Overcoming Regioselectivity Challenges in Iridium Catalyzed C-h Borylation Via Noncovalent Interactions and Advances on Cross Coupling Reactions of Aryl Imidazolylsulfonates

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Total Pages : 879 pages
Book Rating : 4.5/5 (381 download)

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Book Synopsis Overcoming Regioselectivity Challenges in Iridium Catalyzed C-h Borylation Via Noncovalent Interactions and Advances on Cross Coupling Reactions of Aryl Imidazolylsulfonates by : Jose Raul Montero Bastidas

Download or read book Overcoming Regioselectivity Challenges in Iridium Catalyzed C-h Borylation Via Noncovalent Interactions and Advances on Cross Coupling Reactions of Aryl Imidazolylsulfonates written by Jose Raul Montero Bastidas and published by . This book was released on 2021 with total page 879 pages. Available in PDF, EPUB and Kindle. Book excerpt: Direct functionalization of C0́2H bonds reduces the number of synthetic steps for a target molecule enhancing efficiency and avoiding undesired waste material. Iridium catalyzed C-H activation-borylation (CHB) is an established method to access aryl boronic esters. Regioselectivity challenges can arise when multiple hydrogens are present in the molecule. This thesis describes the design of novel strategies to selective direct the CHB to one specific position.Ortho selective CHB has the challenge to go against the traditional CHB selectivity dictated by steric effects. Previously, our group reported a strategy for highly ortho-selective CHB of anilines by using a small B2eg2 (eg = ethanediol) as the borylating reagent. However, the products were unstable and transesterification with pinacol was needed. Chapter 2 builds upon this issue and presents a solution based on the modulation of the size of the boron partner. Small diboron partners retain the high ortho regioselectivity for CHB of aniline but larger borylating reagents generate more stable products. In our estimation, B2bg2 (bg = 1,2-butanediol) represents the best balance of reactivity, regioselectivity and stability.Remote functionalization including para selective reactions are difficult because a potential directing group would be far from the desired reactive site. Chapter 3 details how para CHB of tetraalkylammonium sulfates and sulfamates have been achieved using bipyridine-ligated Ir boryl catalysts. Selectivities can be modulated by both the length of the alkyl groups in the tetraalkylammonium cations and the substituents on the bipyridine ligands. Ion pairing, where the alkyl groups of the cation shield the meta C8́2H bonds in the counteranions, is proposed to account for para selectivity. The 4,4'-dimethoxy-2,2'-bipyridine ligand gave superior selectivities.The next chapter describes how intramolecular hydrogen bonding (IMHB) can lead to steric shielding effects that can direct CHB regiochemistry. Bpin/arene IMHB can promote remote borylations of N-borylated anilines, 2-amino-N-alkylpyridine, tetrahydroquinolines, indoles and 1-borylated naphthalenes. Our studies support molecular geometries with the Bpin orientation controlled by a C-H0́Ø0́Ø0́ØO IMHB. Calculated rotation barriers to displace the Bpin group are above 4 kcal/mol, suggesting that the planar ground conformation of the borylated arenes is retained during CHB. This study informs researchers to evaluate not only inter- but also intramolecular noncovalent interactions as potential drivers of remote CHB regioselectivity.The borylated products from CHB can be further manipulated in Suzuki-Miyaura cross-coupling (SMC) with aryl halides as the typical electrophilic partner. Aryl imidazolylsulfonates are nongenotoxic electrophiles that can be used in palladium catalyzed SMC to avoid halogenated materials. Chapter 5 shows the efforts towards a nickel-catalyzed SMC of aryl imidazolyl-sulfonates. Results show considerable amounts of the corresponding diarylsulfate formed during the reaction. Interestingly, the diaryl sulfa byproducts were found to be competent electrophilic partners for both palladium and nickel-catalyzed SMC.In summary, this thesis presents novel methodologies to access challenging transformations as the para borylations of phenols, anilines and benzyl alcohols. This was possible by the analysis of the different components of the catalytic system: design of ligands, diboron partners and substrate directing groups and how they interact during the reaction. Finally, the potential of aryl imidazolylsulfonates as nongenotoxic pseudohalides in nickel-catalyzed SMC was evaluated.

Frontiers in Iridium-Catalyzed C-H Borylation

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ISBN 13 :
Total Pages : 246 pages
Book Rating : 4.:/5 (994 download)

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Book Synopsis Frontiers in Iridium-Catalyzed C-H Borylation by : Matthew Alan Larsen

Download or read book Frontiers in Iridium-Catalyzed C-H Borylation written by Matthew Alan Larsen and published by . This book was released on 2016 with total page 246 pages. Available in PDF, EPUB and Kindle. Book excerpt: The following dissertation discusses the development of novel methodology for the catalytic borylation of C-H bonds and includes in-depth studies on the mechanism and selectivity of these synthetic transformations. These methods include the borylation of heteroaryl C-H bonds, the selective borylation of benzylic C-H bonds, and the directed and undirected borylation of unactivated alkyl C-H bonds. Chapter 1 contains a comprehensive review of C-H borylation methodology. This review focuses on the initial development of catalytic C-H borylation and on the state-of- the-art of methodology for the undirected and directed borylation of aryl, benzylic, and alkyl C-H bonds. Additionally, this review highlights knowledge gaps and unsolved challenges. Furthermore, this review provides the author's opinion on future directions for research on the borylation of C-H bonds. Chapter 2 describes the study of the iridium-catalyzed borylation of heteroaryl C- H bonds. Contained is an examination of the scope of the borylation of heterocycles containing more than one heteroatom and rules for predicting the site-selectivity of this reaction. Also included are experimental and computational studies that reveal the mechanism of this reaction and the origins of the observed regioselectivity. Chapter 3 discusses the development of the selective borylation of the primary benzylic C-H bonds of methylarenes. Key to this development was the discovery that the combination of a novel iridium catalyst and a silylborane allows for the selective borylation of benzylic C-H bonds over aryl C-H bonds. Experimental and computational studies that investigate the origins of this selectivity are also discussed. Chapter 4 discusses the development of the iridium-catalyzed, hydrosilyl-directed borylation of alkyl C-H bonds. This methodology allows for the diastereoselective borylation of secondary alkyl C-H bonds under relatively mild conditions. Chapter 5 explores the effect of ligand structure on the rates of alkyl C-H borylation catalyzed by Ir-phenanthroline complexes. Experimental and computational studies reveal that in addition to the relative electron-donating ability of phenanthrolines, weak interactions involving the phenanthroline in the transition state of the turnover- limiting step for the borylation of alkyl C-H bonds can have a large impact on the relative rates of alkyl C-H borylation catalyzed by various Ir-phenanthroline complexes.

Computational Studies of Iridium-catalyzed Borylation Reactions and Defying Torquoselectivity in Cyclobutene Ring-opening Via Strain-induced Thermal Selectivity

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ISBN 13 :
Total Pages : 138 pages
Book Rating : 4.:/5 (869 download)

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Book Synopsis Computational Studies of Iridium-catalyzed Borylation Reactions and Defying Torquoselectivity in Cyclobutene Ring-opening Via Strain-induced Thermal Selectivity by : Aaron Gabriel Green

Download or read book Computational Studies of Iridium-catalyzed Borylation Reactions and Defying Torquoselectivity in Cyclobutene Ring-opening Via Strain-induced Thermal Selectivity written by Aaron Gabriel Green and published by . This book was released on 2013 with total page 138 pages. Available in PDF, EPUB and Kindle. Book excerpt: The studies reported in this dissertation illustrate a few selected examples of using density functional theory (DFT) calculations to investigate various aspects of iridium-catalyzed reactions and ring-opening of bicyclic cyclobutene rings. These computational predictions not only reproduce and explain experimental results and offer insights to reaction mechanisms, but also provide theoretical models to predict reactivity, regio- and stereoselectivities. Chapter 1 is a review surveying the literature of iridium-catalyzed borylation reactions. Emphasis is placed on iridium-catalyzed borylation of alkenes and arenes. In particular, I discuss the history leading up to the current catalyst systems for iridium-catalyzed borylation reactions, and regioselectivity of borylation for a number of different substrates. Despite the large amount of work on iridium-catalyzed borylation reactions, this review shows that there is still much to be understood regarding the origins of observed regioselectivities. Chapters 2 and 3 describe theoretical investigations of Ir(III)-catalyzed borylation reactions. The origins of regioselectivities observed in the borylation of pyridine are discussed in Chapter 2. The high selectivity for borylation at the 3- and 4- position of pyridine is attributed to the formation of a Lewis acid-base complex between pyridine and either boron species or iridium species in solution. The origins of regioselectivities for the iridium-catalyzed borylation of substituted arenes and 5-membered heterocycles are discussed in Chapter 3. The distortion/interaction model was employed to understand the origins of the selectivities in these reactions. Computations revealed that regioselectivity is mainly controlled by differences in the interaction energies between the iridium catalyst and arene carbon. Chapter 4 illustrates a theoretical study of ring-opening in strained, trans-substituted cyclobutenes. The torquoselectively preferred outward ring-opening products are unable to form due to ring strain inherent in 9- and 10-membered macrocyclic (E, E)-1,3-dienes. As a result of this study, I propose a general methodology for stereoselective synthesis of macrocyclic (Z, Z)-1,3-dienes termed strain-induced thermal selectivity (SITS).

Iridium Catalyzed C-H Borylation

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ISBN 13 : 9781369755664
Total Pages : 290 pages
Book Rating : 4.7/5 (556 download)

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Book Synopsis Iridium Catalyzed C-H Borylation by : Kristin Anne Gore

Download or read book Iridium Catalyzed C-H Borylation written by Kristin Anne Gore and published by . This book was released on 2017 with total page 290 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Advancing Frontiers in Reactive and Selective Iridium C-h Borylation Catalysis and Targeted Silsesquioxane Synthesis

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ISBN 13 : 9781085673259
Total Pages : 521 pages
Book Rating : 4.6/5 (732 download)

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Book Synopsis Advancing Frontiers in Reactive and Selective Iridium C-h Borylation Catalysis and Targeted Silsesquioxane Synthesis by : Jonathan E. Dannatt

Download or read book Advancing Frontiers in Reactive and Selective Iridium C-h Borylation Catalysis and Targeted Silsesquioxane Synthesis written by Jonathan E. Dannatt and published by . This book was released on 2019 with total page 521 pages. Available in PDF, EPUB and Kindle. Book excerpt: The studies in this dissertation are aimed at uncovering reactive and selective Ir-catalyzed C-H borylation (CHB) catalysts. Due to the high versatility of organoboron species, green methodology to produce the C-B bond is poised to support a myriad of subsequent transformations. These transformations include Suzuki couplings, aminations, oxidations, halogenations, cyanations, and trifluoromethylations.Typical iridium catalyzed CHBs proceed through an iridium trisboryl with a bidentate ligand such as bipyridine or 1,10-phenanthroline. The selectivity of these standard catalysts is generally driven by sterics; however, many methods of overcoming the steric bias have been developed in the two decades since the first thermal catalytic C-H activation borylation. These methods include both inner- and outer-sphere directed mechanisms. Outer-sphere directed borylations have been accomplished by leveraging hydrogen bonding, Lewis acid-base, and ion-pairing as directing elements. In general this reactivity is activated by precise design of the bidentate ligand framework.Herein is reported a subtle electrostatic interaction to direct ortho-borylation of phenols by simply switching boron source from the common B2pin2 (pin = pinacolate) to B2eg2 (eg = ethyleneglycolate). This electrostatic interaction was revealed by a careful computational analysis of key C-H activation transition states. Understanding gained by the computational studies led to the redesign of the boron source which enabled by selectivities of > 99% ortho borylation. This methodology was extended to the highly selective ortho-borylation of anilines, and the underlying mechanism has been interrogated.Currently, iridium based catalysts have been generated to borylate ortho, meta, and even para to a variety of classes of substrates; however, control of selectivity can breakdown in many fluorinated arenes without a directing group. These substrates are challenging because the fluoro moiety being similar in size to a hydrogen offers little in the way of steric bias. While working to overcome these challenges, a serendipitously discovered hydrazone based ligand was discovered. Exploration of the catalysts generated by this ligand revealed not only impressive activity rivaling dtbpy but also incredible selectivity for meta to a fluoro group.In general iridium CHB catalysts selectively activate sp2 C-H bonds leaving all sp3 C-H bonds intact; however, a method to turn on sp3 C-H activation would be desirable. It was reasoned that a directing group able to increase the effective concentration of the iridium catalyst near a C(sp3)-H bond may enable this transformation. Indeed, it was discovered that catalysts able to accept amide directing groups were able to selectively borylate compounds with amide N-methyl substituents.

Advances in Cross-Coupling Reactions

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ISBN 13 : 9783039435685
Total Pages : 234 pages
Book Rating : 4.4/5 (356 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 . This book was released on 2020 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.

Science of Synthesis: Electrochemistry in Organic Synthesis

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Publisher : Thieme
ISBN 13 : 3132442135
Total Pages : 574 pages
Book Rating : 4.1/5 (324 download)

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Book Synopsis Science of Synthesis: Electrochemistry in Organic Synthesis by : L. Ackermann

Download or read book Science of Synthesis: Electrochemistry in Organic Synthesis written by L. Ackermann and published by Thieme. This book was released on 2021-12-10 with total page 574 pages. Available in PDF, EPUB and Kindle. Book excerpt: Applications of Electrochemistry in Synthesis Electrosynthesis represents an increasingly viable platform for molecular synthesis, which is currently undergoing a remarkable renaissance. The use of electricity can, for instance, avoid chemical redox reagents as well as the generation of byproducts derived thereof, setting the stage for improved resource economy. This volume is the defining reference work for this rapidly evolving research arena. It features a collection of the most practical and robust methods of organic electrosynthesis. It introduces the key concepts of electrochemistry and provides all relevant laboratory set-ups, enabling newcomers to the field the effective application of these powerful new tools to molecular syntheses. Innovative strategies that successfully realize topical challenging transformations by the art of electrosynthesis are presented. Pioneers and leaders in the field discuss both the practical and conceptual aspects of this rapidly evolving research field.

Ethics Of Chemistry: From Poison Gas To Climate Engineering

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Publisher : World Scientific
ISBN 13 : 9811233551
Total Pages : 568 pages
Book Rating : 4.8/5 (112 download)

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Book Synopsis Ethics Of Chemistry: From Poison Gas To Climate Engineering by : Joachim Schummer

Download or read book Ethics Of Chemistry: From Poison Gas To Climate Engineering written by Joachim Schummer and published by World Scientific. This book was released on 2021-02-08 with total page 568 pages. Available in PDF, EPUB and Kindle. Book excerpt: 'Overall, this collection of case studies provides an outstanding starting point for understanding the ethics of chemistry. It is an extremely important contribution to the study of chemical ethics … Ethics of Chemistry is a key resource for educators interested in integrating ethics instruction into their chemistry curricula … an important foundation for equipping students with the moral judgement and analytical skills necessary to contend with the ethical issues they are likely to face in their professional lives.'Nature Chemistry'… the book offers a general introduction to many relevant topics concerning the values, responsibilities, and judgements in (and of) chemistry. The volume could be helpful for university students and teachers or even general readers interested in the ethics of chemistry.' [Read Full Review]José Ramón Bertomeu-SánchezAmbixAlthough chemistry has been the target of numerous public moral debates for over a century, there is still no academic field of ethics of chemistry to develop an ethically balanced view of the discipline. And while ethics courses are increasingly demanded for science and engineering students in many countries, chemistry is still lagging behind because of a lack of appropriate teaching material. This volume fills both gaps by establishing the scope of ethics of chemistry and providing a cased-based approach to teaching, thereby also narrating a cultural history of chemistry.From poison gas in WWI to climate engineering of the future, this volume covers the most important historical cases of chemistry. It draws lesson from major disasters of the past, such as in Bhopal and Love Canal, or from thalidomide, Agent Orange, and DDT. It further introduces to ethical arguments pro and con by discussing issues about bisphenol-A, polyvinyl chloride, and rare earth elements; as well as of contested chemical projects such as human enhancement, the creation of artificial life, and patents on human DNA. Moreover, it illustrates chemical engagements in preventing hazards, from the prediction of ozone depletion, to Green Chemistry, and research in recycling, industrial substance substitution, and clean-up. Students also learn about codes of conduct and chemical regulations.An international team of experts narrate the historical cases and analyse their ethical dimensions. All cases are suitable for undergraduate teaching, either in classes of ethics, history of chemistry, or in chemistry classes proper.

Catalytic Hydroarylation of Carbon-Carbon Multiple Bonds

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Publisher : John Wiley & Sons
ISBN 13 : 3527697659
Total Pages : 566 pages
Book Rating : 4.5/5 (276 download)

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Book Synopsis Catalytic Hydroarylation of Carbon-Carbon Multiple Bonds by : Lutz Ackermann

Download or read book Catalytic Hydroarylation of Carbon-Carbon Multiple Bonds written by Lutz Ackermann and published by John Wiley & Sons. This book was released on 2017-10-13 with total page 566 pages. Available in PDF, EPUB and Kindle. Book excerpt: Filling a gap in the literature, this book comprehensively reviews catalytic C-H addition reactions of (hetero)aromatic hydrocarbons across carbon-carbon multiple bonds. In so doing, it summarizes both the scope as well as the limitations of different catalyst systems and building blocks, while highlighting their application to the synthesis of pharmaceuticals as well as commodity chemicals. Focusing on the latest developments, the team of authors comprising leaders in the field covers such topics as the hydroarylation of olefins, alkyne hydroarylation in the presence of transition metal catalysts, reaction of alkynes with arylboronic acids, and allene hydroarylation, as well as the synthesis of functionalized arenes and heteroaromatics. A must-have for synthetic chemists in academia and industry dealing with catalysis, organometallic chemistry, the synthesis of natural products, fine chemicals, pharmaceuticals, products of the chemical industry and organic materials.

Modern Arylation Methods

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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.

C-C Bond Activation

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Publisher : Springer
ISBN 13 : 364255055X
Total Pages : 265 pages
Book Rating : 4.6/5 (425 download)

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Book Synopsis C-C Bond Activation by : Guangbin Dong

Download or read book C-C Bond Activation written by Guangbin Dong and published by Springer. This book was released on 2014-09-18 with total page 265 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

The Mizoroki-Heck Reaction

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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)

Catalysis with Earth-abundant Elements

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Publisher : Royal Society of Chemistry
ISBN 13 : 178801118X
Total Pages : 431 pages
Book Rating : 4.7/5 (88 download)

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Book Synopsis Catalysis with Earth-abundant Elements by : Uwe Schneider

Download or read book Catalysis with Earth-abundant Elements written by Uwe Schneider and published by Royal Society of Chemistry. This book was released on 2020-10-30 with total page 431 pages. Available in PDF, EPUB and Kindle. Book excerpt: Considering the limited resources of our planet, earth-abundant elements will have to be explored increasingly in the future. This book highlights the uses of the most earth-abundant elements in catalysis and will be of interest to graduates, academic researchers and practitioners in catalysis.

Non-Noble Metal Catalysis

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Publisher : John Wiley & Sons
ISBN 13 : 3527340610
Total Pages : 610 pages
Book Rating : 4.5/5 (273 download)

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Book Synopsis Non-Noble Metal Catalysis by : Robertus J. M. Klein Gebbink

Download or read book Non-Noble Metal Catalysis written by Robertus J. M. Klein Gebbink and published by John Wiley & Sons. This book was released on 2019-04-29 with total page 610 pages. Available in PDF, EPUB and Kindle. Book excerpt: An expert overview of current research, applications, and economic and environmental advantages The study and development of new homogeneous catalysts based on first-row metals (Mn, Fe, Co, Ni, and Cu) has grown significantly due to the economic and environmental advantages that non-noble metals present. Base metals offer reduced cost, greater supply, and lower toxicity levels than noble metals?enabling greater opportunity for scientific investigation and increased development of practical applications. Non-Noble Metal Catalysis provides an authoritative survey of the field, from fundamental concepts and computational methods to industrial applications and reaction classes. Recognized experts in organometallic chemistry and homogeneous catalysis, the authors present a comprehensive overview of the conceptual and practical aspects of non-noble metal catalysts. Examination of topics including non-innocent ligands, proton-coupled electron transfer, and multi-nuclear complexes provide essential background information, while areas such as kinetic lability and lifetimes of intermediates reflect current research and shifting trends in the field. This timely book demonstrates the efficacy of base metal catalysts in the pharmaceutical, fine-chemical, and agrochemical industries, addressing both environmental and economic concerns. Providing essential conceptual and practical exploration, this valuable resource: -Illustrates how unravelling new reactivity patterns can lead to new catalysts and new applications -Highlights the multiple advantages of using non-noble metals in homogenous catalysis -Demonstrates how the availability of non-noble metal catalysis reduces costs and leads to immense savings for the chemical industry -Reveals how non-noble metal catalysis are more sustainable than noble metals such as palladium or platinum Non-Noble Metal Catalysis: Molecular Approaches and Reactions is an indispensable source of up-to-date information for catalytic chemists, organic chemists, industrial chemists, organometallic chemists, and those seeking to broaden their knowledge of catalytic chemistry.

Remote C-H Bond Functionalizations

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Publisher : John Wiley & Sons
ISBN 13 : 3527346678
Total Pages : 450 pages
Book Rating : 4.5/5 (273 download)

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Book Synopsis Remote C-H Bond Functionalizations by : Debabrata Maiti

Download or read book Remote C-H Bond Functionalizations written by Debabrata Maiti and published by John Wiley & Sons. This book was released on 2021-04-26 with total page 450 pages. Available in PDF, EPUB and Kindle. Book excerpt: A guide to contemporary advancements in the field of distal C-H functionalizations An important and dynamic topic within the modern field of organic synthesis, selective functionalization of C-H bonds can be used in a variety of applications across the pharmaceutical and agrochemical industries. Remote C-H Bond Functionalizations presents an inclusive account of the most recent developments and potential applications of performing variegated functionalizations selectively at the distal positions of organic compounds. Featuring contributions by an international team of experts, this authoritative volume provides deep insight into distal functionalizations, including detailed discussion of mechanisms, the engineering of templates, and the design of strategies. The text covers a diverse range of topics including C-H functionalization of palladium/norbornene catalysis, ruthenium-catalyzed remote functionalization, the non-directed distal C(sp2)-H, functionalization, transition metal catalyzed distal para-selective C-H functionalization, and much more. Reviewing contemporary advancements in the field while laying the foundation for future research, this important resource: Provides the most recent research and thorough coverage of the subject available in a single volume Offers practical information on C-H functionalizations in various industries Includes an up-to-date introduction to distal C-H functionalizations Remote C-H Bond Functionalizations is a must-read for every synthetic chemist, including chemists working with organometallics, organic chemists and researchers, and industrial chemists.

Experiments in Green and Sustainable Chemistry

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Publisher : Wiley-VCH
ISBN 13 : 9783527325467
Total Pages : 0 pages
Book Rating : 4.3/5 (254 download)

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Book Synopsis Experiments in Green and Sustainable Chemistry by : Herbert W. Roesky

Download or read book Experiments in Green and Sustainable Chemistry written by Herbert W. Roesky and published by Wiley-VCH. This book was released on 2009-06-08 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Encouraging a new attitude and approach to chemistry, this is the first such collection designed for lab courses and experimental teaching. Experts from around the globe present over 40 real-life teaching experiments, all clearly structured and divided into the five main principles of sustainable and green chemistry: catalysis, solvents, high yield and one-pot synthesis, limiting waste and exposure, as well as special topics. With a foreword by Nobel prize winner Jean Marie Lehn.

The Claisen Rearrangement

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Publisher : John Wiley & Sons
ISBN 13 : 3527610553
Total Pages : 591 pages
Book Rating : 4.5/5 (276 download)

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Book Synopsis The Claisen Rearrangement by : Martin Hiersemann

Download or read book The Claisen Rearrangement written by Martin Hiersemann and published by John Wiley & Sons. This book was released on 2007-02-27 with total page 591 pages. Available in PDF, EPUB and Kindle. Book excerpt: The first comprehensive coverage of all facets of the Claisen rearrangement and its variants. As such, this book helps synthetic chemists to exploit the vast potential of this elegant C-C linking reaction, discusses a wealth of catalytic options, and gives those more theory-minded chemists a detailed insight into the mechanistic aspects of the Claisen rearrangement. An invaluable source of information and a ready reference for all organic and catalytic chemists, as well as those working with/on organometallics, and in industry.