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Book Mechanistic Studies of Copper catalyzed Transformations

Download or read book Mechanistic Studies of Copper catalyzed Transformations written by Amanda Elisabeth King and published by . This book was released on 2009 with total page 213 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Copper Catalyzed Asymmetric Synthesis

Download or read book Copper Catalyzed Asymmetric Synthesis written by Alexandre Alexakis and published by John Wiley & Sons. This book was released on 2013-12-30 with total page 467 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book reflects the increasing interest among the chemical synthetic community in the area of asymmetric copper-catalyzed reactions, and introduces readers to the latest, most significant developments in the field. The contents are organized according to reaction type and cover mechanistic and spectroscopic aspects as well as applications in the synthesis of natural products. A whole chapter is devoted to understanding how primary organometallics interact with copper to provide selective catalysts for allylic substitution and conjugate addition, both of which are treated in separate chapters. Another is devoted to the variety of substrates and experimental protocols, while an entire chapter covers the use on non-carbon nucleophiles. Other chapters deal with less-known reactions, such as carbometallation or the additions to imines and related systems, while the more established reactions cyclopropanation and aziridination as well as the use of copper (II) Lewis acids are warranted their own special chapters. Two further chapters concern the processes involved, as determined by mechanistic studies. Finally, a whole chapter is devoted to the synthetic applications. This is essential reading for researchers at academic institutions and professionals at pharmaceutical or agrochemical companies.

Book Oxidative Cross Coupling Reactions

Download or read book Oxidative Cross Coupling Reactions written by Aiwen Lei and published by John Wiley & Sons. This book was released on 2016-08-12 with total page 240 pages. Available in PDF, EPUB and Kindle. Book excerpt: The first handbook on this emerging field provides a comprehensive overview of transition metal-catalyzed coupling reactions in the presence of an oxidant. Following an introduction to the general concept and mechanism of this reaction class, the team of authors presents chapters on C-C cross-coupling reactions using organometallic partners, C-Heteroatom bond forming reactions via oxidative couplings, and C-H couplings via C-H activation. The text also covers such groundbreaking topics as recent achievements in the fields of C-C and C-X bond formation reactions as well as C-H activation involving oxidative couplings. With its novel and concise approach towards important building blocks in organic chemistry and its focus on synthetic applications, this handbook is of great interest to all synthetic chemists in academia and industry alike.

Book Copper catalyzed Reactions of Organoboron Compounds

Download or read book Copper catalyzed Reactions of Organoboron Compounds written by Richard P. Rucker and published by . This book was released on 2013 with total page 167 pages. Available in PDF, EPUB and Kindle. Book excerpt: The discovery, development, scope, and mechanistic studies of three new copper-catalyzed transformations of organoboron compounds are described herein. Specifically, Chapter 1 details the development and scope of the first general method for SN2'-selective substitution of primary allylic chlorides using aryl boronic esters as nucleophiles. The formal anti-Markovnikov hydroamination of 9-alkyl-9-BBN derivatives, which are conveniently prepared from the hydroboration of terminal alkenes, to give tertiary alkyl amines is discussed in Chapter 2. Chapter 3 describes the development, scope, and mechanistic studies of the copper-catalyzed electrophilic amination of aryl boronic esters and its application to the synthesis of hindered N,N-dialkyl anilines.

Book Copper Catalysis in Organic Synthesis

Download or read book Copper Catalysis in Organic Synthesis written by Gopinathan Anilkumar and published by John Wiley & Sons. This book was released on 2020-12-07 with total page 504 pages. Available in PDF, EPUB and Kindle. Book excerpt: The most current information on growing field of copper catalysis Copper Catalysis in Organic Synthesis contains an up-to-date overview of the most important reactions in the presence of copper catalysts. The contributors—noted experts on the topic—provide an introduction to the field of copper catalysis, reviewing its development, scope, and limitations, as well as providing descriptions of various homo- and cross-coupling reactions. In addition, information is presented on copper-catalyzed C–H activation, amination, carbonylation, trifluoromethylation, cyanation, and click reactions. Comprehensive in scope, the book also describes microwave-assisted and multi-component transformations as well as copper-catalyzed reactions in green solvents and continuous flow reactors. The authors highlight the application of copper catalysis in asymmetric synthesis and total synthesis of natural products and heterocycles as well as nanocatalysis. This important book: Examines copper and its use in organic synthesis as a more cost-effective and sustainable for researchers in academia and industry Offers the first up-to-date book to explore copper as a first line catalyst for many organic reactions Presents the most significant developments in the area, including cross-coupling reactions, C–H activation, asymmetric synthesis, and total synthesis of natural products and heterocycles Contains over 20 contributions from leaders in the field Written for catalytic chemists, organic chemists, natural products chemists, pharmaceutical chemists, and chemists in industry, Copper Catalysis in Organic Synthesis offers a book on the growing field of copper catalysis, covering cross-coupling reactions, C–H activation, and applications in the total synthesis of natural products.

Book Mechanistic Studies on Transition Metal Catalyzed C   H Activation Reactions Using Combined Mass Spectrometry and Theoretical Methods

Download or read book Mechanistic Studies on Transition Metal Catalyzed C H Activation Reactions Using Combined Mass Spectrometry and Theoretical Methods written by Gui-Juan Cheng and published by Springer. This book was released on 2017-06-07 with total page 140 pages. Available in PDF, EPUB and Kindle. Book excerpt: This thesis presents detailed mechanistic studies on a series of important C-H activation reactions using combined computational methods and mass spectrometry experiments. It also provides guidance on the design and improvement of catalysts and ligands. The reactions investigated include: (i) a nitrile-containing template-assisted meta-selective C-H activation, (ii) Pd/mono-N-protected amino acid (MPAA) catalyzed meta-selective C-H activation, (iii) Pd/MPAA catalyzed asymmetric C-H activation reactions, and (iv) Cu-catalyzed sp3 C-H cross-dehydrogenative-coupling reaction. The book reports on a novel dimeric Pd-M (M = Pd or Ag) model for reaction (i), which successfully explains the meta-selectivity observed experimentally. For reaction (ii), with a combined DFT/MS method, the author successfully reveals the roles of MPAA ligands and a new C-H activation mechanism, which accounts for the improved reactivity and high meta-selectivity and opens new avenues for ligand design. She subsequently applies ion-mobility mass spectrometry to capture and separate the [Pd(MPAA)(substrate)] complex at different stages for the first time, providing support for the internal-base model for reaction (iii). Employing DFT studies, she then establishes a chirality relay model that can be widely applied to MPAA-assisted asymmetric C-H activation reactions. Lastly, for reaction (iv) the author conducts detailed computational studies on several plausible pathways for Cu/O2 and Cu/TBHP systems and finds a reliable method for calculating the single electron transfer (SET) process on the basis of benchmark studies.

Book Copper Mediated Cross Coupling Reactions

Download or read book Copper Mediated Cross Coupling Reactions written by Gwilherm Evano and published by John Wiley & Sons. This book was released on 2013-09-23 with total page 682 pages. Available in PDF, EPUB and Kindle. Book excerpt: Providing comprehensive insight into the use of copper in cross-coupling reactions, Copper-Mediated Cross-Coupling Reactions provides a complete up-to-date collection of the available reactions and catalytic systems for the formation of carbon-heteroatom and carbon-carbon bonds. This essential reference covers a broad scope of copper-mediated reactions, their variations, key advances, improvements, and an array of academic and industrial applications that have revolutionized the field of organic synthesis. The text also discusses the mechanism of these transformations, the use of copper as cost-efficient alternative to palladium, as well as recently developed methods for conducting copper-mediated reactions with supported catalysts.

Book Mechanistic Studies on the Copper catalysed C N Cross coupling Reaction

Download or read book Mechanistic Studies on the Copper catalysed C N Cross coupling Reaction written by Quintin Lo and published by . This book was released on 2019 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Mechanistic Studies of Copper and Nickel Catalyzed Sp3 C   H Functionalization

Download or read book Mechanistic Studies of Copper and Nickel Catalyzed Sp3 C H Functionalization written by Abolghasem Bakhoda and published by . This book was released on 2019 with total page 516 pages. Available in PDF, EPUB and Kindle. Book excerpt: Recent studies from our laboratory have discovered that C−H functionalization with unactivated amines, anilines or acyl−protected phenols with tBuOOtBu as an oxidant can take place at CuI b−diketiminates under a radical−relay mechanism. Mechanistic studies revealed that while in some cases the copper(II) alkylamide [CuII]−NHR' is capable of HAA, the principle role of the copper intermediates [CuII]−NHR' or [CuII]−OAr is to capture an alkyl radical R• (generated in the HAT of R−H substrate via tBuO• radical) to form R−NHR' or R'OAr, respectively.

Book Transition Metal Catalyzed Oxidative Cross Coupling Reactions

Download or read book Transition Metal Catalyzed Oxidative Cross Coupling Reactions written by Aiwen Lei and published by Springer. This book was released on 2018-12-14 with total page 192 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book is a comprehensive text covering the research and development trends in the booming field of transition metal catalyzed oxidative cross-coupling reactions. Oxidative cross-coupling reaction is a new method to forming chemical bonds besides the traditional cross-coupling reactions. This book provides the answers to how this coupling reaction occurs and what its advantages are. The palladium, copper and iron catalyzed oxidative cross-coupling reactions as the main focuses of interest are described in detail. The oxidative cross-coupling reactions catalyzed by other metals and transition-metal-free oxidative coupling reactions are also introduced.This book provides a useful reference source for researchers and graduates in the field of transition metal catalyzed coupling reactions. It is also valuable to researchers working in pharmaceutical companies, fine organic chemical companies, and etc.

Book Copper catalyzed Transformations for the Synthesis of Carbo  and Heterocycles

Download or read book Copper catalyzed Transformations for the Synthesis of Carbo and Heterocycles written by Kavitha Sudheendran and published by . This book was released on 2014 with total page 90 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Mechanistic Studies for Catalytic Transformation of Small Oxygenates on Transition Metals

Download or read book Mechanistic Studies for Catalytic Transformation of Small Oxygenates on Transition Metals written by Suyash Singh and published by . This book was released on 2014 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Over the past century, heterogeneous catalysis has played a central role in the development of efficient chemical processes for the conversion of fossil resources to fuels and chemicals, and identification of new, sustainable routes to upgrade renewable carbon sources that minimize the ecological footprint. More recently, unprecedented advances in electronic structure theory and related computational methods have provided a major thrust to the efforts that utilize density function theory (DFT) calculations for developing fundamental atomic-level understanding of these processes, and subsequently designing new and improved catalysts. In this dissertation, a combined theoretical and experimental approach is presented to study the reaction mechanisms for the catalytic conversion of formic acid (FA) and propylene oxide on transition metals. An iterative methodology comprising of DFT calculations, reaction kinetics measurements, and mean-field microkinetic modeling is employed to determine the nature of active sites on supported catalysts, explain the experimentally observed trends, and obtain predictions for the surface environment under reaction conditions. A detailed analysis of the DFT derived thermochemistry and kinetics parameters over a wide range of transition metal surfaces is performed to identify the key reactivity descriptors for FA decomposition on transition metal catalysts, and develop semi-empirical linear correlations that are then used to develop a microkinetic modeling based framework for the identification and design of improved (active and selective) bimetallic alloy catalysts. Finally, the possible utilization and applications of these methods and ideas in other key chemical transformations are proposed, and suggestions for future work are included.

Book Development and Applications of Copper I  Hydride Catalysis in Asymmetric Reactions and Heterocycle Synthesis

Download or read book Development and Applications of Copper I Hydride Catalysis in Asymmetric Reactions and Heterocycle Synthesis written by Yujing Zhou (Ph. D.) and published by . This book was released on 2021 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Chapter 2. Enantioselective CuH-Catalyzed Hydroacylation Employing Unsaturated Carboxylic Acids as Aldehyde Surrogates The direct asymmetric copper hydride (CuH)-catalyzed coupling of [alpha],[beta]-unsaturated carboxylic acids to aryl alkenes is developed to access chiral [alpha]-aryl dialkyl ketones. A variety of substrate substitution patterns, sensitive functional groups and heterocycles are tolerated in this reaction, which significantly expands the range of accessible products compared to existing hydroacylation methodology. Although mechanistic studies are ongoing, we propose that CuH-catalyzed silylation of unsaturated acids occurs to access a uniquely effective acyl electrophilic coupling partner. Chapter 3. CuH-Catalyzed Asymmetric Reduction of [alpha],[beta]-Unsaturated Carboxylic Acids to [beta]-Chiral Aldehydes The copper hydride (CuH)-catalyzed enantioselective reduction of [alpha],[beta]-unsaturated carboxylic acids to saturated aldehydes is reported. This protocol provides a new method to access a variety of [beta]-chiral aldehydes in good yields, with high levels of enantioselectivity and broad functional group tolerance. A reaction pathway involving a ketene intermediate is proposed based on preliminary mechanistic studies and density functional theory calculations. Chapter 4. CuH-Catalyzed Asymmetric Reductive Amidation of [alpha],[beta]-Unsaturated Carboxylic Acids The direct enantioselective copper hydride (CuH)-catalyzed synthesis of [beta]-chiral amides from [alpha],[beta]-unsaturated carboxylic acids and secondary amines under mild reaction conditions is reported. The method utilizes readily accessible carboxylic acids, and tolerates a variety of functional groups at [beta]-position including several heteroarenes. A subsequent iridium-catalyzed reduction to [gamma]-chiral amines can be performed in the same flask without purification of the intermediate amides. Chapter 5. CuH-Catalyzed Asymmetric Hydroamidation of Vinylarenes A CuH-catalyzed enantioselective hydroamidation reaction of vinylarenes has been developed using readily accessible 1,4,2-dioxazol-5-ones as electrophilic amidating reagents. This method provides a straightforward and efficient approach to synthesize chiral amides in good yields with high levels of enantiopurity under mild conditions. Moreover, this transformation tolerates substrates bearing a broad range of functional groups. Chapter 6. Enantioselective Allylation Using Allene, a Petroleum Cracking Byproduct Allene (C3H4) gas is produced and separated on million-metric-ton scale per year during petroleum refining but is rarely employed in organic synthesis. Meanwhile, the addition of an allyl group (C3H5) to ketones is among the most common and prototypical reactions in synthetic chemistry. Herein, we report that the combination of allene gas with inexpensive and environmentally benign hydrosilanes, such as PMHS, can serve as a replacement for stoichiometric quantities of allylmetal reagents, which are required in most enantioselective ketone allylation reactions. This process is catalyzed by copper catalyst and commercially available ligands, operates without specialized equipment or pressurization, and tolerates a broad range of functional groups. Furthermore, the exceptional chemoselectivity of this catalyst system enables industrially relevant C3 hydrocarbon mixtures of allene with methylacetylene and propylene to be applied directly. Based on our strategy, we anticipate the rapid development of methods that leverage this unexploited feedstock as an allyl anion surrogate. Chapter 7. Synthesis of Pyrroles through the CuH-Catalyzed Coupling of Enynes and Nitriles Herein, we describe an efficient method to prepare polysubstituted pyrroles via a copper-hydride (CuH)- catalyzed enyne-nitrile coupling reaction. This protocol accommodates both aromatic and aliphatic substituents and a broad range of functional groups, providing a variety of N-H pyrroles in good yields and with high regioselectivity. We propose that the Cu-based catalyst promotes both the initial reductive coupling and subsequent cyclization steps. Density functional theory (DFT) calculations were performed to help elucidate the reaction mechanism.

Book Synthesis  Characterization and Mechanistic Studies of Biomimetic Dinyclear Copper II  Complexes

Download or read book Synthesis Characterization and Mechanistic Studies of Biomimetic Dinyclear Copper II Complexes written by Millaniyage Nuwanthaka Prasad Jayaweera and published by . This book was released on 2019 with total page 136 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Organotransition Metal Chemistry  From Bonding to Catalysis

Download or read book Organotransition Metal Chemistry From Bonding to Catalysis written by John F. Hartwig and published by . This book was released on 2010-02-10 with total page 1172 pages. Available in PDF, EPUB and Kindle. Book excerpt: Based on Collman et al.'s best-selling classic book, Principles and Applications of Organotransition Metal Chemistry, Hartwig's text consists of new or thoroughly updated and restructured chapters and provides an in-depth view into mechanism, reaction scope, and applications. It covers the most important developments in the field over the last twenty years with great clarity with a selective, but thorough and authoritative coverage of the fundamentals of organometallic chemistry, the elementary reactions of these complexes, and many catalytic processes occurring through organometallic intermediates, making this the Organotransition Metal Chemistry text for a new generation of scientists.

Book Copper Catalyzed Amination of Aryl and Alkenyl Electrophiles

Download or read book Copper Catalyzed Amination of Aryl and Alkenyl Electrophiles written by Kevin H. Shaughnessy and published by John Wiley & Sons. This book was released on 2017-01-03 with total page 445 pages. Available in PDF, EPUB and Kindle. Book excerpt: The metal-catalyzed amination of aryl and alkenyl electrophiles has developed into a widely used methodology for the synthesis of natural products, active pharmaceutical ingredients, agricultural chemicals, and materials for molecular electronics. Copper catalysts promote the coupling of a wide range of nitrogen nucleophiles, including amines, amides, and heteroaromatic nitrogen compounds with aryl and alkenyl halides. The reactivity profile of copper catalysts is complementary to that of palladium catalysts in many cases. Copper catalysts are highly effective with less nucleophilic nitrogen nucleophiles, such as amides and azoles, whereas palladium catalysts are more effective with more nucleophilic amine nucleophiles. Copper is an attractive alternative to palladium due to its significantly lower cost. In addition, high activity palladium catalysts require expensive and often air-sensitive ligands, whereas the modern copper systems use relatively stable and inexpensive diamine or amino acid ligands. Copper-catalyzed C N coupling reactions are tolerant of a wide range of functional groups and have been applied to the synthesis of a variety of complex natural products. Significant work has also been done to understand the mechanism of these reactions. Current mechanistic understanding of these methodologies is covered in this monograph. The contents of the book are taken from the comprehensive review of the topic in the Organic Reactions series. Optimal experimental conditions for the amination of aryl and alkenyl halides with all classes of nitrogen nucleophiles are presented. Specific experimental procedures from the literature are provided for the major classes of copper-catalyzed C N coupling reactions. A tabular survey of all examples of Cu-catalyzed arylation and alkenylation of nitrogen nucleophiles is presented in 35 tables organized by nitrogen nucleophile and electrophilic coupling partner. The literature is covered through December 2015 and provides 300 recent citations to supplement the 680 citations of the original hardbound chapter. These latest literature references have been collected in separate sections according to the sequence of the tables in the tabular survey section. In each of the sections, the individual citations have been arranged in alphabetic order of the author names. Copper-Catalyzed Amination of Aryl and Alkenyl Electrophiles is intended to provide organic chemists with an accessible, but detailed, introduction to this important class of transformations.