Relevant bibliographies by topics / Chemistry synthesis

Contents

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

Academic literature on the topic 'Chemistry synthesis'

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

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Journal articles on the topic "Chemistry synthesis"

1

Dai, Mingji, Xinpei Cai, and Yu Bai. "Total Syntheses of Spinosyn A." Synlett 29, no. 20 (2018): 2623–32. http://dx.doi.org/10.1055/s-0037-1610249.

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Spinosyn A is an important polycyclic natural product with impressive insecticidal activity and has been used worldwide in agriculture as the major component of Spinosad. Herein, four chemical total syntheses of spinosyn A are summarized. Its biosynthesis and a chemoenzymatic total synthesis are discussed as well.1 Biosynthesis2 The Evans Synthesis3 The Paquette Synthesis4 The Roush Synthesis5 The Liu Synthesis6 The Dai Synthesis7 Conclusions
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Tauro, Dr Savita J., and Jineetkumar B. Gawad. "Green Chemistry: A Boon to Pharmaceutical Synthesis." International Journal of Scientific Research 2, no. 7 (2012): 67–69. http://dx.doi.org/10.15373/22778179/july2013/22.

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Kaur, Navjeet. "Photochemical Reactions for the Synthesis of Six-Membered O-Heterocycles." Current Organic Synthesis 15, no. 3 (2018): 298–320. http://dx.doi.org/10.2174/1570179414666171011160355.

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Background: The chemists have been interested in light as an energy source to induce chemical reactions since the beginning of the scientific chemistry. This review summarizes the chemistry of photochemical reactions with emphasis of their synthetic applications. The organic photochemical reactions avoid the polluting or toxic reagents and therefore offer perspectives for sustainable processes and green chemistry. In summary, this review article describes the synthesis of a number of six-membered O-heterocycles. Objective: Photochemistry is indeed a great tool synthetic chemists have at their
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Hundekar, Pritee P., Manish R. Deshpande, and Uday D. Joshi. "Basic CS-MCM-41: Synthesis , Characterization and Activity in Synthesis of Methine Dyes as Green Chemistry Approach." Global Journal For Research Analysis 3, no. 6 (2012): 188–90. http://dx.doi.org/10.15373/22778160/june2014/64.

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Metanis, Norman, Reem Mousa, and Post Reddy. "Chemical Protein Synthesis through Selenocysteine Chemistry." Synlett 28, no. 12 (2017): 1389–93. http://dx.doi.org/10.1055/s-0036-1588762.

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Methods for the preparation of small-to-medium-sized proteins by chemical protein synthesis have matured in recent years and proven valuable for protein science. Thanks to the many recent discoveries and developments in the field, proteins up to 300 amino acids can now be prepared in the lab in a matter of days. This technology gives the scientists the flexibility to substitute any atom in the protein sequence; hence synthesis is not constrained to the 20 canonical amino acids. In this Synpacts article we briefly highlight the recent studies on selenocysteine chemistry in the field of chemical
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Petrovčič, Jan, Chad Nicholas Ungarean, and David Sarlah. "Recent Chemical Methodology Advances in the Total Synthesis of Meroterpenoids." Acta Chimica Slovenica 68, no. 2 (2021): 247–67. http://dx.doi.org/10.17344/acsi.2021.6921.

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Heterogeneity of meroterpenoids arising from their dual biosynthetic origins is constantly provoking synthetic chemists to utilize their ingenuity and revise their retrosynthetic logic. By studying recent publications on meroterpenoid synthesis,tremendous advances in the field of synthetic organic chemistry can be witnessed. This feature article covers some of the most intriguing total syntheses and synthetic studies towards the meroterpenoid class of natural products from the last five years.
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Bose, Anima, and Prasenjit Mal. "Mechanochemistry of supramolecules." Beilstein Journal of Organic Chemistry 15 (April 12, 2019): 881–900. http://dx.doi.org/10.3762/bjoc.15.86.

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The urge to use alternative energy sources has gained significant attention in the eye of chemists in recent years. Solution-based traditional syntheses are extremely useful, although they are often associated with certain disadvantages like generation of waste as by-products, use of large quantities of solvents which causes environmental hazard, etc. Contrastingly, achieving syntheses through mechanochemical methods are generally time-saving, environmentally friendly and more economical. This review is written to shed some light on supramolecular chemistry and the synthesis of various supramo
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Swan, Ellen, Kirsten Platts, and Anton Blencowe. "An overview of the cycloaddition chemistry of fulvenes and emerging applications." Beilstein Journal of Organic Chemistry 15 (September 6, 2019): 2113–32. http://dx.doi.org/10.3762/bjoc.15.209.

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The unusual electronic properties and unique reactivity of fulvenes have interested researchers for over a century. The propensity to form dipolar structures at relatively low temperatures and to participate as various components in cycloaddition reactions, often highly selectively, makes them ideal for the synthesis of complex polycyclic carbon scaffolds. As a result, fulvene cycloaddition chemistry has been employed extensively for the synthesis of natural products. More recently, fulvene cycloaddition chemistry has also found application to other areas including materials chemistry and dyna
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Ramachandran, P. Veeraraghavan, M. Venkat Ram Reddy, and Herbert C. Brown. "Tandem allylboration-ring-closing metathesis reactions for the preparation of biologically active molecules." Pure and Applied Chemistry 75, no. 9 (2003): 1263–75. http://dx.doi.org/10.1351/pac200375091263.

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The development of asymmetric synthesis during the past two decades aided organic chemists considerably in the synthesis of complex natural products. Organoborane chemistry continues to play an important role in asymmetric synthesis. One of the important reactions that has become very common in the arsenal of synthetic chemists is allylboration and related reactions. Another important reaction that has recently attained enormous importance in organic chemistry is the ring-closing metathesis (RCM) reaction. Indeed, a combination of allylboration and RCM reactions provides an excellent route to
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Bhandari, Meena, and Seema Raj. "PRACTICAL APPROACH TO GREEN CHEMISTRY." International Journal of Pharmacy and Pharmaceutical Sciences 9, no. 4 (2017): 10. http://dx.doi.org/10.22159/ijpps.2017v9i4.15640.

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Objective: The basic principles of green chemistry addresses various issues related to synthesis of chemical compounds: planning organic synthesis to maximise yield, prevention/minimization of waste, atom economy, the use of less lethal chemicals, use of safer solvents, renewable starting materials, energy efficiency and use of green catalysts. The objective of this study is to elaborate the practical approach of green methods.Methods: In this paper, we elucidate some important common syntheses having green procedures which can be used in the fields of pharmaceutical chemistry and other fields
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Dissertations / Theses on the topic "Chemistry synthesis"

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Lau, Shing Hing. "Organic synthesis : taming chemistry using enabling technologies." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/273347.

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This thesis describes the application of flow chemistry to discovery and development of medicinal compound synthesis and new chemical methodologies respectively. It is divided into three distinct sections. The first section addresses a brief introduction to flow chemistry, highlighting the advantages and challenges that have been faced in the past and present and also the outlook to the future. The second section reports the integration of machine-assisted methods with batch processes to produce two medicinal compounds, a precursor to the sacubitril and OZ439 respectively. In the respect to th
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Polywka, R. "Epoxide chemistry." Thesis, University of Oxford, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.258024.

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Pearson, Christopher I. "Lithiated azetidine and azetine chemistry." Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:cf3c942f-80de-4092-a38d-11006ccbb9ce.

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This work describes developments in new azetidine and azetine chemistry; specifically, methods developed for the introduction of functionality α- to nitrogen in both ring systems, with additionally in situ formation of the latter system, from azetidine substrates. Chapter 1 discusses the growing importance of azetidines, and the current methods available for making substituted azetidines by ring formation. Further discussion comprises of current sp<sup>3</sup> C–H activation approaches α- to nitrogen in heterocyclic compounds as potential methods for sp<sup>3</sup> C–H activation on azetidines
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Coates, Helen Margaret. "Synthetic studies towards stemofoline synthesis." Thesis, University of Southampton, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.238730.

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Ince, Julie. "Synthesis and chemistry of methyleneaziridines." Thesis, University of Exeter, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.267223.

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Al'Issa, Farouk. "Synthesis and chemistry of perfluoroalkylphosphines." Thesis, University of Manchester, 2014. https://www.research.manchester.ac.uk/portal/en/theses/synthesis-and-chemistry-of-perfluoroalkylphosphines(76d4e25b-9ed4-474a-9af1-e47693d7ee42).html.

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The synthesis of new perfluoroalkyl-containing phosphines from the reactions of the perfluoroalkyl iodides n-C3F7I, i-C3F7I, n-C4F9I, sec-C4F9I, cyc-C6F11Br or cyc-C6F11I, n-C6F13I and n-C8F17I with R2PSiMe3 or R2PLi (R = Ph2, t-Bu2, Et2, MePh and EtPh was investigated. The new perfluoroalkyl-containing phosphines were characterised by multinuclear NMR spectroscopy. The reaction between i-Pr2P-Pi-Pr2 and i-C3F7I resulted in some i-Pr2PCF(CF3)2, 11, but an elimination process was dominant. Compound 11 was obtained using a reaction of i-Pr2PCl with i-C3F7I in the presence of MePh2P, dpph, dppm,
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Thomas, David William. "Studies in peptide chemistry." Thesis, University of Oxford, 1988. http://ora.ox.ac.uk/objects/uuid:8cf7679d-1a0b-4163-b9dd-87363c9bf806.

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The thesis discusses the design of potential inhibitors of Angiotensin Converting Enzyme (ACE). The synthesis of pep tide inhibitors containing arginine and histidine-type residues is described. Successful incorporation of these residues during peptide synthesis requires the use of protecting groups on the side-chains* and new developments in this area are described. Ch. 1 reviews the currently available protecting groups for histidine. A methodology for regiospecific introduction of protecting groups of type ROCH<sub>2</sub>-, via their corresponding chloromethyl ethers, is described. A conve
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Ward, G. J. "Imidazolines in peptide chemistry." Thesis, University of Nottingham, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.381082.

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Chen, Yong. "Synthetic Studies on Total Synthesis of Azaspiracid-3." The Ohio State University, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=osu1385895424.

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Pearson, Jem M. "Hydrogen-bonding motifs for non-covalent synthesis." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:f0630898-35b4-4c74-bc31-dfd252c2ee26.

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This work describes the design and synthesis of a set of four organic molecules that are intended to hydrogen-bond to each other in a pairwise manner. The four hydrogen-bonding units, termed ‘A’, ‘B’, ‘C’ and ‘D’, when placed in solution together, are designed so that A binds only to B, and C binds only to D. Each unit does not bind to itself, nor to either of the other two units to which binding is not intended. For example, A binds to B, but not to A, C, or D. Each unit contains an array of four hydrogen-bonds for strong binding to its partner, is designed to be as rigid as possible, as non-
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Books on the topic "Chemistry synthesis"

1

Rahman, Atta-ur. Stereoselective synthesis in organic chemistry. Springer-Verlag, 1993.

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Benoiton, N. Leo. Chemistry of peptide synthesis. Taylor & Francis/CRC Press, 2006.

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Chemistry of peptide synthesis. Taylor & Francis/CRC Press, 2006.

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Volodarsky, Leonid B. Synthetic chemistry of stable nitroxides. CRC Press, 1994.

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Science of synthesis: Water in organic synthesis. Georg Thieme, 2012.

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Andreas, Gansäuer, and SpringerLink (Online service), eds. Radicals in Synthesis III. Springer Berlin Heidelberg, 2012.

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service), ScienceDirect (Online, ed. Modern inorganic synthetic chemistry. Elsevier, 2011.

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service), SpringerLink (Online, ed. Total Synthesis of Plakortide E and Biomimetic Synthesis of Plakortone B. Springer Berlin Heidelberg, 2012.

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Shono, Tatsuya. Electroorganic synthesis. Academic Press, 1991.

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Zvi, Rappoport, and Liebman Joel F, eds. The chemistry of cyclobutanes. Wiley, 2005.

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Book chapters on the topic "Chemistry synthesis"

1

Breslow, R. "Biomimetic Chemistry." In Chemical Synthesis. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0255-8_5.

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Schlosser, Manfred. "Organoalkali Chemistry." In Organometallics in Synthesis. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118484722.ch1.

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Knölker, Hans-Joachim. "Organoiron Chemistry." In Organometallics in Synthesis. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118484722.ch4.

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Bräse, Stefan. "Organopalladium Chemistry." In Organometallics in Synthesis. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118484722.ch5.

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Lipshutz, Bruce H. "Organocopper Chemistry." In Organometallics in Synthesis. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118651421.ch1.

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Ojima, Iwao, Alexandra A. Athan, Stephen J. Chaterpaul, Joseph J. Kaloko, and Yu-Han Gary Teng. "Organorhodium Chemistry." In Organometallics in Synthesis. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118651421.ch2.

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Montgomery, John. "Organonickel Chemistry." In Organometallics in Synthesis. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118651421.ch3.

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Krause, Norbert. "Organogold Chemistry." In Organometallics in Synthesis. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118651421.ch4.

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Smith, Keith. "Organoboron Chemistry." In Organometallics in Synthesis. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118750407.ch6.

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Nozaki, Hitosi. "Organotin Chemistry." In Organometallics in Synthesis. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118750407.ch8.

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Conference papers on the topic "Chemistry synthesis"

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Magalhaes, Elizabeth, and Ray Jones. "About the Royal Society of Chemistry." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-2013-about.

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Lima, Cíntia M. C. F., Maurício M. Victor, Lenilson C. Rocha, Alex H. Jeller, and and André L. M. Porto. "Synthesis of New Triazoles by Click Chemistry." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201391520366.

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Valdomir, Guillermo, José M. Padrón, Juan I. Padrón, Víctor S. Martín, and Danilo Davyt. "New modular structures constructed by click chemistry." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201381919619.

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Kimball, Gregory M., Nathan S. Lewis, and Harry A. Atwater. "Synthesis and surface chemistry of Zn3P2." In 2008 33rd IEEE Photovolatic Specialists Conference (PVSC). IEEE, 2008. http://dx.doi.org/10.1109/pvsc.2008.4922747.

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Hori, Kenji, Michinori Sumimoto, and Toshihiro Murafuji. "Quantum chemistry-assisted synthesis route development." In INTERNATIONAL CONFERENCE OF COMPUTATIONAL METHODS IN SCIENCES AND ENGINEERING 2015 (ICCMSE 2015). AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4938827.

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Sovera, V. de la, A. Bellomo, and D. Gonzalez. "Click Chemistry Approach to Structurally Simplified Pancratistatin Analogs." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0064-1.

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Jakubke, Hans-Dieter. "Enzymatic synthesis." In Future Aspect in Peptide Chemistry - Ringberg Conference. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 1999. http://dx.doi.org/10.1135/css199901047.

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Ducharme, Vincent, Richard Egli, and Claude Y. Legault. "Energy-based Artificial Chemistry Simulator." In International Conference on the Simulation and Synthesis of Living Systems. MIT Press, 2012. http://dx.doi.org/10.7551/978-0-262-31050-5-ch059.

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Valdomir, Guillermo, Juan Ignacio Padrón, Jenny Saldaña, et al. "Synthesis of hybrids compounds by Click Chemistry and their bioactivities." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0081-1.

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Lima, Cíntia Maria Carneiro Franco, and Maurício Moraes Victor. "Synthesis of Triazoles with Potential Antileishmanial Activity by Click Chemistry." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0321-1.

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Reports on the topic "Chemistry synthesis"

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Liu, Zhijian. Novel Aryne Chemistry in Organic Synthesis. Office of Scientific and Technical Information (OSTI), 2006. http://dx.doi.org/10.2172/897369.

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Trogler, William C. Synthesis and Chemistry of Energetic Metallotetraazadienes. Defense Technical Information Center, 1985. http://dx.doi.org/10.21236/ada166923.

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Brennan, J. G. Organoactinide chemistry: synthesis, structure, and solution dynamics. Office of Scientific and Technical Information (OSTI), 1985. http://dx.doi.org/10.2172/6147151.

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Hare, Michael. The synthesis and chemistry of N-chlorosulfenylaziridines. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.6203.

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Lemal, David M. Synthesis and Chemistry of Novel Cyclic Fluorocarbons. Defense Technical Information Center, 1993. http://dx.doi.org/10.21236/ada267148.

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Hidy, George M. Synthesis and Integration of Energy Related Tropospheric Chemistry Research. Office of Scientific and Technical Information (OSTI), 2007. http://dx.doi.org/10.2172/897518.

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Liu, Haitao. Chemistry of the Colloidal Group II-VI Nanocrystal Synthesis. Office of Scientific and Technical Information (OSTI), 2007. http://dx.doi.org/10.2172/918668.

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Kipp, D. O., C. K. Lowe-Ma, and T. A. Vanderah. Crystal Chemistry, Synthesis, and Characterization of Infrared Optical Materials. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada208723.

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Evans, W. J. Synthesis and chemistry of yttrium and lanthanide metal complexes. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/6267724.

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Christe, K. O., W. W. Wilson, A. Vij, V. Vij, and J. A. Sheehy. Use of Fluorine Chemistry for the Synthesis of Polynitrogen Compounds. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada409532.

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