Aziridines and Epoxides in Organic Synthesis. Herausgegeben von Andrei K. Yudin. (Deutsch)
- Neue Suche nach: Gansäuer, Andreas
- Neue Suche nach: Gansäuer, Andreas
In:
Angewandte Chemie
;
118
, 35
;
5863
;
2006
- Aufsatz (Zeitschrift) / Elektronische Ressource
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Titel:Aziridines and Epoxides in Organic Synthesis. Herausgegeben von Andrei K. Yudin.
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Beteiligte:Gansäuer, Andreas ( Autor:in )
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Erschienen in:Angewandte Chemie ; 118, 35 ; 5863
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Verlag:
- Neue Suche nach: WILEY‐VCH Verlag
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Erscheinungsdatum:04.09.2006
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Format / Umfang:1 pages
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ISSN:
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DOI:
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Medientyp:Aufsatz (Zeitschrift)
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Format:Elektronische Ressource
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Sprache:Deutsch
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Schlagwörter:
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Datenquelle:
Inhaltsverzeichnis – Band 118, Ausgabe 35
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Die Inhaltsverzeichnisse werden automatisch erzeugt und basieren auf den im Index des TIB-Portals verfügbaren Einzelnachweisen der enthaltenen Beiträge. Die Anzeige der Inhaltsverzeichnisse kann daher unvollständig oder lückenhaft sein.
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Titelbild: Pd-Catalyzed [alpha]-Arylation of Trimethylsilyl Enol Ethers with Aryl Bromides and Chlorides: A Synergistic Effect of Two Metal Fluorides as Additives (Angew. Chem. 35-2006)Su, Weiping et al. | 2006
- 5847
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Titelbild: Pd‐Catalyzed α‐Arylation of Trimethylsilyl Enol Ethers with Aryl Bromides and Chlorides: A Synergistic Effect of Two Metal Fluorides as Additives (Angew. Chem. 35/2006)Su, Weiping / Raders, Steven / Verkade, John G. / Liao, Xuebin / Hartwig, John F. et al. | 2006
- 5847
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Titelbild: Pd-Catalyzed a-Arylation of Trimethylsilyl Enol Ethers with Aryl Bromides and Chlorides: A Synergistic Effect of Two Metal Fluorides as Additives (Angew. Chem. 35/2006)Su, W. / Raders, S. / Verkade, J. G. / Liao, X. / Hartwig, J. F. et al. | 2006
- 5850
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Graphisches Inhaltsverzeichnis: Angew. Chem. 35/2006| 2006
- 5860
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Design and Size Control of Uniform Zeolite Nanocrystals Synthesized in Adjustable Confined Voids Formed by Recyclable Monodisperse Polymer SpheresYang, Xiaoyu / Feng, Yefei / Tian, Ge / Du, Yunchen / Ge, Xin / Di, Yan / Zhang, Yonglai / Sun, Bo / Xiao, Feng‐Shou et al. | 2006
- 5863
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Aziridines and Epoxides in Organic Synthesis. Herausgegeben von Andrei K. Yudin.Gansäuer, Andreas et al. | 2006
- 5863
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Molecular Physics. Theoretical Principles and Experimental Methods. Von Wolfgang Demtroder.van Wullen, C. et al. | 2006
- 5863
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Molecular Physics. Theoretical Principles and Experimental Methods. Von Wolfgang Demtröder.van Wüllen, Christoph et al. | 2006
- 5866
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Totalsynthesen des antibakteriellen Naturstoffes Abyssomicin CPeters, René / Fischer, Daniel F. et al. | 2006
- 5870
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Selektiver Aufbau achtgliedriger Carbocyclen durch Ringschlussmetathese acyclischer VorstufenMichaut, Antoine / Rodriguez, Jean et al. | 2006
- 5884
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Polypeptide und 100 Jahre Chemie der [alpha]-Aminosäure-N-carboxyanhydrideKricheldorf, Hans R. et al. | 2006
- 5884
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Polypeptide und 100 Jahre Chemie der α‐Aminosäure‐N‐carboxyanhydrideKricheldorf, Hans R. et al. | 2006
- 5884
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Polypeptide und 100 Jahre Chemie der a-Aminosaure-N-carboxyanhydrideKricheldorf, H. R. et al. | 2006
- 5918
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Multilayer Sequential Assembly of Thin Films That Display Room‐Temperature Spin Crossover with HysteresisCobo, Saioa / Molnár, Gábor / Real, José Antonio / Bousseksou, Azzedine et al. | 2006
- 5918
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Multilayer Sequential Assembly of Thin Films That Display Room-Temperature Spin Crossover with Hysteresis. The authors are grateful to L. Rechignat (LCC-CNRS) and G. L. Agusti (ICMol) for experimental help. This work was supported by the Plateforme Technologique du LAAS CNRS (Toulouse, France). J.A.R. is grateful to the Spanish Ministerio de Education y Ciencia (MEC; CTQ 2004-03456-BQU).Cobo, Saioa et al. | 2006
- 5922
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Total Synthesis and Structure Assignment of (+)-Hexacyclinol. We thank Mr. Andrew Germain (Boston University) for helpful discussions, Dr. Friedrich A. Gollmick (Leibniz Institute for Natural Products Research and Infection Biology-Hans-Knöll-Institute, Jena, Germany) for providing spectra of natural hexacyclinol, and Dr. Emil Lobkovsky (Cornell University) for X-ray crystal structure analysis. Financial support from the NIH (GM62842 and P50 GM067041), Bristol-Myers Squibb, Merck, and Novartis is gratefully acknowledged.Porco, John A. et al. | 2006
- 5922
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Total Synthesis and Structure Assignment of (+)‐HexacyclinolPorco, John A. Jr. / Su, Shun / Lei, Xiaoguang / Bardhan, Sujata / Rychnovsky, Scott D. et al. | 2006
- 5924
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Thermally Responsive Vesicles and Their Structural “Locking” through Polyelectrolyte Complex FormationLi, Yuting / Lokitz, Brad S. / McCormick, Charles L. et al. | 2006
- 5924
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Thermally Responsive Vesicles and Their Structural "Locking" through Polyelectrolyte Complex Formation. Paper 123 in a series entitled "Water-Soluble Polymers". We gratefully acknowledge financial support provided by the Department of Energy (DE-FC26-01BC15317) and the MRSEC program of the National Science Foundation (DMR-0213883).Li, Yuting et al. | 2006
- 5928
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Color‐Saturated Green‐Emitting QD‐LEDsSteckel, Jonathan S. / Snee, Preston / Coe‐Sullivan, Seth / Zimmer, John P. / Halpert, Jonathan E. / Anikeeva, Polina / Kim, Lee‐Ann / Bulovic, Vladimir / Bawendi, Moungi G. et al. | 2006
- 5928
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Color-Saturated Green-Emitting QD-LEDs. This work was funded in part by the NSF-MRSEC program (DMR 0213282), by the US Army through the Institute for Soldier Nanotechnologies, under Contract DAAD-19-02-0002 with the US Army Research Office, by the Presidential Early Career Award for Scientists and Engineers (PECASE). QD-LED=quantum dot light-emitting device.Steckel, Jonathan S. et al. | 2006
- 5931
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Sandwich Complexes Containing Bent Palladium ChainsTatsumi, Yasuki / Shirato, Katsunori / Murahashi, Tetsuro / Ogoshi, Sensuke / Kurosawa, Hideo et al. | 2006
- 5931
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Sandwich Complexes Containing Bent Palladium Chains. This work was supported by PRESTO, Japan Science and Technology Agency (JST) and Grants-in-aid for Scientific Research, Ministry of Education, Culture, Sports, Science and Technology of Japan. Y.T. thanks the research fellowships for young scientists from the Japan Society for the Promotion of Science.Tatsumi, Yasuki et al. | 2006
- 5935
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Three Groups Good, Four Groups Bad? Atropisomerism in ortho-Substituted Diaryl Ethers. We are grateful to the Leverhulme Trust, GlaxoSmithKline, and the EPSRC for funding this study.Betson, Mark S. et al. | 2006
- 5935
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Three Groups Good, Four Groups Bad? Atropisomerism in ortho‐Substituted Diaryl EthersBetson, Mark S. / Clayden, Jonathan / Worrall, Christopher P. / Peace, Simon et al. | 2006
- 5939
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A Zinc–Zinc‐Bonded Compound and Its Derivatives Bridged by One or Two Hydrogen Atoms: A New Type of ZnZn BondingZhu, Zhongliang / Wright, Robert J. / Olmstead, Marilyn M. / Rivard, Eric / Brynda, Marcin / Power, Philip P. et al. | 2006
- 5939
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A Zinc-Zinc-Bonded Compound and Its Derivatives Bridged by One or Two Hydrogen Atoms: A New Type of ZnZn Bonding. The authors thank the National Science Foundation for financial support. E.R. thanks NSERC of Canada for a postdoctoral fellowship.Zhu, Zhongliang et al. | 2006
- 5942
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Regioselectivity with Hemispherical Chelators: Increasing the Catalytic Efficiency of Complexes of Diphosphanes with Large Bite Angles. Financial support from the Agence Nationale de la Recherche is gratefully acknowledged.Sémeril, David et al. | 2006
- 5942
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Regioselectivity with Hemispherical Chelators: Increasing the Catalytic Efficiency of Complexes of Diphosphanes with Large Bite AnglesSémeril, David / Jeunesse, Catherine / Matt, Dominique / Toupet, Loïc et al. | 2006
- 5946
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Conductance and Stochastic Switching of Ligand-Supported Linear Chains of Metal Atoms. Thanks to Professor I-C. Chen (NTHU) for fruitful discussions, to Dr. Andy H. Kung (IAMS, Academia Sinica, Taipei) for comments on the manuscript and to collaborators of S.-M.P. for the routine supply of metal string complexes. C.-h.C. acknowledges Professor T.-Y. Luh (NTU) for use of a NanoScope IIIa and the Department of Chemistry (NTHU) for the strong research support. This work was funded by the National Science Council and the Ministry of Education of the Republic of China.Chen, I.-Wen Peter et al. | 2006
- 5946
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Conductance and Stochastic Switching of Ligand‐Supported Linear Chains of Metal AtomsChen, I‐Wen Peter / Fu, Ming‐Dung / Tseng, Wei‐Hsiang / Yu, Jian‐Yuan / Wu, Sung‐Hsun / Ku, Chia‐Jui / Chen, Chun‐hsien / Peng, Shie‐Ming et al. | 2006
- 5950
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Cyclodextrin Bucket Wheels: An Oligosaccharide Assembly Accommodates Metal(IV) CentersBenner, Klaus / Ihringer, Johannes / Klüfers, Peter / Marinov, Danira et al. | 2006
- 5950
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Cyclodextrin Bucket Wheels: An Oligosaccharide Assembly Accommodates Metal(IV) Centers. Polyol metal complexes, Part 53. This work was supported by the Deutsche Forschungsgemeinschaft and the Fachagentur Nachwachsende Rohstoffe. Part 52: M. Hinrichs, F. R. Hofbauer, P. Klüfers, Chem. Eur. J. 2006, 12, 4675-4683.Benner, Klaus et al. | 2006
- 5954
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A Ruthenium Complex with Superhigh Light‐Harvesting Capacity for Dye‐Sensitized Solar CellsChen, Chia‐Yuan / Wu, Shi‐Jhang / Wu, Chun‐Guey / Chen, Jian‐Ging / Ho, Kuo‐Chuan et al. | 2006
- 5954
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A Ruthenium Complex with Superhigh Light-Harvesting Capacity for Dye-Sensitized Solar Cells. This work was financially supported by the National Science Council, Taiwan.Chen, Chia-Yuan et al. | 2006
- 5957
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Fluorescent Organometallic Sensors for the Detection of Chemical-Warfare-Agent Mimics. The material reported herein is based on work supported by the US army research office (Grant No. DAAD19-03-1-0208), the National Science Foundation (Grant No. CAREER-CHE 0133164), and the Case School of Engineering. The authors also thank Eric Giles, Casey Johnson, and Dr. Parameswar K. Iyer for their assistance.Knapton, Daniel et al. | 2006
- 5957
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Fluorescent Organometallic Sensors for the Detection of Chemical‐Warfare‐Agent MimicsKnapton, Daniel / Burnworth, Mark / Rowan, Stuart J. / Weder, Christoph et al. | 2006
- 5961
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Thermodynamic and Kinetic Enhancement of Electrochemical Sensitivity by Chemical Coupling in Microfluidic Systems. This work is supported by Virginia Commonwealth University and the Jeffress Memorial Trust of Virginia.Khalid, Imtiaz M. et al. | 2006
- 5961
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Thermodynamic and Kinetic Enhancement of Electrochemical Sensitivity by Chemical Coupling in Microfluidic SystemsKhalid, Imtiaz M. / Pu, Qiaosheng / Alvarez, Julio C. et al. | 2006
- 5964
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Studies on Iejimalide B: Preparation of the Seco Acid and Identification of the Molecule's "Achilles Heel". Generous financial support from the MPG, the Fonds der Chemischen Industrie, the Alexander-von-Humboldt Foundation (fellowship to C.N.), and the NSERC, Canada (fellowship to M.T.) is gratefully acknowledged. We thank Dr. R. Riveiros for assistance in the initial phase of this project, and Dr. R. Mynott, B. Gabor, and C. Wirtz for their invaluable help with the structure assignment of several key compounds.Fürstner, Alois et al. | 2006
- 5964
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Studies on Iejimalide B: Preparation of the Seco Acid and Identification of the Molecule's “Achilles Heel”Fürstner, Alois / Aïssa, Christophe / Chevrier, Carine / Teplý, Filip / Nevado, Cristina / Tremblay, Martin et al. | 2006
- 5969
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Total Synthesis of Iejimalide BFürstner, Alois / Nevado, Cristina / Tremblay, Martin / Chevrier, Carine / Teplý, Filip / Aïssa, Christophe / Waser, Mario et al. | 2006
- 5969
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Total Synthesis of Iejimalide B. Generous financial support from the MPG, the Fonds der Chemischen Industrie, the Alexander-von-Humboldt Foundation (fellowship to C.N.), the NSERC Canada (fellowship to M.T.), and the Austrian Fonds zur Förderung der Wissenschaftlichen Forschung (fellowship to M.W.) is gratefully acknowledged. We thank Dr. R. Mynott, B. Gabor, and C. Wirtz for their invaluable help with the structure assignment of several key compounds, and R. Leichtweiß for HPLC assistance.Fürstner, Alois et al. | 2006
- 5974
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Osmium-Mediated Hexamerization of Phenylacetylene. This work was supported by the Hong Kong Research Grant Council (HKUST6090-02P).Wen, Ting Bin et al. | 2006
- 5974
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Osmium‐Mediated Hexamerization of PhenylacetyleneWen, Ting Bin / Zhou, Zhong Yuan / Jia, Guochen et al. | 2006
- 5979
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Radical‐Mediated Alkenylation, Alkynylation, Methanimination, and Cyanation of B‐AlkylcatecholboranesSchaffner, Arnaud‐Pierre / Darmency, Vincent / Renaud, Philippe et al. | 2006
- 5979
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Radical-Mediated Alkenylation, Alkynylation, Methanimination, and Cyanation of B-Alkylcatecholboranes. This work was supported by the Swiss National Science Foundation (project 21-103627). We thank BASF Corporation for the generous gift of catecholborane.Schaffner, Arnaud-Pierre et al. | 2006
- 5981
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Enantioselective Oxidation of Olefins Catalyzed by a Chiral Bishydroxamic Acid Complex of Molybdenum. Support for this research was provided by the SORST project of the Japan Science and Technology Agency (JST) and GAANN.Barlan, Allan U. et al. | 2006
- 5981
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Enantioselective Oxidation of Olefins Catalyzed by a Chiral Bishydroxamic Acid Complex of MolybdenumBarlan, Allan U. / Basak, Arindrajit / Yamamoto, Hisashi et al. | 2006
- 5984
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Pd‐Catalyzed α‐Arylation of Trimethylsilyl Enol Ethers with Aryl Bromides and Chlorides: A Synergistic Effect of Two Metal Fluorides as AdditivesSu, Weiping / Raders, Steven / Verkade, John G. / Liao, Xuebin / Hartwig, John F. et al. | 2006
- 5984
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Pd-Catalyzed [alpha]-Arylation of Trimethylsilyl Enol Ethers with Aryl Bromides and Chlorides: A Synergistic Effect of Two Metal Fluorides as Additives. J.G.V. gratefully acknowledges the National Science Foundation for financial support of this investigation, and J.F.H. thanks the NIH (NIGMS GM-58108). The authors thank Professor Robert Angelici for helpful discussions.Su, Weiping et al. | 2006
- 5984
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Pd-Catalyzed a-Arylation of Trimethylsilyl Enol Ethers with Aryl Bromides and Chlorides: A Synergistic Effect of Two Metal Fluorides as AdditivesSu, W. / Raders, S. / Verkade, J. G. / Liao, X. / Hartwig, J. F. et al. | 2006
- 5988
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Guest‐Induced Conformational Switching in a Single CrystalDobrzańska, Liliana / Lloyd, Gareth O. / Esterhuysen, Catharine / Barbour, Leonard J. et al. | 2006
- 5988
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Guest-Induced Conformational Switching in a Single Crystal. We acknowledge financial support from the National Research Foundation (South Africa) and L.D. thanks the Claude Harris Leon Foundation for a postdoctoral fellowship.Dobrzanska, Liliana et al. | 2006
- 5991
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Enantioselective Total Synthesis of (−)‐Acylfulvene and (−)‐IrofulvenMovassaghi, Mohammad / Piizzi, Grazia / Siegel, Dustin S. / Piersanti, Giovanni et al. | 2006
- 5991
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Enantioselective Total Synthesis of (-)-Acylfulvene and (-)-Irofulven. M.M. is a Dale F. and Betty Ann Frey Damon Runyon Scholar supported by the Damon Runyon Cancer Research Foundation (DRS-39-04). M.M. is a Firmenich Assistant Professor of Chemistry. G.P. acknowledges partial support for a postdoctoral fellowship from Universitá degli Studi di Urbino "Carlo Bo". We are grateful to Professors A. H. Hoveyda and E. N. Jacobsen for generous samples of their silylcyanation catalysts. We acknowledge financial support by MIT, Paul M. Cook Fund, and Boehringer Ingelheim Pharmaceutical Inc.Movassaghi, Mohammad et al. | 2006
- 5995
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Enantioselective Cascade Radical Addition–Cyclization–Trapping ReactionsMiyabe, Hideto / Asada, Ryuta / Toyoda, Akira / Takemoto, Yoshiji et al. | 2006
- 5995
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Enantioselective Cascade Radical Addition-Cyclization-Trapping Reactions. This work was supported in part by a Grant-in-Aid for Young Scientists (B) (H.M.) and Scientific Research on Priority Areas 17035043 (Y.T. and H.M.) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan, 21st Century COE Program "Knowledge Information Infrastructure for Genome Science".Miyabe, Hideto et al. | 2006
- 5999
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Design and Synthesis of Multifunctional Materials Based on an Ionic‐Liquid BackboneZhang, Yuanjian / Shen, Yanfei / Yuan, Junhua / Han, Dongxue / Wang, Zhijuan / Zhang, Qixian / Niu, Li et al. | 2006
- 5999
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Design and Synthesis of Multifunctional Materials Based on an Ionic-Liquid Backbone. The authors are grateful to the NSFC, China (grant no. 20475053) and to the Department of Science and Technology of Jilin Province (grant no. 20050102) for financial support.Zhang, Yuanjian et al. | 2006
- 6002
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Total Synthesis of Pseudotrienic Acid B: A Bioactive Metabolite from Pseudomonas sp. MF 381-IODS. We wish to thank the Société de Chimie Thérapeutique-SERVIER for financial support of this work and Dr. D.-H. Caignard for scientific discussions. We also wish to acknowledge Dr. Fisher and Dr. Trimmer from Materia, USA, for a generous gift of the Grubbs-Hoveyda catalyst.Amans, Dominique et al. | 2006
- 6002
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Total Synthesis of Pseudotrienic Acid B: A Bioactive Metabolite from Pseudomonas sp. MF 381‐IODSAmans, Dominique / Bellosta, Véronique / Cossy, Janine et al. | 2006
- 6007
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Vom Inhibitor zum Aktivator: ein Hammerhead‐Ribozym unter der Kontrolle eines G‐QuartettsWieland, Markus / Hartig, Jörg S. et al. | 2006
- 6007
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Vom Inhibitor zum Aktivator: ein Hammerhead-Ribozym unter der Kontrolle eines G-Quartetts. J.S.H. dankt der Volkswagenstiftung für die großzügige Förderung dieser Arbeit im Rahmen einer Lichtenberg-Professur. Wir danken dem Fachbereich Chemie der Universität Konstanz für die Unterstützung.Wieland, Markus et al. | 2006
- 6010
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Gold(III)‐ und Platin(II)‐katalysierte Dominoreaktion aus Heterocyclisierung und 1,2‐Verschiebung: effiziente Synthese von hoch substituierten 3(2H)‐FuranonenKirsch, Stefan F. / Binder, Jörg T. / Liébert, Clémence / Menz, Helge et al. | 2006
- 6010
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Gold(III)- und Platin(II)-katalysierte Dominoreaktion aus Heterocyclisierung und 1,2-Verschiebung: effiziente Synthese von hoch substituierten 3(2H)-Furanonen. Dieses Projekt wurde von der Deutschen Forschungsgemeinschaft (DFG) und dem Fonds der Chemischen Industrie gefördert. Wir danken Andrea Rothballer und Markus Scheerer für hervorragende experimentelle Unterstützung.Kirsch, Stefan F. et al. | 2006
- 6013
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Entwurf und Synthese von 12‐Aza‐Epothilonen (Azathilonen) – “nicht‐natürliche Naturstoffe” mit potenter AntitumorwirkungFeyen, Fabian / Gertsch, Jürg / Wartmann, Markus / Altmann, Karl‐Heinz et al. | 2006
- 6013
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Entwurf und Synthese von 12-Aza-Epothilonen (Azathilonen) - "nicht-naturliche Naturstoffe" mit potenter AntitumorwirkungFeyen, F. / Gertsch, J. / Wartmann, M. / Altmann, K. H. et al. | 2006
- 6013
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Entwurf und Synthese von 12-Aza-Epothilonen (Azathilonen) - "nicht-natürliche Naturstoffe" mit potenter Antitumorwirkung. Bettina Sager, Jaqueline Loretan und Robert Reuter sei herzlich für die exzellente technische Unterstützung gedankt. Wir danken auch dem Elektronenmikroskopie-Zentrum (EMEZ) der ETH Zürich für die hervorragende Zusammenarbeit.Feyen, Fabian et al. | 2006
- 6017
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Synthese und Redoxeigenschaften gemischtvalenter achtkerniger Eisendefekthexacubane und eines (CaCl)-überdachten raumzentrierten Eisen(III)-Sechsflächners. Chelat-Komplexe, 34. Mitteilung. Diese Arbeit wurde von der Deutschen Forschungsgemeinschaft (SFB583, GK312, SPP1137), dem Bayerischen Langzeitprogramm Neue Werkstoffe und dem Fonds der Chemischen Industrie gefördert. Dr. M. Moll, Institut für Anorganische Chemie, Universität Erlangen-Nürnberg, danken wir für die großzügige Bereitstellung eines Cyclovoltammeters und Prof. Dr. H. Burzlaff für seine Hilfe bei der Bezeichnung des Komplexes 3. - 33. Mitteilung: Lit. [7]Prakash, Raju et al. | 2006
- 6017
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Synthese und Redoxeigenschaften gemischtvalenter achtkerniger Eisendefekthexacubane und eines (CaCl)‐überdachten raumzentrierten Eisen(III)‐SechsflächnersPrakash, Raju / Saalfrank, Rolf W. / Maid, Harald / Scheurer, Andreas / Heinemann, Frank W. / Trautwein, Alfred X. / Böttger, Lars H. et al. | 2006
- 6017
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Synthese und Redoxeigenschaften gemischtvalenter achtkerniger Eisendefekthexacubane und eines (CaCl)-uberdachten raumzentrierten Eisen(III)-SechsflachnersPrakash, R. / Saalfrank, R. W. / Maid, H. / Scheurer, A. / Heinemann, F. W. / Trautwein, A. X. / Bottger, L. H. et al. | 2006
- 6023
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Phannomenklatur Teil II: Änderung des Hydrierungsgrades und Substitutionsderivate von Phanstammverbindungen. Copyright© der englischen Fassung, die unter dem Titel "Phane nomenclature. Part II. Modification of the degree of hydrogenation and substitution derivatives of phane parent hydrides" von H. A. Favre (Kanada), D. Hellwinkel (Deutschland), W. H. Powell (USA), H. A. Smith, Jr. (USA) und S. S.-C. Tsay (Taiwan) für die Veröffentlichung in Pure Appl. Chem. 2002, 74, 809-834BIBR HREF="bib9">9 vorbereitet wurde: International Union of Pure and Applied Chemistry, 2002. Die englische Fassung ist auch im Internet unter der Adresse http: www.chem.qmul.ac.uk-iupac-phane2- zugänglich. - Wir danken der IUPAC für die Genehmigung zum Druck einer deutschen Fassung dieser Recommendation. K.-H. H. dankt Dr. W. H. Powell für die elektronische Fassung des englischen Manuskripts sowie Frau Dipl.-Chem. G. Kruse+, Dr. W. Liebscher und Prof. R. Neier für umfangreiche Diskussionen zur Terminologie im Zusammenhang mit der Übertragung neuer FaHellwich, Karl-Heinz et al. | 2006
- 6023
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Phannomenklatur Teil II: Änderung des Hydrierungsgrades und Substitutionsderivate von PhanstammverbindungenHellwich, Karl‐Heinz et al. | 2006
- 6023
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Phannomenklatur Teil II: Anderung des Hydrierungsgrades und Substitutionsderivate von PhanstammverbindungenHellwich, K. H. et al. | 2006
- 6037
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Vorschau: Angew. Chem. 35/2006| 2006