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Relevant bibliographies by topics / Alkenes and Dienes

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Academic literature on the topic 'Alkenes and Dienes'

Author: Grafiati

Published: 6 September 2023

Last updated: 31 July 2025

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Journal articles on the topic "Alkenes and Dienes"

1

Dobrovolná, Zuzana, and Libor Červený. "Competitive Hydrogenation of Unsaturated Hydrocarbons by Hydrogen Transfer from Ammonium Formateon a Palladium Catalyst." Collection of Czechoslovak Chemical Communications 62, no. 9 (1997): 1497–502. http://dx.doi.org/10.1135/cccc19971497.

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Competitive hydrogenation of alkenes (cyclohexene, hex-1-ene, hept-1-ene, oct-1-ene) and dienes (octa-1,7-diene, cyclohexa-1,3-diene) was carried out by catalytic hydrogen transfer from ammonium formate on palladium in methanol. The adsorptivity and reactivity of the hydrocarbons decreased in the series: cyclic diene > linear diene > linear 1-alkene > cyclic alkene.

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2

Madden, Katrina S., Sylvain David, Jonathan P. Knowles, and Andrew Whiting. "Heck–Mizoroki coupling of vinyliodide and applications in the synthesis of dienes and trienes." Chemical Communications 51, no. 57 (2015): 11409–12. http://dx.doi.org/10.1039/c5cc03273c.

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Vinyliodide reacts chemoselectively under Heck–Mizoroki conditions with terminal alkenes to give diene products, including vinyl boronate esters, and the resulting dienylboronate undergoes Suzuki–Miyaura coupling with aryl, heteroaryl and alkenyl halides to access dienes and trienes.

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3

Hussein, Aqeel A. "Ru-catalysed oxidative cyclisation of 1,5-dienes: an unprecedented role for the co-oxidant." RSC Advances 10, no. 26 (2020): 15228–38. http://dx.doi.org/10.1039/d0ra02303e.

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The Ru-mediated oxidative cyclisation of 1,5-dienes to THF-diols proceeds with the intermediacy of NaIO<sub>4</sub>-complexed Ru(vi) species and offers new insights into the Ru-catalysed functionalizations of alkenes and 1,5-dienes.

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Mantrand, Nathalie, and Philippe Renaud. "Azidosulfonylation of alkenes, dienes, and enynes." Tetrahedron 64, no. 52 (2008): 11860–64. http://dx.doi.org/10.1016/j.tet.2008.09.096.

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5

Tsuno, Takashi. "ChemInform Abstract: Alkenes, Alkynes, Dienes, Polyenes." ChemInform 42, no. 38 (2011): no. http://dx.doi.org/10.1002/chin.201138251.

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6

Welker, Mark E. "Boron and Silicon-Substituted 1,3-Dienes and Dienophiles and Their Use in Diels-Alder Reactions." Molecules 25, no. 16 (2020): 3740. http://dx.doi.org/10.3390/molecules25163740.

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Boron and silicon-substituted 1,3-dienes and boron and silicon-substituted alkenes and alkynes have been known for years and the last 10 years have seen a number of new reports of their preparation and use in Diels-Alder reactions. This review first covers boron-substituted dienes and dienophiles and then moves on to discuss silicon-substituted dienes and dienophiles.

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7

Gong, Liu-Zhu, Pu-Sheng Wang, and Meng-Lan Shen. "Transition-Metal-Catalyzed Asymmetric Allylation of Carbonyl Compounds with Unsaturated Hydrocarbons." Synthesis 50, no. 05 (2017): 956–67. http://dx.doi.org/10.1055/s-0036-1590986.

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The asymmetric allylation of carbonyl compounds is an important process for the formation of carbon–carbon bonds, generating optically active homoallylic alcohols that are versatile building blocks with widespread applications in organic synthesis. The use of readily available unsaturated hydrocarbons as allylating reagents in the transition-metal-catalyzed asymmetric allylation has received increasing interest as either a step- or an atom-economy alternative. This review summarizes transition-metal-catalyzed enantioselective allylations on the basis of the ‘indirect’ and ‘direct’ use of simpl

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8

González-Rodríguez, Carlos, and Michael C. Willis. "Rhodium-catalyzed enantioselective intermolecular hydroacylation reactions." Pure and Applied Chemistry 83, no. 3 (2011): 577–85. http://dx.doi.org/10.1351/pac-con-10-09-23.

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Rhodium-catalyzed enantioselective hydroacylation reactions allow rapid access to chiral substituted ketones. However, due to the low reactivity of disubstituted alkenes in intermolecular versions of this process, only a small number of asymmetric intermolecular reactions have been described. Strategies employed to avoid reactivity issues include the use of norbornadienes, linear dienes, acrylamides, and allenes as the alkene components. In addition, our laboratory has recently reported the rhodium-catalyzed enantioselective inter-molecular alkyne hydroacylation reaction, leading to the format

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Trifonov, A. A., I. V. Basalov, and A. A. Kissel. "Use of organolanthanides in the catalytic intermolecular hydrophosphination and hydroamination of multiple C–C bonds." Dalton Transactions 45, no. 48 (2016): 19172–93. http://dx.doi.org/10.1039/c6dt03913h.

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Maeda, Hajime, Hiroshi Takayama, and Masahito Segi. "Photoinduced three-component coupling reactions of electron deficient alkenes, dienes and active methylene compounds." Photochemical & Photobiological Sciences 17, no. 8 (2018): 1118–26. http://dx.doi.org/10.1039/c8pp00239h.

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Dissertations / Theses on the topic "Alkenes and Dienes"

1

Bloom, Andrew Jonathan. "Chemical and electrochemical nitrations of alkenes and dienes." Thesis, University of Southampton, 1986. https://eprints.soton.ac.uk/365569/.

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2

Smith, Dennis. "Gas phase epoxidation of alkenes." Thesis, University of York, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.323493.

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3

Cui, Xiuhua. "Asymmetric hydrogenations of aryl alkenes using imidazol-2-ylidene iridium complexes." Texas A&M University, 2005. http://hdl.handle.net/1969.1/2456.

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A library of iridium complexes featuring oxazoline and imidazol-2-ylidene ligands were synthesized by reaction of a library of imidazoles with a second library of oxazoline iodides. These complexes were active catalysts for hydrogenations of aryl substituted monoenes. Tri- and 1,1-disubstituted alkenes were hydrogenated quantitatively with ee??s up to 99% at 1 atm hydrogen pressure. Catalyst, substrate, temperature and pressure effects were studied. The iridium complexes were also used for the kinetic study of hydrogenation of 2,3- diphenylbutadiene. This hydrogenation is a stepwise reaction:

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4

Keily, John Fraser. "Part A: [2+2] cycloadditions of keteniminium salts with resin bound alkenes : Part B: Permanganate oxidations of 1,5-dienes." Thesis, University of Southampton, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.271633.

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Chan, Mary S. W. "Factors influencing the regiochemistry of nucleophilic addition to the radical cation of alkenes and dienes studied in the context of the photochemical nucleophile-olefin combination, aromatic substitution (photo-NOCAS) reaction." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp02/NQ36574.pdf.

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Tyler-Mahon, Amanda Rhian. "The effect of alkene substitution in the palladium catalysed cycloisomerisation of dienes." Thesis, University of Bristol, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.413611.

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Ghidu, Victor P. "Cationic cyclizations of iron tricarbonyl diene complexes with pendant alkenes and arenes." online version, 2005. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=case1100725837.

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8

Dion, Isabelle. "Intramolecular Cope-Type Hydroamination of Alkenes in the Synthesis of Alkaloids: Total Synthesis of (±)-Coniine and (±)-Desbromoarborescidine A and Studies on a Novel Amination Strategy Towards Manzamine A." Thesis, Université d'Ottawa / University of Ottawa, 2012. http://hdl.handle.net/10393/23059.

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Intramolecular hydroamination represents a potentially general, simple strategy to access various nitrogen heterocycles. While important progress has been accomplished in recent years, six-membered ring formation via alkene hydroamination is typically difficult and limited to terminal alkenes, suggesting that only 2-methylpiperidines can be accessed reliably with current methods. As part of the Beauchemin group efforts on metal-free concerted hydroamination methods, the first part of this thesis describes the development of a Cope-type hydroamination-Meisenheimer rearrangement (CHMR) sequence

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9

Kouklovsky, Cyrille. "Alkenyl-2 oxazolines, nouveaux diénophiles très efficaces dans la réaction de Diels-Alder asymétrique." Paris 11, 1989. http://www.theses.fr/1989PA112317.

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2-Alkenyl oxazolines activated with trifluoroacetic anhydride proved to be very powerful dienophiles towards various dienes including Danishefsky type dienes in the asymmetric Diels-Alder reaction. The reactions were perfonned generally between -100°C and -20°C and the diastereoselectivity is usually better than 90%. The synthesis of two isomerie amino hydroxy bomanes using for one of them an original scheme is first described. The preparation of 2-alkenyl oxazolines by an original route is presented afterwards. In the following chapter, various Diels-Alder cycloadditions with a number of fonc

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Obrecht, Lorenz. "Artificial metalloenzymes in catalysis." Thesis, University of St Andrews, 2015. http://hdl.handle.net/10023/7248.

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This thesis describes the synthesis, characterisation and application of artificial metalloenzymes as catalysts. The focus was on two mutants of SCP-2L (SCP-2L A100C and SCP-2L V83C) both of which possess a hydrophobic tunnel in which apolar substrates can accumulate. The crystal structure of SCP-2L A100C was determined and discussed with a special emphasis on its hydrophobic tunnel. The SCP-2L mutants were covalently modified at their unique cysteine with two different N-ligands (phenanthroline or dipicolylamine based) or three different phosphine ligands (all based on triphenylphosphine) in

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Books on the topic "Alkenes and Dienes"

1

Perekalin, V. V., Z. F. Pavlova, and E. S. Lipina. Conjugated 1,2-and 1,4-Nitrothio(sulfonyl)alkenes and -Dienes (Sulfur Reports). Routledge, 1995.

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2

Dockendorff, Christopher James. New methods for carbon-carbon bond formation and application to organic synthesis: Metal-catalyzed additions of organoborons to activated alkenes and aryne Diels-Alder reactions with acyclic dienes: Y Christopher James Dockendorff. 2006.

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3

Konzelman, James. Acyclic diene metathesis (ADMET) polymerization: A hydrocarbon structure reactivity study. 1993.

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4

Hahn, Norbert D. Steroselektive Pentacarbonylchrom(0)-katalysierte Cyclopropanierung von Alkenen und Dienen mit Diazo-arylessigsäureestern. 2004.

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Book chapters on the topic "Alkenes and Dienes"

1

Kilway, Kathleen V., and Andrew Streitwieser. "Acidity of Alkenes and Polyenes." In The Chemistry of Dienes and Polyenes. John Wiley & Sons, Ltd, 2003. http://dx.doi.org/10.1002/0470857218.ch16.

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2

Dinda, Biswanath. "Photochemistry of Alkenes, Dienes, and Polyenes." In Lecture Notes in Chemistry. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-45934-9_7.

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3

Chambers, R. D., S. L. Jones, S. J. Mullins, A. Swales, P. Telford, and M. L. H. West. "Perfluorinated Alkenes and Dienes in a Diverse Chemistry." In ACS Symposium Series. American Chemical Society, 1991. http://dx.doi.org/10.1021/bk-1991-0456.ch005.

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4

Tsuno, Takashi. "Organic aspects: photochemistry of alkenes, dienes, polyenes (2020–2021)." In Photochemistry. Royal Society of Chemistry, 2022. http://dx.doi.org/10.1039/9781839167676-00067.

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5

Tsuno, Takashi. "Organic aspects: photochemistry of alkenes, dienes, polyenes (2018–2019)." In Photochemistry. Royal Society of Chemistry, 2020. http://dx.doi.org/10.1039/9781839162114-00071.

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6

Tsuno, Takashi. "Organic aspects: photochemistry of alkenes, dienes, polyenes (2016–2017)." In Photochemistry. Royal Society of Chemistry, 2018. http://dx.doi.org/10.1039/9781788013598-00078.

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7

Latscha, Hans Peter, and Helmut Alfons Klein. "Ungesättigte Kohlenwasserstoffe II. Konjugierte Alkene, Diene und Polyene." In Organische Chemie. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-662-09141-8_6.

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Latscha, Hans Peter, and Helmut Alfons Klein. "Ungesättigte Kohlenwasserstoffe II. Konjugierte Alkene, Diene und Polyene." In Organische Chemie. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-662-09142-5_6.

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9

Latscha, Hans Peter, Helmut Alfons Klein, and Klaus Gulbins. "Ungesättigte Kohlenwasserstoffe II. Konjugierte Alkene, Diene und Polyene." In Chemie für Laboranten und Chemotechniker. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-85881-9_6.

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10

Latscha, Hans Peter, Helmut Alfons Klein, and Klaus Gulbins. "Ungesättigte Kohlenwasserstoffe II. Konjugierte Alkene, Diene und Polyene." In Chemie für Laboranten und Chemotechniker. Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-96875-4_6.

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Conference papers on the topic "Alkenes and Dienes"

1

Reihani, Amin, Brent Patterson, John Hoard, et al. "Rapidly Pulsed Reductants for Diesel NOx Reduction With Lean NOx Traps: Comparison of Alkanes and Alkenes as the Reducing Agent." In ASME 2016 Internal Combustion Engine Division Fall Technical Conference. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/icef2016-9475.

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Lean NOx Traps (LNTs) are often used to reduce NOx on smaller diesel passenger cars where urea-based Selective Catalytic Reduction (SCR) systems may be difficult to package. However, the performance of LNTs at temperatures above 400°C needs to be improved. The use of Rapidly Pulsed Reductants (RPR) is a process in which hydrocarbons are injected in rapid pulses ahead of the LNT in order to improve its performance at higher temperatures and space velocities. This approach was developed by Toyota and was originally called Di-Air (Diesel NOx aftertreatment by Adsorbed Intermediate Reductants) [1]

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