Angewandte Chemie International Edition (ANGEW CHEM INT EDIT)

Description

Angewandte Chemie is one of the prime chemistry journals in the world with an ISI-measured Impact Factor higher than those of comparable journals (1999: 7.996). Moreover it is the only journal in the field to have a stimulating mixture of review articles highlights and short communications. The "reviews" written by leading experts summarize the important results of recent research on topical subjects in all branches of chemistry point to unresolved problems and discuss possible developments. The "highlights" provide concise evaluations of current trends in chemical research. The communications are critically selected and report on the latest research results making the journal indispensable to the chemist who wants to stay well informed. Angewandte Chemie also regularly publishes Nobel lectures in chemistry and related fields. Kurztext Auch die internationale Ausgabe der Angewandten Chemie zählt zu den führenden bedeutenden Chemiezeitschrifent weltweit. Chemiker wissen daß sie hier das Neueste aus der Chemie bestens aufbereitet vorfinden. Society Affiliation German Chemical Society ( Gesellschaft Deutscher Chemiker ) Readers Chemists of all disciplines

Publisher details

John Wiley & Sons

Publications in this journal

• Bio-Inspired Phosphole-Lipids: From Highly Fluorescent Organogels to Mechanically Responsive FRET

  Authors: Yi Ren, Wang Hay Kan, Prof. Dr. Venkataraman Thangadurai, Prof. Dr. Thomas Baumgartner

  Angewandte Chemie International Edition.

• Reversible Modification of Epitaxial Graphene

  Authors: Santanu Sarkar, Elena Bekyarova, Robert C. Haddon

  Angewandte Chemie International Edition.

• Reversibly Shape-Shifting Organic Optical Wave Guides: Formation of Organic Nano-Rings (0-D), Nano-Tubes (1D), and Nano-Sheets (2D)**

  Authors: Naisa Chandrasekhar, Rajadurai Chandrasekar

  Angewandte Chemie International Edition.

  Shape-shifting: A method for reversibly transforming the shape of organic wave-guides to form 2D nanosheets, 1D nanotubes, and 0D nanorings has been developed. The nanosheets can be turned intoShape-shifting: A method for reversibly transforming the shape of organic wave-guides to form 2D nanosheets, 1D nanotubes, and 0D nanorings has been developed. The nanosheets can be turned into nanotubes and subsequently into nanorings by adding water to the solvent, whereas ultrasonication changes the nanotubes back into nanosheets. Both nanotubes and nanosheets act as wave-guides and change the direction of incident laser light in a shape-dependent manner.

• Synthesis of the Smallest Axially Chiral Molecule via Asymmetric Carbon-Fluorine Bond Activation

  Authors: M.F. Kuehnel, T. Schlöder, S. Riedel, B. Nieto-Ortega, F.J.Ramírez, J.T. López Navarrete, J. Casado, D. Lentz

  Angewandte Chemie International Edition. 124:2218-2220.

• Nanoscale Growth of Molecular Oxides: Assembly of a {V6} Double Cubane Between Two Lacunary {P2W15} Polyoxometalates

  Authors: Claire Lydon, Christoph Busche, Haralampos N. Miras, Alexander Delf, De-Liang Long, Lesley Yellowlees, Leroy Cronin

  Angewandte Chemie International Edition. 51:2115 –2118.

  POM-in-POM: A Wells–Dawson polyoxometalate sandwich compound with a double cubane core consisting of six vanadium atoms has been synthesized (see structure). Cluster formation was followed by massPOM-in-POM: A Wells–Dawson polyoxometalate sandwich compound with a double cubane core consisting of six vanadium atoms has been synthesized (see structure). Cluster formation was followed by mass spectrometry and the reduction of the double cubane was studied by a novel technique combining mass spectrometry and spectroelectrochemistry.

• Sn4Si[Si(SiMe3)3]4[SiMe3]2: A model compound for the unexpected first order transition from a singlet biradicaloid to a classical bonded molecule.

  Authors: Claudio Schrenk, Adam Kubas, Karin Fink, Andreas Schnepf

  Angewandte Chemie International Edition.

• Insights into Lasalocid A Ring Formation by Chemical Chain Termination In Vivo

  Authors: Manuela Tosin, Luke Smith, Prof. Peter F. Leadlay

  Angewandte Chemie International Edition.

  Caught in the act: Intermediates in the biosynthesis of lasalocid A are captured in vivo by malonyl carba(dethia)-N-acetyl cysteamine probes. These species constitute novel snapshots of the timing ofCaught in the act: Intermediates in the biosynthesis of lasalocid A are captured in vivo by malonyl carba(dethia)-N-acetyl cysteamine probes. These species constitute novel snapshots of the timing of ether and aromatic ring formation, thus providing valuable insights for the reconstruction and the engineering of polyether biosynthetic pathways.

• Intracellular magnetite biomineralization in bacteria proceeds by a distinct pathway involving membrane-bound ferritin and an iron(II) species.

  Authors: Damien Faivre, Lars H Böttger, Berthold F Matzanke, Dirk Schüler

  Angewandte Chemie (International ed. in English). 46(44):8495-9.

• Simple heme dimers with strongly cooperative ligand binding.

  Authors: Daria Khvostichenko, Qing-Zheng Yang, Roman Boulatov

  Angewandte Chemie (International ed. in English). 46(44):8368-70.

• Palladium-catalyzed aminocarbonylation of aryl chlorides at atmospheric pressure: the dual role of sodium phenoxide.

  Authors: Joseph R Martinelli, Thomas P Clark, Donald A Watson, Rachel H Munday, Stephen L Buchwald

  Angewandte Chemie (International ed. in English). 46(44):8460-3.

• Regioselective 1-hexene oligomerization using cationic bis(phenolato) group 4 metal catalysts: switch from 1,2- to 2,1-insertion.

  Authors: Bing Lian, Klaus Beckerle, Thomas P Spaniol, Jun Okuda

  Angewandte Chemie (International ed. in English). 46(44):8507-10.

• Isoenzymes of pig-liver esterase reveal striking differences in enantioselectivities.

  Authors: Anke Hummel, Elke Brüsehaber, Dominique Böttcher, Harald Trauthwein, Kai Doderer, Uwe T Bornscheuer

  Angewandte Chemie (International ed. in English). 46(44):8492-4.

• Poly(anthrylenebutadiynylene)s: precursor-based synthesis and band-gap tuning.

  Authors: Mark S Taylor, Timothy M Swager

  Angewandte Chemie (International ed. in English). 46(44):8480-3.

• A code for lysine modifications of a silica biomineralizing silaffin protein.

  Authors: Manfred Sumper, Robert Hett, Gerhard Lehmann, Stephan Wenzl

  Angewandte Chemie (International ed. in English). 46(44):8405-8.

• Recognition of "mirror-image" DNA by small molecules.

  Authors: Christian Dose, Dominik Ho, Hermann E Gaub, Peter B Dervan, Christian H Albrecht

  Angewandte Chemie (International ed. in English). 46(44):8384-7.

• Cobalt-catalyzed Alder-ene reaction.

  Authors: Gerhard Hilt, Jonas Treutwein

  Angewandte Chemie (International ed. in English). 46(44):8500-2.

• Kinetic resolution of 1,2-diols through highly site- and enantioselective catalytic silylation.

  Authors: Yu Zhao, Aurpon W Mitra, Amir H Hoveyda, Marc L Snapper

  Angewandte Chemie (International ed. in English). 46(44):8471-4.

• Target-selective degradation of oligosaccharides by a light-activated small-molecule-lectin hybrid.

  Authors: Maiko Ishii, Shuichi Matsumura, Kazunobu Toshima

  Angewandte Chemie (International ed. in English). 46(44):8396-9.

• Indium-catalyzed cycloisomerization of omega-alkynyl-beta-ketoesters into six- to fifteen-membered rings.

  Authors: Hayato Tsuji, Ken-ichi Yamagata, Yoshimitsu Itoh, Kohei Endo, Masaharu Nakamura, Eiichi Nakamura

  Angewandte Chemie (International ed. in English). 46(42):8060-2.

• Electrochemical aerobic oxidation of aminocyclopropanes to endoperoxides.

  Authors: Claire Madelaine, Yvan Six, Olivier Buriez

  Angewandte Chemie (International ed. in English). 46(42):8046-9.

• Conformational locking through allylic strain as a device for stereocontrol--total synthesis of grandisine A.

  Authors: David J Maloney, Samuel J Danishefsky

  Angewandte Chemie (International ed. in English). 46(41):7789-92.

• Direct arylation of thiazoles on water.

  Authors: Gemma L Turner, James A Morris, Michael F Greaney

  Angewandte Chemie (International ed. in English). 46(42):7996-8000.

• The renaissance of H/D exchange.

  Authors: Jens Atzrodt, Volker Derdau, Thorsten Fey, Jochen Zimmermann

  Angewandte Chemie (International ed. in English). 46(41):7744-65.

  The increasing demand for stable isotopically labeled compounds has led to an increased interest in H/D-exchange reactions at carbon centers. Today deuterium-labeled compounds are used as internalThe increasing demand for stable isotopically labeled compounds has led to an increased interest in H/D-exchange reactions at carbon centers. Today deuterium-labeled compounds are used as internal standards in mass spectrometry or to help elucidate mechanistic theories. Access to these deuterated compounds takes place significantly more efficiently and more cost effectively by exchange of hydrogen by deuterium in the target molecule than by classical synthesis. This Review will concentrate on the preparative application of the H/D-exchange reaction in the preparation of deuterium-labeled compounds. Advances over the last ten years are brought together and critically evaluated.

• Chemical defense of the crust fungus Aleurodiscus amorphus by a tailor-made cyanogenic cyanohydrin ether.

  Authors: Bernhard L J Kindler, Peter Spiteller

  Angewandte Chemie (International ed. in English). 46(42):8076-8.

• Engineered alkane-hydroxylating cytochrome P450(BM3) exhibiting nativelike catalytic properties.

  Authors: Rudi Fasan, Mike M Chen, Nathan C Crook, Frances H Arnold

  Angewandte Chemie (International ed. in English). 46(44):8414-8.

Data provided are for informational purposes only. Although carefully collected, accuracy cannot be guaranteed. The impact factor represents a rough estimation of the journal's impact factor and does not reflect the actual current impact factor. Publisher conditions are provided by RoMEO. Differing provisions from the publisher's actual policy or licence agreement may be applicable.