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Relevant bibliographies by topics / Metathesis

Academic literature on the topic 'Metathesis'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 May 2024

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Journal articles on the topic "Metathesis"

1

Schindler, Corinna, and Jacob Ludwig. "Lewis Acid Catalyzed Carbonyl–Olefin Metathesis." Synlett 28, no. 13 (May 16, 2017): 1501–9. http://dx.doi.org/10.1055/s-0036-1588827.

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Olefin–olefin metathesis has led to important advances in diverse fields of research, including synthetic chemistry, materials science, and chemical biology. The corresponding carbonyl–olefin metathesis also enables direct carbon–carbon bond formation from readily available precursors, however, currently available synthetic procedures are significantly less advanced. This Synpacts article provides an overview of recent achievements in the field of Lewis acid mediated and Lewis acid catalyzed carbonyl–olefin metathesis reactions.1 Lewis Acid Mediated Carbonyl–Olefin Metathesis2 Lewis Acid Catalyzed Carbonyl–Olefin Metathesis

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Dragutan, V., I. Dragutan, and A. T. Balaban. "Single-Site Ruthenium Metathesis Catalysts." Platinum Metals Review 45, no. 4 (October 1, 2001): 155–63. http://dx.doi.org/10.1595/003214001x454155163.

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This paper presents an up-to-date investigation relating to the design and synthesis of the recently disclosed single-site ruthenium carbene metathesis catalysts. Created as a convenient counterpart of the earlier tungsten and molybdenum carbene catalysts, these novel ruthenium carbene complexes bear specific heterocyclic ligands and display comparable activity and selectivity in metathesis reactions, as well as good tolerance toward organic functionalities, air and moisture. Due to their unique properties, they can be successfully applied in numerous organic and polymer syntheses involving cross-metathesis, ring-opening and ring-closing metatheses, as well as ring-opening metathesis polymerisation. This paper updates our previous review on metathesis reactions published in this Journal last year.

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Sabatino, Valerio, and Thomas R. Ward. "Aqueous olefin metathesis: recent developments and applications." Beilstein Journal of Organic Chemistry 15 (February 14, 2019): 445–68. http://dx.doi.org/10.3762/bjoc.15.39.

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Olefin metathesis is one of the most powerful C–C double-bond-forming reactions. Metathesis reactions have had a tremendous impact in organic synthesis, enabling a variety of applications in polymer chemistry, drug discovery and chemical biology. Although challenging, the possibility to perform aqueous metatheses has become an attractive alternative, not only because water is a more sustainable medium, but also to exploit biocompatible conditions. This review focuses on the progress made in aqueous olefin metatheses and their applications in chemical biology.

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Lambert, Tristan H. "Development of a Hydrazine-Catalyzed Carbonyl-Olefin Metathesis Reaction." Synlett 30, no. 17 (June 5, 2019): 1954–65. http://dx.doi.org/10.1055/s-0039-1689924.

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Carbonyl-olefin metathesis is a potentially powerful yet underexplored reaction in organic synthesis. In recent years, however, this situation has begun to change, most notably with the introduction of several different catalytic technologies. The development of one of those new strategies, based on hydrazine catalysts and a novel [3+2] paradigm for double bond metathesis, is discussed herein. First, the stage is set with a description of some potential applications of carbonyl-olefin metathesis and a discussion of alternative strategies for this intriguing reaction.1 Introduction2 Potential Applications of Carbonyl-Olefin Metathesis3 Carbonyl-Olefin Metathesis Strategies4 Direct (Type I): Non-Catalytic5 Direct (Type I): Acid-Catalyzed6 Indirect (Type II): Metal Alkylidenes7 Indirect (Type III): Hydrazine-Catalyzed8 Conclusion

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Groso, Emilia, and Corinna Schindler. "Recent Advances in the Application of Ring-Closing Metathesis for the Synthesis of Unsaturated Nitrogen Heterocycles." Synthesis 51, no. 05 (February 8, 2019): 1100–1114. http://dx.doi.org/10.1055/s-0037-1611651.

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This short review summarizes recent advances relating to the application of ring-closing olefin-olefin and carbonyl-olefin metathesis reactions towards the synthesis of unsaturated five- and six-membered nitrogen heterocycles. These developments include catalyst modifications and reaction designs that will enable access to more complex nitrogen heterocycles.1 Introduction2 Expansion of Ring-Closing Metathesis Methods3 Evaluation of Catalyst Design4 Indenylidene Catalysts5 Unsymmetrical N-Heterocyclic Carbene Ligands6 Carbonyl-Olefin Metathesis7 Conclusions

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Rogalski, Szymon, and Cezary Pietraszuk. "Application of Olefin Metathesis in the Synthesis of Carbo- and Heteroaromatic Compounds—Recent Advances." Molecules 28, no. 4 (February 9, 2023): 1680. http://dx.doi.org/10.3390/molecules28041680.

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The olefin metathesis reaction has found numerous applications in organic synthesis. This is due to a number of advantages, such as the tolerance of most functional groups and sterically demanding olefins. This article reviews recent advances in the application of the metathesis reaction, particularly the metathetic cyclization of dienes and enynes, in synthesis protocols leading to (hetero)aromatic compounds.

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Sauer, D. F., S. Gotzen, and J. Okuda. "Metatheases: artificial metalloproteins for olefin metathesis." Organic & Biomolecular Chemistry 14, no. 39 (2016): 9174–83. http://dx.doi.org/10.1039/c6ob01475e.

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Kiss, Loránd, Márton Kardos, Csaba Vass, and Ferenc Fülöp. "Application of Metathesis Reactions in the Synthesis and Transformations of Functionalized β-Amino Acid Derivatives." Synthesis 50, no. 18 (July 26, 2018): 3571–88. http://dx.doi.org/10.1055/s-0036-1591600.

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Because of their biological relevance, cyclic β-amino acids have generated increasing interest and had significant impact in drug research over the past two decades. Their preparation and further functionalization towards new types of molecular entities have received large interest in synthetic and medicinal chemistry. Various types of metathesis reactions, such as ring-opening (ROM), ring-closing (RCM), or cross metathesis (CM) are used widely for access to either alicyclic β-amino acids or other densely functionalized derivatives of this group of compounds. This account intends to provide an insight into the most relevant synthetic routes to this class of derivatives with the application of metathesis reactions. The review focuses on the presentation of selective and stereocontrolled methodologies in view of versatility, robustness, limitations and efficiency.1 Introduction2 Synthesis and Transformation of Cyclic β-Amino Acids through Metathesis Reactions2.1 Synthesis of Five- and Six-Membered Cyclic β-Amino Acids by Ring-Closing Metathesis2.2 Synthesis of Five- and Six-Membered Cyclic β-Amino Acids by Cross Metathesis2.3 Synthesis of β-Amino Acids with Larger Ring Systems by Ring- Closing Metathesis2.4 Synthesis of β-Amino Acids with Condensed Ring Systems by Ring-Rearrangement Metathesis2.5 Stereocontrolled One-Step Synthesis of Functionalized Cispentacin and Transpentacin Derivatives2.5.1 Stereocontrolled Synthesis of Functionalized Cispentacin and Transpentacin Derivatives through Ring-Opening Metathesis of Norbornene β-Amino Acid Derivatives2.5.2 Stereocontrolled Synthesis of Functionalized Azetidinones and β-Amino Acid Derivatives from Condensed Ring β-Lactams by Ring-Opening Metathesis2.5.3 Carbon–Carbon Double Bond Functionalization of β-Amino Acid Derivatives and β-Lactams with α,β-Unsaturated Carbonyl Compounds through Cross Metathesis2.5.4 Synthesis of Functionalized β-Amino Acid Derivatives and β-Lactams through Chemoselective Cross Metathesis3 Conclusions and Outlook

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Kotha, Sambasivarao, Shilpi Misra, Gaddamedi Sreevani, and Bandarugattu Babu. "Non-Metathetic Behaviour of Olefin Metathesis Catalysts." Current Organic Chemistry 17, no. 22 (October 1, 2013): 2776–95. http://dx.doi.org/10.2174/13852728113179990118.

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Sarabia, Francisco, and Iván Cheng-Sánchez. "Recent Advances in Total Synthesis via Metathesis Reactions." Synthesis 50, no. 19 (July 18, 2018): 3749–86. http://dx.doi.org/10.1055/s-0037-1610206.

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The metathesis reactions, in their various versions, have become a powerful and extremely valuable tool for the formation of carbon–carbon bonds in organic synthesis. The plethora of available catalysts to perform these reactions, combined with the various transformations that can be accomplished, have positioned the metathesis processes as one of the most important reactions of this century. In this review, we highlight the most relevant synthetic contributions published between 2012 and early 2018 in the field of total synthesis, reflecting the state of the art of this chemistry and demonstrating the significant synthetic potential of these methodologies.1 Introduction2 Alkene Metathesis in Total Synthesis2.1 Total Synthesis Based on a Ring-Closing-Metathesis Reaction2.2 Total Synthesis Based on a Cross-Metathesis Reaction2.3 Strategies for Selective and Efficient Metathesis Reactions of Alkenes2.3.1 Temporary Tethered Ring-Closing Metathesis2.3.2 Relay Ring-Closing Metathesis2.3.3 Stereoselective Alkene Metathesis2.3.4 Alkene Metathesis in Tandem Reactions3 Enyne Metathesis in Total Synthesis3.1 Total Syntheses Based on a Ring-Closing Enyne-Metathesis Reaction3.2 Total Syntheses Based on an Enyne Cross-Metathesis Reaction3.3 Enyne Metathesis in Tandem Reactions4 Alkyne Metathesis in Total Synthesis4.1 Total Synthesis Based on a Ring-Closing Alkyne-Metathesis Reaction4.2 Other Types of Alkyne-Metathesis Reactions5 Conclusions

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Dissertations / Theses on the topic "Metathesis"

1

Salim, Sofia Saima. "Synthesis of sulfamides using ring closing diene metathesis and enyne metathesis." Thesis, University of Southampton, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.417402.

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Nieczypor, Piotr. "Immobilisation of Ru-based metathesis catalysts and related aspects of olefin metathesis." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2004. http://dare.uva.nl/document/74260.

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Rountree, S. M. "Metal catalysed olefin metathesis." Thesis, Queen's University Belfast, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.517512.

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Oakley, Garrett W. "Solid-state olefin metathesis." [Gainesville, Fla.] : University of Florida, 2004. http://purl.fcla.edu/fcla/etd/UFE0007900.

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Courchay, Florence C. "Metathesis and isomerization activity of ruthenium carbene catalysts in acyclic diene metathesis polymerization." [Gainesville, Fla.] : University of Florida, 2005. http://purl.fcla.edu/fcla/etd/UFE0012985.

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Vernall, Andrea J. "Cross Metathesis and Ring-Closing Metathesis Reactions of Modified Amino Acids and Peptides." Thesis, University of Canterbury. Chemistry, 2005. http://hdl.handle.net/10092/5798.

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This thesis investigates the application of cross metathesis and ring-closing metathesis to amino acid and peptide-based substrates that are suitably modified to contain an olefin tether. Chapter One introduces olefin metathesis, describes the mechanism of cross metathesis (CM) and ring-closing metathesis (RCM), and outlines the catalysts that can be used for these transformations. The application of CM and RCM to amino acid and peptide-based systems is reviewed. Chapter Two describes the CM coupling between modified lysine- (2.34 - 2.37, 2.43), serine- (2.45, 2.46), and cysteine-based (2.48, 2.49a, 2.51) amino acids and dipeptides (2.54, 2.57) to a terminal alkene (2.61, 2.65), carbohydrate (1.51b), or fatty acid (2.76) target compound using catalyst 1.17. The amino acid and dipeptide-based CM substrates were prepared by side-chain acylation of the parent amino acid with carboxylic acids containing variable but controllable olefin tether lengths. A CM model study in which these amino acid-based substrates were coupled to terminal alkene 2.61 and 2.65 gave CM products 2.66 - 2.74. CM was then carried out between amino acid-based substrates and a carbohydrate (1.51b) or fatty acid derivative (2.76), that afforded a novel series of glycoamino acids (2.80 - 2.85) and lipoamino acids (2.94 - 2.101). Chapter Three describes the synthesis of amino acid dimers by CM. Two serine-based (3.22 - 3.23) and two cysteine-based (3.24 - 3.25) symmetrical dimers along with two unsymmetrical serine-cysteine dimers (3.26 - 3.27) were prepared from the same side-chain acylated amino acid substrates described in chapter 2. These compounds are examples of novel cross-linked amino acid-based dimers, and further illustrate the versatility of the CM methodology developed in this thesis. Chapter Four describes the synthesis of cyclic amino acids and dipeptides via RCM of acyclic precursors that are suitably modified with acyl olefin tethers of variable length. Cyclic compounds based on lysine (4.6, 4.13), serine (4.31, 4.33), and cysteine (4.40, 4.42) single amino acid residues, and compounds based on lysine (4.16, 4.21, 4.27), serine (4.37), and cysteine (4.45, 4.46) dipeptides were prepared. All these compounds were constructed using the same, versatile general method, which involves acylation of the natural amino acid substrate with a carboxylic acid of controllable olefin tether length followed by RCM with catalyst 1.17 to give cyclic products containing variable ring sizes.

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Alheritiere, Cyrille. "Electrodialysis applied to metathesis reactions." Thesis, Georgia Institute of Technology, 1995. http://hdl.handle.net/1853/11697.

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Al-Samak, Basma. "Alternating ring-opened metathesis copolymers." Thesis, Queen's University Belfast, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343280.

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Thompson, Jillian Margaret. "Olefin metathesis polymers and copolymers." Thesis, Queen's University Belfast, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.314162.

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Tyler, Michelle A. "Mechanistic studies of metathesis polymerisations." Thesis, Aston University, 1987. http://publications.aston.ac.uk/14525/.

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Books on the topic "Metathesis"

1

Grela, Karol, ed. Olefin Metathesis. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118711613.

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Buchmeiser, Michael R., ed. Metathesis Polymerization. Berlin, Heidelberg: Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/b101315.

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Imamoglu, Yavuz, Valerian Dragutan, and Solmaz Karabulut, eds. Metathesis Chemistry. Dordrecht: Springer Netherlands, 2007. http://dx.doi.org/10.1007/978-1-4020-6091-5.

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R, Buchmeiser Michael, ed. Metathesis polymerization. Berlin: Springer, 2005.

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Grubbs, Robert H., Anna G. Wenzel, Daniel J. O'Leary, and Ezat Khosravi, eds. Handbook of Metathesis. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527674107.

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Dragutan, Valerian, Albert Demonceau, Ileana Dragutan, and Eugene Sh Finkelshtein, eds. Green Metathesis Chemistry. Dordrecht: Springer Netherlands, 2010. http://dx.doi.org/10.1007/978-90-481-3433-5.

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H, Grubbs Robert, ed. Handbook of metathesis. Weinheim, Germany: Wiley-VCH, 2003.

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8

Coccolo, Sebastien. Study on metathesis reactions. Birmingham: University of Birmingham, 1998.

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Fürstner, Alois, ed. Alkene Metathesis in Organic Synthesis. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/3-540-69708-x.

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İmamoğlu, Yavuz, Birgül Zümreoğlu-Karan, and Allan J. Amass, eds. Olefin Metathesis and Polymerization Catalysts. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-3328-9.

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Book chapters on the topic "Metathesis"

1

Żukowska, Karolina, and Karol Grela. "Cross Metathesis." In Olefin Metathesis, 37–83. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118711613.ch2.

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Thiel, Oliver R. "Metathesis Reactions." In Applications of Transition Metal Catalysis in Drug Discovery and Development, 215–55. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118309872.ch5.

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Mori, Miwako. "Enyne Metathesis." In Topics in Organometallic Chemistry, 133–54. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/3-540-69708-x_5.

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Gibson, Susan E., and Stephen P. Keen. "Cross-Metathesis." In Topics in Organometallic Chemistry, 155–81. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/3-540-69708-x_6.

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Stewart, Ian C. "Degenerate Metathesis." In Handbook of Metathesis, 305–22. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527674107.ch10.

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O'Leary, Daniel J., and Gregory W. O'Neil. "Cross-Metathesis." In Handbook of Metathesis, 171–294. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527674107.ch16.

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Li, Jingwei, and Daesung Lee. "Enyne Metathesis." In Handbook of Metathesis, 381–444. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527674107.ch19.

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Basset, Jean-Marie, Emmanuel Callens, and Nassima Riache. "Alkane Metathesis." In Handbook of Metathesis, 33–70. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527674107.ch2.

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Fürstner, Alois. "Alkyne Metathesis." In Handbook of Metathesis, 445–501. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527674107.ch20.

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Yoshida, Kazuhiro. "Metathesis Reactions." In Transition-Metal-Mediated Aromatic Ring Construction, 719–42. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118629871.ch26.

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Conference papers on the topic "Metathesis"

1

Richaud, Emmanuel, Jing Huang, and Pierre Yves Le Gac. "Thermosets synthesized by metathesis: Multiscale lifetime approach." In THE 9TH INTERNATIONAL CONFERENCE ON STRUCTURAL ANALYSIS OF ADVANCED MATERIALS - ICSAAM 2019. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5140307.

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Karpov, Gleb O., Ilya L. Borisov, Boris A. Bulgakov, Maxim V. Bermeshev, Sergey R. Sterlin, Vladimir V. Volkov, and Eugene Sh Finkelshtein. "Synthesis and metathesis polymerization of fluorine-containing tricyclononenes." In 9TH INTERNATIONAL CONFERENCE ON “TIMES OF POLYMERS AND COMPOSITES”: From Aerospace to Nanotechnology. Author(s), 2018. http://dx.doi.org/10.1063/1.5046031.

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Gisemba, Solomon A., and Jane V. Aldrich. "Peptide Ring Closing Metathesis: Minimizing Side Reactions in Arodyn Analogs." In The 24th American Peptide Symposium. Prompt Scientific Publishing, 2015. http://dx.doi.org/10.17952/24aps.2015.177.

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Grubbs, Robert H. "Synthesis of functional materials using olefin metathesis catalysts and initiators." In 2010 IEEE 10th Conference on Nanotechnology (IEEE-NANO). IEEE, 2010. http://dx.doi.org/10.1109/nano.2010.5698062.

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Dirk, Shawn M., Patricia S. Sawyer, Jill Wheeler, Mark Stavig, and Bruce Tuttle. "High temperature polymer dielectrics from the ring opening metathesis polymerization (ROMP)." In 2009 IEEE Pulsed Power Conference (PPC). IEEE, 2009. http://dx.doi.org/10.1109/ppc.2009.5386251.

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Muke, A. M., N. S. Ugemuge, and S. V. Moharil. "Photoluminescence study of Tb3+ doped CaCO3 synthesized by solid state metathesis." In INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC 2015): Proceeding of International Conference on Condensed Matter and Applied Physics. Author(s), 2016. http://dx.doi.org/10.1063/1.4946375.

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Yurpalov, V. L., T. R. Karpova, M. A. Moiseenko, V. A. Drozdov, E. A. Buluchevskiy, and A. V. Lavrenov. "Ex situ EPR investigation of MoO3/Al2O3 catalysts for propylene metathesis." In INTERNATIONAL CONFERENCE ON PHYSICS AND CHEMISTRY OF COMBUSTION AND PROCESSES IN EXTREME ENVIRONMENTS (COMPHYSCHEM’20-21) and VI INTERNATIONAL SUMMER SCHOOL “MODERN QUANTUM CHEMISTRY METHODS IN APPLICATIONS”. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0032830.

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Jones, Brad. "Polyurethanes Rendered Depolymerizable by Introduction of a Metathesis Cleavable Co-Monomer." In Proposed for presentation at the Pacifichem 2021 in ,. US DOE, 2021. http://dx.doi.org/10.2172/2001626.

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Leguizamon, Samuel, Jeffrey Foster, Brad Jones, and Leah Appelhans. "Olefin Metathesis ? Opening the Door to New Materials for Additive Manufacturing." In Proposed for presentation at the PolyMac in ,. US DOE, 2022. http://dx.doi.org/10.2172/2003524.

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Debnath, Pradip. "Regioselective Synthesis of Spiro-Oxindoles via a Ruthenium-Catalyzed Metathesis Reaction." In ECSOC 2023. Basel Switzerland: MDPI, 2023. http://dx.doi.org/10.3390/ecsoc-27-16131.

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Reports on the topic "Metathesis"

1

Schrock, Richard R. Ring Opening Metathesis Polymerization. Fort Belvoir, VA: Defense Technical Information Center, January 1992. http://dx.doi.org/10.21236/ada244693.

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Low, Tammy K., and Eric Enholm. Ring-Closing Metathesis of Macrocyclic Compounds and Cross-Metathesis of Allyl Esters of Amino Acids Leading to Peptidominetics. Fort Belvoir, VA: Defense Technical Information Center, March 2005. http://dx.doi.org/10.21236/ada431183.

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Grubbs, Robert H. The generation of efficient supported (Heterogeneous) olefin metathesis catalysts. Office of Scientific and Technical Information (OSTI), April 2013. http://dx.doi.org/10.2172/1072952.

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Schrock, Richard S., Steven A. Krouse, Konrad Knoll, Jerald Feldman, John S. Murdzek, and Dominic C. Yang. Controlled Ring-Opening Metathesis Polymerization by Molybdenum and Tungsten Alkylidene Complexes. Fort Belvoir, VA: Defense Technical Information Center, July 1988. http://dx.doi.org/10.21236/ada198073.

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Lambeth, Robert H., Joseph M. Dougherty, Joshua A. Orlicki, Adam M. Rawlett, Robert C. Hoffman, Timothy Pritchett, and Andrew G. Mott. Synthesis and Purification of Tunable High Tg Electro-Optical Polymers by Ring Opening Metathesis Polymerization. Fort Belvoir, VA: Defense Technical Information Center, September 2011. http://dx.doi.org/10.21236/ada549234.

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Wallace, Kevin C., Andy H. Liu, John C. Dewan, and Richard R. Schrock. Preparation and Reactions of Tantalum Alkylidene Complexes Containing Bulky Phenoxide or Thiolate Ligands. Controlling Ring-Opening Metathesis Polymerization Activity and Mechanism Through Choice of Anionic Ligand. Fort Belvoir, VA: Defense Technical Information Center, July 1988. http://dx.doi.org/10.21236/ada198293.

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Bazan, G. C., E. Khosravi, R. R. Schrock, W. J. Feast, and V. C. Gibson. Living Ring-Opening Metathesis Polymerization of 2,3-Difunctionalized- Norbornadienes by Mo(CH-t-Bu)(N-2,6-C(6)H(3)-i-Pr(2)(O-t-Bu)(2). Fort Belvoir, VA: Defense Technical Information Center, August 1990. http://dx.doi.org/10.21236/ada225986.

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Komiya, Zen, Coleen Pugh, and Richard R. Schrock. Synthesis of Side Chain Liquid Crystal Polymers by Living Ring Opening Metathesis Polymerization. 1. Influence of Molecular Weight, Polydispersity, and Flexible Spacer Length (n=2-8) on the Thermotropic behavior of the Resulting Polymers. Fort Belvoir, VA: Defense Technical Information Center, March 1992. http://dx.doi.org/10.21236/ada248699.

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