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Oxidative Palladiumii Catalyzed Arene C H Bond Functionalization And Progress Towards The Total Synthesis Of 6 Deoxyerythronolide B
Download Oxidative Palladiumii Catalyzed Arene C H Bond Functionalization And Progress Towards The Total Synthesis Of 6 Deoxyerythronolide B full books in PDF, epub, and Kindle. Read online Oxidative Palladiumii Catalyzed Arene C H Bond Functionalization And Progress Towards The Total Synthesis Of 6 Deoxyerythronolide B ebook anywhere anytime directly on your device. Fast Download speed and no annoying ads. We cannot guarantee that every ebooks is available!
Book Synopsis Oxidative Palladium(II)-catalyzed Arene C-H Bond Functionalization and Progress Towards the Total Synthesis of 6-Deoxyerythronolide B. by : Nadine Borduas
Download or read book Oxidative Palladium(II)-catalyzed Arene C-H Bond Functionalization and Progress Towards the Total Synthesis of 6-Deoxyerythronolide B. written by Nadine Borduas and published by . This book was released on 2012 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Oxidative Palladium(II)-Catalyzed Arene Carbon-Hydrogen Bond Functionalization And Progress Towards The Total Synthesis of 6-Deoxyerythronolide B. by : Nadine Borduas
Download or read book Oxidative Palladium(II)-Catalyzed Arene Carbon-Hydrogen Bond Functionalization And Progress Towards The Total Synthesis of 6-Deoxyerythronolide B. written by Nadine Borduas and published by . This book was released on 2013 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Strategies for Palladium-Catalyzed Non-directed and Directed C bond H Bond Functionalization by : Anant R. Kapdi
Download or read book Strategies for Palladium-Catalyzed Non-directed and Directed C bond H Bond Functionalization written by Anant R. Kapdi and published by Elsevier. This book was released on 2017-05-23 with total page 502 pages. Available in PDF, EPUB and Kindle. Book excerpt: Strategies for Palladium-Catalyzed Non-directed and Directed C-H Bond Functionalization portrays the complete scope of these two aspects of C-H bond functionalization in a single volume for the first time. Featured topics include the influence of palladacyclic systems in C-H bond functionalization (need for newer catalytic systems for better efficiency), mechanistic aspect of the functionalization strategies leading to better systems, and applications of these methodologies to natural product synthesis and material synthesis. - Addresses the involvement of catalytic systems (palladacycles) for better functionalization of (hetero)arenes to emphasize the need for developing better, more selective systems - Covers the use of powerful mechanistic tools for understanding and assisting the development of better functionalization strategies - Discusses the finer aspects of C-H bond functionalization, such as control of regioselectivity with or without directing groups - Includes a chapter detailing the synthesis of naturally occurring molecules or functional molecules via both pathways for assessing the applicability of the functionalization strategies
Book Synopsis Higher Oxidation State Organopalladium and Platinum Chemistry by : Allan J. Canty
Download or read book Higher Oxidation State Organopalladium and Platinum Chemistry written by Allan J. Canty and published by Springer. This book was released on 2011-02-25 with total page 195 pages. Available in PDF, EPUB and Kindle. Book excerpt: Kyle A. Grice, Margaret L. Scheuermann and Karen I. Goldberg: Five-Coordinate Platinum(IV) Complexes.- Jay A. Labinger and John E. Bercaw: The Role of Higher Oxidation State Species in Platinum-Mediated C-H Bond Activation and Functionalization.- Joy M. Racowski and Melanie S. Sanford: Carbon-Heteroatom Bond-Forming Reductive Elimination from Palladium(IV) Complexes.- Helena C. Malinakova: Palladium(IV) Complexes as Intermediates in Catalytic and Stoichiometric Cascade Sequences Providing Complex Carbocycles and Heterocycles.- Allan J. Canty and Manab Sharma: h1-Alkynyl Chemistry for the Higher Oxidation States of Palladium and Platinum.- David C. Powers and Tobias Ritter: Palladium(III) in Synthesis and Catalysis.- Marc-Etienne Moret: Organometallic Platinum(II) and Palladium(II) Complexes as Donor Ligands for Lewis-Acidic d10 and s2 Centers.
Book Synopsis Weak Coordination as a Powerful Means for Developing Useful Palladium (II)-catalyzed C-H Activation Reactions by : Tian-Sheng Mei
Download or read book Weak Coordination as a Powerful Means for Developing Useful Palladium (II)-catalyzed C-H Activation Reactions written by Tian-Sheng Mei and published by . This book was released on 2011 with total page 846 pages. Available in PDF, EPUB and Kindle. Book excerpt: Achieving direct and selective functionalization of carbon-hydrogen (C-H) bonds to give carbon-carbon (C-C) or carbon-heteroatom (C-Y) bonds is a significant and long-standing goal in chemistry. C-H bonds are attractive reaction partners because they are ubiquitous in organic molecules. Thus, C-H functionalization methods could potentially expedite the synthesis of target molecules by providing new disconnections in retrosynthetic analysis. Among the numerous methods to affect this transformation, palladium-catalyzed C-H functionalization is one of most promising methods to construct C-C and C-Y bonds in term of versatile reactivity. The major challenges of palladium-catalyzed C-H functionalization are developing reactions that work with common and useful structural motifs and discovering new transformation, such as C-N or C-F bond formation. This thesis explores palladium-catalyzed C-H bond functionalization with substrates containing simple functional groups such as carboxylic acids and triflamides, which direct C-H cleavage through weak coordination with the metal catalyst. Chapter one introduces different types of C-H bond functionalization and focuses on Pd(II)/Pd(IV) catalysis. Chapter two covers Pd-catalyzed C-H iodination of arene carboxylic acids enabled by the discovery of coutercation-promoted C-H activation. Weak coordination has also been found to enable versatile reactivity of simple arene carboxylic acids. Chapter three focuses on the development of practical and useful C-H fluorination using triflamide as a weakly coordinating directing group that can be easily manipulated to a wide range of useful and common aryl halides. Chapter four describes applications of bystanding F+ oxidants to promote selective C-N reductive elimination in Pd(II)/Pd(IV) catalysis.
Book Synopsis Palladium and Nickel Catalyzed Transformations Forming Functionalized Heterocycles by : Hyung Yoon
Download or read book Palladium and Nickel Catalyzed Transformations Forming Functionalized Heterocycles written by Hyung Yoon and published by Springer Nature. This book was released on 2020-09-02 with total page 236 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book presents Pd- and Ni-catalyzed transformations generating functionalized heterocycles. Transition metal catalysis is at the forefront of synthetic organic chemistry since it offers new and powerful methods to forge carbon–carbon bonds in high atom- and step-economy. In Chapter 1, the author describes a Pd- and Ni-catalyzed cycloisomerization of aryl iodides to alkyl iodides, known as carboiodination. In the context of the Pd-catalyzed variant, the chapter explores the production of enantioenriched carboxamides through diastereoselective Pd-catalyzed carboiodination. It then discusses Ni-catalyzed reactions to generate oxindoles and an enantioselective variant employing a dual ligand system. Chapter 2 introduces readers to a Pd-catalyzed diastereoselective anion-capture cascade. It also examines diastereoselective Pd-catalyzed aryl cyanation to synthesize alkyl nitriles, a method that generates high yields of borylated chromans as a single diastereomer, and highlights its synthetic utility. Lastly, Chapter 3 presents a Pd-catalyzed domino process harnessing carbopalladation, C–H activation and π-system insertion (benzynes and alkynes) to generate spirocycles. It also describes the mechanistic studies performed on these reactions.
Book Synopsis Palladium Catalyzed Transformations of Allenes and Progress Towards the Total Synthesis of Nogalamycin by : Logan Vine (Ph.D.)
Download or read book Palladium Catalyzed Transformations of Allenes and Progress Towards the Total Synthesis of Nogalamycin written by Logan Vine (Ph.D.) and published by . This book was released on 2022 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Transition metal-catalyzed transformations of allenes are underexplored compared to other unsaturated functional groups. However, the consecutive, orthogonal double bonds of allenes represent an extremely valuable functional handle that can be manipulated to rapidly build molecular complexity. The first section of this work (Chapter 2) describes how targeted changes to the reaction conditions enable control over the mechanism of Pd-catalyzed allene cross-coupling/cyclization and cycloisomerization, irrespective of the allene substitution pattern. Both enantioenriched cyclopropanes and cyclopentenes can be obtained through axis-to-center chirality transfer from the allene precursor at room temperature. The next section (Chapter 4) demonstrates a highly stereoselective Pd-catalyzed Heck-type reaction of allenes to form 1,3-dienes in which the stereochemistry of both olefins is set simultaneously. The stereodetermining factors and a plausible mechanism for this work are proposed and both inter- and intramolecular trapping of the Ï0-allyl intermediate with an oxygen nucleophile are demonstrated. The final portion of this work will be focused on progress towards the total synthesis of Nogalamycin (NOG) (Chapter 6). NOG is a member of the glycosidic anthracyclines and shows a unique dumbbell type binding to DNA. Toxicity and relatively low antineoplastic activity have prevented NOG from clinical use, but semisynthetically accessed derivatives have shown great potential, leading to the need for a highly modular synthetic approach to access new analogs and further probe SARs. A complex bicyclic aminosugar motif creates a significant challenge for the synthesis of NOG, as there are no reliable synthetic methods to install the C℗Ơaryl-Cglycoside bond late stage. In this section, we propose a late-stage chemoenzymatic installation of the C℗Ơaryl-Cglycoside bond inspired by the biosynthetic pathway. The synthesis of the tetracyclic anthracycline core includes a key boron-directed cycloaddition, a novel SmI2 mediated ring opening of an oxanorbornadiene, and a proposed Ni-catalyzed cross electrophile coupling.
Book Synopsis Palladium Catalyzed Transformations of Allenes and Progress Towards the Total Synthesis of Nogalamycin by : Logan Vine (Ph.D.)
Download or read book Palladium Catalyzed Transformations of Allenes and Progress Towards the Total Synthesis of Nogalamycin written by Logan Vine (Ph.D.) and published by . This book was released on 2022 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Transition metal-catalyzed transformations of allenes are underexplored compared to other unsaturated functional groups. However, the consecutive, orthogonal double bonds of allenes represent an extremely valuable functional handle that can be manipulated to rapidly build molecular complexity. The first section of this work (Chapter 2) describes how targeted changes to the reaction conditions enable control over the mechanism of Pd-catalyzed allene cross-coupling/cyclization and cycloisomerization, irrespective of the allene substitution pattern. Both enantioenriched cyclopropanes and cyclopentenes can be obtained through axis-to-center chirality transfer from the allene precursor at room temperature. The next section (Chapter 4) demonstrates a highly stereoselective Pd-catalyzed Heck-type reaction of allenes to form 1,3-dienes in which the stereochemistry of both olefins is set simultaneously. The stereodetermining factors and a plausible mechanism for this work are proposed and both inter- and intramolecular trapping of the Ï0-allyl intermediate with an oxygen nucleophile are demonstrated. The final portion of this work will be focused on progress towards the total synthesis of Nogalamycin (NOG) (Chapter 6). NOG is a member of the glycosidic anthracyclines and shows a unique dumbbell type binding to DNA. Toxicity and relatively low antineoplastic activity have prevented NOG from clinical use, but semisynthetically accessed derivatives have shown great potential, leading to the need for a highly modular synthetic approach to access new analogs and further probe SARs. A complex bicyclic aminosugar motif creates a significant challenge for the synthesis of NOG, as there are no reliable synthetic methods to install the C℗Ơaryl-Cglycoside bond late stage. In this section, we propose a late-stage chemoenzymatic installation of the C℗Ơaryl-Cglycoside bond inspired by the biosynthetic pathway. The synthesis of the tetracyclic anthracycline core includes a key boron-directed cycloaddition, a novel SmI2 mediated ring opening of an oxanorbornadiene, and a proposed Ni-catalyzed cross electrophile coupling.
Book Synopsis Rhodium Catalyzed C-H Bond Functionalization by : Andy Siu-Chun Tsai
Download or read book Rhodium Catalyzed C-H Bond Functionalization written by Andy Siu-Chun Tsai and published by . This book was released on 2011 with total page 174 pages. Available in PDF, EPUB and Kindle. Book excerpt: Chapter 1. A sequence of research projects beginning with studies in diastereoselective C-H bond functionalization applied to the synthesis of ( - )-incarvaillateine to the Rh(III) catalyzed arylation of imines, are described. Some theory and mechanistic considerations are discussed in relation to the genesis of these projects. Research directions are summarized and rationalized. Chapter 2. The synthesis of ( - )-incarvillateine utilizing a key C-H bond alkylation step is described as a means to highlight the synthetic utility of a newly reported olefinic C-H bond functionalization methodology. Elements of diastereoselectivity are also explored in the key step which allows for the concise, stereoselective synthesis of the natural product. Progress in the area of enantioselective C-H alkylations are also summarized as it applies to the synthesis of other natural products. Chapter 3. A method for the enantioselective cyclization of N-allylimidazoles is developed. The reaction is thought to proceed via a novel, reactive N-heterocyclic carbene. High enantioselectivities are achieved, which is unusual in view of the elevated temperatures of the reaction. Chapter 4. The first general method for the oxidative coupling of unactivated alkenes via C-H bond functionalization is reported using a methyl oxime directing group. A silver abstractor is important to obtain reactivity. Several functional groups are compatible with the reaction and no precautions to exclude air are required. Chapter 5. A rare example of C-H activation and intermolecular coupling to N-protected-imines is achieved using a cationic Rh(III) catalyst. The reaction is directed by pyridines and related heterocycles and produces a variety of aryl-branched amines. The reaction accommodates several reactive functional groups and is mild enough to even couple with sensitive alkyl N-sulfonyl-imines.
Book Synopsis Investigations in Iron, Copper, and Palladium-catalyzed C-H Bond Functionalization by : Ly Dieu Tran
Download or read book Investigations in Iron, Copper, and Palladium-catalyzed C-H Bond Functionalization written by Ly Dieu Tran and published by . This book was released on 2013 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Transition metal-catalyzed functionalization of C-H bonds has been used as a powerful tool for the construction of C-C and C-heteroatom bonds. Within this dissertation, methods that allow functionalization of C-H bonds via iron and copper catalysis have been developed. Additionally, functionalization of sp3 C-H bonds in amino acid derivatives using auxiliary-assisted palladium-catalyzed methodology is also demonstrated. A method for iron-catalyzed alkylation of arenes and heterocycles containing acidic C-H bonds has been developed. Various heterocycles such as pyridine, furan, thiophene and electron deficient arenes can be coupled with both alkyl bromides and iodides. Magnesium amide base is required for the reaction. Similarly, the deprotonative dimerization of arenes and heterocycles can be effected in the presence of an iron catalyst. Thus, the method allows direct functionalization of arenes and heterocycles. Additionally, the use of an iron catalyst is an advantage compared with existing methods. Methods for copper-catalyzed direct sulfenylation and amination of sp2 C-H bonds have been developed. Using 8-aminoquinoline auxiliary and copper catalyst, ortho C-H bonds of benzoic acid amides can be sulfenylated by disulfides. The method provides an alternative, milder way for the preparation of aryl trifluoromethylsulfides. Furthermore, ortho C-H bonds of benzoic acid amides can be aminated by reaction with simple amines using 8-aminoquinoline directing group and a copper catalyst. Sulfenylation and amination of g-C-H bonds of benzyl amine derivatives using picolinic acid auxiliary were also demonstrated. Broad substrate scope, high regioselectivity, and good functional group tolerance were observed. The use of a copper catalyst and a removable directing group are significant improvements compared with the existing methods. Finally, a novel way for synthesis of non-natural amino acids via auxiliary-assisted, palladium-catalyzed C-H functionalization methodology was developed. Under palladium catalysis, 2-methyl thioaniline auxiliary allows the monoarylation of b-C-H bonds of alanine derivatives generating, after directing group removal, substituted phenylalanines. In contrast, using 8-aminoquinoline auxiliary, methylene groups in phenylalanine, leucine, and lysine derivatives can be arylated. Methods for alkylation and acetoxylation were also reported. The directing group can be removed without significant erosion of enantiomeric excess. The method provides a straight-forward way to synthesize non-natural amino acids from the chiral pool.
Book Synopsis The Mizoroki-Heck Reaction by : Martin Oestreich
Download or read book The Mizoroki-Heck Reaction written by Martin Oestreich and published by John Wiley & Sons. This book was released on 2009-02-11 with total page 608 pages. Available in PDF, EPUB and Kindle. Book excerpt: Exploring the importance of Richard F. Heck’s carbon coupling reaction, this book highlights the subject of the 2010 Nobel Prize in Chemistry for palladium-catalyzed cross couplings in organic synthesis, and includes a foreword from Nobel Prize winner Richard F. Heck. The Mizoroki-Heck reaction is a palladium-catalyzed carbon–carbon bond forming process which is widely used in organic and organometallic synthesis. It has seen increasing use in the past decade as chemists look for strategies enabling the controlled construction of complex carbon skeletons. The Mizoroki-Heck Reaction is the first dedicated volume on this important reaction, including topics on: mechanisms of the Mizoroki-Heck reaction intermolecular Mizoroki-Heck reactions focus on regioselectivity and product outcome in organic synthesis waste-minimized Mizoroki-Heck reactions intramolecular Mizoroki-Heck reactions formation of heterocycles chelation-controlled Mizoroki-Heck reactions the Mizoroki-Heck reaction in domino processes oxidative heck-type reactions (Fujiwara-Moritani reactions) Mizoroki-Heck reactions with metals other than palladium ligand design for intermolecular asymmetric Mizoroki-Heck reactions intramolecular enantioselective Mizoroki-Heck reactions desymmetrizing Mizoroki-Heck reactions applications in combinatorial and solid phase syntheses, and the development of modern solvent systems and reaction techniques the asymmetric intramolecular Mizoroki-Heck reaction in natural product total synthesis Several chapters are devoted to asymmetric Heck reactions with particular focus on the construction of otherwise difficult-to-obtain sterically congested tertiary and quaternary carbons. Industrial and academic applications are highlighted in the final section. The Mizoroki-Heck Reaction will find a place on the bookshelves of any organic or organometallic chemist. “I am convinced that this book will rapidly become the most important reference text for research chemists in academia and industry who seek orientation in the rapidly growing and – for the layman – confusing field described as the “’Mizoroki–Heck reaction’.” (Synthesis, March 2010)
Book Synopsis Amide Bond Activation by : Michal Szostak
Download or read book Amide Bond Activation written by Michal Szostak and published by MDPI. This book was released on 2019-07-12 with total page 466 pages. Available in PDF, EPUB and Kindle. Book excerpt: The amide bond represents a privileged motif in chemistry. The recent years have witnessed an explosion of interest in the development of new chemical transformations of amides. These developments cover an impressive range of catalytic N–C bond activation in electrophilic, Lewis acid, radical, and nucleophilic reaction pathways, among other transformations. Equally relevant are structural and theoretical studies that provide the basis for chemoselective manipulation of amidic resonance. This monograph on amide bonds offers a broad survey of recent advances in activation of amides and addresses various approaches in the field.
Book Synopsis Ruthenium in Organic Synthesis by : Shun-Ichi Murahashi
Download or read book Ruthenium in Organic Synthesis written by Shun-Ichi Murahashi and published by John Wiley & Sons. This book was released on 2006-03-06 with total page 398 pages. Available in PDF, EPUB and Kindle. Book excerpt: In this comprehensive book, one of the leading experts, Shun-Ichi Murahashi, presents all the important facets of modern synthetic chemistry using Ruthenium, ranging from hydrogenation to metathesis. In 14 contributions, written by an international authorship, readers will find all the information they need about this fascinating and extraordinary chemistry. The result is a high quality information source and a indispensable reading for everyone working in organometallic chemistry. From the contents: Introduction (S.-I. Murahashi) Hydrogenation and Transfer Hydrogenation (M. Kitamura and R. Noyori) Oxidations (S.-I. Murahashi and N. Komiya) Carbon-Carbon Bond Formations via Ruthenacycle Intermediates (K. Itoh) Carbon-Carbon Bond Formation via pi-Allylruthenium Intermediates (T. Mitsudo) Olefin Metathesis (R. H. Grubbs) Cyclopropanation (H. Nishiyama) Nucleophilic Addition to Alkynes and Reactions via Vinylidene Intermediates (P. Dixneuf) Reactions via C-H Activation (N. Chatani) Lewis Acid Reactions (E. P. Kundig) Reactions with CO and CO2 (T. Mitsudo) Isomerization of Organic Substrates Catalyzed by Ruthenium Complexes (H. Suzuki) Radical Reactions (H. Nagashima) Bond Cleavage Reactions (S. Komiya)
Book Synopsis Macrocycles in Drug Discovery by : Jeremy I Levin
Download or read book Macrocycles in Drug Discovery written by Jeremy I Levin and published by Royal Society of Chemistry. This book was released on 2015 with total page 526 pages. Available in PDF, EPUB and Kindle. Book excerpt: This series provides a comprehensive resource for postgraduate students and for scientists in academia or industry wanting to learn topics outside their own areas of expertise.
Book Synopsis Site-Selective Catalysis by : Takeo Kawabata
Download or read book Site-Selective Catalysis written by Takeo Kawabata and published by Springer. This book was released on 2016-02-23 with total page 237 pages. Available in PDF, EPUB and Kindle. Book excerpt: The series Topics in Current Chemistry presents critical reviews of the present and future trends in modern chemical research. The scope of coverage is all areas of chemical science including the interfaces with related disciplines such as biology, medicine and materials science.The goal of each thematic volume is to give the non-specialist reader, whether in academia or industry, a comprehensive insight into an area where new research is emerging which is of interest to a larger scientific audience.Each review within the volume critically surveys one aspect of that topic and places it within the context of the volume as a whole. The most significant developments of the last 5 to 10 years are presented using selected examples to illustrate the principles discussed. The coverage is not intended to be an exhaustive summary of the field or include large quantities of data, but should rather be conceptual, concentrating on the methodological thinking that will allow the non-specialist reader to understand the information presented. Contributions also offer an outlook on potential future developments in the field.Review articles for the individual volumes are invited by the volume editors.Readership: research chemists at universities or in industry, graduate students
Download or read book Palladacycles written by Anant Kapdi and published by Elsevier. This book was released on 2019-06-15 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Palladacycles: Catalysis and Beyond provides an overview of recent research in palladacycles in catalysis for cross-coupling and similar reactions. In the quest for developing highly efficient and robust palladium-based catalysts for C-C bond formation via cross-coupling reactions, palladacycles have played a significant role. In recent years, they have found a wide variety of applications, ranging from catalysts for cross-coupling and related reactions, to their more recent application as anticancer agents. This book explores early examples of the use of palladacyclic complexes in catalysis employing azobenzene and hydrazobenzene as coordinating ligands. Its applications in processes such as selective reduction of alkenes, alkynes, or nitroalkanes are also covered. Palladacycles: Catalysis and Beyond reveals the tremendous advances that have taken place in the potential applications of palladacycles as versatile catalysts in academia and industry. It is a valuable resource for synthetic chemists, organometallic chemists, and chemical biologists.
Book Synopsis Computational Methods in Organometallic Catalysis by : Yu Lan
Download or read book Computational Methods in Organometallic Catalysis written by Yu Lan and published by John Wiley & Sons. This book was released on 2021-06-28 with total page 50 pages. Available in PDF, EPUB and Kindle. Book excerpt: Computational Methods in Organometallic Catalysis Discover recent advances in the mechanistic study of organometallic catalysis In Computational Methods in Organometallic Catalysis: From Elementary Reactions to Mechanisms, distinguished chemist and author Yu Lan delivers a synthesis of the use of calculation methods and experimental techniques to improve the efficiency of reaction and yield of product and to uncover the factors that control the selectivity of product. Providing not only a theoretical overview of organometallic catalysis, the book also describes computational studies for the mechanism of transition-metal-assisted reactions. You’ll learn about Ni-, Pd-, Pt-, Co-, Rh-, Ir-, Fe-, Ru-, Mn-, Cu-, Ag-, and Au- catalysis. You’ll also discover many of the experimental and theoretical advances in organometallic catalysis reported in the recent literature. The book summarizes and generalizes the advances made in the mechanistic study of organometallic catalysis. Readers will also benefit from the inclusion of: A thorough introduction to computational organometallic chemistry, including a brief history of the discipline and the use of computational tools to study the mechanism of organometallic chemistry An exploration of computational methods in organometallic chemistry, including density functional theory methods and basis sets and their application in mechanism studies A practical discussion of elementary reactions in organometallic chemistry, including coordination and dissociation, oxidative addition, reductive elimination, insertion, elimination, transmetallation, and metathesis A concise treatment of the theoretical study of transition-metal catalysis. Perfect for organic, catalytic, complex, and structural chemists, Computational Methods in Organometallic Catalysis will also earn a place in the libraries of theoretical chemists seeking a one-stop organometallic catalysis resource with a focus on the mechanism of transition-metal-assisted reactions.
