalyzed reactions represents one of the most economically and environmentally viable options

Appl. Organometal. Chem. for many organic transformations. In this review, recent developments of DOI: 10.1002/aoc.2931 Sonogashira reaction in water or aqueous media will be disclosed.

Binuclear meta-xylyl-linked Ag(I)-N-heterocyclic carbene complexes of N-alkyl/aryl-alkyl- substituted bis-benzimidazolium salts: synthesis, crystal structures and in vitro anticancer studies Rosenani A. Haque*, Muhammad Adnan Iqbal, Srinivasa Budagumpi, Mohamed B. Khadeer Ahamed, Amin M. S. Abdul Majid, Noorhafizah Hasanudin Meta-xylyl-bridged symmetrically substituted Ag(I)-N-heterocyclic carbene complexes were prepared and have been tested for their anticancer activity using human colorectal (HCT 116) cancer cell lines. Ag(I)-carbene Appl. Organometal. Chem. complexes showed exceptionally good activity (0.2-1.3 µM) against tested DOI: 10.1002/aoc.2953 cancer cell lines.

Basic CuCO3/ligand as a new catalyst for ‘on water’ borylation of Michael acceptors, alkenes and alkynes: application to the efficient asymmetric synthesis of β-alcohol type sitagliptin side chain Gaj Stavber, Zdenko Časar* “On water” β-borylation: Simple and efficient catalytic system based on basic copper carbonate and various ligands including D-glucosamine as a green ligand was developed for “on water” accelerated β-borylation of variety of organic compounds. The presented methodology is also for the first time applied for water-based asymmetric β-borylation with excellent Appl. Organometal. Chem. enantioselectivity as demonstrated by the synthesis of β-borylated target DOI: 10.1002/aoc.2957 sitagliptin side chain precursor.

Synthesis, characterization and catalytic activity of peripherally tetra-substituted Co(II) phthalocyanines for cyclohexene oxidation Ece Tugba Saka, Zekeriya Biyiklioglu, Halit Kantekin*, İbrahim Kani Synthesis and characterization of cobalt(II) phthalocyanines. Cobalt(II) phthalocyanines 2 and 6 are employed as catalyst for the oxidation of cyclohexene using tert-butyl hydroperoxide (TBHP), m-chloroperoxybenzoic

acid (m-CPBA), aerobic oxygen and hydrogen peroxide (H2O2) as oxidant. Appl. Organometal. Chem. DOI: 10.1002/aoc.2939

7 All Aspects of Topical A journal of Inorganic Chemistry in

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Editorial Board: Enzo Alessio, Università degli Studi di Trieste, Italy Jean-François Carpentier, Université de Rennes 1, France Lutz Gade, University of Heidelberg, Germany Yann Garcia, Université Catholique de Louvain-la-Neuve, Belgium Pedro J. Pérez, Universidad de Huelva, Spain International Advisory Board: Ana Albéniz, Universidad de Valladolid, Spain Lucia Banci, Università degli Studi di Firenze, Italy Koen Binnemans, KU Leuven, Belgium Mauro Botta, Università degli Studi del Piemonte Orientale, Alessandria, Italy Elisabeth Bouwman, Universiteit Leiden, The Netherlands Wesley R. Browne, Rijksuniversiteit Groningen, The Netherlands Christopher L. Cahill, George Washington University, Washington DC, USA Juan Cámpora, Consejo Superior de Investigaciones Científicas, Spain Luigi Casella, Università degli Studi di Pavia, Italy Editor-in-Chief: Remi Chauvin, CNRS, Toulouse, France Xiao-Ming Chen, Sun Yat-Sen University, Guangzhou, China Alberto Credi, Università degli Studi di Bologna, Italy Pascal D. C. Dietzel, Universitetet i Bergen, Norway Bryan W. Eichhorn, University of Maryland, College Park, USA Toshiaki Enoki, Tokyo Institute of Technology, Japan Juan C. Fontecilla-Camps, Commissariat à l’énergie Atomique et aux énergies Alternatives, Grenoble, France M. Concepción Gimeno, Universidad de Zaragoza, Spain Karen Hindson William T. A. Harrison, University of Aberdeen, UK Susumu Kitagawa, Kyoto University, Japan Editorial Board Chairman: Bert Klein Gebbink, Universiteit Utrecht, The Netherlands Moshe Kol, Tel Aviv University, Israel Janusz Lewiński, Politechnika Warszawska, Poland Ivan Lukeš, Univerzita Karlova, Praha, Czech Republic Eric Meggers, Philipps-Universität Marburg, Germany Karsten Meyer, Universität Erlangen-Nürnberg, Germany Nadia Mösch-Zanetti, Karl-Franzens-Universität Graz, Austria Srinivasan Natarajan, Indian Institute of Science, Bangalore, India Manuel Ocaña, Instituto de Ciencia de Materiales de Sevilla (CSIC-US), Spain Lahcéne Ouahab, Université de Rennes 1, France Bas de Bruin Shie-Ming Peng, National Taiwan University, Taipei, Taiwan Universiteit van Amsterdam, Spyros Perlepes, University of Patras, Greece The Netherlands Anna Proust, Université Pierre et Marie Curie, Paris, France Highlights: Joost N. H. Reek, Universiteit van Amsterdam, The Netherlands Kay Severin, école Polytechnique Fédérale de Lausanne, Switzerland • App available: bit.ly/CHEMAPPS Andreas Taubert, Universität Potsdam, Germany Tito Trindade, Universidade de Aveiro, Portugal • Free colour Felix Tuczek, Christian-Albrechts-Universität zu Kiel, Germany Luis F. Veiros, Universidade Técnica de Lisboa, Portugal Wing-Tak Wong, University of Hong Kong, China 8 Synthesis, Characterisation and Modelling of a Ferromagnetically Coupled Chromium(III) Dimer: Di-μ-hydroxobis[tetrakis(isothiocyanato)chromate(III)] Thorbjørn J. Morsing*, Høgni Weihe, Jesper Bendix* The di-μ-hydroxobis[tetrakis(isothiocyanato)chromate(III)] ion has been isolated and investigated by EPR spectroscopy. The magnetic susceptibility was measured in the temperature range 2–300 K. Both experiments show this system to be ferromagnetically coupled with a septet ground state. This is III Eur. J. Inorg. Chem. the third example of a ferromagnetically coupled Cr dimer, the DOI: 10.1002/ejic.201402779 first to be investigated by EPR.

Encapsulation of Bimetallic Nanoparticles into a Metal–Organic Framework: Preparation and Microstructure Characterization of Pd/Au@ZIF-8 Christoph Rösler, Daniel Esken, Christian Wiktor, Hirokazu Kobayashi, Tomokazu Yamamoto, Syo Matsumura, Hiroshi Kitagawa*, Roland A. Fischer* The imidazolate-based framework ZIF-8 was loaded with catalytically active mono- and bimetallic nanoparticles (Au, Pd, Pd/Au) by a seed-and-growth concept. Characterization of the synthesized materials was carried out by

powder X-ray diffraction, N2 sorption, and advanced transmission electron Eur. J. Inorg. Chem. microscopy.The catalytic activity towards aerobic alcohol oxidations DOI: 10.1002/ejic.201402409 was studied.

New Lithium–Containing Pnictides with 1-D Infinite Chains of Supertetrahedral Clusters: Synthesis, Crystal and Electronic Structure of

Ba4Li2Cd3Pn6 (Pn = P, As and Sb) Julien P. A. Makongo, Tae-Soo You, Hua He, Nian-Tzu Suen, Svilen Bobev* Three new Zintl phases have been synthesized for the first time, and their crystal structures have been established by single-crystal X-ray diffraction. They crystallize with their own-structure type in the orthorhombic space

Eur. J. Inorg. Chem. group Cmcm (Pearson code oC60) and their crystal structure is based on

DOI: 10.1002/ejic.201402434 one-dimensional infinite chains of supertetrahedral clusters, [Cd4Pn10].

O–S Bond Activation in Structures Isoelectronic with Ferric Peroxide Species Known in O–O‐ Activating Enzymes: Relevance for Sulfide Activation and Sulfite Reductases Mihai Surducan*, Sergei V. Makarov, Radu Silaghi-Dumitrescu* Described herein is the proton-driven activation of O–S bonds at heme centers, which is of relevance for sulfite reductases and globins, and contrasts with peroxidases, heme oxygenases, and cytochrome P450. Eur. J. Inorg. Chem. DOI: 10.1002/ejic.201402657

9 Free Your International Source Sample Copy for Inorganic and General Chemistry www.zaac.wiley-vch.de

Chairs of the Editorial Board:

Prof. Dr. Thomas Prof. Dr. Thomas Prof. Dr. F. Fässler, M. Klapötke, Christian Limberg, Technical University, Ludwig-Maximilians Humboldt University, Berlin Munich University, Munich

International Advisory Board:

Evgeny V. Antipov, Moscow, Russia Gerd Meyer, Köln, Germany Johannes Beck, Bonn, Germany Gordon J. Miller, Ames, IA, USA Wolgang Bensch, Kiel, Germany Srinivasan Natarajan, Bangalore, Eugenio Coronado, Valencia, Spain India Stefanie Dehnen, Marburg, Germany Reinhard Nesper, Zürich, Switzerland Hans-Jörg Deiseroth, Siegen, Rainer Pöttgen, Münster, Germany Germany Peter W. Roesky, Karlsruhe, Frank T. Edelmann, Magdeburg, Germany Germany Matthew J. Rosseinsky, Liverpool, UK Dieter Fenske, Karlsruhe, Germany Michael Ruck, Dresden, Germany Helmer Fjellvag, Oslo, Norway Masahiro Sadakane, Hiroshima, Song Gao, Beijing, China Japan Bernd Harbrecht, Marburg, Germany Manfred Scheer, Regensburg, Sjoerd Harder, Erlangen, Germany Germany Highlights: Evamarie Hey-Hawkins, Leipzig, Thomas Schleid, Stuttgart, Germany Germany Wolfgang Schnick, München, • Free color Christoph Janiak, Düsseldorf, Germany Germany Hansgeorg Schnöckel, Karlsruhe, • Pioneering fully electronic services Cameron Jones, Monash, Australia Germany • App available: bit.ly/CHEMAPPS Peter C. Junk, Townsville, Australia Won-Kyung Seok, Seoul, Korea Mercouri Kanatzidis, Evanston, IL, Konrad Seppelt, Berlin, Germany USA Christian Serre, Versailles, France Rhett Kempe, Bayreuth, Germany William S. Sheldrick, Bochum, Peter Klüfers, München, Germany Germany Rüdiger Kniep, Dresden, Germany Dirk Steinborn, Halle/S., Germany Robert L. LaDuca, East Lansing, Douglas W. Stephan, Toronto, MI, USA Canada Sven Lidin, Lund, Denmark Werner Uhl, Münster, Germany Antoine Maignan, Caen, France Mathias S. Wickleder, Oldenburg, Thomas Maschmeyer, Sydney, Germany Australia Michael Veith, Saarbrücken, Germany 10 Molybdenum L-Edge XAS Spectra of MoFe Nitrogenase Ragnar Bjornsson, Mario U. Delgado-Jaime, Frederico A. Lima, Daniel Sippel, Julia Schlesier, Thomas Weyhermüller, Oliver Einsle, Frank Neese, Serena DeBeer*

Z. anorg. allg. Chem. DOI: 10.1002/zaac.201400446

Impact of Crystal Chemistry upon Spin Orientation Transitions in Magnetic Perovskites Bernard Raveau*, Md. Motin Seikh

Z. anorg. allg. Chem. DOI: 10.1002/zaac.201400348

How to Prepare a Good Cu/ZnO Catalyst or the Role of Solid State Chemistry for the Synthesis of Nanostructured Catalysts Malte Behrens*, Robert Schlögl*, Vadim A. Soloshonok*

Z. anorg. allg. Chem. DOI: 10.1002/zaac.201300356

Syntheses, Structural Characterization, and Properties of Mixed‐valent CoIICoIII and ZnII Coordination Polymers from 5- (4- arboxybenzylamino)isophthalic Acid Hai-Wei Kuai*, Xiao-Chun Cheng*, Liang-Dong Feng, Xiao-Hong Zhu

Z. anorg. allg. Chem. DOI: 10.1002/zaac.201300280

Chemical Reactions followed by in situ Neutron Powder Diffraction Thomas C. Hansen*, Holger Kohlmann*

Z. anorg. allg. Chem. DOI: 10.1002/zaac.201400359

11 Publishing the spectrum of A journal of contemporary chemistry www.eurjoc.org Free Sample Copy

Editorial Board Editor-in-Chief: Chairman:

Haymo Ross Cesare Gennari, Università di Milano, Italy Editorial Board: Jesús Jiménez-Barbero, Madrid, Spain Burkhard König, Germany Jean Rodriguez, Pessac, France Floris Rutjes, The Netherlands Highlights: Christian Stevens, Belgium International Advisory Board: • App available: bit.ly/CHEMAPPS Alessandro Abbotto, Milano, Italy Yannick Landais, Bordeaux, France • Competitive Impact Factor of 3.154 Alexandre Alexakis, Genève, Annemieke Madder, Gent, Brussels • Microreviews - highly focused overviews Switherland Martin E. Maier, Tübingen, Germany Isabel Arends, Delft, The Netherlands Uday Maitra, Bangalore, India of a variety of topics Jeffrey Aubé, Lawrence, USA Ilan Marek, Haifa, Israel • A journal of ChemPubSoc Europe Corinne Aubert, Paris, France Rubén Martín, Tarragona, Spain Pablo Ballester, Tarragona, Spain Adriaan Minnaard, Groningen, supported by ACES Geert-Jan Boons, Athens, USA The Netherlands • Colour graphics free when essential Bernhard Breit, Freiburg, Germany Christina Moberg, Kungliga Tekniska Albert Manfred Brouwer, Högskolan, Stockholm Amsterdam, The Netherlands Martin Oestreich, Berlin, Germany Sukbok Chang, Daejeon, Korea Herman Overkleeft, Leiden, Fernando Cossío, San Sebastián – The Netherlands Donostia, Spain Maurizio Prato, Triest, Italy Dennis Curran, Pittsburgh, USA Amelia Rauter, Lisbon, Portugal Maria Valeria D’Auria, Naples, Italy Hans-Günther Schmalz, Cologne, Jonathan Ellman, New Haven, USA Germany Véronique Gouverneur, Oxford, UK Carsten Schmuck, Duisburg/Essen, Karol Grela, Warszawa, Poland Germany Dennis Hall, Edmonton, Canada Miguel Sierra, Madrid, Spain Yujiro Hayashi, Sendai, Japan Tibor Soós, Budapest, Hungary Piet Herdewijn, Leuven, Belgium Brian Stoltz, USA Lukas Hintermann, München Armido Studer, Münster, Germany Pei-Qiang Huang, Xiamen University, Jan van Maarseveen, Amsterdan, P. R. China The Netherlands Ivan Huc, Pessac, France Georgios Vassilikogiannakis, Kazuaki Ishihara, Nagoya University Iraklion, Greece Sambasivarao Kotha, Mumbai, India Guido Verniest, Brussels, Belgium Martin Kotora, Prague, Czech Wen-Jing Xiao, Wuhan, P. R. China Wolfgang Kroutil, Graz, Austria Jieping Zhu, Lausanne, France 12 Design Strategies for Enhanced Hydrogen-Bond Donor Catalysts Tyler J. Auvil, Andrew G. Schafer, Anita E. Mattson* Since initial reports of organocatalysis through hydrogen bonding interactions, a number of strategies have emerged to allow access to enhanced hydrogen-bond donor (HBD) organocatalysts. These strategies range from augmentation of existing HBDs to the design and synthesis of new HBD catalysts. Eur. J. Org. Chem. The effects of recent dual HBD designs on catalyst performance are described. DOI: 10.1002/ejoc.201400035

Fluorescence Enhancement of a Porphyrin–Viologen Dyad by Pseudorotaxane Formation with Cucurbit[7]uril Maher Fathalla, Nathan L. Strutt, Jonathan C. Barnes, Charlotte L. Stern, Chenfeng Ke, J. Fraser Stoddart The electron-transfer processes within a donor–acceptor dyad can be readily controlled through the formation of a pseudorotaxane between a viologen acceptor and cucurbit[7]uril. Eur. J. Org. Chem. DOI: 10.1002/ejoc.201402018

Direct Trifluoromethylthiolation Reactions: The “Renaissance” of an Old Concept Fabien Toulgoat, Sébastien Alazet, Thierry Billard

The CF3S group, owing to its high lipophilicity, has continuously received attention. In the past, trifluoromethylthiolation reactions were performed by using mainly two complementary reagents, that – + is, CF3SCl and CF3S M . Recently, the organic chemist’s toolbox has Eur. J. Org. Chem. gained new efficient methods based on transition-metal catalysis and DOI: 10.1002/ejoc.201301857 new easy-to-handle reagents.

Resorcin[4]arene-Based Molecular Baskets and Water-Soluble Container Molecules: Synthesis and 1H NMR Host–Guest Complexation Studies Daniel Fankhauser, Dušan Kolarski, Wolfram R. Grüning, François Diederich* 1H NMR binding studies of novel resorcin[4]arene-based molecular baskets and water-soluble container molecules have been performed with small molecular guests. Sequences of complexation strength for structurally similar heteroalicyclic Eur. J. Org. Chem. guests differ in organic and aqueous media. Guest inclusion rigidifies the water- DOI: 10.1002/ejoc.201402140 soluble hosts and rotation of the capping bridge slows, revealing planar chirality.

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Editor-in-Chief:

Richard Threlfall Editorial Board Chairs:

Sung Ho Kang Keiji Maruoka Deqing Zhang Korea Advanced Institute Kyoto University Chinese Academy of of Science and Technology, Sciences, Key Laboratory of Daejeon Organic Solids, Beijing

Highlights: Editorial Board Members: Naoto Chatani (Osaka University) • Next day publication of accepted articles Chien-Hong Cheng (National Tsing Hua University) Hyun-Joon Ha (Hankuk University of Foreign Studies) • Articles featured on facebook and Twitter Chun-Cheng Lin (National Tsing Hua University and Academia Sinica) • International readers and authors Teck Peng Loh (Nanyang Technological University) Uday Maitra (Indian Institute of Science, Bangalore) • An Asian Chemical Editorial Society Michio Murata (Osaka University) (ACES) journal supported by Shin-Ichiro Nishimura (Hokkaido University) Takashi Ooi (Nagoya University) ChemPubSoc Europe Ganesh Pandey (Centre of Biomedical Magnetic Resonance, Lucknow) Michael Sherburn (Australian National University) • Editor’s tips for writing scientific papers Young-Ger Suh (Seoul National University) (http://bit.ly/AJOCTips) and presentations Zhenfeng Xi (Peking University) (http://bit.ly/AJOCPresentationTips) Shuli You (Shanghai Institute of Organic Chemistry) Biao Yu (Shanghai Institute of Organic Chemistry) • Fast online publication of accepted Zhi-Xiang Yu (Peking University) articles Honory Board Members: • App available: bit.ly/CHEMAPPS Lixin Dai (Shanghai Institute of Organic Chemistry) Eun Lee (Seoul National University) • One-year Impact Factor: 2.292 (2013) Goverdhan Mehta (University of Hyderabad) Teruaki Mukaiyama (Kitasato University) Koji Nakanishi (Columbia University) Ei-ichi Negishi (Purdue University) Ryoji Noyori (RIKEN and Nagoya University) Akira Suzuki (Hokkaido University) Chi-Huey Wong (Scripps Research Institute) Daoben Zhu (Institute of Chemistry, Chinese Academy of Sciences) International Advisory Board: Comprising 58 world-renowned scientists, from all around the globe. 14 Domino Knoevenagel Condensation/Aza- Ene Addition/N- Cyclization Route to Functionalized Imidazo[1,2-a]pyridines and Pyrido[1,2-a]pyrimidines Sathiyamoorthi Sivakumar, Raju Ranjith Kumar* One-pot wonder! The syntheses of imidazo[1,2-a]pyridines and pyrido[1,2-a]pyrimidines were carried out by using a one-pot three- component protocol. The reaction proceeds in a single step through a domino Knoevenagel condensation/aza-ene addition/imine-enamine Asian Journal of tautomerization/chemoselective N-cyclization sequence of reactions Organic Chemistry (In=indolyl). DOI: 10.1002/ajoc.201402100

A Two-Photon Probe for Near-Membrane Zinc Ions Kailash Rathore, Chang Su Lim, Young Lee, Hee Jung Park, Bong Rae Cho* It takes two to probe: A two-photon probe for near-membrane zinc ions is reported. This probe is derived from a fluorene derivative that has a long-chain hydrocarbon tail and a zinc ion receptor. It predominantly stains the plasma membrane and emits strong two-photon excited fluorescence upon binding with zinc ions. Asian Journal of Organic Chemistry DOI: 10.1002/ajoc.201402112

Chameleonic Binding of the Dimethyldiazaperopyrenium Dication by Cucurbit[8]uril Karel J. Hartlieb, Ashish N. Basuray, Chenfeng Ke, Amy A. Sarjeant, Henri-Pierre Jacquot de Rouville, Takashi Kikuchi, Ross S. Forgan, Josh W. Kurutz, J. Fraser Stoddart* Two are better than one: The diazaperopyrenium dication acts as both a viologen-like electron-poor and an electron-rich guest, resulting in the formation of a 1:2 complex with cucurbit[8]uril. This chameleonic binding facilitates deaggregation of the dications from aqueous Asian Journal of Organic Chemistry solutions, leading to an increase in the fluorescence quantum yield of DOI: 10.1002/ajoc.201200187 the diazaperopyrenium dication.

Application of “Click” Chemistry to the Construction of Supramolecular Functional Systems Liang Xu, Yongjun Li*, Yuliang Li** Click! The click reaction forms 1,4-disubstituted 1,2,3-triazoles regioselectively. By incorporating a CH hydrogen-bond donor these triazoles can be used as anion receptors, and with their atom arrangement and electronic properties similar to those of a peptide bond, they can be used in the synthesis of bioactive macrocycles. Because of the unique mode of cyclization and recognition sites, Asian Journal of they can also be used in the construction of molecular machines. Organic Chemistry DOI: 10.1002/ajoc.201300245

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Editor:

Lyle W. Castle Associate Editor: Nancy Barta

Editorial Associates: Jerome Karle, Naval Research Laboratory J.-M. Lehn, Collège de France

Assistant Editor: Gary E. Martin

Editorial Board: J. Becher, Odense, Denmark R. Beckert, Jena, Germany J. Bergman, Huddinge, Sweden G. Bernáth, Szeged, Hungary D. L. Boger, La Jolla, CA J. Bradshaw, Provo, UT M. Brimble, Auckland, New Zealand P. Chiu, Hong Kong P. D. Cook, Carlsbad, CA J.-L. Imbach, Montpellier, France O. Kappe, Graz, Austria D. H. Kim, Pohang, Korea J. Liebscher, Berlin, Germany G. E. Martin, Kalamazoo, MI W. Pfleiderer, Konstanz, Germany G. Queguiner, Mont Saint Aignan, France S. W. Schneller, Auburn, AL D.-Q. Shi, Jiangsu, China B. Stanovnik, Ljubljana, Slovenia S.-J. Tu, Jiangsu, China 16 Synthesis and Starting from carbonic acid diethyl ester, a series of 1,2,4-triazole Antifungal Activity of derivatives containing 1,2,3-thiadiazole were synthesized. Reactions Novel 1,2,4-Triazole were performed by microwave irradiation or ultrasonic irradiation as well as by conventional heating. The structure of title compounds Derivatives Containing 1 1,2,3-Thiadiazole Moiety was characterized by H-NMR, MS, and elemental analyses. The fungicidal activities of these compounds were tested in vivo. Cheng-Xia Tan, Yan-Xia Shi, Most of title compounds exhibited good antifungal activity against Jian-Quan Weng, Xing-Hai Liu, Pseudoperonospora cubensis. Some of title compounds displayed Wei-Guang Zhao, Bao-Ju Li moderate antifungal activities against Fusarium oxysporum,

J. Heterocyclic Chem. 2014, 51, 690–694, Pseudoperonospora cubensis, Sphaerotheca fuligenea, Corynespora DOI: 10.1002/jhet.1656 cassiicola, and Xanthomonas axonopodis.

Microwave-Assisted Synthesis of Some Novel Benzimidazole Derivatives Containing Imine Function and Evaluation of Their Antimicrobial Activity Bahittin Kahveci, Fatih Yılmaz, Emre Menteşe, Musa Özil, Şengül Alpay Karaoğlu

4-Bromo-o-phenylenediamine and ethylimido-p- bromophenylacetate, 1, were subjected to microwave irradiation to synthesize benzimidazole derivative, compound 2. Ester derivative, 3, and hydrazide derivative, 4, of compound 2 were also synthesized, respectively. Finally, compound 4 was treated with 11 different aromatic aldehydes to obtain benzimidazole derivatives containing imine function. All reactions were carried out with microwave irradiation and conventional heating, and results were compared. Some of the newly synthesized compounds showed moderate antimicrobial activity against some tested organisms.

vJ. Heterocyclic Chem. 2014, 51, 982–990, DOI: 10.1002/jhet.1593

One-Pot Synthesis of A simple and highly efficient protocol for the one-pot synthesis of a 3-[(N-Alkylanilino)(aryl)methyl] series of 3-[(N-alkylanilino)(aryl)methyl]indoles has been developed indoles via a Transition Metal based on low-cost and environmentally benign zirconium oxychloride Assisted Three-Component octahydrate and copper chloride dihydrate catalysts via three- Condensation at Room component condensation between indoles, aromatic aldehydes, and Temperature N-alkylanilines at room temperature under neat condition. Mild reaction conditions, operational simplicity, high atom-economy, good yields in Goutam Brahmachari, Suvankar Das relatively shorter reaction times, and use of low-cost and eco-friendly J. Heterocyclic Chem. 2014, 51, E140–E145, catalysts are the key advantages of the present protocol. DOI: 10.1002/jhet.1909

17 Free Personal Accounts by Sample Copy Leading Experts wileyonlinelibrary.com/journal/poc

Editor-in-Chief:

Luis Echegoyen University of Texas – El Paso, TX, USA

Editorial Board: T. Bally, University of Fribourg, Switzerland Associate Editors: I. P. Beletskaya, Moscow State University, Russia NORTH AMERICA E. L. Clennan, University of Wyoming, USA Christopher J. Cramer, University of Minnesota, J. B. Engberts, University of Groningen, The Netherlands MN, USA D. E. Falvey, University of Maryland, USA Richard Johnson, University of New Hampshire, S. J. Grabowski, Euskal Herriko University, Euskadi (Spain) Durham, NH, USA J. P. Guthrie, University of Western Ontario, Canada ASIA E. Humeres, Universidade Federal de Santa Catarina, Brazil Jian-Bo Wang, College of Chemistry, Peking E. Juaristi, National Polytechnic Institute of Mexico, Mexico University, Beijing, China M. Kira, Tohoku University, Japan Takeshi Akasaka, Center for Tsukuba Advanced H. Mayr, Ludwig-Maximilians-University, Germany Research Alliance, Tsukuba, Japan B. Meunier, PALUMED S. A., France K. Müllen, Max Planck Institute for Polymer Research, Germany EUROPE K. Nakatani, Laboratory of Supramolecular and Macromolecular Mirjana Eckert-Maksic, Rudjer Boskovic Potophysic and Photochemistry (PPSM), France Institute, Zagreb, Croatia A. Nangia, University of Hyderabad, India Michael Schmittel, Universität Siegen, J. Nitschke, University of Cambridge, UK Siegen, Germany M. N. Paddon-Row, University of New South Wales, Australia Jaume Veciana, Campus Universidad Autónoma M. I. Page, University of Huddersfield, UK de Barcelona, Barcelona, Spain C. L. Perrin, University of California at San Diego, USA D. L. Philips, University of Hong Kong, China Reviews Editor: M. S. Platz, Ohio State University, USA Rik Tykwinski, Friedrich-Alexander-Universität J. P. Richard, University at Buffalo, USA Erlangen-Nürnberg, Erlangen, Germany I. Pojarkieff, Bulgarian Academey of Sciences, Bulgaria W. Sander, Ruhr-Universität Bochum, Germany P. R. Schreiner, Justus-Liebig University, Germany S. Shaik, Hebrew University, Jerusalem, Israel J. S. Siegel, Universität Zürich, Switzerland J. A. Sordo, Universidad de Oviedo, Spain M. Speranza, University ‘La Sapienza’, Roma, Italy C. Tung, Chinese Academy of Sciences, Beijing, China O. Wiest, University of Notre Dame, USA 18 Acidities of strong neutral Brønsted acids in different media Elin Raamat, Karl Kaupmees, Gea Ovsjannikov, Aleksander Trummal, Agnes Kütt, Jaan Saame, Ivar Koppel, Ivari Kaljurand, Lauri Lipping, Toomas Rodima, Viljar Pihl, Ilmar A. Koppel, Ivo Leito Acidity orders of acids are different in water, acetonitrile, 1,2-dichloroethane, and gas phase. The acidity order trends of acids depend on the extent of charge delocalization in their anions and can be interpreted using the weighted average J. Phys. Org. Chem. DOI: 10.1002/poc.2946 positive sigma parameters of the anions.

Buckyball maracas: exploring the inside and outside properties of endohedral fullerenes Danisha M. Rivera-Nazario, Julio R. Pinzón, Steven Stevenson, Luis A. Echegoyen* Our research group has contributed to the discovery, functionalization, and characterization of new and interesting compounds that have been explored in different applications, but mainly in the field of organic photovoltaics. Here, we report the

J. Phys. Org. Chem. contribution and progress of our research group in the field of DOI: 10.1002/poc.3009 buckyball “maracas”.

Carbon-rich nanostructures: the conversion of acetylenes into materials Erin T. Chernick, Rik R. Tykwinski* The carbon–carbon triple bond is a high-energy precursor that serves as a unique starting point for the directed synthesis of carbon-based nanomaterials that are important for applications in materials science. This contribution will highlight several recent examples that use acetylenes (or polyynes) as building J. Phys. Org. Chem. blocks in templated synthetic transformations to form carbon- DOI: 10.1002/poc.3160 based nanomaterials.

1,3,5-tricorannulenylbenzene: stereochemistry, reduction and supramolecular dimerization of a branched oligocorannulene David Eisenberg, Jennifer M. Quimby, Lawrence T. Scott*, Roy Shenhar* A novel branched oligocorannulene is synthesized, and its redox J. Phys. Org. Chem. and supramolecular chemistry are elucidated using experimental DOI: 10.1002/poc.2951 and theoretical methods.

19 Free Flavour and Fragrance Sample Copy wileyonlinelibrary/journal/ffj

Editor-in-Chief:

Alain Chaintreau University of Texas – El Paso, TX, USA Editorial Board Chairs:

Carlo Bicchi Gerhard Buchbauer Gary Reineccius Highlights: Universita Degli Studi di University of Vienna, Centre of University of Torino, Italy Pharmacy, Austria Minnesota, USA • Original research articles, reviews and Reviews Editor: special reports on all aspects of flavour and fragrance from academia and industry • Includes composition, analysis and synthesis of flavours and fragrances, as well as essential oils, extracts, natural/ naturally derived and related synthetic products Elisabeth Guichard Vincente Ferreira Daniel Joulain Unité Mixte de Recherches University of Zaragoza, Les Micocouliers-F3, France • All natural or synthetic products eliciting INRA-ENESAD-UB, France Spain or influencing a sensory stimulus related to gustation or olfaction; sensory Editorial Board: evaluation, definition and classification TY. Asakawa, Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Japan • High scientific standards and international R.G. Berger, Institut für Lebensmittelchemie, Hannover, Germany character ensured by a strict refereeing W. Bredie, Department of Food Science, University of Copenhagen, Denmark K. Cadwallader, Department of Food Science and Human Nutrition, University of system managed by an editorial team Illinois, USA representing the multidisciplinary J. Casanova, Université de Corse, CNRS Equipe Chimie et Biomasse, Ajaccio, expertise of the field of research France F. David, R.I.C. BVBA, Kortrijk, Belgium • Recommended Practice articles focus P. Dugo, Faculty of Science, University of Messina, Italy special attention on the quality of A.C. Figueiredo, Centro de Biotechnologia Vegetal, Lisbon, Portugal C. Franz, Institut für Angewandte Botanik, Veterinrmedizinische Universitt Wien, analytical techniques Austria A.Natsch, Givaudan Schweiz AG, Switzerland Y. Noma, Faculty of Human Life Sciences, Tokushima Bunri University, Japan R. A. Raguso, Dept. of Neurobiology and Behavior, Cornell University, USA P. Rubiolo, Faculty of Pharmacy, Università degli Studi di Torino, Italy A. J. Taylor, Department of Applied Biochemistry and Food Science, University of Nottingham, England 20 T. Thomas-Danguin, Centre des Sciences du Goût et de l’Alimentation, France Preparation and characterization of chitosan nanoparticles as the delivery system for tuberose fragrance Zuobing Xiao, Ting Tian, Jing Hu*, Mingxi Wang, Rujun Zhou Fragrance can be encapsulated inside chitosan nanoparticles via the ionic gelification. The thermal stability and antibacterial activity of the nanoparticles have been improved in compared with fragrance. chitosan nanoparticles would be a promising Flavour Fragr. J. 2014, 29, 22–34 controlled-release carrier of fragrance. doi: 10.1002/ffj.3174

Production of ferulic acid and coniferyl alcohol by conversion of eugenol using a recombinant strain of Saccharomyces cerevisiae Fanny Lambert*, Joseph Zucca, Frédérique Ness, Michel Aigle Development of a single-step biotransformation process for natural ferulic acid production from eugenol using a recombinant yeast. Flavour Fragr. J. 2014, 29, 14–21 doi: 10.1002/ffj.3173

Chemical variability and antioxidant activity of Eryngium maritimum L. essential oils from Corsica and Sardinia Florent Darriet, Stéphane Andreani, Marie-Cécile De Cian, Jean Costa, Alain Muselli* The study of the chemical variability of Corsican and Sardinian Eryngium maritimum essential oils showed a direct correlation between the island origins of the sample essential oils and their chemical compositions. Corsican samples exhibited higher amounts of hydrocarbon terpenes than did Sardinian samples. Both E. maritimum essential oils exhibited original compositions with uncommon sesquiterpene aldehydes. No meaningful Flavour Fragr. J. 2014, 29, 3–13 activity could be attributed to sesquiterpene aldehydes but E. maritimum doi: 10.1002/ffj.3160 essential oil demonstrated strong antioxidant properties.

Sensory profile of pink port wines: Development of a flavour lexicon Bebiana Monteiro, Alice Vilela*, Elisete Correia Sensory profile of pink port wines from five different brands. Identification and selection of descriptors for pink port wines, development of references and training of the panel. Data analysis by multivariate non-parametric statistics (non- parametric MANOVA and categorical principal components analysis). Flavour Fragr. J. 2014, 29, 50–58 doi: 10.1002/ffj.3178

21 Free Journal of Peptide Science Sample Copy wileyonlinelibrary.com/journal/jpepsci

Deputy Associate Editor-in-Chief: Editor-in-Chief:

Luis Moroder Ulf Diederichsen Max Planck Institute of Biochemistry, Insitut fur Organische und Germany Biomolekulare Chemie, Germany

Highlights: www.eurpepsoc.com Editors: • The official journal of the European Peptide Society, recognised throughout the world as a premier research resource for all peptide scientists, building bridges between physical chemistry and the bioscience communities Michael Chorev Yoshiaki Kiso Paolo Rovero • Original articles, rapid communications, Harvard Medical School, Nagahama Institute of Universita di Firenze, Italy Cambridge, USA Bio-Science and invited reviews, special issues and Technology, Japan major peptide conference abstract/ supplement issues • International research from institutions of excellence throughout North America, Asia and Europe

Ernest Giralt John Wade Institut de Recerca Biomèdica Howard Florey Institute, de Barcelona, Spain Australia

International Advisory Board: Comprising 49 world-renowned scientists, from all around the globe.

22 Self-assembling amphiphilic peptides Ashkan Dehsorkhi, Valeria Castelletto, Ian W. Hamley* The self-assembly of amphiphilic peptides including surfactant- like peptides and lipopeptides is reviewed, focusing on modes and mechanisms of self-assembly as well as applications in biomedicine and materials science.

J. Pept. Sci. 2014, 20, 453–467, doi: 10.1002/psc.2633

Development of a neuromedin U–human serum albumin conjugate as a long-acting candidate for the treatment of obesity and diabetes. Comparison with the PEGylated peptide Philippe Neuner, Andrea M. Peier, Fabio Talamo, Paolo Ingallinella, Armin Lahm, Gaetano Barbato, Annalise Di Marco, Kunal Desai, Karolina Zytko, Ying Qian, Xiaobing Du, Davide Ricci, Edith Monteagudo, Ralph Laufer, Alessandro Pocai, Elisabetta Bianchi, Donald J. Marsh*, Antonello Pessi* Conjugation of the endogenous peptide neuromedin U to J. Pept. Sci. 2014, 20, 7–19, albumin yields a compound with long-lasting body-weight doi: 10.1002/psc.2582 lowering and glucose-tolerance improving effects.

BOP-OXy, BOP-OBt, and BOP-OAt: novel organophosphinic coupling reagents useful for solution and solid-phase peptide synthesis Ayman El-Faham*, Sherine N. Khattab, Ramon Subirós- Funosas, Fernando Albericio* BOP-OXy, BOP-OBt, and BOP-OAt coupling reagents show efficient performance in solution and SPPS. BOP-OXy shows

J. Pept. Sci. 2014, 20, 1–6, the additional advantage of being highly soluble in DMF and doi: 10.1002/psc.2579 even fairly soluble in CH3CN.

Evaluation of acid-labile S-protecting groups to prevent Cys racemization in Fmoc solid-phase peptide synthesis Hajime Hibino, Yasuyoshi Miki, Yuji Nishiuchi* The 4,4’-dimethoxydiphenylmethyl and 4-methoxybenzyloxymethyl groups were shown to be acid-labile S-protecting groups that can suppress racemization of Cys to an acceptable level (<1.0%) even when its Fmoc derivatives are incorporated via the standard

J. Pept. Sci. 2014, 20, 30–35, SPPS protocol of phosphonium or uronium reagents with the aid doi: 10.1002/psc.2585 of DIEA in DMF.

23 Free All aspects of Sample Copy Chiral Molecules wileyonlinelibrary.com/journal/chir

Editors:

Prof. John Caldwell Prof. Nina Berova University of Liverpool Columbia University

Chiral 3D Open-Framework Material

Ni(D-cam)(H2O)2 Used as GC Stationary Phase Shengming Xie, Bangjin Wang, Xinhuan Zhang, Junhui Zhang, Mei Zhang, Liming Yuan

Chirality DOI: 10.1002/chir.22260

Chromatographic Separation and Assignment of Absolute Configuration of Hydroxywarfarin Isomers Erik L. Regalado, Edward C. Sherer, Mitchell D. Green, Derek W. Hendersonl, R. Thomas Williamson, Leo A. Joyce, Christopher J. Welchu

Chirality DOI: 10.1002/chir.22274

Development and Mechanism of an Enantioselective Bromocycloetherification Reaction via Lewis Base/Chiral Brønsted Acid Cooperative Catalysis Scott E. Denmark, Matthew T. Burk

Chirality DOI: 10.1002/chir.22259

24 Free Concentrating on Sample Copy Heteroatoms wileyonlinelibrary.com/journal/hc

Editor in Chief:

Derek P. Gates University of British Columbia

Bifunctionalized Allenes, Part XI: Competitive Electrophilic Cyclization and Addition Reactions of 4-Phosphorylated Allenecarboxylates Ivaylo K. Ivanov, Ivaylo D. Parushev, Valerij Ch. Christov*, Mei Zhang, Liming Yuan

Heteroatom Chem. 2014, 25, 60–71 DOI: 10.1002/hc.21136

Syntheses of Chiral Phosphazenes with Stereogenic Centers: NMR Behavior in the Presence of a Chiral Solvating Agent Nuran Asmafiliz*

Heteroatom Chem. 2014, 25, 83–94 DOI: 10.1002/hc.21139

Double Asymmetric Induction in the Synthesis of Enantiomeric α-Aminophosphonic Acids Mediated by Sulfinimines Piotr Łyżwa*

Heteroatom Chem. 2014, 25, 15–19 DOI: 10.1002/hc.21130

25 Good Things NEW come in threes

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Video: Carbonate Looping Elmar Zimmermann, Vera Köster (Video Editing: Lynsey Geldeard) 28 www.chempubsoc.eu Conference onCoordination Chemistry, Organometal- ChemPubSoc Europe Owners Meeting1999,Madrid lic Chemistry andCatalysis 2012,MétabiefMontd’Or www.chemeurj.org K. A.Jørgensen etal.K. Hydrogen-Bonding inAminocatalysis: From Proline andBeyond Concept CEUJED 20 (2) 337–612 (2014)·ISSN0947-6539 Vol. 20·No.CEUJED 20(2)337–612 2·2014 Speakers Launched Launched Launched Launched Launched Launched CPCHFT 14 (9) 1749 CPCHFT 14(9)1749 – 2004 (2013)·ISSN1439-4235 Vol. 14·No. 9·June2013 2000 200 1995 Symposium 2005,Strasbourg 8 Chemistry –AEuropean Journal 2014-20/2 A Journalof Launched Launched Launched Launched Launched Launched CHEMK3 6 (1) 1–362 (2014)·ISSN1867-3880Vol.6No.1January,2014 CHEMK3 6(1)1–362 2014 2009 2010

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ChemPubSoc Europe Owners Meeting2004,Lisbon EJOCFK (33) 7437–7636 (2013) · ISSN 1434-193X · No. 33/2013 No. · 1434-193X ISSN · (2013) 7437–7636 (33) EJOCFK A sister journal of journal sister A Open 2013·39 – 76 ·OnlineISSN2191-1363Vol.2No.April2013 Recent Developments in Amide Synthesis Amide in Developments Recent Rachel M. Lanigan and Tomand Lanigan Sheppard M. D. Rachel Microreviews Tetra(2-thienyl)ethyleneDerivatives Clara Baldoli, Emanuela Licandro et al. et Licandro Emanuela Baldoli, Clara CoverPicture Asian Journal of Organic Chemistry Organic of Journal Asian Wissenschaftsforum Chemie2013,Darmstadt Eur Enantioselective ArtiﬁcialMetalloenzymes Speakers (K. Tschulik,R.G.Compton) Nanoparticle Agglomeration CBCHFX 14(17)2221– 2376 (2013)·ISSN1439-4227 Vol. 14·No. 17·November 2013 Communication: Launched Launched Launched Launched Launched Launched (J. Eppinger) Full Paper: JOC Organic Chemistry Organic of Journal European 2012 1998 2000 Symposium 2010,Paris ChemBioChem /ChemPhysChem www.eurjoc.org 2/2013 3rd November Issue November 3rd 33 D55712 /2013 D 6093 D EJICFK (25) 4353–4525 (2013) · ISSN 1099-0682 · No. 25/2013 No. · 1099-0682 ISSN · (2013) 4353–4525 (25) EJICFK Biologically Relevant Silver(I)–N-Heterocyclic CarbeneComplexesSilver(I)–N-Heterocyclic Relevant Biologically Srinivasa Budagumpi et al. et Budagumpi Srinivasa Microreview White-Emitting CaWhite-Emitting Jun Lin et al. et Lin Jun CoverPicture Eur Cover Picture: Nanodiamond–TiO Minireview: Full Paper: Energy-Transfer inIr Mechanisms 9 MgNa(PO ChemPlusChem 78 (8) 749–884 (2013)·ISSN2192-6506Vol.78No.8August2013 ChemPlusChem 78(8)749–884 The Piers–Rubinsztajn (R. Reaction Wakabayashi Kuroda) andK. Launched Launched 4 Launched Launched ) 7 CHEMGX 8(8)1229 –1420 (2013)·ISSN1860-7179 Vol. 8·No. 8·August, 2013 Launched Launched :Ce 3+ /Tb JIC www.chempluschem.org 3+ 8/2013 2012 Inorganic Chemistry Inorganic of Journal European /Mn 2005 1998 2 Composites for Photocatalysis (A. M. T. Silvaetal.) 2+ Phosphors III –Eu www.eurjic.org III Complexes (Z.Bianetal.)

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