Organic Synthesis via Organometallics OSM 5: Proceedings of the Fifth Symposium in Heidelberg, September 26 to 28, 1996

Author:   Günter Helmchen ,  Jörg Dibo ,  Dietmar Flubacher ,  Burkhard Wiese
Publisher:   Springer-Verlag Berlin and Heidelberg GmbH & Co. KG
Edition:   Softcover reprint of the original 1st ed. 1997
ISBN:  

9783642493508


Pages:   376
Publication Date:   21 April 2012
Format:   Paperback
Availability:   Manufactured on demand   Availability explained
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Organic Synthesis via Organometallics OSM 5: Proceedings of the Fifth Symposium in Heidelberg, September 26 to 28, 1996


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Overview

Interdisciplinarity is an important aspect of modem science. A convincing example is pro­ vided by organometallic chemistry, a discipline at the interface of inorganic and organic chemistry. Over the last 20 years, organometallic chemistry has served as an inexhaustible source of new methods of ever increasing value to organic synthesis both in the laboratory and in large scale industrial plants using transition metal catalysts. In order to strengthen collaboration between inorganic and organic chemists the ""Vokswagen-Stiftung"" started a new program ""Organic Synthesis via Organometallics"" in 1986. This program grew up to more than 60 projects over a period of six years. In addi­ tion to its main topic organic synthesis it covered mechanistic and structural aspects of organometallic chemistry. Scientists participating in the program met with other experts from academia and industry in a series of five symposia held in Hamburg (February 1986), WUrzburg (October 1988), Marburg (July 1990) and Aachen (November 1992). The fifth and final symposium took place in Heidelberg from September 26 to 28, 1996.

Full Product Details

Author:   Günter Helmchen ,  Jörg Dibo ,  Dietmar Flubacher ,  Burkhard Wiese
Publisher:   Springer-Verlag Berlin and Heidelberg GmbH & Co. KG
Imprint:   Springer-Verlag Berlin and Heidelberg GmbH & Co. K
Edition:   Softcover reprint of the original 1st ed. 1997
Dimensions:   Width: 17.00cm , Height: 2.00cm , Length: 24.40cm
Weight:   0.668kg
ISBN:  

9783642493508


ISBN 10:   3642493505
Pages:   376
Publication Date:   21 April 2012
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Paperback
Publisher's Status:   Active
Availability:   Manufactured on demand   Availability explained
We will order this item for you from a manufactured on demand supplier.

Table of Contents

Carbon-Rich Organoruthenium and Selective Catalytic Transformations of Alkynes.- Polymer Synthesis with Organometallic Intermediates.- Organoaluminum and Organogallium Complexes as Efficient and Selective Alkylating Agents.- Nickel Mediated Cyclobutabenzenes Syntheses.- Organometallics-Aided “SO”, “S2” and “S” Transfer in the Synthesis of Small-Membered Heterocycles.- Stereoselective Reactions of Transition Metal Carbonyl Complexes.- Metal-Centered Coupling Reactions of C1-Ligands Analogous to Carbon Monoxide.- The Synthesis of Indoles by Transition Metal Catalyzed Addition of Alkynes to 1,2-Diazenes.- Polycyclic Ring Systems via Palladacycles as Reactive Intermediates.- Substrate Directed Diastereoselective Hydroformylation of Methallylic Alcohols.- Parahydrogen and in situ NMR-Spectroscopy as Mechanistic Tools in Catalysis.- Chiral Ligands and Chiral Pockets. Some Thoughts on Enantioselective Homogeneous Catalysis.- Application of High Pressure in Palladium Catalysis.- Asymmetric Reactions Catalyzed by Palladium-MOP Complexes.- New Chiral Ferrocenyl Ligands in Asymmetric Catalysis: Applications and Mechanistic Studies.- Mechanisms of the Catalyzed Mukaiyama Cross-Aldol Reaction.- New Rhodium Hydroformylation Catalysts.- Development of Transition Metal Complexes as Redox Reagents and Redox Catalysts.- Synthesis of Highly Enantioenriched Compounds via Iron Mediated Allylic Substitutions.- Syntheses of Biologically Relevant Target Molecules by Transition Metal-Induced C-C-Bond Formation.- Pd(II)-Catalyzed Carbonylation of Unsaturated Polyols and Aminopolyols.- New Organometallic Solutions to Problems in Polyene Natural and Unnatural Products Synthesis.

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