Готові списки джерел за темами / Alkynyl

Добірка наукової літератури з теми "Alkynyl"

Автор: Grafiati
Опубліковано: 10 грудня 2022
Оновлено: 28 січня 2023

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Статті в журналах з теми "Alkynyl"

1

Matsumura, Mio, Kaho Tsukada, Kiwa Sugimoto, Yuki Murata, and Shuji Yasuike. "Synthesis of novel alkynyl imidazopyridinyl selenides: copper-catalyzed tandem selenation of selenium with 2-arylimidazo[1,2-a]pyridines and terminal alkynes." Beilstein Journal of Organic Chemistry 18 (July 19, 2022): 863–71. http://dx.doi.org/10.3762/bjoc.18.87.

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Alkynyl selenides have attracted considerable research interest recently, owing to their applications in the biological and pharmaceutical fields. The Cu-catalyzed tandem reaction for the synthesis of novel alkynyl imidazopyridinyl selenides is presented. A one-pot synthesis route afforded alkynyl imidazopyridinyl selenides in moderate to good yields. This was achieved by a two-step reaction between terminal alkynes and diimidazopyridinyl diselenides, generated from imidazo[1,2-a]pyridines and Se powder, using 10 mol % of CuI and 1,10-phenanthroline as the catalytic system under aerobic conditions. The C(sp2)–Se and C(sp)–Se bond-formation reaction can be performed in one-pot by using inexpensive and easy to handle Se powder as the Se source. The reaction proceeded with terminal alkynes having various substitutions, such as aryl, vinyl, and alkyl groups. The obtained alkynyl imidazopyridinyl selenide was found to undergo nucleophilic substitution reaction on Se atom using organolithium reagents and 1,3-dipolar azide–alkyne cycloaddition based on the alkyne moiety.
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2

Sewald, Norbert, та Klaus Burger. "α-Trifluormethylsubstituierte α-Hydroxysäuren mit Alkinfunktionen in der Seitenkette / α-Trifluoromethyl Substituted α-Hydroxy Acids with Alkyne Functions in the Side Chain". Zeitschrift für Naturforschung B 45, № 6 (1 червня 1990): 871–75. http://dx.doi.org/10.1515/znb-1990-0619.

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Trifluoromethyl substituted α-hydroxy acids with alkyne functions in the side chain are obtained on reaction of trifluoro pyruvates with alkynyl Grignard reagents and alkali metal salts of alkynes, respectively.
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3

Heredia, Adrián A., and Alicia B. Peñéñory. "Transition-metal-free one-pot synthesis of alkynyl selenides from terminal alkynes under aerobic and sustainable conditions." Beilstein Journal of Organic Chemistry 13 (May 16, 2017): 910–18. http://dx.doi.org/10.3762/bjoc.13.92.

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Alkynyl selenides were synthesized by a straightforward one-pot and three-step methodology, without the need of diselenides as starting reagents, under an oxygen atmosphere and using PEG 200 as the solvent. This procedure involves the in situ generation of dialkyl diselenides through a K3PO4-assisted reaction of an alkyl selenocyanate obtained by a nucleophilic substitution reaction between KSeCN and alkyl halides. Successive reaction with terminal alkynes in the presence of t-BuOK affords the corresponding alkyl alkynyl selenide in moderate to good yields. Finally, this methodology allowed the synthesis of 2-alkylselanyl-substituted benzofuran and indole derivatives starting from convenient 2-substituted acetylenes.
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4

Wu, Ge, Lin Min, Hongchen Li, Wenxia Gao, Jinchang Ding, Xiaobo Huang, Miaochang Liu, and Huayue Wu. "Metal-free synthesis of alkynyl alkyl selenides via three-component coupling of terminal alkynes, Se, and epoxides." Green Chemistry 20, no. 7 (2018): 1560–63. http://dx.doi.org/10.1039/c8gc00341f.

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Анотація:
A metal-free three-component coupling reaction of alkynes, Se powder and epoxides is described, providing an efficient, straightforward route for the preparation of alkynyl alkyl selenides via a double C–Se bond formation process.
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5

Reinus, Brandon, and Sean Kerwin. "Preparation and Utility of N-Alkynyl Azoles in Synthesis." Molecules 24, no. 3 (January 24, 2019): 422. http://dx.doi.org/10.3390/molecules24030422.

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Анотація:
Heteroatom-substituted alkynes have attracted a significant amount of interest in the synthetic community due to the polarized nature of these alkynes and their utility in a wide range of reactions. One specific class of heteroatom-substituted alkynes combines this utility with the presence of an azole moiety. These N-alkynyl azoles have been known for nearly 50 years, but recently there has been a tremendous increase in the number of reports detailing the synthesis and utility of this class of compound. While much of the chemistry of N-alkynyl azoles mirrors that of the more extensively studied N-alkynyl amides (ynamides), there are notable exceptions. In addition, as azoles are extremely common in natural products and pharmaceuticals, these N-alkynyl azoles have high potential for accessing biologically important compounds. In this review, the literature reports of N-alkynyl azole synthesis, reactions, and uses have been assembled. Collectively, these reports demonstrate the growth in this area and the promise of exploiting N-alkynyl azoles in synthesis.
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6

Li, Qingjiang, Jiatong Guo, and Zhongwu Guo. "Direct access to various C3-substituted sialyl glycal derivatives from 3-iodo-sialyl glycals." Organic & Biomolecular Chemistry 19, no. 46 (2021): 10169–73. http://dx.doi.org/10.1039/d1ob01977e.

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Sialyl glycal C3-aryl, alkyl, alkenyl, and alkynyl derivatives useful for sialylidase inhibitor discovery were efficiently synthesized by a new method based on the cross-coupling of 3-iodo-sialyl glycal with boronic acids, alkenes, and alkynes.
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7

Jover, Jesús. "Copper-Catalyzed Eglinton Oxidative Homocoupling of Terminal Alkynes: A Computational Study." Journal of Chemistry 2015 (2015): 1–8. http://dx.doi.org/10.1155/2015/430358.

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Анотація:
The copper(II) acetate mediated oxidative homocoupling of terminal alkynes, namely, the Eglinton coupling, has been studied with DFT methods. The mechanism of the whole reaction has been modeled using phenylacetylene as substrate. The obtained results indicate that, in contrast to some classical proposals, the reaction does not involve the formation of free alkynyl radicals and proceeds by the dimerization of copper(II) alkynyl complexes followed by a bimetallic reductive elimination. The calculations demonstrate that the rate limiting-step of the reaction is the alkyne deprotonation and that more acidic substrates provide faster reactions, in agreement with the experimental observations.
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8

Frontier, Alison J., Shukree Abdul-Rashed, and Connor Holt. "Alkynyl Prins and Alkynyl Aza-Prins Annulations: Scope and Synthetic Applications." Synthesis 52, no. 14 (April 9, 2020): 1991–2007. http://dx.doi.org/10.1055/s-0039-1690869.

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Анотація:
This review focuses on alkynyl Prins and alkynyl aza-Prins cyclization­ processes, which involve intramolecular coupling of an alkyne with either an oxocarbenium or iminium electrophile. The oxocarbenium or iminium species can be generated through condensation- or elimination-type processes, to achieve an overall bimolecular annulation that enables the synthesis of both oxygen- and nitrogen-containing­ saturated heterocycles with different ring sizes and substitution patterns. Also discussed are cascade processes in which alkynyl Prins heterocyclic adducts react to trigger subsequent pericyclic reactions, including [4+2] cycloadditions and Nazarov electrocyclizations, to rapidly construct complex small molecules. Finally, examples of the use of alkynyl Prins and alkynyl aza-Prins reactions in the synthesis of natural products are described. The review covers the literature through the end of 2019.1 Introduction1.1 Alkyne-Carbonyl Coupling Pathways1.2 Coupling/Cyclization Cascades Using the Alkynyl Prins Reaction2 Alkynyl Prins Annulation (Oxocarbenium Electrophiles)2.1 Early Work2.2 Halide as Terminal Nucleophile2.3 Oxygen as Terminal Nucleophile2.4 Arene as Terminal Nucleophile (Intermolecular)2.5 Arene Terminal Nucleophile (Intramolecular)2.6 Cyclizations Terminated by Elimination3 Synthetic Utility of Alkynyl Prins Annulation3.1 Alkynyl Prins-Mediated Synthesis of Dienes for a [4+2] Cyclo­- addition­-Oxidation Sequence3.2 Alkynyl Prins Cyclization Adducts as Nazarov Cyclization Precursors3.3 Alkynyl Prins Cyclization in Natural Product Synthesis4 Alkynyl Aza-Prins Annulation4.1 Iminium Electrophiles4.2 Activated Iminium Electrophiles5 Alkynyl Aza-Prins Cyclizations in Natural Product Synthesis6 Summary and Outlook
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9

Sun, Fenggang, Miao Li, and Zhenhua Gu. "Pd/norbornene-catalyzed sequential ortho-C–H alkylation and ipso-alkynylation: a 1,1-dimethyl-2-alkynol strategy." Organic Chemistry Frontiers 3, no. 3 (2016): 309–13. http://dx.doi.org/10.1039/c5qo00391a.

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Анотація:
A palladium/norbornene-catalyzedortho-C–H alkylation andipso-alkynylation reaction for the synthesis of 2-alkyl-1-alkynyl arenes was reported, where the use of bulky 1,1-dimethyl-2-alkynols led to significant suppression of the formation ofO-alkylation and norbornene alkynylation by-products.
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10

Chowdhury, Roomi Mohima, and Jonathan D. Wilden. "An improved transition-metal-free synthesis of aryl alkynyl sulfides via substitution of a halide at an sp-centre." Organic & Biomolecular Chemistry 13, no. 21 (2015): 5859–61. http://dx.doi.org/10.1039/c5ob00494b.

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A simple high-yielding preparation of aryl alkynyl sulfides is presented. The reaction of a chloroacetylene with a thiolate salt in the presence of an amine mediator (dimethylamine or N,N′-dimethylethylenediamine) yields the alkynyl sulfides in excellent yields. The alkynyl chloride is easily prepared from the parent alkyne.
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Дисертації з теми "Alkynyl"

1

George, Darren Shawn Allen. "Alkyne and alkynyl complexes of rhodium and iridium." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0025/NQ39530.pdf.

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2

Yasui, Hiroto. "Studies on Addition to 1-Aryl-1-alkynes and N-Alkynyl Amides." 京都大学 (Kyoto University), 2008. http://hdl.handle.net/2433/57271.

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Анотація:
Kyoto University (京都大学)
0048
新制・課程博士
博士(工学)
甲第13827号
工博第2931号
新制||工||1433(附属図書館)
26043
UT51-2008-C743
京都大学大学院工学研究科材料化学専攻
(主査)教授 大嶌 幸一郎, 教授 檜山 爲次郎, 教授 松原 誠二郎
学位規則第4条第1項該当
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3

Bailey, Austin Lou. "Alkynyl and isocyanobiphenyls : new thermotropic liquid crystals." Thesis, University of British Columbia, 1989. http://hdl.handle.net/2429/27388.

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The presence of mesomorphism in 4-n-alkyl-4'-isocyanobiphenyls 4 and 4-n-alkyl-4'-alkynylbiphenyls 5 was investigated, based on the liquid-crystallinity of the cyanobiphenyls 2 (R = n-alkyl). Compound 4 (R = n-butyl) is non-mesomorphic, whereas 4 (R = n-pentyl) is a virtual liquid crystal melting at 34-35°C and supercooling to a nematic phase at 30°C, and 4 (R = n-hexyI) is a nematic liquid crystal from 9 to 19°C. Compounds of structure 5 (R = n-pentyl, X = Si(CH₃)₃, H, CH₃, CI) are not liquid crystals. The corresponding bromo- and iodoalkynes (5, R = n-pentyl, X = Br, I) are liquid crystals with mesomorphic ranges of 88-108°C and 110-119°C, respectively. [See Thesis for Diagram]
Science, Faculty of
Chemistry, Department of
Graduate
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4

Ballisai, Antonio. "Synthesis of rigid-rod metal-alkynyl complexes." Thesis, Imperial College London, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.433302.

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5

Chan, Yew Boon Colin. "Synthesis and reactivity of platinum alkynyl complexes." Thesis, Imperial College London, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.395761.

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6

Eaves, Samantha Grace. "Trans-bis(alkynyl) ruthenium complexes : synthesis, structure and reactivity." Thesis, Durham University, 2015. http://etheses.dur.ac.uk/11444/.

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This Thesis describes the synthesis and characterisation of a series of trans-bis(alkynyl) ruthenium complexes, trans-[Ru(C≡CR)2(L)4], to better understand how the variation of the metal ancillary ligands (L) affect electronic structure and spectroscopic properties, chemical reactivity, and behaviour in metal|molecule|metal junctions. Reactions of cis-[RuCl2(dppm)2] with terminal alkyne HC≡CC6H4-4-R, in the presence of TlBF4 and base, gives into trans-bis(alkynyl) complexes, trans-[Ru(C≡CC6H4-4-R)2(dppm)2], for electron withdrawing R groups or cationic η3-butenynyl complexes, E-­[Ru(η3-{HC(C6H4-4-R)=CC≡C(C6H4-4-R)})(dppm)2]+ for electron donating R groups. Reactions of cis-[RuCl2(dppm)2] with di-terminal alkynes HC≡CC6H4-2,5-X2-4-C≡CH, in the presence of TlBF4 and [NnBu4]Cl, gives trans-[RuCl(C≡CC6H2-2,5-X2-4-CCl=CH2)(dppm)2], inferring a quinoidal cumulene intermediate. Multi-metallic trans-bis(alkynyl) {Ru(dppe)2} complexes, varying in binding groups and bridging ligands, have been prepared. Reversible oxidation processes, whilst corresponding to the number of integrated metal centres, exhibit a high degree of alkynyl character in all cases. The vibrational and electronic spectra of both neutral and oxidised complexes are complicated by the presence of numerous spectroscopically distinct rotamer conformations and redox isomers. For example in the case of mono-oxidised complexes, a principal low-energy (π-π*) NIR band is exhibited along with multiple higher energy (MLCT-type) NIR bands, which can be assigned by comparison with smaller model systems. Finally, trans-bis(alkynyl) {Ru{P(OEt)3}4} complexes have been synthesised. As a result of the increased (pseudo D4h) molecular symmetry and consequent fewer distinct rotamer conformations, a lesser number of NIR bands are exhibited for trans­[Ru(C≡CR)2{P(OEt)3}4]+ than bis-chelating dppm and dppe derivatives. Between trans-[Ru(C≡CR)2(PPʹ)] (PPʹ = (dppe)2, {P(OEt)3}4) complexes, the {Ru(dppe)2} derivatives give rise to conductance histograms with additional features. These features are attributed to contacts formed at or across the dppe-phenyl rings, leading to suggestions that phosphite complexes might be novel ‘insulated’ molecular wires.
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7

Wang, Ruiping. "Indenyl nickel complexes bearing alkynyl, alkenyl and triflate ligands." [Montréal] : Université de Montréal, 2003. http://wwwlib.umi.com/cr/umontreal/fullcit?pNQ82764.

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Thèse (Ph. D.)--Université de Montréal, 2003.
"NQ-82764." "Thèse présentée à la faculté des études supérieures en vue de l'obtention du grade de philosophiae doctor (Ph. D.) en chimie." Version électronique également disponible sur Internet.
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8

Shen, Lixin. "Design and synthesis of 3,3'-disubstituted-binaphthyl alkynyl boron reagents for asymmetric conjugate addition of alkynyl groups to enones and 1,2-addition to aldehydes." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0006/NQ44782.pdf.

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9

Weisner, Andrew John. "SONOGASHIRA COUPLING ROUTES TO ortho-ALKYNYL- AND FUSED-RING SYDNONES." Wright State University / OhioLINK, 2003. http://rave.ohiolink.edu/etdc/view?acc_num=wright1054924552.

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10

Humphrey, Mark Graeme. "Aspects of organometallic chemistry, particularly metal alkynyl and cluster chemistry." Title page, contents and abstract only, 2002. http://web4.library.adelaide.edu.au/theses/09SD/09sdh9267.pdf.

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Includes bibliographical references. Details research carried out into the nonlinear optical properties of metal alkynyls, chiefly organoruthenium complexes, showing that these complexes can be designed to have very large NLO coefficients. Also demonstrates the utility of spectroscopic, electrochemical and copmutational aids as predictive tools for NLO materials. Also examines cluster synthesis, reactivity and physical properties using ruthenium clusters and hard-donor ligands, affording a series of cluster complrxes that provide structural models for industrially-important hydrotreating intermediates.
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Книги з теми "Alkynyl"

1

1933-, Tebby John C., ed. Alkynes in cycloadditions. Chichester, West Sussex: Wiley, 2014.

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2

Alexandrovna, Maretina I., Boris I. Ionin, and John C. Tebby. Alkynes in Cycloadditions. Chichester, UK: John Wiley & Sons Ltd, 2013. http://dx.doi.org/10.1002/9781118709313.

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3

Assis, Cecy de. Alkymya de assustos: Poesia. Rio de Janeiro, RJ: Philobiblion, 1987.

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4

Trost, Barry M., and Chao-Jun Li, eds. Modern Alkyne Chemistry. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527677894.

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5

Greenhalgh, Mark. Iron-Catalysed Hydrofunctionalisation of Alkenes and Alkynes. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-33663-3.

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6

Marsh, K. N., ed. Densities of Aliphatic Hydrocarbons: Alkenes, Alkadienes, Alkynes. Berlin/Heidelberg: Springer-Verlag, 1996. http://dx.doi.org/10.1007/b59735.

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7

Hellwig, Raphael. Alkyne‐Based Nanostructures on Silver Substrates. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-00997-7.

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8

Imamoglu, Yavuz, ed. Metathesis Polymerization of Olefins and Polymerization of Alkynes. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5188-7.

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9

Simonneau, Antoine. Gold-Catalyzed Cycloisomerization Reactions Through Activation of Alkynes. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-06707-0.

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10

Imamoglu, Yavuz. Metathesis Polymerization of Olefins and Polymerization of Alkynes. Dordrecht: Springer Netherlands, 1998.

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Частини книг з теми "Alkynyl"

1

Smith, Lowell R. "Alkyl, Alkenyl and Alkynyl Indoles." In Chemistry of Heterocyclic Compounds: A Series Of Monographs, 65–126. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186930.ch2.

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2

Hellwig, Raphael. "Metal Alkynyl $$\pi $$ Complexes." In Springer Theses, 75–103. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-00997-7_5.

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3

Yam, Vivian Wing-Wah, and Keith Man-Chung Wong. "Luminescent Molecular Rods — Transition-Metal Alkynyl Complexes." In Molecular Wires and Electronics, 1–32. Berlin, Heidelberg: Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/b136069.

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4

"Alkynyl Compounds." In Substance index, edited by Backes, Fröhlich, and Padeken. Stuttgart: Georg Thieme Verlag, 2001. http://dx.doi.org/10.1055/b-0035-113707.

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5

"Alkynyl-, sec.-Alkyl-, prim.-Alkyl Hafnium Compounds." In Houben-Weyl Methods of Organic Chemistry Vol. E 23d/1, 4th Edition Supplement, edited by Backes, Fröhlich, and Padeken. Stuttgart: Georg Thieme Verlag, 2001. http://dx.doi.org/10.1055/b-0035-113846.

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6

De Wildeman, S., and N. Sereinig. "Dialkyl, Alkyl Alkenyl, and Alkyl Alkynyl Ketones." In Stereoselective Reactions of Carbonyl and Imino Groups, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-202-00068.

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7

"Alkynyl-, Alkenyl-, sec.-Alkyl Zinc Compounds." In Houben-Weyl Methods of Organic Chemistry Vol. E 23d/1, 4th Edition Supplement, edited by Backes, Fröhlich, and Padeken. Stuttgart: Georg Thieme Verlag, 2001. http://dx.doi.org/10.1055/b-0035-113866.

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8

Gandon, V., and M. Malacria. "Allylzinc Intermediates from Alkynyl Sulfoxides and Alkynyl Sulfones." In Cumulenes and Allenes, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-044-00181.

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9

"Alkynyl Oxygen Compounds." In Substance index, edited by Backes, Fröhlich, and Padeken. Stuttgart: Georg Thieme Verlag, 2001. http://dx.doi.org/10.1055/b-0035-113776.

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10

"Alkynyl Tellurium Compounds." In Houben-Weyl Methods of Organic Chemistry Vol. E 23d/1, 4th Edition Supplement, edited by Backes, Fröhlich, and Padeken. Stuttgart: Georg Thieme Verlag, 2001. http://dx.doi.org/10.1055/b-0035-113849.

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Тези доповідей конференцій з теми "Alkynyl"

1

Sahraoui, B., J. Luc, A. Meghea, R. Czaplicki, J. L. Fillaut, and A. Migalska-Zalas. "Alkynyl-ruthenium complexes for nonlinear optical applications." In 2008 2nd ICTON Mediterranean Winter (ICTON-MW). IEEE, 2008. http://dx.doi.org/10.1109/ictonmw.2008.4773092.

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2

Mihaly, Joseph J., David J. Stewart, Tod A. Grusenmeyer, Alexis T. Phillip, Joy E. Haley, and Thomas G. Gray. "Excited-State Properties of (Alkynyl)Gold(I) Fluorenyls." In 2021 IEEE Research and Applications of Photonics in Defense Conference (RAPID). IEEE, 2021. http://dx.doi.org/10.1109/rapid51799.2021.9521375.

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3

Thorley, Karl J., Micai Benford, Yang Song, Sean R. Parkin, Chad Risko, and John E. Anthony. "Group 14 effects in alkynyl acene small molecule semiconductors." In 2021 IEEE International Flexible Electronics Technology Conference (IFETC). IEEE, 2021. http://dx.doi.org/10.1109/ifetc49530.2021.9580518.

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4

Levashov, Andrey S., Dmitrii S. Buryi, and Valeriy V. Konshin. "New approaches to the synthesis of alkynyl ketones using tin tetraalkynylides." In PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON AUTOMOTIVE INNOVATION GREEN ENERGY VEHICLE: AIGEV 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5087365.

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5

Aguilar, Enrique, Alexandra Pérez-Anes, Patricia García-García, and Manuel Fernández-Rodríguez. "Microwave-Accelerated Multi-Component Cascade Reactions Involving Fischer Alkoxy Alkynyl Carbene Complexes." In The 12th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01264.

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6

Padwa, Albert. "Synthesis of Polycyclic Ring Systems Using Transition Metal Catalyzed Cyclizations of Diazo Alkynyl Ketones." In The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01782.

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7

Van Steerteghem, Nick, Stijn Van Cleuvenbergen, Noor Aisyah Ahmad Shah, Mark G. Humphrey, Thierry Verbiest, and Koen Clays. "Investigation of the second hyperpolarizability of Ru-alkynyl complexes by z-scan and nonlinear scattering." In SPIE Organic Photonics + Electronics, edited by Joy E. Haley, Jon A. Schuller, Manfred Eich, and Jean-Michel Nunzi. SPIE, 2016. http://dx.doi.org/10.1117/12.2237203.

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8

Karakas, A., T. Dag, A. Migalska-Zalas, Jean-Luc Fillaut, and B. Sahraoui. "Determination of dipole polarizabilities and second hyperpolarizabilities in alkynyl-ruthenium complexes using quantum-chemical calculations." In 2013 15th International Conference on Transparent Optical Networks (ICTON). IEEE, 2013. http://dx.doi.org/10.1109/icton.2013.6602902.

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9

Ford, M. J., R. C. Hoft, J. D. Gale, and A. M. Mcdonagh. "A new class of self-assembled monolayers on gold using an alkynyl group as a linker." In 2006 International Conference on Nanoscience and Nanotechnology. IEEE, 2006. http://dx.doi.org/10.1109/iconn.2006.340700.

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10

Godoi, Marcelo, Eduardo Wronscki Ricardo, Tiago Elias Frizon, Devender Singh, and Antonio Luiz Braga. "An Efficient Synthesis of Alkynyl Selenides and Telurides from Terminal Acetylenes and Diorganoyl Dichalcogenides Catalyzed by Copper Oxide Nanopowder." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0115-1.

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Звіти організацій з теми "Alkynyl"

1

Atwood, Jim, D. Catalytic Hydration of Alkenes and Alkynes. Office of Scientific and Technical Information (OSTI), March 2003. http://dx.doi.org/10.2172/808955.

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2

Parsons, Brendon Andrew. Per/Polyfluoro Alkyl Substances (PFAS). Office of Scientific and Technical Information (OSTI), November 2019. http://dx.doi.org/10.2172/1573986.

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3

Winter, Rolf. Chemistry of Pentafluorothio (SF5) Alkyl Derivatives. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.1280.

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4

Jordan, Richard F. Electrophilic metal alkyl chemistry in new ligand environments. Office of Scientific and Technical Information (OSTI), September 2002. http://dx.doi.org/10.2172/805469.

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5

Jordan, Richard F. Electrophilic Metal Alkyl Chemistry in New Ligand Environments. Office of Scientific and Technical Information (OSTI), June 2013. http://dx.doi.org/10.2172/1087361.

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6

Jordan, R. F. Electrophilic metal alkyl chemistry in new ligand environments. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/6905640.

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7

Moriarty, Robert M. Alkyl Azides, Diazides, Haloazides and Bridged Polycyclic Diazides. Fort Belvoir, VA: Defense Technical Information Center, May 1991. http://dx.doi.org/10.21236/ada236202.

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8

Downer, Nancy W., Jianguo Li, Leslie W. DeLuca, Elizabeth M. Penniman, and H. G. Smith. Surface-Bound Alkyl Monolayers: Electrochemical and Structural Characterization. Fort Belvoir, VA: Defense Technical Information Center, June 1991. http://dx.doi.org/10.21236/ada237604.

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9

Allcock, Harry R. Synthesis of Alkyl and Aryl Phosphazene High Polymers. Fort Belvoir, VA: Defense Technical Information Center, November 1990. http://dx.doi.org/10.21236/ada229369.

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10

Jordan, R. F. Synthesis and chemistry of cationic d sup 0 metal alkyl complexes. Office of Scientific and Technical Information (OSTI), January 1991. http://dx.doi.org/10.2172/6020649.

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