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Among the many types of transition-metal-catalyzed C-C bond-forming reactions, olefin metathesis has come to the fore in recent years owing to the wide range of transformations that are possible with commercially available and easily handled catalysts. Consequently, olefin metathesis is now widely considered as one of the most powerful synthetic tools in organic chemistry. Until recently the intermolecular variant of this reaction, cross-metathesis, had been neglected despite its potential. With the evolution of new catalysts, the selectivity, efficiency, and functional-group compatibility of this reaction have improved to a level that was unimaginable just a few years ago. These advances, together with a better understanding of the mechanism and catalyst-substrate interactions, have brought us to a stage where more and more researchers are employing cross-metathesis reactions in multistep procedures and in the synthesis of natural products. The recent inclusion of alkynes and hindered bicyclic olefins as viable substrates for bimolecular metathesis coupling, the discovery of enantioselective cross-metathesis and cross-metathesis in water, and the successful marriage of metathesis and solid-phase organic synthesis has further widened the scope of this versatile reaction. 相似文献
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Dr. Benedikt W. Grau Alexander Neuhauser Dr. Sadig Aghazada Prof. Dr. Karsten Meyer Prof. Dr. Svetlana B. Tsogoeva 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(62):e202201414
The “metathesis reaction” is a straightforward and often metal-catalyzed chemical reaction that transforms two hydrocarbon molecules to two new hydrocarbons by exchange of molecular fragments. Alkane, alkene and alkyne metathesis have become an important tool in synthetic chemistry and have provided access to complex organic structures. Since the discovery of industrial olefin metathesis in the 1960s, many modifications have been reported; thus, increasing scope and improving reaction selectivity. Olefin metathesis catalysts based on high-valent group six elements or Ru(IV) have been developed and improved through ligand modifications. In addition, significant effort was invested to realize olefin metathesis with a non-toxic, bio-compatible and one of the most abundant elements in the earth′s crust; namely, iron. First evidences suggest that low-valent Fe(II) complexes are active in olefin metathesis. Although the latter has not been unambiguously established, this review summarizes the key advances in the field and aims to guide through the challenges. 相似文献
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Miguel ngel Rivero‐Crespo María Tejeda‐Serrano Horacio Prez‐Snchez Jos Pedro Cern‐Carrasco Antonio Leyva‐Prez 《Angewandte Chemie (International ed. in English)》2020,59(10):3846-3849
The carbonyl–olefin metathesis reaction has experienced significant advances in the last seven years with new catalysts and reaction protocols. However, most of these procedures involve soluble catalysts for intramolecular reactions in batch. Herein, we show that recoverable, inexpensive, easy to handle, non‐toxic, and widely available simple solid acids, such as the aluminosilicate montmorillonite, can catalyze the intermolecular carbonyl–olefin metathesis of aromatic ketones and aldehydes with vinyl ethers in‐flow, to give alkenes with complete trans stereoselectivity on multi‐gram scale and high yields. Experimental and computational data support a mechanism based on a carbocation‐induced Grob fragmentation. These results open the way for the industrial implementation of carbonyl–olefin metathesis over solid catalysts in continuous mode, which is still the origin and main application of the parent alkene–alkene cross‐metathesis. 相似文献
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Dr. Miguel Ángel Rivero-Crespo María Tejeda-Serrano Dr. Horacio Pérez-Sánchez Dr. José Pedro Cerón-Carrasco Dr. Antonio Leyva-Pérez 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(10):3874-3877
The carbonyl–olefin metathesis reaction has experienced significant advances in the last seven years with new catalysts and reaction protocols. However, most of these procedures involve soluble catalysts for intramolecular reactions in batch. Herein, we show that recoverable, inexpensive, easy to handle, non-toxic, and widely available simple solid acids, such as the aluminosilicate montmorillonite, can catalyze the intermolecular carbonyl–olefin metathesis of aromatic ketones and aldehydes with vinyl ethers in-flow, to give alkenes with complete trans stereoselectivity on multi-gram scale and high yields. Experimental and computational data support a mechanism based on a carbocation-induced Grob fragmentation. These results open the way for the industrial implementation of carbonyl–olefin metathesis over solid catalysts in continuous mode, which is still the origin and main application of the parent alkene–alkene cross-metathesis. 相似文献
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Keitz BK Endo K Patel PR Herbert MB Grubbs RH 《Journal of the American Chemical Society》2012,134(1):693-699
Several new C-H-activated ruthenium catalysts for Z-selective olefin metathesis have been synthesized. Both the carboxylate ligand and the aryl group of the N-heterocyclic carbene have been altered and the resulting catalysts evaluated using a range of metathesis reactions. Substitution of bidentate with monodentate X-type ligands led to a severe attenuation of metathesis activity and selectivity, while minor differences were observed between bidentate ligands within the same family (e.g., carboxylates). The use of nitrato-type ligands in place of carboxylates afforded a significant improvement in metathesis activity and selectivity. With these catalysts, turnover numbers approaching 1000 were possible for a variety of cross-metathesis reactions, including the synthesis of industrially relevant products. 相似文献
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Hoveyda AH Gillingham DG Van Veldhuizen JJ Kataoka O Garber SB Kingsbury JS Harrity JP 《Organic & biomolecular chemistry》2004,2(1):8-23
The discovery and development of a new class of Ru-based catalysts for olefin metathesis is described. These catalysts, particularly those that do not bear a phosphine ligand, have been demonstrated to promote unique levels of reactivity in a variety of olefin metathesis reactions. The design and development of supported and chiral optically pure variants of this class of Ru catalysts for use in enantioselective metathesis are discussed as well. All catalysts are air stable, reusable, and can be employed with unpurified solvents. 相似文献
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Dr. Amit A. Nagarkar Mohammad Yasir Dr. Aurelien Crochet Prof. Dr. Katharina M. Fromm Prof. Dr. Andreas F. M. Kilbinger 《Angewandte Chemie (International ed. in English)》2016,55(40):12343-12346
Use of a tandem ring‐opening–ring‐closing metathesis (RORCM) strategy for the synthesis of functional metathesis catalysts is reported. Ring opening of 7‐substituted norbornenes and subsequent ring‐closing metathesis forming a thermodynamically stable 6‐membered ring lead to a very efficient synthesis of new catalysts from commercially available Grubbs’ catalysts. Hydroxy functionalized Grubbs’ first‐ as well as third‐generation catalysts have been synthesized. Mechanistic studies have been performed to elucidate the order of attack of the olefinic bonds. This strategy was also used to synthesize the ruthenium methylidene complex. 相似文献
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Grubbs' carbene complex [Cl(2)(Cy(3)P)(2)Ru=CHPh] and its second-generation counterpart [Cl(2)(Im)(Cy(3)P)Ru=CHPh] have demonstrated remarkable efficiency metathesizing olefins. Furthermore, a growing number of newly discovered catalytic processes mediated by this complex broaden its synthetic utility beyond olefin metathesis. In addition, the ready availability of these stable ruthenium-based catalysts coupled with their tolerance toward a wide variety of common functional groups make Grubbs' catalysts very convenient synthetic tools. This paper presents recent advances in the non-metathetic behavior patterns of Grubbs' carbene. 相似文献
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Olefin metathesis catalyst: stabilization effect of backbone substitutions of N-heterocyclic carbene
Ruthenium olefin metathesis catalysts bearing an N-phenyl-substituted N-heterocyclic carbene (NHC) ligand that are resistant to decomposition through C-H activation have been prepared and tested in ring closing metathesis (RCM), cross metathesis (CM), and ROMP reactions. The N, N'-diphenyl-substituted NHC complex proved to be one of the most efficient catalysts in RCM to form tetrasubstituted olefins. 相似文献
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Fürstner A 《Angewandte Chemie (International ed. in English)》2000,39(17):3012-3043
The advent of well-defined catalysts for olefin metathesis which combine high activity, durability, and excellent tolerance towards polar functional groups has revolutionized the field. The past decade has seen the rapid embrace of these reagents as tools for advanced organic and polymer chemistry and the success of this development is witnessed by a plethora of elegant applications to the synthesis of natural and nonnatural products. This review article provides an overview of these developments and intends to familiarize the reader with some very recent advances which hold the promise to expand the scope of the reaction even further. Moreover, the positive impact of metathesis on the fundamental logic of retrosynthetic planning is demonstrated by means of typical examples. Finally, it will be shown that metathesis is by no means restricted to alkenes as substrates, and some comments on metathesis reactions following unconventional mechanistic pathways will also be presented. 相似文献
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[reaction: see text] A series of ruthenium-based metathesis catalysts with N-heterocyclic carbene (NHC) ligands have been prepared in which the N-aryl groups have been changed from mesityl to mono-ortho-substituted phenyl (e.g., tolyl). These new catalysts offer an exceptional increase in activity for the formation of tetrasubstituted olefins via ring-closing metathesis (RCM), while maintaining high levels of activity in ring-closing metathesis (RCM) reactions that generate di- and trisubstituted olefins. 相似文献
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Carl A. Denard Dr. Hua Huang Dr. Mark J. Bartlett Lu Lu Dr. Yichen Tan Prof. Huimin Zhao Prof. John F. Hartwig 《Angewandte Chemie (International ed. in English)》2014,53(2):465-469
Although chemical and enzymatic catalysts have been combined, reactions in which an organometallic catalyst and a metalloenzyme work cooperatively to create products, which cannot be generated with either catalyst alone or in comparable yields by sequential reactions of the two catalysts, have not been reported. Such reactions are challenging to achieve, in part because the milieu in which these catalysts operate are typically different. Herein, two classes of catalysts are demonstrated to react cooperatively in the same system. Combination of a metathesis catalyst and a P450 enzyme lead to a dynamic equilibration of alkenes and a selective epoxidation of the cross‐metathesis products. These results show the potential of combining the two classes of catalysts for synthetic transformations. 相似文献
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Christophe Copret Zachariah J. Berkson Ka Wing Chan Jordan de Jesus Silva Christopher P. Gordon Margherita Pucino Pavel A. Zhizhko 《Chemical science》2021,12(9):3092
Since its early days, olefin metathesis has been in the focus of scientific discussions and technology development. While heterogeneous olefin metathesis catalysts based on supported group 6 metal oxides have been used for decades in the petrochemical industry, detailed mechanistic studies and the development of molecular organometallic chemistry have led to the development of robust and widely used homogeneous catalysts based on well-defined alkylidenes that have found applications for the synthesis of fine and bulk chemicals and are also used in the polymer industry. The development of the chemistry of high-oxidation group 5–7 alkylidenes and the use of surface organometallic chemistry (SOMC) principles unlocked the preparation of so-called well-defined supported olefin metathesis catalysts. The high activity and stability (often superior to their molecular analogues) and molecular-level characterisation of these systems, that were first reported in 2001, opened the possibility for the first direct structure–activity relationships for supported metathesis catalysts. This review describes first the history of SOMC in the field of olefin metathesis, and then focuses on what has happened since 2007, the date of our last comprehensive reviews in this field.Surface organometallic chemistry bridges the gap between homogeneous and heterogeneous olefin metathesis catalysts. 相似文献
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Samojłowicz C Bieniek M Pazio A Makal A Woźniak K Poater A Cavallo L Wójcik J Zdanowski K Grela K 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(46):12981-12993
A study concerning the effect of using a fluorinated aromatic solvent as the medium for olefin metathesis reactions catalysed by ruthenium complexes bearing N-heterocyclic carbene ligands is presented. The use of fluorinated aromatic hydrocarbons (FAH) as solvents for olefin metathesis reactions catalysed by standard commercially available ruthenium pre-catalysts allows substantially higher yields of the desired products to be obtained, especially in the case of demanding polyfunctional molecules, including natural and biologically active compounds. Interactions between the FAH and the second-generation ruthenium catalysts, which apparently improve the efficiency of the olefin metathesis transformation, have been studied by X-ray structure analysis and computations, as well as by carrying out a number of metathesis experiments. The optimisation of reaction conditions by using an FAH can be regarded as a complementary approach for the design of new improved ruthenium catalysts. Fluorinated aromatic solvents are an attractive alternative medium for promoting challenging olefin metathesis reactions. 相似文献
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Cationic Silica‐Supported N‐Heterocyclic Carbene Tungsten Oxo Alkylidene Sites: Highly Active and Stable Catalysts for Olefin Metathesis 下载免费PDF全文
Margherita Pucino Dr. Victor Mougel Roman Schowner Dr. Alexey Fedorov Prof. Dr. Michael R. Buchmeiser Prof. Dr. Christophe Copéret 《Angewandte Chemie (International ed. in English)》2016,55(13):4300-4302
Designing supported alkene metathesis catalysts with high activity and stability is still a challenge, despite significant advances in the last years. Described herein is the combination of strong σ‐donating N‐heterocyclic carbene ligands with weak σ‐donating surface silanolates and cationic tungsten sites leading to highly active and stable alkene metathesis catalysts. These well‐defined silica‐supported catalysts, [(≡SiO)W(=O)(=CHCMe2Ph)(IMes)(OTf)] and [(≡SiO)W(=O)(=CHCMe2Ph)(IMes)+][B(ArF)4?] [IMes=1,3‐bis(2,4,6‐trimethylphenyl)‐imidazol‐2‐ylidene, B(ArF)4=B(3,5‐(CF3)2C6H3)4] catalyze alkene metathesis, and the cationic species display unprecedented activity for a broad range of substrates, especially for terminal olefins with turnover numbers above 1.2 million for propene. 相似文献
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Clavier H Grela K Kirschning A Mauduit M Nolan SP 《Angewandte Chemie (International ed. in English)》2007,46(36):6786-6801
Ruthenium-catalyzed olefin metathesis reactions represent an attractive and powerful transformation for the formation of new carbon-carbon double bonds. This area is now quite familiar to most chemists as numerous catalysts are available that enable a plethora of olefin metathesis reactions. Nevertheless, with the exception of uses in polymerization reactions, only a limited number of industrial processes use olefin metathesis. This is mainly due to difficulties associated with removing ruthenium from the final products. In this context, a number of studies have been carried out to develop procedures for the removal of the catalyst or the products of catalyst decomposition, however, none are universally attractive so far. This situation has resulted in tremendous activity in the area dealing with supported or tagged versions of homogeneous catalysts. This Review summarizes the numerous studies focused on developing cleaner ruthenium-catalyzed metathesis processes. 相似文献
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Martin A. Dolan Alexandre D.C. Dixon John D. Chisholm Daniel A. Clark 《Tetrahedron letters》2018,59(51):4471-4474
Ruthenium–catalyzed enyne metathesis is a reliable and efficient method for the formation of 1,3-dienes, a common structural motif in synthetic organic chemistry. The development of new transition-metal complexes competent to catalyze enyne metathesis reactions remains an important research area. This report describes the use of ruthenium (IV) dihydride complexes with the general structure RuH2Cl2(PR3)2 as new catalysts for enyne metathesis. These ruthenium (IV) dihydrides have been largely unexplored as catalysts in metathesis-based transformations. The reactivity of these complexes with 1,6 and 1,7-enynes was investigated. The observed reaction products are consistent with the metathesis activity occurring through a ruthenium vinylidene intermediate. 相似文献
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Chelating Ruthenium Phenolate Complexes: Synthesis,General Catalytic Activity,and Applications in Olefin Metathesis Polymerization 下载免费PDF全文
Anna Kozłowska Dr. Maciej Dranka Prof. Janusz Zachara Eva Pump Prof. Dr. Christian Slugovc Krzysztof Skowerski Prof. Dr. Karol Grela 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(43):14120-14125
Cyclic Ru‐phenolates were synthesized, and these compounds were used as olefin metathesis catalysts. Investigation of their catalytic activity pointed out that, after activation with chemical agents, these catalysts promote ring‐closing metathesis (RCM), enyne and cross‐metathesis (CM) reactions, including butenolysis, with good results. Importantly, these latent catalysts are soluble in neat dicyclopentadiene (DCPD) and show good applicability in ring‐opening metathesis polymeriyation (ROMP) of this monomer. 相似文献
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[reaction: see text] The cross metathesis reactivities of alpha-methylene-gamma-butyrolactone and an alpha-methylene-delta-lactone have been investigated. alpha-Methylene-gamma-butyrolactone undergoes rapid and efficient olefin isomerization in the presence of second-generation metathesis catalysts. However, cross metathesis can be achieved with the additive 2,6-dichlorobenzoquinone. In contrast, the alpha-methylene-delta-lactone neither isomerizes nor couples under similar conditions. 相似文献