Download or read book Nickel Precatalysts as Enabling Tools for Catalytic Coupling Reactions written by Eric Alan Standley and published by . This book was released on 2015 with total page 527 pages. Available in PDF, EPUB and Kindle. Book excerpt: [Chemical formula] A series of air-stable nickel complexes of the form L2Ni(aryl)X (L = monodentate phosphine, X = Cl, Br) and LNi(aryl)X (L = bis-phosphine) have been synthesized and are presented as a library of precatalysts suitable for a wide variety of nickel-catalyzed transformations. These complexes are easily synthesized from low-cost NiCl2-6H2O or NiBr2-3H2O and the desired ligand followed by addition of 1 equiv of Grignard reagent. A selection of these complexes were characterized by single-crystal X-ray diffraction, and an analysis of their structural features is provided. [Chemical formula] The air-stable nickel(II) complex trans-(PCy2Ph)2Ni(o-tolyl)Cl was employed as a precatalyst for the Mizoroki-Heck-type, room temperature, internally selective coupling of substituted benzyl chlorides with terminal alkenes. This reaction, which employs a terminal alkene as an alkenylmetal equivalent, provides rapid, convergent access to substituted allylbenzene derivatives in high yield and with regioselectivity greater than 95:5 in nearly all cases. The reaction is operationally simple, can be carried out on the benchtop with no purification or degassing of solvents or reagents, and requires no exclusion of air or water during setup. Synthesis of the precatalyst is accomplished through a straightforward procedure that employs inexpensive, commercially available reagents, requires no purification steps, and proceeds in high yield. [Chemical formula] The nickel-catalyzed cross-coupling of aliphatic N-tosylaziridines with aliphatic organozinc reagents is described. The reaction protocol displays complete regioselectivity for reaction at the less hindered C-N bond, and the products are furnished in good to excellent yield for a broad selection of substrates. An air-stable nickel(II) chloride/ligand precatalyst was also developed and employed for the reaction. In addition to increasing the activity of this catalyst system, this also greatly improves the practicality of this reaction, as the use of the very air-sensitive Ni(cod)2 is avoided. Finally, mechanistic investigations, including deuterium-labeling studies, show that the reaction proceeds with overall inversion of configuration at the terminal position of the aziridine by way of aziridine ring opening by Ni (inversion), transmetallation (retention), and reductive elimination (retention).
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.
Download or read book Advances in Palladium and Nickel Catalyzed Cross Coupling Reactions written by Ryan Sawatzky and published by . This book was released on 2017 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Homogeneous organometallic complexes have become an indispensable tool as they are employed as catalysts for a large number of chemical transformations. Ancillary ligands, organic molecules that bind to the metal center, are critical for fine tuning the performance of these catalysts. The initial portion of this thesis describes a comparative survey of several state-of-the-art ligands for Pd catalyzed C-O cross-coupling reactions. As part of this survey two sets of conditions are employed: reactions carried out at 90 °C, using 1 mol % Pd, and room temperature reactions, using 7 mol % Pd. In these comparisons, it was found that Rockphos was the ligand of choice for reactions at room temperature, as well for electron rich electrophiles. The Josiphos variant, CyPF-tBu, was the optimal ligand for reactions at elevated temperatures, as well as for activated electrophiles. Many ligands that have found use in Pd chemistry have been repurposed for use in Ni catalysis. While this an effective strategy, it is not necessarily ideal. The bisphosphine PAd-Dalphos has been tailored for Ni catalyzed monoarylation of ammonia, and primary amines. Here, ammonium, methylamine, and ethylamine salts are successfully used as cross-coupling partners employing microwave heating. High yielding reactions, utilizing as little as 1 mol % Ni can be completed in as little as 5 minutes under these conditions. In an effort to establish trends of reactivity in Ni catalysis, the complex (DPEphos)Ni(mesityl)Br was developed for both C-N, C-C cross-coupling reactions. This complex was first established in the cross-coupling of secondary amines, and azoles with activated aryl chlorides. The observation of PhB(OH)2 required as a catalyst activator lead to the development of this complex as a catalyst for C-C cross-coupling using unstable 5-membered heterocyclic boronic acids for challenging biheteroaryl formation. Here reactions conducted at room temperature were found to be comparable to the previous state-of-the-art Ni catalysis. In addition, 3-pyridinyl-boronic acids were also successfully employed. While the scope of reactivity with such challenging substrates was modest, the work herein represents a step forward as only a small handful of examples exist for Ni catalyzed reactions.
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.
Download or read book Reaction Discovery Using Nickel Catalysis and Total Syntheses of Indolactam Alkaloids written by Noah Frederick Fine Nathel and published by . This book was released on 2015 with total page 574 pages. Available in PDF, EPUB and Kindle. Book excerpt: Transition metal-catalyzed cross-coupling reactions are useful tools to assemble carbon-carbon (C-C) and carbon-heteroatom (C-X) bonds. Traditionally, electrophilic halides and pseudohalides have been cross-coupled to their nucleophilic counterparts with palladium. Recently, however, the implementation of nickel as a catalyst for cross-coupling reactions has enabled the use of less reactive cross-coupling partners, such as carbamates, sulfamates, and amides. This dissertation describes the development of nickel-catalyzed cros-couplings of untraditional electrophiles to forge carbon-heteroatom (C-X) bonds. Additionally, the total syntheses of four indolactam alkaloids, indolactam V, pendolmycin, lyngbyatoxin A1 and teleocidin A-2, using both a key distortion-controlled indolyne reaction and palladium-catalyzed sp2-sp3 C-C bond construction, are described. Chapters one and two describe the development of nickel-catalyzed amination reactions of aryl electrophiles to form carbon-nitrogen (C-N) bonds. The amination reaction of aryl carbamates to form aryl amines is discussed. Subsequently, the development of green cross-couplings of aryl sulfamates and chlorides to similarly form aryl amines is reported. Chapter three introduces a means to accomplish a controlled cine substitution. This two-step process is comprised of a carbamate-directed ortho-lithiation/functionalization of an arene, followed by a nickel-catalyzed reductive deoxygenation of the directing group. This sequence provides a new strategy for synthesis and complements the more commonly employed ipso substitution in arene functionalization. Chapter four concerns the utility of amides as electrophilic cross-coupling partners. These traditionally unreactive moieties are activated by nickel and coupled to alcohols to form acyl C--O bonds. This study suggests that amides may serve as useful building blocks to construct C-X and C-C bonds. Chapter five describes the total syntheses of ( - )-indolactam V and its C7-substituted natural product derivatives, ( - )-pendolmycin, ( - )-lyngbyatoxin A1 and ( - )-teleocidin A-2. The C4-N linkage is constructed with a distortion-controlled indolyne functionalization. The total synthesis of ( - )-indolactam V provides a platform for the divergent syntheses of the other three natural products via a palladium-catalyzed cross-coupling to functionalize C7 and introduce a quaternary center.
Download or read book Enabling Tools and Techniques for Organic Synthesis written by Stephen G. Newman and published by John Wiley & Sons. This book was released on 2023-09-26 with total page 500 pages. Available in PDF, EPUB and Kindle. Book excerpt: Provides the practical knowledge of how new technologies impact organic synthesis, enabling the reader to understand literature, evaluate different techniques, and solve synthetic challenges In recent years, new technologies have impacted organic chemistry to the point that they are no longer the sole domain of dedicated specialists. Computational chemistry, for example, can now be used by organic chemists to help predict outcomes, understand selectivity, and decipher mechanisms. To be prepared to solve various synthetic problems, it is increasingly important for chemists to familiarize themselves with a range of current and emerging tools and techniques. Enabling Tools and Techniques for Organic Synthesis A Practical Guide to Experimentation, Automation, and Computation provides a broad overview of contemporary research and new technologies applied to organic synthesis. Detailed chapters, written by a team of experts from academia and industry, describe different state-of-the-art techniques such as computer-assisted retrosynthesis, spectroscopy prediction with computational chemistry, high throughput experimentation for reaction screening, and robotic and automated data collection methods. Emphasizing real-world practicality, the book includes chapters on programming for synthetic chemists, Machine Learning (ML) in chemical synthesis, concepts and applications of computational chemistry, and more. Highlights the most recent methods in organic synthesis and describes how to employ these techniques in a reader’s own research Familiarize readers with the application of computational chemistry and automation technology in organic synthesis Introduces synthetic chemists to electrochemistry, photochemistry, and flow chemistry Helps readers comprehend the literature, assess the strengths and limitations of each technique, and apply those tools to solve synthetic challenges Provides case studies and guided examples with graphical illustrations in each chapter Enabling Tools and Techniques for Organic Synthesis: A Practical Guide to Experimentation, Automation, and Computation is an invaluable reference for scientists needing an up-to-date introduction to new tools, graduate students wanting to expand their organic chemistry skills, and instructors teaching courses in advanced techniques for organic synthesis.
Download or read book C N Bond Formation Employing Palladium and Nickel Precatalysts Containing Anionic Phosphinobenzimidazole Ligands written by Joseph P. Tassone and published by . This book was released on 2016 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: In this investigation, the catalytic utility of anionic, phosphinobenzimidzoles [Li(THF)2][1a] and [Li(THF)4][1b] in effecting the Buchwald-Hartwig amination reaction was examined. Specifically, the coordination chemistry of ligands [Li(THF)2][1a] and [Li(THF)4][1b] with palladium was studied in an attempt to synthesize a distinct precatalyst containing either 1a or 1b that could be screened for catalytic activity in the reaction of interest. Additionally, the screening of a Pd/[Li(THF)4][1b] catalyst system for activity in the Buchwald-Hartwig amination reaction was conducted concurrently. Complex 6, containing 1a, and complexes 7-12, containing 1b, were successfully synthesized, and characterized using multi-nuclear NMR spectroscopy. An optimized [Pd(cinnamyl)Cl]2/[Li(THF)4][1b] catalyst system was also developed, and performed the coupling of activated and deactivated aryl bromides with a selection of amines in moderate to excellent yields (36-97%). A preference for primary vs. secondary amine coupling partners, as well as a high selectivity for the monoarylated product, was observed during the course of these studies. To highlight the remarkable potential of anionic ligands in catalysis, the catalytic efficiency of the [Pd(cinnamyl)Cl]2/[Li(THF)4][1b] catalyst system was compared with a corresponding system utilizing the related, neutral phosphinobenzimidazole 2, with the anionic system displaying superior catalytic activity in the Buchwald-Hartwig amination reaction in almost all cases. This phenomenon was attributed to the more electron-rich catalytic intermediates present in the anionic system, enabling more rapid oxidative addition, and thus more efficient catalysis. Further screening of the anionic precatalyst [PPh4][PdCl2(k2-1b)] (10) and neutral precatalyst [PdCl2(k2-2)] (13) corroborated these results. Finally, preliminary studies examining the potential of 1b as an ancillary ligand in Ni-catalyzed C-N bond formation was undertaken. The coordination chemistry of 1b with nickel was explored, resulting in the formation of complex 14, whose tentative structure was assigned on the basis of NMR spectroscopic evidence. Furthermore, initial screening of a NiCl2(DME)/[Li(THF)4][1b] catalyst system in the cross-coupling of chlorobenzene and aniline did not result in observable product formation under various reaction conditions.
Download or read book Exploring Ligand Enabled Nickel Catalyzed Cross Coupling of Sulfur Based Nucleophiles written by Connor Simon and published by . This book was released on 2022 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: The catalytic synthesis of C(sp2)-N linkages is of utmost significance in modern synthetic chemistry, predominantly due to their prevalence in active pharmaceutical ingredients and natural products. Pd-catalyzed cross-couplings of this type, known colloquially as Buchwald-Hartwig amination (BHA), represent a tremendously important class of reactions in research and industrial settings. The success achieved by BHA can largely be attributed to the rational design of ancillary ligands specifically configured to exploit the natural electronic characteristics of the Pd metal centre. Research efforts surrounding the BHA reaction have enabled the scope of suitable coupling partners to grow rapidly, encompassing a vast array of (hetero)aryl (pseudo)halides and NH couplings partners. Notwithstanding the value of the BHA reaction, concerns over the rising costs of Pd and subsequent sustainability issues have prompted researchers to seek economical methods for accessing these linkages. One of the most promising alternatives to Pd-catalysis is the developing field of its 3d congener, Ni. However, given the relatively underdeveloped nature of Ni-catalyzed C-N bond formation, many questions regarding the mechanistic underpinnings and scope limitations remain unanswered. In this thesis, my contributions include experimental investigations into the elementary steps of a successful Ni-catalyzed cross-coupling. The successful synthesis and characterization of primary Ni-NHR catalytic intermediates reveal previously undocumented C-N bond-forming pathways, and the implementation of the mechanistic lessons learned from these studies allow for the discovery of new ligand-enabled Ni-catalyzed C-N cross-couplings.
Download or read book Challenging Nickel Catalyzed Cross Couplings Enabled by Ligand Design written by Ryan McGuire and published by . This book was released on 2022 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Carbon-nitrogen linkages are highly prevalent in bioactive molecules, and as such, the development of sustainable methodologies for their formation is of immense importance to both the pharmaceutical and agricultural industries. Within this realm, the advent of homogeneous transition metal catalysis has allowed significant progress to be made in the development of routes toward the formation of these linkages, encompassing a wide range of different carbon and nitrogen-containing organic reagents. Specifically, the development of Pd-catalyzed C(sp2)-N (herein, C-N) cross-coupling (i.e. Buchwald-Hartwig-Amination, BHA) has transformed the way chemists approach solving synthetic problems. Indeed, research efforts in BHA over the past 25 years have allowed for the development of several catalytic systems, encompassing a large array of both (hetero)aryl (pseudo)halide and NH-bearing substrates. Successes in BHA can be largely attributed to the rational design of ancillary ligands, which are able to dramatically influence the reactive properties of Pd through a combination of steric and electronic effects. Despite the utility of BHA, researchers have now turned to more Earth-abundant sources for effecting these transformations, including the implementation of Cu for improved versions of well-known Ullmann-coupling, and the implementation of Ni, both as alternatives to precious Pd. In this thesis, my contributions toward the rational design, syntheses and use of appropriate ancillary ligands for enabling Ni-catalyzed C-N cross-coupling are described. Included are the development of new phosphonite/phosphine ligands such as Phen-DalPhos and related variants, along with the application of Ni-based pre-catalysts for the cross-coupling of ammonia, (hetero)anilines, indoles, sulfonamides, fluoroalkylamines and amides with (hetero)aryl (pseudo)halides under unprecedently mild conditions in Ni-based catalysis.
Download or read book Nickel Catalyzed Cross Coupling Reactions written by Luke Edward Hanna and published by . This book was released on 2016 with total page 333 pages. Available in PDF, EPUB and Kindle. Book excerpt: Cross-coupling technology has become an indispensable tool for the rapid and efficient synthesis of complex molecules. Over the past few decades a foundational understanding of organometallic chemistry has been laid using palladium and other precious metals. Recent research on first row base metal catalysts such as nickel, cobalt and iron has uncovered new and complementary modes of reactivity compared to their more well-studied precious metal counterparts. While nickel sits one row above palladium on the periodic table, ongoing research has illustrated that nickel possesses a unique reactivity profile. Thus, while nickel is commonly thought of as a cheaper alternative to palladium, research in the field of nickel catalysis has demonstrated far more potential than this. The unique propensity of nickel to undergo single electron chemistry as well as its ability to break strong carbon oxygen bonds make research into nickel reactivity an immensely beneficial endeavor to the fields of inorganic, organometallic and synthetic organic chemistry.Chapter 1 describes the development of a stereospecific Suzuki coupling of benzylic carbamates and pivalates with aryl- and heteroarylboronic esters. The reaction proceeds with selective inversion or retention at the electrophilic carbon, depending on the identity of the ligand used. Tricyclohexylphosphine ligand provides products with retention of configuration at the electrophilic carbon, while an N-heterocyclic carbene ligand SIMes provides products with inversion.Chapter 2 discusses the development of a regio- and stereoselective nickel-catalyzed hydroarylation of alkynes using propargylic carbamates as directing groups. The reaction proceeds under mild reaction conditions using arylboronic acids in the absence of base. A range of heterocycles and functional groups are tolerated under the reaction conditions. Additionally, the method is applied to the synthesis of tamoxifen.Chapter 3 details a nickel-catalyzed cross-electrophile coupling reaction of benzylic esters and aryl halides. Both inter- and intramolecular variants proceed under mild reaction conditions. A range of heterocycles and functional groups are tolerated under the reaction conditions. Additionally, the first example of a stereospecific cross-electrophile coupling of a secondary benzylic ester is described.Chapter 4 presents secondary benzylzinc reagents generated from 2-pyridylcarbinols using a nickel catalyst and diethylzinc. Substrates are activated in situ using a chlorophosphate reagent. Quenching the organozinc reagents allows for facile deoxygenation of 2-pyridylcarbinols in a one-pot reaction with straightforward incorporation of a deuterium label from deuteromethanol. An intramolecular conjugate addition of a secondary benzylzinc reagent with an alpha,beta-unsaturated ester is also demonstrated.
Download or read book Synthesis of Biaryls written by Ivica Cepanec and published by Elsevier. This book was released on 2010-07-07 with total page 365 pages. Available in PDF, EPUB and Kindle. Book excerpt: Organic chemistry is one of the most rapidly growing sciences. There is a wide variety of applications of organic compounds, for instance, pharmaceutically active substances, agrochemicals, optoelectronics, etc. Within this group there are hundereds and thousands of new compounds synthesized or isolated from natural sources. Such important organic chemistry developments are accompanied by the profound break-through of new reactions, increasingly efficient methodologies, reagents and catalysts. The chemistry of biaryls is one of the most interesting fields in organic chemistry, this book looks at these reactions both new and old. Synthesis of Biaryls presents the description of a given method for the synthesis of biaryls: short introduction, reaction mechanism, application, representative synthetic procedures, conclusion and literature references. This book will be of interest to organic chemists in industry and academia. A topic of growing importance in organic synthesis The FIRST book to cover all reactions for the synthesis of biaryls, including the most recent The book provides detailed applications of each method described
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).
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.
Download or read book Olefin Polymerization written by Walter Kaminsky and published by Wiley-VCH. This book was released on 2006-08-18 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: With an enormous velocity, olefin polymerization has expanded to one of the most significant fields in polymers since the first industrial use about 50 years ago. In 2005, 100 million tons of polyolefins were produced - the biggest part was catalyzed by metallorganic compounds. The Hamburg Macromolecular Symposium 2005 with the title "Olefin Polymerization" involved topics such as new catalysts and cocatalysts, kinetics, mechanism and polymer reaction engineering, synthesis of special polymers, and characterization of polyolefins. The conference combined scientists from different disciplines to discuss latest research results of polymers and to offer each other the possibility of cooperation. This is reflected in this volume, which contains invited lectures and selected posters presented at the symposium.
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)
Download or read book Synthesis and Use of Bench stable Precatalysts with Heck type Activation and Progress Towards the Continuous flow Synthesis of Atorvastatin written by Jessica Marie Weber and published by . This book was released on 2019 with total page 393 pages. Available in PDF, EPUB and Kindle. Book excerpt: [color illustrations] We introduce a new class of bench-stable N-heterocyclic carbene nickel precatalysts for homogeneous nickel-catalysis. The nickel(II) complexes are readily activated to Ni0 in situ under mild conditions, via a proposed Heck-type mechanism. The precatalysts are able to facilitate carbonyl-ene, hydroalkenylation, and amination reactions. [color illustrations] Herein, we report the synthesis and characterization of a new class of air- and moisture-stable triphenylphosphine nickel(II) precatalysts, which activate through a Heck-type mechanism. The activity of these precatalysts is demonstrated with a carbonyl-ene coupling reaction.
Download or read book Photocatalysis written by Dionysios D Dionysiou and published by Royal Society of Chemistry. This book was released on 2016-03-30 with total page 395 pages. Available in PDF, EPUB and Kindle. Book excerpt: From environmental remediation to alternative fuels, this book explores the numerous important applications of photocatalysis. The book covers topics such as the photocatalytic processes in the treatment of water and air; the fundamentals of solar photocatalysis; the challenges involved in developing self-cleaning photocatalytic materials; photocatalytic hydrogen generation; photocatalysts in the synthesis of chemicals; and photocatalysis in food packaging and biomedical and medical applications. The book also critically discusses concepts for the future of photocatalysis, providing a fascinating insight for researchers. Together with Photocatalysis: Fundamentals and Perspectives, these volumes provide a complete overview to photocatalysis.
