Advancements In Nickel Catalyzed Cross Electrophile Coupling

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Nickel Catalysis in Organic Synthesis

Author : Sensuke Ogoshi
Publisher : John Wiley & Sons
ISBN 13 : 3527344071
Total Pages : 348 pages
Book Rating : 4.5/5 (273 download)

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Book Synopsis Nickel Catalysis in Organic Synthesis by : Sensuke Ogoshi

Download or read book Nickel Catalysis in Organic Synthesis written by Sensuke Ogoshi and published by John Wiley & Sons. This book was released on 2020-03-09 with total page 348 pages. Available in PDF, EPUB and Kindle. Book excerpt: A comprehensive reference to nickel chemistry for every scientist working with organometallic catalysts Written by one of the world?s leading reseachers in the field, Nickel Catalysis in Organic Synthesis presents a comprehensive review of the high potential of modern nickel catalysis and its application in synthesis. Structured in a clear and assessible manner, the book offers a collection of various reaction types, such as cross-coupling reactions, reactions for the activation of unreactive bonds, carbon dioxide fixation, and many more. Nickel has been recognized as one of the most interesting transition metals for homogeneous catalysis. This book offers an overview to the recently developed new ligands, new reaction conditions, and new apparatus to control the reactivity of nickel catalysts, allowing scientists to apply nickel catalysts to a variety of bond-forming reactions. A must-read for anyone working with organometallic compounds and their application in organic synthesis, this important guide: -Reviews the numerous applications of nickel catalysis in synthesis -Explores the use of nickel as a relatively cheap and earth-abundant metal -Examines the versatility of nickel catalysis in reactions like cross-coupling reactions and CH activations -Offers a resource for academics and industry professionals Written for catalytic chemists, organic chemists, inorganic chemists, structural chemists, and chemists in industry, Nickel Catalysis in Organic Synthesis provides a much-needed overview of the most recent developments in modern nickel catalysis and its application in synthesis.

Advancements in Nickel-catalyzed Cross-electrophile Coupling

Author : Keywan Alexander Johnson
Publisher :
ISBN 13 :
Total Pages : 154 pages
Book Rating : 4.:/5 (111 download)

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Book Synopsis Advancements in Nickel-catalyzed Cross-electrophile Coupling by : Keywan Alexander Johnson

Download or read book Advancements in Nickel-catalyzed Cross-electrophile Coupling written by Keywan Alexander Johnson and published by . This book was released on 2019 with total page 154 pages. Available in PDF, EPUB and Kindle. Book excerpt: In this thesis, the extension of cross-electrophile coupling to engage vinyl halides, organic chlorides, and dihalides for cyclization will be described in detail. Chapter 1 will provide an introduction to cross-electrophile coupling and the current state of the art for these transformations. Chapter 2 describes the development of improved coupling conditions for the nickel-catalyzed cross-electrophile coupling of vinyl halides with alkyl halides. The application of these conditions to aryl-alkyl coupling, substrate scope and limitations, and preliminary mechanistic insights are also discussed. Chapter 3 describes studies performed for the coupling of aryl and alkyl chlorides. The effects of a dual ligand system on reaction selectivity, as well as implications of dimethoxyethane and diglyme nickel precatalysts are also conferred. Chapter 4 provides a survey of macrocyclization methodologies and details the application of cross-electrophile coupling to the synthesis of macrocyclic rings. Efforts towards the total synthesis of (+/-)-Recifeiolide are also discussed.

Development of Nickel-catalyzed Cross-electrophile Coupling of Aryl Chlorides and Triflates with Alkyl Halides

Author : Seoyoung Kim (Ph.D.)
Publisher :
ISBN 13 :
Total Pages : 0 pages
Book Rating : 4.:/5 (141 download)

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Book Synopsis Development of Nickel-catalyzed Cross-electrophile Coupling of Aryl Chlorides and Triflates with Alkyl Halides by : Seoyoung Kim (Ph.D.)

Download or read book Development of Nickel-catalyzed Cross-electrophile Coupling of Aryl Chlorides and Triflates with Alkyl Halides written by Seoyoung Kim (Ph.D.) and published by . This book was released on 2023 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Cross-coupling is one of the most commonly used reactions in synthetic chemistry. While palladium-catalyzed cross-coupling is well-developed and established, cross-electrophile coupling is significantly younger field of study. In this approach two carbon electrophiles are directly coupled under reductive conditions, avoiding the need to prepare organometallic reagents. This is an attractive strategy because these reactions proceed through mild conditions, have high functional group tolerance, and employ readily available coupling partners. Nickel-catalyzed cross-electrophile couplings have seen considerable success in the past decade, initially in the coupling of organic iodides and later organic bromides. Despite these advances, the cross-coupling with the more abundant and inexpensive organic chlorides remain elusive due to their low reactivity. Furthermore the nickel-catalyzed cross-coupling of aryl triflates presents analogous challenges due to their differential reactivity. This thesis presents our studies to address these limitations. Through a combination of: (1) new ligand application, (2) fine tuning of alkyl electrophile reactivity through in situ halide exchange, (3) detailed mechanistic investigation of elementary steps, we demonstrate the nickel-catalyzed cross-electrophile coupling of these traditionally inert organic coupling partner. This dissertation is presented as follows: Chapter 1 is an introduction to cross-coupling strategies. Common palladium-catalyzed cross-coupling methods are discussed and their origin of cross-selectivity is highlighted. This is contrasted to cross-electrophile approaches of which mechanism is less well-understood. Early reports on nickel-catalyzed cross-electrophile coupling are presented and how mechanistic studies have elucidated the origin of cross-selectivity in these processes. Finally, the challenges of applying aryl chlorides in these first generation approaches are briefly discussed. Chapter 2 describes the development of nickel-catalyzed cross-electrophile coupling of aryl chlorides with primary alkyl chlorides to form C(sp2)-C(sp3) bonds. Investigation of ligands on selectivity and in situ halide exchange on the activation of C(sp3)-Cl bonds are detailed. Chapter 3 discusses a strategy for nickel-catalyzed cross-electrophile coupling of aryl triflates with alkyl halides. The development of reaction conditions for differing aryl electronics and mechanistic insights are described in detail. Mechanistically driven optimization and the extent of halide exchange to modulate alkyl halide reactivity are also discussed.

Computational Approaches to Improve Catalyst Design in Nickel-catalyzed Cross-electrophile Coupling

Author : Michelle Elizabeth Akana
Publisher :
ISBN 13 :
Total Pages : 0 pages
Book Rating : 4.:/5 (144 download)

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Book Synopsis Computational Approaches to Improve Catalyst Design in Nickel-catalyzed Cross-electrophile Coupling by : Michelle Elizabeth Akana

Download or read book Computational Approaches to Improve Catalyst Design in Nickel-catalyzed Cross-electrophile Coupling written by Michelle Elizabeth Akana and published by . This book was released on 2024 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: This dissertation will discuss advancements made toward understanding the intrinsic reactivity of nitrogenous ligands in nickel-catalyzed cross-electrophile coupling, as well as their impacts on reaction selectivities.Chapter 1 will introduce cross-electrophile coupling, highlight the importance of ligands in promoting diverse elementary steps, and discuss strategies to search for, understand, and improve ligand architecture. Chapter 2 describes our initial investigation utilizing descriptors from a diverse set of ligands and ligand-like molecules to predict reaction yield and selectivity. This investigation provided critical insight into experimental design, construction of a training set, and determining project outcomes. The results of these efforts informed our studies that are detailed in successive chapters. Chapter 3 summarizes the application of statistical methods to develop a model for selectivity in bipyridine-nickel-catalyzed cross-electrophile coupling. The resulting model was used to rationalize experimental outcomes, develop mechanistic insight, and design improved ligands in silico. Chapter 4 summarizes initial insights into the relationships between the structure of other classes of heterocycle-based L2 dinitrogen ligands and their corresponding experimental outcomes. These investigations provide a basis for understanding the performance of these ligands and expands on the insights described in Chapter 3. A plan for ongoing research informed by these results is proposed. Chapter 5 describes additional computationally informed projects that were undertaken by the author. These projects utilize computed catalyst structures and energies to rationalize the impact of ligand binding on the reactivity of novel 2,2'- bipyridine-6-carbonitrile ligands, as well as the relationship of ligand structure to selectivity in decarbonylative cross-electrophile coupling.

Modern Organonickel Chemistry

Author : Yoshinao Tamaru
Publisher : John Wiley & Sons
ISBN 13 : 3527604235
Total Pages : 346 pages
Book Rating : 4.5/5 (276 download)

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Book Synopsis Modern Organonickel Chemistry by : Yoshinao Tamaru

Download or read book Modern Organonickel Chemistry written by Yoshinao Tamaru and published by John Wiley & Sons. This book was released on 2006-03-06 with total page 346 pages. Available in PDF, EPUB and Kindle. Book excerpt: Organonickel chemistry plays an increasingly important role in organic chemistry, and interest in this topic is now just as keen as in organopalladium chemistry. While there are numerous, very successful books on the latter, a book specializing in organonickel chemistry is long overdue. Edited by one of the leading experts in the field, this volume covers the many discoveries made over the past 30 years, and previously scattered throughout the literature. Active researchers working at the forefront of organonickel chemistry provide a comprehensive review of the topic, including cross-coupling reactions, asymmetric synthesis and heterogeneous catalysis reaction types. A must-have for both organometallic chemists and synthetic organic chemists.

Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions

Author : Lucas William Erickson
Publisher :
ISBN 13 : 9780355307122
Total Pages : 321 pages
Book Rating : 4.3/5 (71 download)

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Book Synopsis Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions by : Lucas William Erickson

Download or read book Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions written by Lucas William Erickson and published by . This book was released on 2017 with total page 321 pages. Available in PDF, EPUB and Kindle. Book excerpt: In recent years, the Jarvo lab has developed the field of stereospecific nickel-catalyzed cross-coupling reactions of benzylic electrophiles. This chemistry allows for straightforward synthesis of asymmetric C--C bonds. The focus of this dissertation is on the study of the mechanism of these transformations, and the development of reductive cross-electrophile coupling reactions.First, the mechanism of the nickel-catalyzed Kumada cross-coupling reaction was studied via a 13C kinetic isotope effect experiment. This experiment indicated that oxidative addition of the nickel catalyst into the C--O sigma bond was the rate limiting step. Combining this data with a rate law allowed us to propose a catalytic cycle for this reaction. Additionally, the nickel-catalyzed deoxygenation of benzylic ethers was optimized for the formation of diaryl methanes. Deoxygenation performed best with a proton-rich Grignard reagent. We demonstrated that these Grignard reagents act as the hydride source for the reduction reaction.Next, an intramolecular nickel-catalyzed reductive cross-electrophile coupling reaction of benzylic ethers and alkyl chlorides was developed. This reaction proceeds with a variety of extended aromatic and heteroaromatic groups to produce cyclopropane rings in great yields and diastereoselectivity. This is the first example of a stereospecific reductive cross-electrophile coupling reaction, as well as the first to employ alkyl ethers and alkyl halides as the electrophiles.Finally, the work on nickel-catalyzed reductive cross-electrophile coupling reactions was expanded to synthesize vinylcyclopropanes from allylic ethers and alkyl halides. This reaction occurs with both alkyl fluorides and alkyl chlorides. To the best of our knowledge, this is the first reported cross-electrophile coupling reaction of an alkyl fluoride. Ring contraction proceeds with high stereospecificity, providing selective synthesis of either diastereomer of di- and tri-substituted cyclopropanes. The utility of this methodology is demonstrated by several synthetic applications including the synthesis of the natural product dictyopterene A. 2-Vinyl-4-fluorotetrahydrofurans also undergo stereospecific ring contractions, providing access to synthetically useful hydroxymethyl cyclopropanes.

Ni- and Fe-Based Cross-Coupling Reactions

Author : Arkaitz Correa
Publisher : Springer
ISBN 13 : 3319497847
Total Pages : 342 pages
Book Rating : 4.3/5 (194 download)

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Book Synopsis Ni- and Fe-Based Cross-Coupling Reactions by : Arkaitz Correa

Download or read book Ni- and Fe-Based Cross-Coupling Reactions written by Arkaitz Correa and published by Springer. This book was released on 2016-11-26 with total page 342 pages. Available in PDF, EPUB and Kindle. Book excerpt: The series Topics in Current Chemistry Collections presents critical reviews from the journal Topics in Current Chemistry organized in topical volumes. 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.

The Mizoroki-Heck Reaction

Author : Martin Oestreich
Publisher : John Wiley & Sons
ISBN 13 : 9780470716069
Total Pages : 608 pages
Book Rating : 4.7/5 (16 download)

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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)

Nickel-catalyzed Electrophile Cross-coupling of Aryl Halides with Alkyl Halides

Author : Daniel A. Everson
Publisher :
ISBN 13 :
Total Pages : 264 pages
Book Rating : 4.:/5 (925 download)

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Book Synopsis Nickel-catalyzed Electrophile Cross-coupling of Aryl Halides with Alkyl Halides by : Daniel A. Everson

Download or read book Nickel-catalyzed Electrophile Cross-coupling of Aryl Halides with Alkyl Halides written by Daniel A. Everson and published by . This book was released on 2013 with total page 264 pages. Available in PDF, EPUB and Kindle. Book excerpt: "This thesis details the author's contributions to the emerging field of electrophile cross-couplings. This new field is related to the well-established field of conventional cross-coupling that uses transition metal-catalysts to facilitate coupling reactions between electrophile-nucleophile pairs. Electrophile cross-coupling uses a conceptually different approach because it seeks to selectively join two different electrophiles with a transition metal-catalyst. The issue of developing cross-selective reactions is the central challenge addressed. Chapter 1 details recent advances and the state-of-the-art in conventional cross-coupling only for the purpose of conceptual comparison to electrophile cross-coupling. Additionally, a review of similar coupling reactions and their mechanisms are presented with the earliest examples of the unique reactivity that guided development of the reactions in this thesis. Chapter 2 details the first cross-selective nickel-catalyzed electrophile cross-coupling of iodoarenes with iodoalkanes. The new method displays exceptional functional group compatibility (-C(O)Me, -NHBoc, 1° and 2° alkyls, -OH) and the catalyst shows chemoselective reaction at C-I bonds over C-B bonds on bifunctional substrates. Mechanistic studies reveal that the reaction likely proceeds without the intermediacy of a carbon nucleophile, and that dimeric by-products arise from disproportionation of nickel intermediates. Chapter 2 also summarizes a detailed mechanistic study conducted in our lab that indicates the cross-coupled product is formed by a radical chain mechanism. Chapter 3 expands on the results of Chapter 2 by increasing the scope of the method to include bromo- and chloroarenes for the first time. Additional competition experiments reveal that the new catalysts and reaction conditions are chemoselective for the cross-coupling of two electrophilic C-Br bonds over conventional cross coupling of C-Br bonds with C-B, C-Sn, or C-Si bonds. Further mechanistic work reveals that [upsilon] [is proportional to] [bromoalkane][^x][catalyst][^y]/[bromoarene][^z] (x, y, and z are positive numbers and could be non-integers). Chapter 4 presents the first electrophile cross-couplings of halogenated pyridines with alkyl bromides. Scope and limitations are discussed in the context of improving the method. Chapter 5 details the effect of additives on other related electrophile coupling reactions"--Pages vii-viii.

Advances in Cross-Coupling Reactions

Author : José Pérez Sestelo
Publisher : MDPI
ISBN 13 : 3039435671
Total Pages : 234 pages
Book Rating : 4.0/5 (394 download)

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Book Synopsis Advances in Cross-Coupling Reactions by : José Pérez Sestelo

Download or read book Advances in Cross-Coupling Reactions written by José Pérez Sestelo and published by MDPI. This book was released on 2020-12-03 with total page 234 pages. Available in PDF, EPUB and Kindle. Book excerpt: In this Special Issue, recent advances in cross-coupling reactions are presented in the form of original research articles, reviews, and short communications. These contributions cover different topics in this area, including novel coupling reactions, reaction conditions, synthetic alternatives, metal ligands, and applications for new pharmaceutical compounds and organic materials. In particular, the reviews deal with methodologies such as the synthesis of diarylketones through palladium catalysis and the most relevant examples of Suzuki–Miyaura and Buchwald–Hartwig coupling reactions in the synthesis of bioactive compounds. The synthetic utility of cross-coupling reactions for the synthesis of medium-size rings and the utility of Stille and Suzuki coupling reactions for the synthesis of new molecular machines based on sterically hindered anthracenyl trypticenyl units are also summarized. The original research articles present the synthesis of 2-alkynylpyrrols by inverse Sonogashira coupling and the synthesis of indoles under oxidative dearomative cross-dehydrogenative conditions. The efficient combination of iridium-catalyzed C–H borylation of aryl halides with the Sonogashira coupling and a sequential iridium-catalyzed borylation of NH-free pyrroles followed by a Suzuki–Miyaura reaction are included. The synthesis of aryl propionic acids, a common structural motif in medicinal chemistry, and the synthesis of new organic dyes are also covered.

Modern Arylation Methods

Author : Lutz Ackermann
Publisher : John Wiley & Sons
ISBN 13 : 3527627332
Total Pages : 561 pages
Book Rating : 4.5/5 (276 download)

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Book Synopsis Modern Arylation Methods by : Lutz Ackermann

Download or read book Modern Arylation Methods written by Lutz Ackermann and published by John Wiley & Sons. This book was released on 2009-04-22 with total page 561 pages. Available in PDF, EPUB and Kindle. Book excerpt: Today, arylation methods are belonging to the most important reaction types in organic synthesis. Lutz Ackermann, a young and ambitious professor has gathered a number of top international authors to present the first comprehensive book on the topic. Starting from a historical review, the book covers hot topics like Palladium-catalyzed arylation of N-H and alpha-C-H-acidic Bonds, Copper-catalyzed arylation of N-H and O-H Bonds, direct arylation reactions, carbanion aromatic synthesis, arylation reactions of alkenes, alkynes and much more. This compact source of high quality information is indispensable to synthetic chemists and those working in the pharmaceutical and chemical industry.

Cross-Coupling Reactions

Author : Norio Miyaura
Publisher : Springer
ISBN 13 : 354045313X
Total Pages : 253 pages
Book Rating : 4.5/5 (44 download)

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Book Synopsis Cross-Coupling Reactions by : Norio Miyaura

Download or read book Cross-Coupling Reactions written by Norio Miyaura and published by Springer. This book was released on 2003-07-01 with total page 253 pages. Available in PDF, EPUB and Kindle. Book excerpt: In 1972, a very powerful catalytic cycle for carbon-carbon bond formation was 2 first discovered by the coupling reaction of Grignard reagents at the sp -carbon. Over the past 30 years, the protocol has been substantially improved and expanded to other coupling reactions of Li,B,N,O,Al,Si,P,S,Cu,Mn,Zn,In,Sn, and Hg compounds. These reactions provided an indispensable and simple methodology for preparative organic chemists. Due to the simplicity and rel- bility in the carbon-carbon, carbon-heteroatom, and carbon-metalloid bo- formations,as well as high efficiency of the catalytic process,the reactions have been widely employed by organic chemists in various fields. Application of the protocol ranges from various syntheses of complex natural products to the preparation of biologically relevant molecules including drugs, and of sup- molecules, and to functional materials. The reactions on solid surfaces allow robot synthesis and combinatorial synthesis. Now, many organic chemists do not hesitate to use transition metal complexes for the transformation of org- ic molecules. Indeed, innumerable organic syntheses have been realized by the catalyzed reactions of transition metal complexes that are not achievable by t- ditional synthetic methods. Among these, the metal-catalyzed cross-coupling reactions have undoubtedly contributed greatly to the development of such a new area of “metal-catalyzed organic syntheses”. An excellent monograph for the cross-coupling reactions and other met- catalyzed C-C bond-forming reactions recently appeared in Metal-catalyzed Cross-coupling Reactions (Wiley-VCH,1998).

Applied Cross-Coupling Reactions

Author : Yasushi Nishihara
Publisher : Springer Science & Business Media
ISBN 13 : 3642323685
Total Pages : 247 pages
Book Rating : 4.6/5 (423 download)

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Book Synopsis Applied Cross-Coupling Reactions by : Yasushi Nishihara

Download or read book Applied Cross-Coupling Reactions written by Yasushi Nishihara and published by Springer Science & Business Media. This book was released on 2012-12-14 with total page 247 pages. Available in PDF, EPUB and Kindle. Book excerpt: “Applied Cross-Coupling Reactions” provides students and teachers of advanced organic chemistry with an overview of the history, mechanisms and applications of cross-coupling reactions. Since the discovery of the transition-metal-catalyzed cross-coupling reactions in 1972, numerous synthetic uses and industrial applications have been developed. The mechanistic studies of the cross-coupling reactions have disclosed that three fundamental reactions: oxidative addition, transmetalation, and reductive elimination, are involved in a catalytic cycle. Cross-coupling reactions have allowed us to produce a variety of compounds for industrial purposes, such as natural products, pharmaceuticals, liquid crystals and conjugate polymers for use in electronic devices. Indeed, the Nobel Prize for Chemistry in 2010 was awarded for work on cross-coupling reactions. In this book, the recent trends in cross-coupling reactions are also introduced from the point of view of synthesis design and catalytic activities of transition-metal catalysts.

Metal-catalyzed Cross-coupling Reactions

Author : François Diederich
Publisher : John Wiley & Sons
ISBN 13 : 3527612203
Total Pages : 540 pages
Book Rating : 4.5/5 (276 download)

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Book Synopsis Metal-catalyzed Cross-coupling Reactions by : François Diederich

Download or read book Metal-catalyzed Cross-coupling Reactions written by François Diederich and published by John Wiley & Sons. This book was released on 2008-07-11 with total page 540 pages. Available in PDF, EPUB and Kindle. Book excerpt: Carbon-carbon bond forming reactions are arguably the most important processes in chemistry, as they represent key steps in the building of complex molecules from simple precursors. Among these reactions, metal-catalyzed cross-coupling reactions are extensively employed in a wide range of areas of preparative organic chemistry, ranging from the synthesis of complex natural products, to supramolecular chemistry, and materials science. In this work, a dozen internationally renowned experts and leaders in the field bring the reader up to date by documenting and critically analyzing current developments and uses of metal-catalyzed cross-coupling reactions. A particularly attractive and useful feature, that enhances the practical value of this monograph, is the inclusion of key synthetic protocols, in experimental format, chosen for broad utility and application. This practice-oriented book can offer the practitioner short cuts to ensure they remain up-to-date with the latest developments.

Nickel-catalyzed Reductive Coupling of Aryl Halides with Alkyl Electrophiles

Author : Lukiana L. Anka-Lufford
Publisher :
ISBN 13 :
Total Pages : 208 pages
Book Rating : 4.:/5 (11 download)

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Book Synopsis Nickel-catalyzed Reductive Coupling of Aryl Halides with Alkyl Electrophiles by : Lukiana L. Anka-Lufford

Download or read book Nickel-catalyzed Reductive Coupling of Aryl Halides with Alkyl Electrophiles written by Lukiana L. Anka-Lufford and published by . This book was released on 2015 with total page 208 pages. Available in PDF, EPUB and Kindle. Book excerpt: "The direct transition-metal catalyzed cross-coupling of two different electrophiles is a fast emerging synthetic method, as it avoids the use of carbon nucleophiles. Despite being a synthetically valuable strategy, a central challenge of cross-electrophile coupling is achieving selectivity for cross-coupled product over dimerization products. This thesis details the author's work towards the development of cross-selective methods for the formation of Csp2-Csp3 bonds. Chapter 1 introduces the conventional cross-coupling method of forming C-C bonds and highlights the advantages of using the reductive cross-electrophile coupling approach instead. The selectivity challenges associated with reductive cross-coupling and the origins of selectivity in the cross-coupling reactions of aryl halides with allylic acetates and benzyl mesylates are discussed. Motivations towards the adaptation of our cross-electrophile coupling methods to more environmentally responsible solvents and reductants are also described. Chapter 2 details a general protocol for the coupling of aryl halides with allylic acetates and shows that high cross-selectivity can be achieved with the use of a terpyridine nickel catalyst. Strength's of the method are presented such tolerance for electrophilic (ketone (71%), aldehyde (70%)) and acidic (sulfonamide (73%), trifluoroacetamide (64%)) substrates and the ability to couple with a variety of substituted allylic acetates. The reductive method addresses the regioselectivity and substrate availability limitations observed in past approaches to allylated arenes. Chapter 3 presents the first synthesis of diarylmethanes from benzyl mesylates and aryl halides using cobalt phthalocyanine (Co(Pc)), a new co-catalyst for radical generation that is compatible with nickel-catalysis. Studies are shown demonstrating the orthogonal reactivity of (dtbbpy)Ni and Co(Pc) and the application of this selectivity to the coupling of functionalized benzyl mesylates with aryl halides. The adaptation of the method to the less reactive benzyl phosphate ester and an enantioconvergent reaction are also presented. Chapter 4 shows studies towards the adaptation of cross-electrophile coupling to more environmentally friendly solvents and reductants. Here, a homogeneous, two electronic organic reductant, 1,2,2-tetrakis(dimethylamino)ethylene (TDAE), is shown to be effective for nickel-catalyzed cross-electrophile coupling in various green solvents such as propylene carbonate and acetonitrile. These reactions are close in yield to our best-reported results in amide or urea solvents using zinc or manganese as the reductant. Chapter 5 describes initial studies towards nickel-catalyzed decarbonylative coupling reactions of acid chloride derivatives with aryl and alkyl halides and nickel-catalyzed coupling reactions of aryl halides with small cyclic alkyl bromides and oxetane tosylate. Further optimization strategies are presented."--Pages viii-ix.

Development of Nickel-Catalyzed Coupling Reactions

Author : Mikhail Olegovich Konev
Publisher :
ISBN 13 : 9780355308976
Total Pages : 503 pages
Book Rating : 4.3/5 (89 download)

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Book Synopsis Development of Nickel-Catalyzed Coupling Reactions by : Mikhail Olegovich Konev

Download or read book Development of Nickel-Catalyzed Coupling Reactions written by Mikhail Olegovich Konev and published by . This book was released on 2017 with total page 503 pages. Available in PDF, EPUB and Kindle. Book excerpt: Transition metal catalyzed reactions are ubiquitous in the realm of synthetic chemistry, allowing for the strategic construction of complex molecular frameworks of pharmaceuticals, natural products, and synthetic materials. Palladium-catalyzed cross-coupling reactions are part of the foundation of these transformations, insofar as they were recognized with the 2010 Nobel Prize in chemistry. Traditionally, these reactions have relied on aryl and vinyl electrophiles, whereas the alkyl counterparts have only recently begun to emerge in the literature. Nickel has been on the forefront of enantioconvergent alkyl cross--coupling reactions due to its propensity to undergo single electron chemistry. However, under special conditions, it has a unique ability to break strong carbon--oxygen bonds in a stereospecific manner, making research into its reactivity a valuable endeavor to the field of organometallic chemistry.Chapter 1 describes the development of a stereospecific intramolecular alkyl-Heck cyclization of benzylic ethers. The reaction proceeds with inversion at the electrophilic carbon, for the synthesis of methylenecyclopentanes of both extended pi-electron and simple aromatic systems. The enantioenriched products can be effectively derivatized to cyclic alpha-aryl ketones in good yields with good transfer of chirality. Avenues to expand the utility of this reaction have been identified and further studies are ongoing.Chapter 2 discusses the development of nickel-catalyzed cross-electrophile coupling reactions of benzylic esters and aryl halides. An intermolecular reaction proceeds in high yields for primary benzylic esters for the synthesis of pharmacologically relevant diarylmethanes. The corresponding intramolecular cyclization proceeds under mild conditions, demonstrating the first example of a stereospecific cross-electrophile coupling of secondary benzylic esters. A variety of heterocyclic and functionalized substrates are tolerated under the reaction conditions.Chapter 3 examines the development a regio- and stereoselective nickel-catalyzed hydroarylation of alkynes with arylboronic acids. The reaction is facilitated by propargyl carbamates as directing groups. The reaction is tolerant of a range of functional groups and heterocycles. Mechanistic studies reveal that the acidic protons of the arylboronic acid coupling partner serve as the origin of hydrogen. Furthermore, the synthesis of tamoxifen can be completed in two steps from a simple hydroarylation product.

Amide Bond Activation

Author : Michal Szostak
Publisher : MDPI
ISBN 13 : 3039212036
Total Pages : 466 pages
Book Rating : 4.0/5 (392 download)

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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.