Relevant bibliographies by topics / Organic chemistry - Synthesis

Contents

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

Academic literature on the topic 'Organic chemistry - Synthesis'

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

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Journal articles on the topic "Organic chemistry - Synthesis"

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Dai, Mingji, Xinpei Cai, and Yu Bai. "Total Syntheses of Spinosyn A." Synlett 29, no. 20 (September 7, 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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Kaur, Navjeet. "Photochemical Reactions for the Synthesis of Six-Membered O-Heterocycles." Current Organic Synthesis 15, no. 3 (April 27, 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 disposal. The formation of byproducts was diminished under photochemical substrate activation that usually occurred without additional reagents. Photochemical irradiation is becoming more interesting day by day because of easy purification of the products as well as green chemistry. Conclusion: This review article represents the high applicability of photochemical reactions for organic synthesis and research activities in organic photochemistry. The synthesis of heterocyclic molecules has been outlined in this review. Traditional approaches require expensive or highly specialized equipment or would be of limited use to the synthetic organic chemist due to their highly inconvenient approaches. Photochemistry can be used to prepare a number of heterocycles selectively, efficiently and in high yield.
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Muldakhmetov, Z. М. "Institute of Organic Synthesis and Coal Chemistry: the present state and development prospects." Bulletin of the Karaganda University. "Chemistry" series 94, no. 2 (June 28, 2019): 88–104. http://dx.doi.org/10.31489/2019ch2/88-104.

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Elgemeie, Galal H., and Doaa M. Masoud. "Recent trends in microwave assisted synthesis of fluorescent dyes." Pigment & Resin Technology 45, no. 6 (November 7, 2016): 381–407. http://dx.doi.org/10.1108/prt-04-2015-0036.

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Purpose This paper aims to focus on the most popular technique nowadays, the use of microwave irradiation in organic synthesis; in a few years, most chemists will use microwave energy to heat chemical reactions on a laboratory scale. Also, many scientists use microwave technology in the industry. They have turned to microwave synthesis as a frontline methodology for their projects. Microwave and microwave-assisted organic synthesis (MAOS) has emerged as a new “lead” in organic synthesis. Design/methodology/approach Using microwave radiation for synthesis and design of fluorescent dyes is of great interest, as it decreases the time required for synthesis and the synthesized dyes can be applied to industrial scale. Findings The technique offers many advantages, as it is simple, clean, fast, efficient and economical for the synthesis of a large number of organic compounds. These advantages encourage many chemists to switch from the traditional heating method to microwave-assisted chemistry. Practical implications This review highlights applications of microwave chemistry in organic synthesis for fluorescent dyes. Fluorescents are a fairly new and very heavily used class of organics. These materials have many applications, as a penetrant liquid for crack detection, synthetic resins, plastics, printing inks, non-destructive testing and sports ball dyeing. Originality/value The aim value of this review is to define the scope and limitation of microwave synthesis procedures for the synthesis of novel fluorescent dyes via a simple and economic way.
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Huang, Jianhui, Caifeng Li, Liu Liu, and Xuegang Fu. "Norbornene in Organic Synthesis." Synthesis 50, no. 15 (June 25, 2018): 2799–823. http://dx.doi.org/10.1055/s-0037-1610143.

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The norbornene skeleton possesses an alkene functionality with a fixed conformation, and represents unique reactivity. The use of norbornene and analogues as substrates is overviewed; reactivities are discussed as well as the role of norbornenes as ligands assisting modern organic transformations.1 Introduction2 Synthesis of Substituted Norbornenes2.1 Preparation of Functionalized Norbornenes by Deprotonation and Substitution Reactions2.2 Preparation of Functionalized Norbornenes under Palladium-Catalyzed­ Reaction Conditions2.3 Alkylation of Norbornene2.4 Multistep Synthesis3 Synthesis of Substituted Norbornanes3.1 Three-Membered-Ring Formation3.2 Formation of Four-Membered Rings3.3 Five- and Six-Membered Ring Formation3.4 Syntheses of Difunctionalized Norbornanes4 Synthesis of Cyclopentanes4.1 Oxidation Reactions4.2 Ring-Opening Cross Metathesis (ROCM)4.3 Ring-Opening Metathesis Polymerization (ROMP)4.4 Palladium-Catalyzed Ring-Opening of Norbornene5 Norbornene-Mediated Reactions5.1 Palladium Insertion into Carbon–Halide Bonds5.2 Palladium Insertion into N–H and C–H Bonds5.3 Norbornene as Ligand in Mediated Reactions6 Conclusion
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Ley, Steven V., Richard J. Ingham, Matthew O’Brien, and Duncan L. Browne. "Camera-enabled techniques for organic synthesis." Beilstein Journal of Organic Chemistry 9 (May 31, 2013): 1051–72. http://dx.doi.org/10.3762/bjoc.9.118.

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A great deal of time is spent within synthetic chemistry laboratories on non-value-adding activities such as sample preparation and work-up operations, and labour intensive activities such as extended periods of continued data collection. Using digital cameras connected to computer vision algorithms, camera-enabled apparatus can perform some of these processes in an automated fashion, allowing skilled chemists to spend their time more productively. In this review we describe recent advances in this field of chemical synthesis and discuss how they will lead to advanced synthesis laboratories of the future.
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Takahashi, Takashi, and Takayuki Doi. "Combinatorial Chemistry in Organic Synthesis." Journal of Synthetic Organic Chemistry, Japan 60, no. 5 (2002): 426–33. http://dx.doi.org/10.5059/yukigoseikyokaishi.60.426.

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Hong, Ro Bin, and Hong Mei Wang. "Development of Experimental System in Organic Synthesis." Advanced Materials Research 490-495 (March 2012): 3207–10. http://dx.doi.org/10.4028/www.scientific.net/amr.490-495.3207.

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Organic synthesis chemistry is a very fast-growing discipline and it plays a very important role in chemistry. With the development of organic synthetic chemistry, organic synthesis device has also made greater development. At the same time, advances of organic synthesis device further promote the development of organic synthetic chemistry. This paper describes the working principle and system architecture of organic synthesis device and takes a case of di-n-butyl phthalate (DBP). At last, I foresee great prospect for organic synthesis
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Meng, Yan-Ping, Shi-Meng Wang, Wan-Yin Fang, Zhi-Zhong Xie, Jing Leng, Hamed Alsulami, and Hua-Li Qin. "Ethenesulfonyl Fluoride (ESF) and Its Derivatives in SuFEx Click Chemistry and More." Synthesis 52, no. 05 (December 9, 2019): 673–87. http://dx.doi.org/10.1055/s-0039-1690038.

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The sulfur(VI) fluoride exchange reaction (SuFEx), developed by Sharpless and co-workers in 2014, is a new category of click reaction that creates molecular connections with absolute reliability and unprecedented efficiency through a sulfur(VI) hub. Ethenesulfonyl fluoride (ESF), as one of the most important sulfur(VI) hubs, exhibits extraordinary reactivity in SuFEx click chemistry and organic synthesis. This review summarizes the chemical properties and applications of ESF in click chemistry, organic chemistry, materials science, medicinal chemistry and in many other fields related to organic synthesis.1 Introduction2 Chemical Transformations of ESF3 Chemical Transformations of 2-Arylethenesulfonyl Fluorides4 Novel SuFEx Reagents Derived from ESF5 Applications of ESF Derivatives in Medicinal Chemistry6 Applications of ESF Derivatives in Materials Science7 Conclusion
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Salame, Issa I., Pauline Casino, and Natasha Hodges. "Examining Challenges that Students Face in Learning Organic Chemistry Synthesis." International Journal of Chemistry Education Research 3, no. 3 (May 22, 2020): 1–9. http://dx.doi.org/10.20885/ijcer.vol4.iss1.art1.

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Organic chemistry is the offered after general chemistry and is the course that many find it challenging and difficult. Synthesis is first introduced in organic chemistry I course and is widely considered as one of the topics in which students struggle with and is evident in their performance in the topic. Our method of data collection is a Likert-type and open-ended questionnaire that was distributed at the end organic chemistry I course in an anonymous fashion. The collected data enabled us to examine the challenges students face in learning organic chemistry synthesis. Our findings support the notion that students have many difficulties with multistep organic chemistry synthesis including challenges recalling all of the varied required reactions, the amount of content and topics covered in organic chemistry, conceptual understanding of needed important topics such as mechanisms, acids and bases, nucleophiles and electrophiles, and stereochemistry, and problem-solving competency. Students view organic chemistry synthesis as challenging because of their reliance on memorization of a large number of reactions, reagents, and rules, poor conceptual understanding of the topics, ineffective teaching methods which lacks active learning and student engagement, and the myriad number of possible pathways to solve synthesis problems. Our participants suggest that memorization and rote-learning plays an important role in the learning of multistep organic synthesis, which might cause a hindrance to process of learning and can impede students’ problem-solving ability.
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Dissertations / Theses on the topic "Organic 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 the precursor to sacubritil, a flow-batch integrated synthesis is developed to provide the desired product in 54% yield over 7 steps from commercially available 4-iodophenyl. In particular, a tube-in-tube gas flow reactor was employed in three gas-liquid reactions without the need for installing a costly highpressure autoclave. These gas-lquid reactions were an ethylene Heck coupling reaction, an anti-Markovnikov Wacker oxidation and a rhodium-catalysed stereoselective hydrogenation respectively. In addition, a diastereoselective Reformatsky-type carbethoxyallylation using zinc metal was also highlighted in this synthesis to install an important stereocentre. A new antimalarial agent, OZ439 containing a trioxolane unit as the main structural feature, has the unique property of providing a single-dose cure for malaria in humans and has recently completed phase IIb trials. A machine-enabled process for the preparation of OZ439 was developed in 33% overall yield over 5 steps without the need of column chromatography purification. This preparation features a selective continuous hydrogrenation, Griesbaum ozonlysis and a Zn-catalysed amide reduction in the present of triethoxylsilane. The third section contains the development of two new methodologies of diazo compounds with organoboron compounds. The first methodology involves an in situ generation of transient allylic boronic species by reacting TMSCHN2 and E-vinyl boronic acids in flow, followed by subsequent trapping with a range of aldehydes (15 examples, 55-97% yield) and on a large scale (10 mmol) to provide homoallylic alcohols with high diastereoselectivity (>20:1 dr confirmed by 1H NMR). This multicomponent metal-free reaction could also be applied under batch conditions (20 further examples, 60-82% yield). The second methodology involves the preparation of an organodimetallic compound, α-trimethylsilyl benzylboronic acid pinacol esters, by reacting TMSCHN2 and phenylboronic anhydrides (21 examples, 60-91% yield), and the development of their applications as bifunctional building blocks to complex structures.
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Liu, Zhijian. "Novel aryne chemistry in organic synthesis." [Ames, Iowa : Iowa State University], 2006.

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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 sp3 C–H activation approaches α- to nitrogen in heterocyclic compounds as potential methods for sp3 C–H activation on azetidines to give substituted azetidines. Previous work by the Hodgson group in this area is detailed. Chapter 2 describes the advance made towards 2,3-disubstituted azetidines using the thiopivaloyl protecting/activating group, where the latter plays a key role. Optimisation, scope, selectivity and mechanistic insight into the α-deprotonation–electrophile trapping of a 3-hydroxy azetidine system is discussed, which successfully gives access to a range of 3-hydroxy-2-substituted azetidines. Preliminary investigations with 3-alkyl-2-substituted azetidines are also described. Chapter 3 describes the development of a straightforward protocol to make 2-substituted-2- azetines, a rarely studied and difficult to access 4-membered azacycle subclass, from readily accessible azetidine starting materials using α-deprotonation–in situ elimination followed by further α-lithiation–electrophile trapping. Extension of this methodology by transmetallation from the intermediate organolithium to the organocuprate, resulting in greater electrophile scope, is also described.
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Roper, Kimberley Ann. "New flow chemistry methods for organic synthesis." Thesis, University of Cambridge, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607846.

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Short, Robert Paul 1951. "Organoboranes in organic synthesis." Thesis, Massachusetts Institute of Technology, 1989. http://hdl.handle.net/1721.1/14204.

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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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Tilliet, Mélanie. "Synthesis and study of new oxazoline-based ligands." Doctoral thesis, KTH, Organisk kemi, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4858.

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This thesis deals with the study of oxazoline-based ligands in metal-catalyzed asymmetric reactions. The first part describes the synthesis of six new bifunctinal pyridine-bis(oxazoline) ligands and their applications in asymmetric metal-catalysis. These ligands, in addition to a Lewis acid coordination site, are equipped with a Lewis basic part in the 4-position of the oxazoline rings. Dual activation by means of this system was probed in cyanide addition to aldehydes. The second part is concerned with the synthesis of two pyridine-bis(oxazoline) ligands bearing bulky triazole groups in the 4-position of the oxazoline rings and a macrocyclic ligand consisting of a pyridine-bis(oxazoline) moiety and a diaza-18-crown-6 ether. The synthesis of these compounds benefits from the use of “click chemistry”. The ligands thus obtained were tested in different asymmetric catalytic reactions. Complexation studies with different bifunctional molecules that could bind into the cavity of the macrocycle were carried out using NMR spectroscopy. A third chapter is devoted to the synthesis of a supported pyridine-bis(oxazoline) catalyst and its use in catalysis. The pyridine-bis(oxazoline) ligand was efficiently connected to a polystyrene resin via a robust triazole linker. This resin could be employed in different metal-catalyzed asymmetric reactions and good results were obtained in terms of yield and enantioselectivity. Moreover, this polymer-bound ligand could be easily and efficiently recycled. Finally, the last part deals with the use of a hydroxy-containing phosphinooxazoline ligand in the hydrosilylation of imines and in the asymmetric intermolecular Heck reaction. A cationic iridium complex of this ligand was studied by NMR spectroscopy.
QC 20100914
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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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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-tautomeric as possible, and utilises a staggered non-symmetrical architecture. Of the four intended compounds, three were successfully synthesised (A, B and D). Units B and D were soluble in CDCl3, but Unit A was not. Therefore, the design and synthesis of Unit A was amended, and two variants of Unit A that are both soluble in CDCl3 were successfully synthesised. 1H NMR binding experiments were performed between Unit B and each of the two variants of Unit A. Their binding behaviour was described. A binding constant could not be calculated because the units did not bind in a 1:1 fashion.
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Kang, G. S. "Applications of boron chemistry to organic synthesis." Thesis, Swansea University, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.637757.

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Chapter 1 deals with an investigation into the synthesis of α-aminoboronic acids and their attempted incorporation into targeted peptides. This approach, developed by Matteson, is the only methodology for the preparation of α-aminoboronates. Chapter 2 deals with an alternative route, developed by the author, to the synthesis of α-aminoboronates; an approach which is based upon the hydroboration of a nitrogen-substituted carbon-carbon double bond with a range of achiral and chiral dialkylboranes of varying steric requirement. Chapter 3 introduces the subject of boron-stabilised carbanions, with a discussion of structure, stabilisation, methods for their preparation and their application to general organic synthesis. Chapter 4 discusses methods for the production of less bulky boron stabilised carbanions derived from B-alkyl-9-borabicyclo[3.3.1]nonane by utilising a range of hindered bases. In addition, this chapter deals with the development of an alternative route to the generation of boron-stabilised carbanions via the use of gem-dimetallic compounds and their reactions with a range of enolisable and non-enolisable ketones. Chapter 5 reports on the use of alkylditripylhydroborates, a novel class of highly hindered reducing agents and specifically on the use of lithium ethylditripylhydroborate as a reagent for the reduction of a range of organic compounds containing representative functional groups. The catalytic properties of the hydroborate in the reduction of haloalkanes in the presence of metal hydride are also discussed.
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Books on the topic "Organic chemistry - Synthesis"

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

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Atta-ur-Rahman and Zahir Shah. Stereoselective Synthesis in Organic Chemistry. New York, NY: Springer New York, 1993. http://dx.doi.org/10.1007/978-1-4613-8327-7.

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Dianion chemistry in organic synthesis. Boca Raton: CRC Press, 1994.

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Mukaiyama, Teruaki. Challenges in synthetic organic chemistry. Oxford: Clarendon, 1990.

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1966-, Thomas Russell J., ed. Exercises in synthetic organic chemistry. Oxford: Oxford University Press, 1997.

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

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Serratosa, Fèlix. Organic chemistry in action: The design of organic synthesis. 2nd ed. Amsterdam: Elsevier, 1996.

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Josep, Xicart, ed. Organic chemistry in action: The design of organic synthesis. Amsterdam: Elsevier, 1990.

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Wong, Chi-Huey. Enzymes in synthetic organic chemistry. Oxford, U.K: Pergamon, 1994.

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Shōno, T. Electro-organic synthesis. London: Academic, 1991.

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Book chapters on the topic "Organic chemistry - Synthesis"

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Jacquesy, Jean-Claude. "Organic Synthesis in Superacids." In Carbocation Chemistry, 359–76. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9780471678656.ch14.

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Bazureau, Jean Pierre, Ludovic Paquin, Daniel Carrié, Jean Martial L'Helgoual'ch, Solène Guihéneuf, Karime Wacothon Coulibaly, Guillaume Burgy, Sarah Komaty, and Emmanuelle Limanton. "Microwaves in Heterocyclic Chemistry." In Microwaves in Organic Synthesis, 673–735. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527651313.ch16.

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Bogdal, Dariusz, and Urszula Pisarek. "Polymer Chemistry Under Microwave Irradiation." In Microwaves in Organic Synthesis, 1013–57. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527651313.ch22.

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Rasmussen, Brian, Anne Sørensen, Sophie R. Beeren, and Michael Pittelkow. "Dynamic Combinatorial Chemistry." In Organic Synthesis and Molecular Engineering, 393–436. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118736449.ch14.

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Feuerbacher, Nina, and Fritz Vögtle. "Iterative Synthesis in Organic Chemistry." In Dendrimers, 1–18. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/3-540-69779-9_1.

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Ahluwalia, V. K., and M. Kidwai. "Biocatalysts in Organic Synthesis." In New Trends in Green Chemistry, 88–107. Dordrecht: Springer Netherlands, 2004. http://dx.doi.org/10.1007/978-1-4020-3175-5_11.

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Hoffmann, Reinhard W. "Biomimicry in Organic Synthesis." In Bioinspiration and Biomimicry in Chemistry, 419–53. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118310083.ch14.

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Fürstner, Alois. "Alkyne Metathesis in Organic Synthesis." In Modern Alkyne Chemistry, 69–112. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527677894.ch4.

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Lubineau, A., J. Augé, and Y. Queneau. "Carbonyl additions and organometallic chemistry in water." In Organic Synthesis in Water, 102–40. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-4950-1_4.

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Nagaki, Aiichiro, and Jun-Ichi Yoshida. "Microreactor Technology in Lithium Chemistry." In Lithium Compounds in Organic Synthesis, 491–512. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.ch17.

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Conference papers on the topic "Organic chemistry - Synthesis"

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Magalhaes, Elizabeth, and Ray Jones. "About the Royal Society of Chemistry." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: 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. São Paulo: 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. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201381919619.

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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. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0064-1.

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Valdomir, Guillermo, Juan Ignacio Padrón, Jenny Saldaña, José Manuel Padrón, Gloria Serra, Eduardo Manta, Victor S. Martín, and Danilo Davyt. "Synthesis of hybrids compounds by Click Chemistry and their bioactivities." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: 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. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0321-1.

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Neier, Reinhard. "A Novel Synthesis of Porphobilinogen: Synthetic and Biosynthetic Studies." In The 3rd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1999. http://dx.doi.org/10.3390/ecsoc-3-01765.

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Moreira, Bárbara V., and Cristiano Raminelli. "Synthesis of 3-hydroxy-2-(trimethylsilyl)phenyl trifluoromethanesulfonate as a versatile intermediate in preparative organic chemistry." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201391593549.

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Toledo, P. R. S., D. M. Oliveira, J. G. Ferreira, D. M. S. Leotério, S. Alves Jr, and J. L. Princival. "Synthesis of novel optically active ligants to coordination chemistry and its application in the organic reactions." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0368-1.

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10

Wallace, Owen. "Automated Synthesis of Small, Organic Therapeutics." In The 2nd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1998. http://dx.doi.org/10.3390/ecsoc-2-01691.

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Reports on the topic "Organic chemistry - Synthesis"

1

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

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Bump, Charles, Kesete Ghebreyessus, Edmund M. Ndip, Godson C. Nwokogu, and Michelle K. Waddell. Purchase of Microwave Reactors for Implementation of Small-scale Microwave-accelerated Organic Chemistry Laboratory Program in Undergraduate Curriculum and Synthetic Chemistry Research at HU. Fort Belvoir, VA: Defense Technical Information Center, April 2015. http://dx.doi.org/10.21236/ad1001096.

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