Relevant bibliographies by topics / Organic synthesis ; organometallic chemistry ; transition metal catalysis

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Organic synthesis ; organometallic chemistry ; transition metal catalysis'

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Published: 4 June 2021
Last updated: 3 February 2022

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Journal articles on the topic "Organic synthesis ; organometallic chemistry ; transition metal catalysis"

1

Dong, Zhi-Bing, and Jin-Quan Chen. "Recent Progress in Utilization of Functionalized Organometallic Reagents in Cross Coupling Reactions and Nucleophilic Additions." Synthesis 52, no. 24 (2020): 3714–34. http://dx.doi.org/10.1055/s-0040-1706550.

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AbstractOrganometallic compounds have become increasingly important in organic synthesis because of their high chemoselectivity and excellent reactivity. Recently, a variety of organometallic reagents were found to facilitate transition-metal-catalyzed cross-coupling reactions and nucleophilic addition reactions. Here, we have summarized the latest progress in cross-coupling reactions and in nucleophilic addition reactions with functionalized organometallic reagents present to illustrate their application value. Due to the tremendous contribution made by the Knochel group towards the development of novel organometallic reagents, this review draws extensively from their work in this area in recent years.Introduction1 Transition-Metal-Catalyzed Cross Couplings Involving Organo­zinc Reagents2 Transition-Metal-Catalyzed Cross Couplings Involving Organomagnesium Reagents3 Transition-Metal-Free Cross Couplings Involving Zn and Mg ­Organometallic Reagents4 Nucleophilic Additions Involving Zn and Mg Organometallic Reagents5 Cross-Coupling Reactions or Nucleophilic Additions Involving Mn, Al-, La-, Li-, Sm- and In-Organometallics6 Conclusion
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Alexakis, Alexandre. "Preface." Pure and Applied Chemistry 78, no. 2 (2006): vi. http://dx.doi.org/10.1351/pac20067802vi.

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The 13th IUPAC International Symposium on Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS-13<http://omcos13.unige.ch/>) was held in Geneva, Switzerland, from 17-21 July 2005.The aim of this series of symposia is to bring together chemists from academia and industry to define and discuss the most recent developments in the areas of catalysis, new organometallic reagents and reactions, and new materials chemistry. In 2001, Sharpless, Noyori, and Knowles received the Nobel Prize for their work in this area of chemistry; and the high profile has been maintained by the award of the 2005 Nobel Prize in Chemistry to Chauvin, Grubbs, and Schrock for the development of the metathesis method in organic synthesis.OMCOS-13 had a record number of nearly 1200 participants from 41 countries, and there was an encouragingly high proportion of young scientists in attendance. Very strong Asian participation at this conference reflected the outstanding level of research and leadership in this field from countries such as Japan, China, South Korea, and Taiwan.Prof. Shengming Ma, from the Shanghai Institute of Organic Chemistry of the Chinese Academy of Science and the Department of Chemistry, Zhejiang University, China received the OMCOS-13 Award (sponsored by the Yen Chuang Foundation and Springer Verlag). The prize was awarded for his creative research contributions in the field of transition-metal-catalyzed reactions of allenes.Apart from the OMCOS-13 Award lecture, there were 23 plenary lectures and 20 oral communications that dealt with aspects of reactivity and chemoselectivity of main group and transition-metal organometallics. Stereoselectivity issues also figured prominently with a particular emphasis on asymmetric synthesis and catalysis. Mechanistic insights, new reagents for synthesis, new catalyst and ligand design, and ligand effects were other important topics.The quality of the 620 posters that were on display during the entire conference was also outstanding. This extraordinary poster session was highlighted with the Monday evening "poster party" and culminated in the awarding of 37 poster prizes.OMCOS-13 was held as a single session conference in an impressive lecture theater and a large exhibition area in the center of Geneva at a superb lakefront location. It was a fitting venue for the firstclass science that was presented.Thirty-seven lecturers of OMCOS-13 present their chemistry in this issue of Pure and Applied Chemistry and provide a fine recollection of last summer's conference. The 14th edition of OMCOS will be held in Nara, Japan (2-6 August 2007) under the chairmanship of Prof. Koichiro Oshima.Alexandre AlexakisOMCOS-13 Co-chairE. Peter KündigOMCOS-13 Co-chair
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Silva, Eduarda, Artur Silva, and Djenisa Rocha. "Diels–Alder Reactions of 1,2-Dihydropyridines: An Efficient Tool for the Synthesis of Isoquinuclidines." Synthesis 50, no. 09 (2018): 1773–82. http://dx.doi.org/10.1055/s-0037-1609418.

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The Diels–Alder reaction of 1,2-dihydropyridines with different dienophiles is a well-established and straightforward method for the synthesis of isoquinuclidines. Nevertheless, the enantioselective preparation of isoquinuclidines using organocatalysts or organometallic catalysts is rather unexplored. This succinct review offers readers an overall perspective of the most important recent developments and concepts related to this topic.1 Introduction2 Asymmetric Diels–Alder Reaction of 1,2-Dihydropyridines2.1 Transition-Metal-Catalyzed Reactions2.2 Organocatalyzed Reactions3 Diels–Alder Reaction of 1,2-Dihydropyridines in the Synthesis of Biologically Valuable Compounds4 Conclusion
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Piccardi, Riccardo, Serge Turcaud, Erica Benedetti, and Laurent Micouin. "Synthesis and Reactivity of Mixed Dimethylalkynylaluminum Reagents." Synthesis 51, no. 01 (2018): 97–106. http://dx.doi.org/10.1055/s-0037-1610392.

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Organoaluminum derivatives are mostly appreciated for their Lewis acidity properties, but generally not considered as reagents of choice in synthetic transformations involving the creation of C–C bonds. Among these species, dimethylalkynylaluminum reagents represent a special class of compounds, with, in many cases, unique reactivity. This review summarizes the preparation and reactivity of these organometallic reagents with a focus on their synthetic potential.1 Introduction2 Preparation of Dimethylalkynylaluminum Reagents3 Reactivity of Dimethylalkynylaluminum Reagents3.1 Reactions with Csp3 Electrophiles3.2 Reactions with Csp2 Electrophiles4 Transition-Metal-Catalyzed Reactions4.1 Addition to α,β-Unsaturated Enones4.2 Coupling Reactions5 Triple Bond Reactivity6 Conclusion
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Arisawa, Mieko, and Masahiko Yamaguchi. "Rhodium-Catalyzed Synthesis of Organosulfur Compounds Involving S-S Bond Cleavage of Disulfides and Sulfur." Molecules 25, no. 16 (2020): 3595. http://dx.doi.org/10.3390/molecules25163595.

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Organosulfur compounds are widely used for the manufacture of drugs and materials, and their synthesis in general conventionally employs nucleophilic substitution reactions of thiolate anions formed from thiols and bases. To synthesize advanced functional organosulfur compounds, development of novel synthetic methods is an important task. We have been studying the synthesis of organosulfur compounds by transition-metal catalysis using disulfides and sulfur, which are easier to handle and less odiferous than thiols. In this article, we describe our development that rhodium complexes efficiently catalyze the cleavage of S-S bonds and transfer organothio groups to organic compounds, which provide diverse organosulfur compounds. The synthesis does not require use of bases or organometallic reagents; furthermore, it is reversible, involving chemical equilibria and interconversion reactions.
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Nicholas, Kenneth M., and Chandrasekhar Bandari. "Deoxygenative Transition-Metal-Promoted Reductive Coupling and Cross-Coupling of Alcohols and Epoxides." Synthesis 53, no. 02 (2020): 267–78. http://dx.doi.org/10.1055/s-0040-1707269.

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AbstractThe prospective utilization of abundant, CO2-neutral, renewable feedstocks is driving the discovery and development of new reactions that refunctionalize oxygen-rich substrates such as alcohols and polyols through C–O bond activation. In this review, we highlight the development of transition-metal-promoted reactions of renewable alcohols and epoxides that result in carbon–carbon bond-formation. These include reductive self-coupling reactions and cross-coupling reactions of alcohols with alkenes and arene derivatives. Early approaches to reductive couplings employed stoichiometric amounts of low-valent transition-metal reagents to form the corresponding hydrocarbon dimers. More recently, the use of redox-active transition-metal catalysts together with a reductant has enhanced the practical applications and scope of the reductive coupling of alcohols. Inclusion of other reaction partners with alcohols such as unsaturated hydrocarbons and main-group organometallics has further expanded the diversity of carbon skeletons accessible and the potential for applications in chemical synthesis. Catalytic reductive coupling and cross-coupling reactions of epoxides are also highlighted. Mechanistic insights into the means of C–O activation and C–C bond formation, where available, are also highlighted.1 Introduction2 Stoichiometric Reductive Coupling of Alcohols3 Catalytic Reductive Coupling of Alcohols3.1 Heterogeneous Catalysis3.2 Homogeneous Catalysis4 Reductive Cross-Coupling of Alcohols4.1 Reductive Alkylation4.2 Reductive Addition to Olefins5 Epoxide Reductive Coupling Reactions6 Conclusions and Future Directions
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Diao, Tianning, Qiao Lin, and Gregory Dawson. "Experimental Electrochemical Potentials of Nickel Complexes." Synlett 32, no. 16 (2021): 1606–20. http://dx.doi.org/10.1055/s-0040-1719829.

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AbstractNickel-catalyzed cross-coupling and photoredox catalytic reactions has found widespread utilities in organic synthesis. Redox processes are key intermediate steps in many catalytic cycles. As a result, it is pertinent to measure and document the redox potentials of various nickel species as precatalysts, catalysts, and intermediates. The redox potentials of a transition-metal complex are governed by its oxidation state, ligand, and the solvent environment. This article tabulates experimentally measured redox potentials of nickel complexes supported on common ligands under various conditions. This review article serves as a versatile tool to help synthetic organic and organometallic chemists evaluate the feasibility and kinetics of redox events occurring at the nickel center, when designing catalytic reactions and preparing nickel complexes.1 Introduction1.1 Scope1.2 Measurement of Formal Redox Potentials1.3 Redox Potentials in Nonaqueous Solution2 Redox Potentials of Nickel Complexes2.1 Redox Potentials of (Phosphine)Ni Complexes2.2 Redox Potentials of (Nitrogen)Ni Complexes2.3 Redox Potentials of (NHC)Ni Complexes
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Manners, Ian. "Article." Canadian Journal of Chemistry 76, no. 4 (1998): 371–81. http://dx.doi.org/10.1139/v98-054.

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Ring-opening polymerization (ROP) of strained ring-tilted metallocenophanes can be achieved thermally, via anionic or cationic initiation, or by the use of transition-metal catalysts and provides access to a wide range of high molecular weight (Mw = 105-106, Mn > 105) poly(metallocenes). These materials possess a variety of interesting properties and many are very easy to prepare. This article provides an overview of our work, giving background to and an account of the initial discovery, and discusses work on the synthesis and properties of new poly(metallocenes) and related materials with particular emphasis on recent research directions.Key words: metallocene, ring-opening polymerization, ferrocenophane, organometallic polymer.
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Butenschön, Holger. "Transition Metal Arene π-Complexes in Organic Synthesis and Catalysis. (Series: Topics in Organometallic Chemistry, Vol. 7.). Edited by E. Peter Kündig." Angewandte Chemie International Edition 44, № 11 (2005): 1591–92. http://dx.doi.org/10.1002/anie.200485231.

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Fui, Choong Jian, Mohd Sani Sarjadi, Shaheen M. Sarkar, and Md Lutfor Rahman. "Recent Advancement of Ullmann Condensation Coupling Reaction in the Formation of Aryl-Oxygen (C-O) Bonding by Copper-Mediated Catalyst." Catalysts 10, no. 10 (2020): 1103. http://dx.doi.org/10.3390/catal10101103.

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Transition metal-catalyzed chemical transformation of organic electrophiles and organometallic reagents belong to the most important cross coupling reaction in organic synthesis. The biaryl ether division is not only popular in natural products and synthetic pharmaceuticals but also widely found in many pesticides, polymers, and ligands. Copper catalyst has received great attention owing to the low toxicity and low cost. However, traditional Ullmann-type couplings suffer from limited substrate scopes and harsh reaction conditions. The introduction of homogeneous copper catalyst with presence of bidentate ligands over the past two decades has totally changed this situation as these ligands enable the reaction promoted in mild condition. The reaction scope has also been greatly expanded, rendering this copper-based cross-coupling attractive for both academia and industry. In this review, we will highlight the latest progress in the development of useful homogeneous copper catalyst with presence of ligand and heterogeneous copper catalyst in Ullmann type C-O cross-coupling reaction. Additionally, the application of Ullmann type C-O cross coupling reaction will be discussed.
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Dissertations / Theses on the topic "Organic synthesis ; organometallic chemistry ; transition metal catalysis"

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Benedetto, Elena. "Synthesis and reactivity of allylic fluorides under transition metal catalysis." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:8c9965ef-2694-4792-a0ef-932e4eff6c7b.

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In this thesis, C-F bond activation and C-F bond construction under platinum and iridium catalysis is described. Chapter 1 provides a general introduction on the use of transition metal catalysis for the formation and activation of Csp³-F bonds in organofluorine compounds. In Chapter 2, an investigation on the reactivity of allylic fluorides, under platinum and palladium catalysed alkylation conditions, is presented. The relative reactivity of fluoride versus other commonly used leaving groups was compared via internal competition experiments. Fluoride showed a different reactivity profile, when subjected to Pt and Pd catalytic systems. Based on the observed reactivity trend, a Pd-catalysed fluorination reaction of allylic alcohol derivatives was successfully developed, within the group. In Chapter 3, a new iridium catalysed fluorination using branched, E- or Z-linear allylic carbonates is described. The catalyst [Ir(COD)Cl]₂ leads to an unexpected regio- and stereoretentive selectivity, affording fluorinated products not accessible via palladium catalysis. The effect of a fluoride additive on the selectivity of the Ir-catalysed alkylation reaction is also presented. A highly efficient <sup>18</sup>F-fluorination variant for this new catalytic transformation is reported. Chapter 4 gives full experimental procedures and characterisation data for all compounds.
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Hopkinson, Matthew Neil. "Transition metal catalysis in the presence of fluorinating reagents." Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:4f29607a-7aad-473b-aabc-af320ea2b1e5.

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In this thesis, the effect of fluorinating reagents on a selection of transition metal-mediated organic transformations was investigated. The first four chapters are focused on gold-catalysed nucleophilic addition processes performed in the presence of “F⁺” sources. Chapter 1 provides a general introduction to homogeneous gold catalysis and summarises the aims and objectives of the project. The effect of the electrophilic fluorinating reagent Selectfluor (82) on the gold-catalysed rearrangement of propargyl acetates 85 is discussed in Chapter 2. α-Fluoroenones 92 resulting from fluorodeacetylation of an allenyl acetate intermediate were delivered as the major products of these reactions (Scheme i). [Scheme i Gold-Catalysed Rearrangement-Fluorodeacetylation of Propargyl Acetates 85.] By contrast, performing the gold(I)-catalysed cyclisation of allenoates 102 in the presence of Selectfluor (82) led to products of oxidative coupling. The “F⁺” source in these processes most likely acts as an external oxidant in an Au<sup>I</sup</Au<sup>III</sup> redox cycle. In Chapter 3, the cascade cyclisation-intramolecular arylation of benzyl-substituted substrates is discussed whilst the extension of the methodology towards intermolecular homocoupling and intermolecular alkynylation is presented in Chapter 4 (Scheme ii). [Scheme ii Gold-Catalysed Cyclisation-Oxidative Coupling of tert-Butyl Allenoates 102.] In Chapter 5, the feasibility of palladium-catalysed allylic [<sup>18</sup>F]radiofluorination was investigated using high-specific-activity [<sup>18</sup>F]fluoride. This study led to the development of the first transition metal-mediated C-<sup>18</sup>F bond-forming process of relevance for the preparation of radiotracers for PET imaging (Scheme iii). [Scheme iii Palladium-Catalysed Allylic [18F]Radiofluorination of Allylic Methyl Carbonate 227b.] Chapter 6 gives full experimental procedures and characterisation data for all compounds.
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Deeming, Alex. "Applications of DABSO for the delivery of sulfur dioxide in organic synthesis." Thesis, University of Oxford, 2015. http://ora.ox.ac.uk/objects/uuid:ae0a6c5c-57a1-48bc-b219-ad22678d51ca.

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This thesis documents the development of novel synthetic methodologies for the incorporation of sulfur dioxide into organic molecules employing the amine-sulfur dioxide complex DABSO (vide infra). These developed processes serve to access a range of sulfonyl-containing (-SO<sub>2</sub>-) compounds including sulfones and sulfonamides, via sulfinic acid precursors. <b>Chapter 1</b> provides an overview of the synthesis and applications of sulfonyl-containing compounds and the organic chemistry of sulfur dioxide. A comprehensive introduction to the developed uses of sulfur dioxide surrogates in organic chemistry is given. The synthetic utility of metal sulfinates towards accessing sulfonyl-containing compounds is also discussed. <b>Chapter 2</b> details the development of a one-pot sulfone synthesis via metal sulfinates generated from organometallic reagents and DABSO. Alkyl, alkenyl and (hetero)aryl sulfinates prepared from organolithium and Grignard reagents can be efficiently coupled with a range of electrophiles to access a range of products including diaryl, aryl-heteroaryl and &beta;-hydroxy sulfones. <b>Chapter 3</b> describes an array-compatible, one-pot sulfonamide synthesis employing metal sulfinates and N-chloroamines as in situ-generated intermediates. This employs DABSO and sodium hypochlorite (bleach) as simple reagents and organolithium, organozinc and Grignard reagents along with amines as readily-accessible building blocks. The robust nature of this methodology and its potential application in discovery chemistry is demonstrated with a 65-compound array synthesis. <b>Chapter 4</b> documents the development of a palladium-catalysed sulfination reaction of boronic acids to access a range of sulfonyl-containing compounds. This involved the establishment of a one-pot/one step synthesis of sulfones leading to the discovery of a redox-neutral, ligand-free sulfination procedure using DABSO and palladium(II) catalysis. Sulfinic acid derivatives can be generated and subsequently trapped in situ with a variety of electrophiles to furnish sulfones and sulfonamides. <b>Chapter 5</b> summarises the research and the potential future work. <b>Chapter 6</b> provides experimental details and data.
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Perego, Luca Alessandro. "Transition metal-catalyzed reactions : mechanistic studies and methodology developments." Thesis, Paris Sciences et Lettres (ComUE), 2018. http://www.theses.fr/2018PSLEE003/document.

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Dans cette thèse les mécanismes de trois réactions catalysées par des complexes de palladium et de cuivre ont été étudiés en utilisant des méthodes expérimentales et théoriques. La première réaction est la synthèse d’amides à partir d’halogénoarènes, d’isonitriles et d’eau, qui est un exemple de couplage catalysé par le palladium impliquant l’insertion d’un isonitrile. Cette dernière molécule sert à la fois de ligand et de substrat, et son influence sur chaque étape du cycle catalytique a été mise en évidence. La deuxième réaction est l’ouverture des benzofuranes conduisant à des dérivés indoliques catalysée par des sels de palladium. Les conditions opératoires ont été optimisées et les étapes clés du mécanisme ont été élucidées.La dernière réaction étudiée, qui est le sujet principal de cette thèse, est l’addition d’amines sur des allènes catalysée par des sels de cuivre (hydroamination). La caractérisation des espèces catalytiques de cuivre(I) et l’étude théorique du mécanisme ont permis d’étendre cette réaction à différents substrats (allénamides, N-allénylazoles, N-allénylsulfamides) dans des conditions particulièrement douces et efficaces<br>In this thesis, the mechanism of three organic reactions catalyzed by palladium and copper complexes has been elucidated by the use of both experimental and theoretical methods. The first reaction is the synthesis of amides from haloarenes, isocyanides and water as an example of the broad family of palladium-catalyzed imidoylative couplings. Multiple roles of the isocyanide as both a ligand and a substrate in the different steps of the catalytic cycle have been disclosed. The second transformation is the palladium-catalyzed ring opening of benzofurans leading to indoles. Optimal conditions for this transformation have been found and the key aspects of its mechanism clarified. The last reaction, which is the main topic of this thesis, is the addition of amines to allenes catalyzed by copper salts (hydroamination). A characterization of the catalytically active copper(I) species and insight from theoretical calculations suggested how to extend this reaction to other substrates (allenamides, N-allenylazoles, N-allenylsulfonamides) under mild and efficient conditions
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Truscott, Fiona Rosemary. "Transition metal catalysed C-C bond formation via C-H functionalisation." Thesis, University of Oxford, 2012. http://ora.ox.ac.uk/objects/uuid:6a1ef296-8d63-470d-96bd-3e01a887c81f.

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The functionalisation of C-H bonds has been widely studied in organic synthesis. This work presents the results of investigation into two areas of current research, copper-catalysed aromatic C-H functionalisation and rhodium-catalysed hydroacylation. Chapter 1 presents the development of palladium- and copper-catalysed aromatic C-H functionalisation with particular attention paid to regiocontrol. Chapter 2 describes the development of copper-catalysed cross-coupling of perfluorinated arenes and alkenyl halides along with efforts to expand this methodology to a more general reaction. In Chapter 3 the development of chelation-controlled rhodium-catalysed hydroacylation is discussed. Chapter 4 outlines the utilisation of amino acid derived N-methylthiomethyl aldehydes in rhodium-catalysed hydroacylation methodology.
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Elliott, Mark Christopher. "Transition metal catalysis : application to the synthesis of novel heterocycles." Thesis, Loughborough University, 1994. https://dspace.lboro.ac.uk/2134/13422.

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Larabi, Cherif. "Surface organometallic chemistry on Metal Organic Frameworks (MOF) : synthesis, characterization and their application in catalysis." Thesis, Lyon 1, 2011. http://www.theses.fr/2011LYO10008/document.

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Les structures organométalliques poreuses (Metal Organic Framework, MOF) sont une nouvelle classe de matériaux, composées d'ions métalliques ou de clusters liés à des ligands organiques ou des complexes organométalliques dans des réseaux cristallins 1D, 2D ou 3D. Au cours de cette thèse la possibilité de construire de nouveaux MOF a été illustrée par le développement de matériaux MOF à base d’imidazolium, précurseur important pour la synthèse de catalyseurs. En outre, ce travail démontre l’utilité de la modification post-synthèse des MOFs par chimie organométallique de surface à visée catalytique : i) un MOF connu, UiO-66, avec des pores relativement petits a été fonctionnalisé avec un groupement amino et ses capacités d'adsorption de gaz ont été étudiées. ii) la synthèse de MOF a structure poreuse, CPO-27, MOF a été optimisée et utilisée comme précurseur pour produire un catalyseur d'hydrodésulfuration après l'introduction d'espèces actives, via la chimie organométallique de surface, dont les performances catalytiques ont été évaluées<br>Metal organic frameworks (MOF) are a new class of material, which consist of metal ions or clusters coordinated to organic ligands or metal-organic complexes and result in 1D, 2D or 3D crystalline networks. The possibility of constructing new MOF has been exemplified in this thesis by development of imidazolium based MOF, a highly important ligand system in catalysis. Moreover, this work has performed post synthesis modification via surface organometallic chemistry on existing MOF: i) a known MOF, UiO-66, with relatively small pores has been functionalized with amino group and its gas adsorption capacity has been investigated, ii) the syntheses of a 3D open structure MOF, CPO-27, MOFs have been optimized and used as a precursor to produce a hydrodesulfurization catalyst after introducing active species via surface organometallic chemistry approach, whose catalytic performances have been measured
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Shen, Di. "Transition metal catalyzed alkylation and synthesis of biotin derivatives." Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:1467ba98-846c-46e6-9620-e4639ed07e43.

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<b>Transition Metal Catalyzed Alkylation</b> We have reported methodology for the use of methanol as an alkylation reagent using catalytic rhodium or iridium species for the formation of branched products from methyl ketones. The synthetic utility of the dialkylated products was enhanced by performing a regioselective Baeyer-Villiger oxidation which allowed access to ester products. A range of different phosphine ligands were screened, and sterically hindered and electron rich phosphine ligands were found to favour the formation of enone and methoxy adducts under an O2 atmosphere. This interrupted hydrogen borrowing reaction enabled the in situ addition of a nucleophile to give more complex products. A range of tetrasubsitituted pyridines were then synthesized from 1, 5-dicarbonyl compounds formed in the methylenation/conjugate addition sequence. Finally, deuteration experiments suggest that the reaction proceeds via a monohydride mechanism, and the possibilities for the beneficial effect of O2 were discussed. <b>Synthesis of biotin derivatives</b> The streptavidin-biotin system was chosen for the studies of protein/ligand interactions at molecular level. A series of modified biotin ligands were designed and synthesized to introduce repulsive interations with streptavidin. The protein/ligand complexes were analyzed at high resolution by X-ray crystallography.
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Brookings, Daniel Christopher. "The design, synthesis and application to asymmetric catalysis of chiral transition metal cyclopentadienyl complexes." Thesis, University of Southampton, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273849.

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Leon, Robert. "Stereoselective Transition-Metal-Free Diboration of Alkenes." Thesis, Boston College, 2016. http://hdl.handle.net/2345/bc-ir:106845.

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Thesis advisor: James Morken<br>Boronates are extremely useful in synthesis due to the ability of carbon-boron bonds to be transformed into carbon-oxygen, carbon-nitrogen, or carbon-carbon bonds stereospecifically. This makes the stereoselective construction of carbon-boron bonds especially useful. The development of transition-metal catalyzed diboration of alkenes gave synthetic organic chemists a way to quickly make not one, but two carbon-boron bonds in a stereoselective fashion. However, there are many drawbacks to transition-metal catalysis, such as high cost of catalysts and chiral ligands, and air and moisture sensitivity of catalysts. These issues, in addition to difficulties in removing trace amounts of metal contaminants from reaction products have prevented transition-metal-catalysis from being used on the industrial scale. Discussed in this thesis are two different methods for stereoselective, transition-metal-free diboration of alkenes developed by the Morken group. Also discussed is the pioneering work in the area of transition-metal-free diboration done by the Fernández group, which inspired these methodologies<br>Thesis (BS) — Boston College, 2016<br>Submitted to: Boston College. College of Arts and Sciences<br>Discipline: Departmental Honors<br>Discipline: Chemistry
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Books on the topic "Organic synthesis ; organometallic chemistry ; transition metal catalysis"

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Kazmaier, Uli. Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis. Springer-Verlag Berlin Heidelberg, 2012.

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Ikariya, Takao. Bifunctional Molecular Catalysis. Springer-Verlag Berlin Heidelberg, 2011.

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D, Ittel Steven, ed. Homogeneous catalysis: The applications and chemistry of catalysis by soluble transition metal complexes. 2nd ed. Wiley, 1992.

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Aldrich-Wright, Janice. Metallointercalators: Synthesis and Techniques to Probe Their Interactions with Biomolecules. Springer-Verlag/Wien, 2011.

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Peter, Kündig E., and Böttcher A, eds. Transition metal arene [pi]-complexes in organic synthesis and catalysis. Springer-Verlag, 2004.

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Kazmaier, Uli. Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis. Springer, 2013.

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Comprehensive Organometallic Chemistry II : Transition Metal Organometallics in Organic Synthesis (Comprehensive Organometallic Chemistry II). Pergamon, 1995.

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Hiyama, Tamejiro, Robert H. Crabtree, and D. M. P. Mingos. Comprehensive Organometallic Chemistry III Vol. 11: Applications III - Transition Metal Compounds in Organic Synthesis 2. Elsevier Science & Technology Books, 2006.

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Ikariya, Takao, and Masakatsu Shibasaki. Bifunctional Molecular Catalysis. Springer, 2011.

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Ikariya, Takao, and Masakatsu Shibasaki. Bifunctional Molecular Catalysis. Springer, 2013.

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Book chapters on the topic "Organic synthesis ; organometallic chemistry ; transition metal catalysis"

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Oost, Rik, James D. Neuhaus, Jérémy Merad, and Nuno Maulide. "Sulfur Ylides in Organic Synthesis and Transition Metal Catalysis." In Modern Ylide Chemistry. Springer International Publishing, 2017. http://dx.doi.org/10.1007/430_2017_14.

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Day, Victor W., Walter G. Klemperer, Curtis Schwartz, and Ren-Chain Wang. "Molecular Models of Early Transition Metal Oxides: Polyoxoanions as Organic Functional Groups." In Surface Organometallic Chemistry: Molecular Approaches to Surface Catalysis. Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-2971-5_9.

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Subramaniann, H., and M. P. Sibi. "2.12 Asymmetric Catalysis of Radical Reactions." In Free Radicals: Fundamentals and Applications in Organic Synthesis 2. Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/sos-sd-233-00202.

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AbstractSynthetic methodologies based on radical chemistry are efficient and powerful tools for the construction of carbon–carbon and carbon–heteroatom bonds. This chapter highlights the significance of asymmetric catalysis in free-radical reactions. Several asymmetric catalytic principles, ranging from early chiral Lewis acid and organocatalytic activation to recent photoredox and transition-metal-based asymmetric catalytic systems, are discussed.
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Ikariya, Takao, and Ryoji Noyori. "Advances in Homogeneous, Heterogeneous, and Biphasic Metal-Catalyzed Reactions in Dense-Phase Carbon Dioxide." In Green Chemistry Using Liquid and Supercritical Carbon Dioxide. Oxford University Press, 2004. http://dx.doi.org/10.1093/oso/9780195154832.003.0006.

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The use of compressed carbon dioxide as a reaction medium, either as a liquid or a supercritical fluid (sc CO2), offers the opportunity not only to replace conventional hazardous organic solvents but also to optimize and potentially control the effect of solvent on chemical synthesis. Although synthetic chemists, particularly those employing catalysis, may be relative latecomers to the area of supercritical fluids, the area of catalysis in carbon dioxide has grown significantly since around 1975 to the point that a number of excellent reviews have appeared (Baiker et al., 1999; Buelow et al., 1998; Jessop and Leitner, 1999; Jessop et al., 1995c, 1999; Morgenstern et al., 1996). Developing and understanding catalytic processes in dense-phase carbon dioxide could lead to “greener” processing at three levels: (1) solvent replacement, (2) improved chemistry (e.g., higher reactivity, selectivity, less energy), and (3) new chemistry (e.g., use of CO2 as a C-1 source). In this chapter, we will highlight a number of examples from the literature in homogeneous and heterogeneous transition-metal catalysis, as well as the emerging area of biphasic catalysis in H2O/sc CO2 mixtures. The intent is to provide an illustrative rather than a comprehensive overview to four classes of catalytic transformations: acid catalysis, reduction via hydrogenation, selective oxidation catalysis, and catalytic carbon–carbon bond-forming reactions. The reader is referred to other chapters in this book and other reviews (King and Bott, 1993) for discussion of uncatalyzed reactions, phase-transfer catalysis, polymerization, and radical reactions in sc CO2. From a synthetic chemist’s viewpoint, sc CO2 has a number of potential advantages that one would like to capitalize upon. • Solvent Replacement Carbon dioxide is a nontoxic, nonflammable, inexpensive alternative to hazardous organic solvents. Simple solvent replacement will not be a sufficient driver for all chemical reactions; however, as described below, the use of carbon dioxide could lead to better chemistry for certain reactions. • Gas Miscibility Gases such as H2, O2, and CO are sparingly soluble in liquid solvents but they are highly miscible with sc CO2.
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Conference papers on the topic "Organic synthesis ; organometallic chemistry ; transition metal catalysis"

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Rutjes, Floris, Sape Kinderman, Jetze van Beijma, Larissa Wolf, Hans Schoemaker, and Henk Hiemstra. "Synthesis of Enantiomerically Pure Pipecolic Acid Derivatives via Combination of Biocatalysis and Transition Metal Catalysis." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01816.

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