Relevant bibliographies by topics / Cumulenes; organic compounds synthesis

Academic literature on the topic 'Cumulenes; organic compounds synthesis'

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Published: 10 December 2022
Last updated: 28 January 2023

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Journal articles on the topic "Cumulenes; organic compounds synthesis"

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Mai, Juri, and Sascha Ott. "The Fascinating World of Phosphanylphosphonates: From Acetylenic Phosphaalkenes to Reductive Aldehyde Couplings." Synlett 30, no. 16 (August 13, 2019): 1867–85. http://dx.doi.org/10.1055/s-0039-1690129.

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This account highlights the versatility of phosphanylphosphonates, which can be used for the preparation of phosphorus-containing π-systems and as reagents for the reductive coupling of carbonyl compounds to alkenes. Phosphanylphosphonates with metal fragments coordinated to the P-lone pair have been known for a long time and they have been used for the synthesis of phosphaalkenes by means of the phospha-Horner–Wadsworth–Emmons reaction. With the original aim of incorporating phosphorus heteroatoms into classical all-carbon ethynylethene scaffolds, we entered the field of phosphanylphosphonates with the discovery that these compounds engage in complex cascade reactions with acetylenic ketones, forming 1,2-oxaphospholes, cumulenes, and bisphospholes. Later, we synthesized the first metal-free phosphanylphosphonate, which reacts with aldehydes to yield phosphaalkenes, but gives phospholones when diacetylenic ketones are used as substrates. In the final part of the account, we outline our discovery and the development of an unprecedented carbonyl–carbonyl cross-coupling reaction. This protocol offers a straightforward method for the synthesis of nonsymmetric 1,2-disubstituted alkenes directly from two dissimilar aldehydes.1 Combining Acetylenes with Phosphaalkenes2 Synthetic Examples of Acetylenic Phosphaalkenes3 The Phospha-Horner–Wadsworth–Emmons Approach to Phosphaalkenes3.1 Metal-Coordinated Phosphanylphosphonates3.2 Mechanism of the Phospha-Horner–Wadsworth–Emmons Reaction3.3 The First Metal-Free Phosphanylphosphonate and Its Reactivity with Aldehydes4 Reactions with Acetylenic Ketones4.1 Metal-Coordinated Phosphanylphosphonate and Monoacetylenic Ketones4.2 Metal-Coordinated Phosphanylphosphonate and Diacetylenic Ketones4.3 Metal-Free Phosphanylphosphonate and Diacetylenic Ketones5 Metal-Free Phosphanylphosphonate as a Coupling Reagent for Aldehydes6 E-Alkenes by the Reductive Coupling of Two Aldehydes7 Conclusions and Outlook
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Hopf, Henning, and Georgios Markopoulos. "The chemistry of bisallenes." Beilstein Journal of Organic Chemistry 8 (November 15, 2012): 1936–98. http://dx.doi.org/10.3762/bjoc.8.225.

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This review describes the preparation, structural properties and the use of bisallenes in organic synthesis for the first time. All classes of compounds containing at least two allene moieties are considered, starting from simple conjugated bisallenes and ending with allenes in which the two cumulenic units are connected by complex polycyclic ring systems, heteroatoms and/or heteroatom-containing tethers. Preparatively the bisallenes are especially useful in isomerization and cycloaddition reactions of all kinds leading to the respective target molecules with high atom economy and often in high yield. Bisallenes are hence substrates for generating molecular complexity in a small number of steps (high step economy).
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Santos, Jose, Pavel Jelínek, David Ecija, and Nazario Martin. "(Invited) On-Surface Synthesis of Acene Polymers." ECS Meeting Abstracts MA2022-01, no. 11 (July 7, 2022): 811. http://dx.doi.org/10.1149/ma2022-0111811mtgabs.

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The design and study of π-conjugated polymers has received great attention along the last decades. The relevant optical and electronic properties stemming from their delocalised π-electrons allow for a number of applications in the emerging field of organic electronics. However, the inherent limited solubility of planar π-conjugated systems hinders their development, forcing chemists to introduce ancillary solubilising side-chains. On the other hand, ultrahigh-vacuum on-surface synthesis has become a powerful discipline that enables designing with atomistic precision a new plethora of molecular compounds, polymers, and nanomaterials that otherwise are unachievable by conventional organic chemistry. Herein we present a novel on-surface chemical transformation that allows obtaining π-conjugated acene polymers from simple aromatic molecules carrying =CBr2 functionalities. The deposition of such precursors on an Au(111) surface gives rise to close-packed assemblies. Thermal annealing promotes the debromination of the species that thereafter homocouple and give rise to long anthracene wires linked by acetylene bridges, featuring a bandgap of 1.5 eV (see figure below). When larger acenes or periacenes are used (i.e. pentacene, bisanthene, peripentacene) the resulting polymers undergo dramatic structural and electronic changes. Non-contact-AFM evince that the benzoid subunits evolve from aromatic (anthracene) to quinoid (pentacene, bisanthene...), while the alkyne linkers turn into cumulenic. The STM images allow witnessing the HOMO-LUMO levels crossing from anthracene to pentacene. This swap destabilises the aromatic structure and enables a biradical-quinoid one, that permit almost vanishing bandgaps below 0.35 eV. These findings can also be rationalised by topological band gap theory: DFT, tight binding and GW calculations predict that polymers these quasi-metallic polymers exhibit a topologically non-trivial electronic structure. Our results herald novel pathways to engineer π-conjugated polymers on solid surfaces, addressing the relevant family of acenes and, thus, contributing to develop the field of on-surface chemistry and to steer the design of modern low bandgap polymers. Figure 1
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Gawel, Przemyslaw, Elias A. Halabi, David Schweinfurth, Nils Trapp, Laurent Ruhlmann, Corinne Boudon, and François Diederich. "Synthesis of Dicyano-Substituted Benzo[c]fluorenes from Tetraaryl[3]cumulenes." European Journal of Organic Chemistry 2016, no. 17 (May 30, 2016): 2919–24. http://dx.doi.org/10.1002/ejoc.201600470.

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Yranzo, Gloria I., José Elguero, Robert Flammang, and Curt Wentrup. "Formation of Cumulenes, Triple-Bonded, and Related Compounds by Flash Vacuum Thermolysis of Five-Membered Heterocycles." European Journal of Organic Chemistry 2001, no. 12 (June 2001): 2209–20. http://dx.doi.org/10.1002/1099-0690(200106)2001:12<2209::aid-ejoc2209>3.0.co;2-x.

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MURAHASHI, Shun-Ichi, and Takeshi NAOTA. "Organic synthesis using ruthenium compounds." Journal of Synthetic Organic Chemistry, Japan 46, no. 10 (1988): 930–42. http://dx.doi.org/10.5059/yukigoseikyokaishi.46.930.

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KUSAMA, Hiroyuki, and Koichi NARASAKA. "Rhenium Compounds in Organic Synthesis." Journal of Synthetic Organic Chemistry, Japan 54, no. 8 (1996): 644–53. http://dx.doi.org/10.5059/yukigoseikyokaishi.54.644.

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SHINOKUBO, Hiroshi, and Koichiro OSHIMA. "Organic Synthesis Using Organomanganese Compounds." Journal of Synthetic Organic Chemistry, Japan 57, no. 1 (1999): 13–23. http://dx.doi.org/10.5059/yukigoseikyokaishi.57.13.

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Negishi, Ei-ichi, and Tamotsu Takahashi. "Organozirconium Compounds in Organic Synthesis." Synthesis 1988, no. 01 (1988): 1–19. http://dx.doi.org/10.1055/s-1988-27453.

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Sadekov, Igor D., B. B. Rivkin, and Vladimir I. Minkin. "Organotellurium Compounds in Organic Synthesis." Russian Chemical Reviews 56, no. 4 (April 30, 1987): 343–54. http://dx.doi.org/10.1070/rc1987v056n04abeh003275.

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Dissertations / Theses on the topic "Cumulenes; organic compounds synthesis"

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Fitzgerald, Mark. "The mass spectrometric and theoretical study of some cumulene oxides of potential interstellar significance : submitted for the degree of Doctor of Philosophy (Ph.D.) /." Title page, table of contents and abstract only, 2004. http://web4.library.adelaide.edu.au/theses/09PH/09phf5531.pdf.

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Newington, Ian M. "Azo-anions in organic synthesis." Thesis, University of Oxford, 1985. http://ora.ox.ac.uk/objects/uuid:690ab891-be13-4582-a029-47974d20adac.

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Novel synthetic applications of ambident azo-anions derived from hindered hydrazones have been investigated. Reaction with electrophiles occurred predominantly at carbon as the N-addition pathway was sterically retarded. Trityl, diphenyl-4-pyridylmethyl (DPP) benzhydryl, and t-butyldiphenylmethyl (BDP) hydrazones of various aldehydes and ketones were prepared in good yields from the corresponding hydrazines and carbonyls in aqueous methanol. The lithium salts derived from trityl and DPP hydrazones, by treatment with methyl lithium at -55°C, reacted with aldehydes and ketones to generate azo-alkoxides. These could be diverted to alcohols,by sequential protonation and spontaneous homolysis (about -20°C) in the presence of ethanethiol, or to alkenes,by treatment with phosphorus trichloride at -78 G followed by azo-homolysis. The reactions enabled efficient reductive cross-coupling of aldehydes and ketones. The mechanism of the alkene forming reaction was investigated. Anions of benzhydryl hydrazones were found to react inefficiently by a G-addition pathway giving mainly N-addition products. Anions of BDP hydrazones conveniently gave excellent yields of azo-alkanes upon treatment with alkyl halides,but no products were obtained on reaction with carbonyl electrophiles. The azo-alkanes could be isolated and purified and acted as key intermediates for several synthetically useful transformations. Homolysis in refluxing benzene with thiophenol gave alkanes in good yields. Phenylselenenyl-, bromo-, and chloro-alkanes,and β-alkylstyrenes were generated when thiol was replaced by diphenyl diselenide, N-bromosuccinimide, N-chlorosuccinimide and β-nitrostyrene respectively. Treatment of the azo-alkanes with trifluoroacetic acid generated benzophenone alkylhydrazones. These were dissolved in ethanol with concentrated hydrochloric acid, thereafter hydrolysis yielded alkylhydrazines or treatment with hydrogen (1 atm., 50°C, 20h) over 10% Pd/C generated primary amines by a novel use of carbonyls as α-aminocarbanion equivalents.
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Reynolds, Stephen J. "Carbamoylcobalt (III) compounds in organic synthesis." Thesis, University of Nottingham, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.280294.

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This thesis describes the development and use of organocobalt (III) compounds in the formation of carbon-carbon and carbon-heteroatom bonds and, in particular, details the application of this chemistry for the synthesis of functionalised amides and ~, 1" and 8-lactams. Organocobalt chemistry was born from the isolation and characterisation of the vitamin B12 coenzyme (2) in the 1950s and early 1960s. The introduction to this thesis covers the search for vitamin B12 and briefly describes its biological role. Next, the considerable development of the simple vitamin B12 analogues, i.e. organocobalt (II) salophens (10), is outlined. Finally, the exploitation of organocobalt (III) complexes in synthetic organic chemistry is detailed. The preparation of nitrogen heterocycles is initially addressed, with a study of the viability of carbamoylcobalt (III) salophen compounds, i.e. (68), as sources of carbamoyl radicals, i.e. (73), in Chapter 1 of the thesis. Thus, radical quenching, employing several heteroatom trapping agents, successfully afforded the amide derivatives (74) and (75). In addition, carbamoyl radicals were induced to undergo intermolecular oxidative additions to deactivated alkenes, under both thermal and photolytic conditions, to secure the cinnamamides (77) and (78). A unique approach to /3-, y- and o-lactams using cobalt-mediated radical chemistry is described in Chapter 2. Thus, the carbamoylcobalt (m) salophen (111) underwent sequential homolysis, 4-exo-trigonal radical cyclisation, and radical-cobalt (II) recombination, to create the unusual azetidin-2-one (114), which was subsequently transformed into the alcohol (125). Computer generated molecular modelling calculations supporting the novel radical cyclisation are presented. Next, analogous cyclisations are described with the homologous carbamoylcobalt (III) salophens (138) and (150). Subsequent in situ dehydrocobaltation secured the y-lactams (140) and (141), and the 8-lactams (151) and (152). Results concerning the introduction of oxygenation in tandem with cyclisation are also presented in Chapter 2. Chapter 3 of the thesis describes a novel synthetic approach to the broad-spectrum antibiotic (+)-thienamycin (56), harnessing a cobaltmediated 4-exo radical cyclisation as the key step. Model studies showed that the cyclisation would tolerate a range of substitution around the precursor, i.e. (165) and (179), and that the stereochemical outcome delivers the required 3,4-trans geometry for thienamycin, i.e. (187)~(182). Our initial synthetic target towards (56) was the acid (196), but the route was abandoned when the carbamoyl chloride (193) failed to yield the organocobalt (III) compound (194) on treatment with sodium cobalt (I) salophen (12). However, our second approach was successful and culminated in the preparation of the /J-lactam (200), which constituted a fonnal synthesis of (+)-thienamycin. Our synthetic route to (200) involved: (i) the preparation of the amine (197) via Wittig methodology, i.e. (203)~(205); (ii) conversion of (197) to the radical precursor (198); (iii) a 4-exo radical cyclisation to afford the 3,4-transazetidin- 2-one (199) and finally, (iv) a two step sequence to yield the /3- lactam (200).
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Kim, Byeongmoon 1957. "Asymmetric organic synthesis using organoboron compounds." Thesis, Massachusetts Institute of Technology, 1987. http://hdl.handle.net/1721.1/14679.

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Haughey, Simon Anthony. "Chemoenzymatic synthesis of organosulfur compounds." Thesis, Queen's University Belfast, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318731.

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Kou, Xiaodi. "Synthesis, characterization and reactivity of organic bismuth compounds." Fort Worth, Tex. : Texas Christian University, 2007. http://etd.tcu.edu/etdfiles/available/etd-07312007-125631/unrestricted/kou.pdf.

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Buckley, Anne Margaret. "Inorganic-organic layer compounds : synthesis and properties." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.253398.

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Hamilton, A. L. "Applications of lithium compounds in organic synthesis." Thesis, Swansea University, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.637209.

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The lithiation and subsequent condensation with an electrophile is a useful reaction in many 'total' syntheses. This study was undertaken to investigate the lithiation reactions of several organic molecules. In Chapters 2 and 3, the lithiation of a range of N-pivaloyl-o-toluidines was studied, with the resultant formation of indoles (Chapter 2) and reaction with carbon monoxide to form a carbonylated product (Chapter 3). The lithiation reaction was then applied to 2,5-dimethyl-1,4-phenylene-di-N-pivaloylamine as an attempt to effect quadruple lithiation. However, only double lithiation was observed. In Chapter 4, the attempted lithiation of trifluoroacetylanilines, was studied to see whether it is possible to effect lithiation on the aromatic ring to yield a dianion. Both alkyl and aryllithium reagents were observed to act as nucleophiles towards the substrates, resulting in displacement of the trifluoromethyl group. In Chapters 5, 6 and 7, lithiation of pyridones was investigated. Lithiation and electrophile trapping were found to readily occur for 3-methyl- (Chapter 6) and 6-methyl-2-pyridone (Chapter 5). However, the research on 4-methyl-2-pyridone (Chapter 6) showed that n-butyllithium caused either (i) lithiation at the 4-position in the ring or (ii) acted as a nucleophile, with the addition of a butyl group at the 6-position in the ring. The reaction of n-butyllithium and 3-cyano-6-methyl-2-pyridone was studied (Chapter 7). n-Butyllithium was found to act as a nucleophile towards 3-cyano-6-methyl-2-pyridone, resulting in the addition of a butyl group.
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Wang, Haofan. "Synthesis and reactions of organoiron compounds." Diss., The University of Arizona, 2003. http://hdl.handle.net/10150/289994.

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The multistep synthesis of the redox active adenine analog [e]-ferrocenyl-4-aminopyrimidine is reported. The redox active system will be incorporated into oligonucleotides to study the electron transfer through the molecular pi-system of DNA in future studies. Attempts were made to synthesize a cyclopenta-4-aminopyrimidine derivative which possesses an endocyclic double bond in the cyclopentane ring. This intermediate can be subsequently coupled with cyclopentadienyl iron dicarbonyl (Fp) group and, after thermal decarbonylation, form the desired ferrocene ring. Many double bond precursors are prepared, including dibromide, acetate, alcohol, ketone and phenylseleno derivatives of cyclopentapyrimidine. However efforts to form an endocyclic double bond turned out to be unsuccessful. Exocyclic double bond derivatives of cyclopentapyrimidine have also been prepared. An improved chiral synthesis of [e]-ferrocenyl-4-aminopyrimidine is achieved, in which a Curtius rearrangement to form an O-benzylcarbamate was done using a formyl ferrocene carboxylic acid. The yield of the final cyclization step was also greatly improved. The synthesis of methyl-(2,5-dimethoxy-4-fluorophenyl)-acetate, a thymine isostere precursor, is reported. It will be used as a substitute for a thymine base in a peptide nucleic acid (PNA) synthesis in the future. Regioselective bromination of 2-fluoro-hydroquinone introduced a bromo group at the desired position. After protection of hydroxyl groups in this product, a carboxylic acid ethyl ester group was introduced. Finally, an Arndt-Eistert reaction was used to extend the carboxylic acid by one carbon to the corresponding phenyl acetic acid ethyl ester. A chemical model mimicking the biosynthesis of the cyanide ligand in the enzyme hydrogenase is developed. In this model a thiocarbamate is first formed and subsequently dehydrated by polyphosphate ethyl ester(PPE) to make a thiocyanate. Finally, the cyanide moiety is transferred to the metal center. The direct dehydration of a carboxamidoiron species to form a cyano ligand is also reported.
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Ikegami, Toru. "Hypervalent Organobismuth Compounds : Synthesis, Reaction, and Applications to Organic Synthesis." 京都大学 (Kyoto University), 1997. http://hdl.handle.net/2433/86484.

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Books on the topic "Cumulenes; organic compounds synthesis"

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Brandsma, L. Preparative acetylenic chemistry. 2nd ed. Amsterdam: Elsevier, 1988.

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Brandsma, L. Preparative acetylenic chemistry. 2nd ed. Amsterdam: Elsevier, 1988.

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Willis, Christine L. Organic synthesis. Oxford: Oxford University Press, 1995.

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Organic synthesis. 2nd ed. Boston: McGraw-Hill, 2002.

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Organic synthesis. New York: McGraw-Hill, 1994.

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M, Trost Barry, and International Union of Pure and Applied Chemistry., eds. Stereocontrolled organic synthesis. Oxford: Blackwell Scientific Publications, 1994.

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Smith, Michael B. Organic synthesis. New York: McGraw-Hill, 1994.

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Jean-Paul, Quintard, and Rahm Alain, eds. Tin in organic synthesis. London: Butterworths, 1987.

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1937-, Murahashi Shunʾichi, ed. Ruthenium in organic synthesis. Weinheim: Wiley-VCH, 2004.

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Renu, Aggarwal, ed. Organic synthesis: Special techniques. Boca Raton, FL: CRC Press, 2001.

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Book chapters on the topic "Cumulenes; organic compounds synthesis"

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Ahluwalia, V. K. "Stereoselective Synthesis." In Stereochemistry of Organic Compounds, 505–61. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-84961-0_18.

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Volke, Jiří, and František Liška. "Reactions of Organic Compounds at Electrodes." In Electrochemistry in Organic Synthesis, 45–139. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-78699-0_3.

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Fagnoni, Maurizio. "CHAPTER 6. Colored Compounds for Eco-sustainable Visible-light Promoted Syntheses." In Sustainable Organic Synthesis, 150–80. Cambridge: Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781839164842-00150.

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Norman, Richard, and James M. Coxon. "The syntheses of some naturally occurring compounds." In Principles of Organic Synthesis, 728–90. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2166-8_22.

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Norman, Richard, and James M. Coxon. "The synthesis of five-and six-membered heterocyclic compounds." In Principles of Organic Synthesis, 676–727. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2166-8_21.

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Kostikov, Rafael R., Alexandr P. Molchanov, and Henning Hopf. "Gem-Dihalocyclopropanes in organic synthesis." In Small Ring Compounds in Organic Synthesis IV, 41–80. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/3-540-52422-3_2.

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Carl, Elena, and Dietmar Stalke. "Structure-Reactivity Relationship in Organolithium Compounds." In Lithium Compounds in Organic Synthesis, 1–32. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.ch1.

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Harrison-Marchand, Anne, and Jacques Maddaluno. "Advances in the Chemistry of Chiral Lithium Amides." In Lithium Compounds in Organic Synthesis, 297–328. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.ch10.

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Minko, Yury, and Ilan Marek. "Advances in Carbolithiation." In Lithium Compounds in Organic Synthesis, 329–50. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.ch11.

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Azzena, Ugo, and Luisa Pisano. "Reductive Lithiation and Multilithiated Compounds in Synthesis." In Lithium Compounds in Organic Synthesis, 351–74. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.ch12.

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Conference papers on the topic "Cumulenes; organic compounds synthesis"

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Monçalves, Matias, Mariana M. Bassaco, Marcos A. Villetti, and Claudio C. Silveira. "Novel Divinyl Sulfides: Potential Luminescent Compounds." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0308-1.

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Martins, Lucimara J., Wanessa F. Altei, Cristiane S. Schwalm, Adriano D. Andricopulo, and Fernando Coelho. "Synthesis of new biologically actived azaspiro compounds." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013917144424.

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Ali, Bakhat, Hélio A. Stefani, and Fernando P. Ferreira. "Addition of Amino Acids to oxopyrrolidin compounds." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20131014161751.

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Silva, Anderson B. da, and Juliana A. Vale. "Rapid synthesis of di-1,2,4-oxadiazoles pyridyl compounds." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0031-1.

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Silva, Anderson B. da, and Juliana A. Vale. "Rapid synthesis of di-1,2,4-oxadiazoles pyridyl compounds." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0317-1.

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Carneiro, Paula F., Maria do Carmo F. R. Pinto, Tatiane S. Coelho, Antonio V. Pinto, Kelly C. G. Moura, Pedro A. da Silva, and Eufrânio N. da Silva Júnior. "Quinonoid and phenazine compounds: synthesis of new antimycobacterial prototypes." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0224-1.

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Barbosa, Flavio A. R., Rômulo F. S. Canto, and Antonio L. Braga. "Synthesis of novel 6-seleno-dihydropyrimidinones: Potentially bioactive compounds." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013819222620.

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Rafique, Jamal, Sumbal Saba, Rômulo F. S. Canto, Waseem Hassan, João B. T. Rocha, and Antonio L. Braga. "Synthesis of Diselenide Based Picolylamide Derivatives: Biologically Potential Compounds." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013822125235.

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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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Brondani, Patrícia B., Gonzalo de Gonzalo, Marco W. Fraaije, and Leandro H. Andrade. "Selective oxidations of organoboron compounds catalyzed by Baeyer-Villiger monooxygenases." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0097-2.

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Reports on the topic "Cumulenes; organic compounds synthesis"

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Wiemers, K. D., H. Babad, R. T. Hallen, L. P. Jackson, and M. E. Lerchen. An Assessment of the Stability and the Potential for In-Situ Synthesis of Regulated Organic Compounds in High Level Radioactive Waste Stored at Hanford, Richland, Washington. Office of Scientific and Technical Information (OSTI), January 1999. http://dx.doi.org/10.2172/2535.

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