Relevant bibliographies by topics / Macrocyclic chemistry

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Academic literature on the topic 'Macrocyclic chemistry'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Macrocyclic chemistry"

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Singh, Kartikey, and Rama Pati Tripathi. "An Overview on Glyco-Macrocycles: Potential New Lead and their Future in Medicinal Chemistry." Current Medicinal Chemistry 27, no. 20 (2020): 3386–410. http://dx.doi.org/10.2174/0929867326666190227232721.

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Macrocycles cover a small segment of molecules with a vast range of biological activity in the chemotherapeutic world. Primarily, the natural sources derived from macrocyclic drug candidates with a wide range of biological activities are known. Further evolutions of the medicinal chemistry towards macrocycle-based chemotherapeutics involve the functionalization of the natural product by hemisynthesis. More recently, macrocycles based on carbohydrates have evolved a considerable interest among the medicinal chemists worldwide. Carbohydrates provide an ideal scaffold to generate chiral macrocycl
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Kallert, Uwe, and Rainer Mattes. "Komplexe 17-gliedriger Dibenzo-Makrocyclen mit N3O2- bzw. N3S2-Donorzentren Strukturen von [Zn(′N3O2′)Cl]2ZnCl4 und [Hg(′N3S2′)Br2] / Complexes of 17-Membered Dibenzo Macrocycles with N3O2 or N3S2 Donor Sets Crystal and Molecular Structures of [Zn(′N3O2′)Cl]2ZnCl4 and [Hg(′N3S2′)Br2]." Zeitschrift für Naturforschung B 47, no. 9 (1992): 1271–75. http://dx.doi.org/10.1515/znb-1992-0910.

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The macrocyclic complexes [Zn(′N3O2')Cl]2ZnCl4 (1) und [Hg(′N3S2')Br2] (2) have been prepared and their crystal structures determined. Zn(II) is incorporated into the macrocyclic cavity of the ′N3O2′ ligand and primarly coordinated to the three nitrogen donors of the macrocycle and to a chloride ion. Weaker interactions occur with the oxygen donors of the macrocycle. The Zn—O distances are 296,4(5) and 322,4(6) pm. In complex 2 Hg(II) lies outside the macrocyclic cavity. The donor set comprises two secondary amine nitrogen atoms and a thioether sulfur atom of the macrocycle, and two bromide an
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Shurpik, Dmitriy N., Alan A. Akhmedov, Peter J. Cragg, Vitaliy V. Plemenkov, and Ivan I. Stoikov. "Progress in the Chemistry of Macrocyclic Meroterpenoids." Plants 9, no. 11 (2020): 1582. http://dx.doi.org/10.3390/plants9111582.

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In the last decade, the chemistry of meroterpenoids—conjugated molecules formed from isoprenyl fragments through biosynthetic pathways—has developed rapidly. The class includes some natural metabolites and fully synthetic fragments formed through nonbiological synthesis. In the field of synthetic receptors, a range of structures can be achieved by combining fragments of different classes of organic compounds into one hybrid macrocyclic platform which retains the properties of these fragments. This review discusses the successes in the synthesis and practical application of both natural and syn
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Abdelraheem, Eman, Shabnam Shaabani, and Alexander Dömling. "Artificial Macrocycles." Synlett 29, no. 09 (2018): 1136–51. http://dx.doi.org/10.1055/s-0036-1591975.

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Artificial macrocycles recently became popular as a novel research field in drug discovery. As opposed to their natural twins, artificial macrocycles promise to have better control on synthesizability and control over their physicochemical properties resulting in druglike properties. Very few synthetic methods allow for the convergent, fast but diverse access to large macrocycles chemical space. One synthetic technology to access artificial macrocycles with potential biological activity, multicomponent reactions, is reviewed here, with a focus on our own work. We believe that synthetic chemist
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Roberge, Jacques Y., Pierre Giguere, Pierre Soucy, Yves L. Dory, and Pierre Deslongchamps. "First transannular Diels–Alder reactions involving tetrasubstituted non-activated dienophiles." Canadian Journal of Chemistry 72, no. 8 (1994): 1820–29. http://dx.doi.org/10.1139/v94-231.

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Transannular Diels–Alder reactions of four 14-membered macrocyclic trienes (27, 28, 43, and 44) possessing a dimethyl tetrasubstituted dienophile have been investigated. Macrocycles having a cis-trans-cis (CTC) (27), a CTT (43), and a TTT (44) geometry produced the predicted trans-syn-cis (TSC) (45), cis-anti-cis (CAC) (48), and TAC (49) tricycles, respectively. The TTC macrocycle (28) gave exclusively the TST tricycle (46), no CSC tricycle (47) being observed. TTT macrocycle (44) underwent macrocyclization at a lower temperature than the TTC isomer (28).
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Ghosh Roy, Tapashi. "Macrocyclic Chemistry." Acta Scientific Pharmaceutical Sciences 4, no. 3 (2020): 01. http://dx.doi.org/10.31080/asps.2020.04.0500.

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IZATT, R. M. "Macrocyclic Chemistry: The Chemistry of Macrocyclic Ligand Complexes." Science 246, no. 4932 (1989): 942. http://dx.doi.org/10.1126/science.246.4932.942.

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Lodeiro, Carlos, Rufina Bastida, Emilia Bértolo, and Adolfo Rodríguez. "A new family of NxOy pyridine-containing macrocycles: Synthesis and characterization of their Y(III), Ln(III), Zn(II), and Cd(II) coordination compounds." Canadian Journal of Chemistry 82, no. 3 (2004): 437–47. http://dx.doi.org/10.1139/v03-214.

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Reaction between 2,6-bis(2-formylphenoxymethyl)pyridine and N,N-bis(3-aminopropyl)methylamine or tris(2-aminoethyl)amine has been used as the starting point for the synthesis of seven oxa-aza macrocyclic ligands, five of them never reported previously. They all feature different pendant arms, which provide a wide range of coordination possibilities. The Schiff base macrocycles L1 and L4 and their reduced ligands L2 and L5 are derived from 2,6-bis(2-formylphenoxymethyl)pyridine and tris(2-aminoethyl)amine or N,N-bis(3-aminopropyl)methylamine, respectively. The reaction of L1 with salicylaldehyd
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Chi, Xiaodong, Jinya Tian, Dan Luo, Han-Yuan Gong, Feihe Huang, and Jonathan L. Sessler. "“Texas-Sized” Molecular Boxes: From Chemistry to Applications." Molecules 26, no. 9 (2021): 2426. http://dx.doi.org/10.3390/molecules26092426.

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The design and synthesis of novel macrocyclic host molecules continues to attract attention because such species play important roles in supramolecular chemistry. However, the discovery of new classes of macrocycles presents a considerable challenge due to the need to embody by design effective molecular recognition features, as well as ideally the development of synthetic routes that permit further functionalization. In 2010, we reported a new class of macrocyclic hosts: a set of tetracationic imidazolium macrocycles, which we termed “Texas-sized” molecular boxes (TxSBs) in homage to Stoddart
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Archibald, Stephen J. "Macrocyclic coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 103 (2007): 264. http://dx.doi.org/10.1039/b612865n.

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Dissertations / Theses on the topic "Macrocyclic chemistry"

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Tuffin, Rachel Patricia. "Macrocyclic liquid crystals." Thesis, University of Hull, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.337245.

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Nicholson, Patrick Edmund. "Synthetic macrocyclic ionophores." Thesis, Durham University, 1989. http://etheses.dur.ac.uk/6321/.

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14-Crown-4 derivatives bearing either one or two oxymethyl, benzyl- oxymethyl, methoxycarbonylmethyl or carbamoylmethyl substituents have been prepared in an attempt to obtain selective ionophores for lithiumions. Complexation has been monitored by IR, (^13)C NMR, Fast Atom Bombardment Mass Spectrometry, and solvent polymeric membranes have been fabricated and evaluated using the fixed interference method. Improved lithium selectivities of the disubstituted 14-crown-4 ligands compared to the monosubstituted analogues in the potentiometric experiments, bears out the premise that there is a need
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Kyte, A. B. "Chiral macrocyclic receptors." Thesis, University of Liverpool, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.354552.

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Martí-Centelles, Vicente, M. Isabel Burguete, and Santiago V. Luis. "Chemistry inspired by nature: macrocyclic pseudopeptides design." Revista de Química, 2013. http://repositorio.pucp.edu.pe/index/handle/123456789/100172.

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El diseño molecular fundamentado en la imitación de las complejas estructuras y procesos que se encuentran en la naturaleza se conoce como Química bioinspirada o Química biomimética. Una de las aproximaciones utilizadas en esta disciplina es la preparación de compuestos seudopeptídicos macrocíclicos a partir de aminoácidos naturales y componentes abióticos. En la naturaleza existen proteínas con propiedades muy específicas y diversas. El uso de la información codificada en las cadenas laterales de los aminoácidos es un factor clave que, a su vez, puede utilizarse con ventaja para el diseño de
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Göransson, Ulf. "Macrocyclic polypeptides from plants." Doctoral thesis, Uppsala University, Department of Medicinal Chemistry, 2002. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-1956.

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<p>The aim of this work was to explore the structural and functional diversity of polypeptides that are found in plants. Expanding knowledge of simililarities between plant use of these compound and animal use promises exceptional opportunities for finding, from plant research, new structures with biomedical and biotechnological potential.</p><p>A fractionation protocol was developed and applied to many plant species, providing fractions enriched in polypeptides, amenable to chemical and biological evaluation. From one species, the common field pansy (<i>Viola arvensis</i>), a 29-amino-acid re
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Richtzenhain, Heiko. "Macrocyclic liquid crystals." Thesis, University of Nottingham, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243475.

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Salek, Spencer N. "Macrocyclic tridentate phosphathia ligands." Thesis, University of Kent, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.242928.

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Lippolis, Vito. "Studies on the coordination chemistry of macrocyclic ligands." Thesis, University of Nottingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311755.

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Rawle, Simon Charles. "The coordination chemistry of some multidentate thioether ligands." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.329963.

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Tei, Lorenzo. "Studies on functionalised macrocyclic ligands." Thesis, University of Nottingham, 2001. http://eprints.nottingham.ac.uk/12386/.

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The work presented in this thesis hinges on three main topics: a) the coordination chemistry of symmetric and asymmetric derivatives of [9]aneN3 towards lanthanide ions; b) the transition metal co-ordination chemistry of nitrile and amino derivatives of [9]aneN3 and [15]aneN3O2; c) the use of macrocyclic ligands for the synthesis of polymeric Ag' complexes. Chapter 3 describes the Ln"' complexes of the ligand obtained by Schiffbase condensation of 1,4,7-tris(2-aminoethyl)-1,4,7-triazacyclononane (L) with three molar equivalents of sodium pyruvate using the Ln0' ion as templating agent. The mon
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Books on the topic "Macrocyclic chemistry"

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Gloe, Karsten, ed. Macrocyclic Chemistry. Springer Netherlands, 2005. http://dx.doi.org/10.1007/1-4020-3687-6.

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Izatt, Reed M., ed. Macrocyclic and Supramolecular Chemistry. John Wiley &;#38; Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119053859.

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Coordination chemistry of macrocyclic compounds. Oxford University Press, 1999.

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Gėrbėlėu, Nikolaĭ Vasilʹevich. Template synthesis of macrocyclic compounds. Wiley-VCH, 1999.

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The chemistry of macrocyclic ligand complexes. Cambridge University Press, 1989.

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Macrocyclic chemistry: Aspects of organic and inorganic supramolecular chemistry. VCH, 1993.

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Séamus, Higson, and Wiley online library, eds. Macrocycles: Construction, chemistry, and nanotechnology applications. Wiley, 2011.

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Sikanyika, Harrison. The synthesis and co-ordination chemistry of redox-active macrocyclic receptor molecules. University of Birmingham, 1989.

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Lehn, J. M. Aspects de la chimie des compose s macrocycliques: Notes re dige es, augmente es et actualise es. InterEditions, 1991.

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International Symposium on Macrocyclic Chemistry (20th 1995 Jerusalem, Israel). Invited lectures presented at the 20th InternationalSymposium on Macrocyclic Chemistry held in Jerusalem, Israel, 2-7 July 1995. Edited by Meyerstein D and Shanzer A. Blackwell Science, 1996.

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Book chapters on the topic "Macrocyclic chemistry"

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Moyer, Bruce A., Joseph F. Birdwell, Peter V. Bonnesen, and Laetitia H. Delmau. "Use of Macrocycles in Nuclear-Waste Cleanup: A Realworld Application of a Calixcrown in Cesium Separation Technology." In Macrocyclic Chemistry. Springer Netherlands, 2005. http://dx.doi.org/10.1007/1-4020-3687-6_24.

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Chidchob, Pongphak, and Hanadi Sleiman. "Supramolecular Chemistry with DNA." In Macrocyclic and Supramolecular Chemistry. John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119053859.ch2.

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Newkome, G. R., V. K. Gupta, and J. D. Sauer. "Macrocyclic Pyridines." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186701.ch3.

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Meadows, Margaret K., and Eric V. Anslyn. "Three Tales of Supramolecular Analytical Chemistry." In Macrocyclic and Supramolecular Chemistry. John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119053859.ch5.

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Kim, Kimoon, Dinesh Shetty, and Kyeng Min Park. "Robust Host-Guest Chemistry of Cucurbit[n]uril." In Macrocyclic and Supramolecular Chemistry. John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119053859.ch6.

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Izatt, Reed M., Jerald S. Bradshaw, Steven R. Izatt, and Roger G. Harrison. "The Izatt-Christensen Award in Macrocyclic and Supramolecular Chemistry." In Macrocyclic and Supramolecular Chemistry. John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119053859.ch1.

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Leigh, David A. "Making the Tiniest Machines." In Macrocyclic and Supramolecular Chemistry. John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119053859.ch11.

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Nolte, Roeland J. M., Alan E. Rowan, and Johannes A. A. W. Elemans. "Clipping an Angel's Wings." In Macrocyclic and Supramolecular Chemistry. John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119053859.ch12.

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Sanders, Jeremy K. M. "From Lanthanide Shift Reagents to Molecular Knots." In Macrocyclic and Supramolecular Chemistry. John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119053859.ch13.

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Sessler, Jonathan L. "Texaphyrins." In Macrocyclic and Supramolecular Chemistry. John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119053859.ch14.

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Conference papers on the topic "Macrocyclic chemistry"

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Keserű, György M., and Mihály Nógrádi. "Structure and activity of macrocyclic diarylheptanoids isolated from Garuga species." In The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47717.

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Vasilevich, Natalya, Anna Aksenova, Elena Aksenova, and Ilya Afanasyev. "Design and Synthesis of Macrocyclic Scaffolds for Compounds with Potential Antituberculosis/Antibacterial Activity and Improved CYP450 Properties." In 2nd International Electronic Conference on Medicinal Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecmc-2-a013.

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Pérez-Mayoral, Elena, Elena Soriano, Sebastián Cerdán, and Paloma Ballesteros. "Experimental and Theoretical Study of Lanthanide Complexes Based on Linear and Macrocyclic Polyaminopolycarboxylic Acids with Pyrazolylethyl Arms." In The 9th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01506.

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Schrader, Thomas, Paolo Finocchiaro, Thomas Grawe, Salvatore Failla, and Giuseppe Consiglio. "A New Receptor Molecule for Lysine and Histidine in Water � Strong Binding of Basic Amino Acids by a Macrocyclic Host." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01919.

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Shutalev, Anatoly, Anastasia Fesenko, Dmitry Albov, Vladimir Chernyshev, and Ilia Zamilatskov. "Novel 14-Membered Hexaaza Macrocycles." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a042.

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Dalager, Michael, and Stefan Vogel. "Towards a DNA based asymmetric catalyst based on a tetraaza crown ether macrocycle." In XVIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2014. http://dx.doi.org/10.1135/css201414242.

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Lamelas, Rodrigo, Alejandro Macías, Elena Labisbal, Maria Teresa Pereira, Paula Munin, and Francisco Reigosa. "Synthesis of macrocycles with pendant arms derived from 2- (2-bromoethyl) -1,3-dioxolane." In The 21st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04788.

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Bischoff, I., and M. Senge. "Conformationally Designed Biomimetic Macrocycles - Synthesis of Porphyrins and Porphodimethenes with Mixed Substitution Pattern and Distortion Modes." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01922.

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Shutalev, Anatoly, Anastasia Fesenko, and Alexander Yankov. "Novel Semicarbazone-Based Amidoalkylation Reagents: Preparation and Application to the Stereoselective Synthesis of 14-Membered Hexaaza Macrocycles." In The 21st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04765.

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Martí, Vicente, M. Burguete, and Santiago Luis. "Understanding the Cyclization Step for the Preparation of Pseudopeptidic Macrocycles. Optimization of the Process Trough a Theoretical Analysis." In The 12th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01290.

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Reports on the topic "Macrocyclic chemistry"

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Davis, Jeffery T. 8th International Symposium on Supramolecular and Macrocyclic Chemistry. Office of Scientific and Technical Information (OSTI), 2015. http://dx.doi.org/10.2172/1215453.

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