Relevant bibliographies by topics / Ene reaction

Contents

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

Academic literature on the topic 'Ene reaction'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 September 2023

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Ene reaction.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Ene reaction"

1

Bakhtiari, Atefeh, and Javad Safaei-Ghomi. "Effects of Chiral Ligands on the Asymmetric Carbonyl-Ene Reaction." Synlett 30, no. 15 (July 23, 2019): 1738–64. http://dx.doi.org/10.1055/s-0037-1611875.

Full text
Abstract:
The carbonyl-ene reaction is one of the most well-known reactions for C–C bond formation. Based on frontier molecular orbitals (FMO), carbonyl-ene reactions occur between the highest occupied molecular orbital (HOMO) of the ene compound bearing an active hydrogen atom at the allylic center and the lowest unoccupied molecular orbital (LUMO) of the electron-deficient enophile, which is a carbonyl compound. A high activation barrier enforces the concerted ene reaction rather than a Diels–Alder reaction at high temperature. Employing a catalytic system can eliminate defects in the ene reaction, and chiral catalysts promote the reaction under mild conditions to produce optically active compounds. In this account, we highlight investigations on the effects of various classes of chiral ligands on intermolecular and intramolecular carbonyl-ene reactions.1 Introduction2 Biaryl-Type Chiral Ligands3 C 1- and C 2-Symmetric Bis(oxazoline) Ligands4 Schiff Base Ligands5 N,N′-Dioxide Ligands6 Conclusions
APA, Harvard, Vancouver, ISO, and other styles
2

Clarke, Matthew L., and Marcia B. France. "The carbonyl ene reaction." Tetrahedron 64, no. 38 (September 2008): 9003–31. http://dx.doi.org/10.1016/j.tet.2008.06.075.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Cossy, J., A. Bouzide, and M. Pfau. "Asymmetric intramolecular Ene-reaction." Tetrahedron Letters 33, no. 34 (August 1992): 4883–84. http://dx.doi.org/10.1016/s0040-4039(00)61223-6.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Niu, Dawen, and Thomas R. Hoye. "The aromatic ene reaction." Nature Chemistry 6, no. 1 (November 17, 2013): 34–40. http://dx.doi.org/10.1038/nchem.1797.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Achmatowicz, Osman, Jacek Rozwadowski, Barbara Szechner, and Jan Szymoniak. "Lewis acid catalysis of the ene addition of dimethyl oxomalonate and butyl glyoxylate to olefins: Formation of cyclic ethers and lactones." Collection of Czechoslovak Chemical Communications 56, no. 5 (1991): 1011–18. http://dx.doi.org/10.1135/cccc19911011.

Full text
Abstract:
The Lewis acid (SnCl4, TiCl4) catalyzed ene addition of dimethyl oxomalonate and butyl glyoxylate to pent-1-ene and 3-methylbut-1-ene has been investigated. Side reactions have been noted leading variously to the formation of δ-lactones and/or cyclic esters (tetrahydrofurans). The effect on the reaction course of the structure of the substrates has been discussed.
APA, Harvard, Vancouver, ISO, and other styles
6

Lee, Chi-Sing, Guangyan Du, Gaopeng Wang, Wenjing Ma, Qianqian Yang, Wenli Bao, Xuefeng Liang, and Lizhi Zhu. "Syntheses of Diverse Natural Products via Dual-Mode Lewis Acid Induced Cascade Cyclization Reactions." Synlett 28, no. 12 (April 6, 2017): 1394–406. http://dx.doi.org/10.1055/s-0036-1588777.

Full text
Abstract:
The σ/π-binding properties of a series of Lewis acids was studied using DFT calculations. The results led to the identification of Zn(II)/In(III) as a suitable dual-mode Lewis acid for use in promoting cascade cyclization reactions. Based on this finding, we developed three new types of dual-mode Lewis acid induced cascade cyclization reactions and have demonstrated the utilities of each process in natural product synthesis.1 Introduction2 Dual-Mode Lewis Acids3 Prins/Conia-Ene Cascade Reaction and its Applications4 Diels–Alder/Carbocyclization Cascade Reaction and Applications4.1 First Generation Diels–Alder/Carbocyclization Cascade Reaction and its Application4.2 Second Generation Diels–Alder/Carbocyclization Cascade Reaction and its Applications5 Michael/Conia-Ene Cascade Reaction and its Applications6 Conclusion
APA, Harvard, Vancouver, ISO, and other styles
7

Kanase, Vanita, and Diptesh T Patil. "EVALUATION OF IN VIVO IMMUNOMODULATORY ACTIVITY OF AQUEOUS AND ETHANOLIC EXTRACT OF EULOPHIA NUDA L." Asian Journal of Pharmaceutical and Clinical Research 11, no. 12 (December 7, 2018): 374. http://dx.doi.org/10.22159/ajpcr.2018.v11i12.27051.

Full text
Abstract:
Objective: The aim of this study was to evaluate the in vivo immunomodulatory activity of an aqueous and ethanolic extract of dried tubers of Eulophia nuda (ENA and ENE).Methods: Effect of both the extracts was evaluated on delayed-type hypersensitivity (DTH) response, serum antibody response, and cyclophosphamide-induced myelosuppression in Swiss albino mice.Results: The extracts showed stimulation of DTH reaction in mice in response to T-cell dependent antigen by both ENE () and ENA (); significant increase in serum antibody titer at of ENA (768.01) and ENE (768.33) extract at 200 mg/kg, compared to control group (213.33); Combined treatment of ENA+Cytochromes P450 [CYP]-25 mg/kg and ENE+CYP-25mg/kg (50, 100, and 200 mg/kg) doses of ENA and ENE each with 25 mg/kg resulted in restoration of bone marrow activity as compared with CYP treatment alone.Conclusion: Both specific and non-specific immunostimulating properties of the ENE and ENA tubers in in vivo experimental methods suggest its therapeutic usefulness in immunocompromised conditions.
APA, Harvard, Vancouver, ISO, and other styles
8

Ollevier, Thierry, and Di Meng. "Fe(BF4)2-Catalyzed Inter- and Intramolecular Carbonyl-Ene Reaction of Trifluoropyruvate." Synlett 29, no. 05 (December 13, 2017): 640–44. http://dx.doi.org/10.1055/s-0036-1591858.

Full text
Abstract:
Inter- and intramolecular carbonyl-ene reactions have been developed using 5 mol% Fe(BF4)2 as catalyst, affording homoallylic alcohols in 36–87% isolated yields. This catalyst, prepared from FeCl2 and AgBF4, is the first FeII Lewis acid reported for the carbonyl-ene reaction using ethyl trifluoropyruvate. The method was successfully applied to the reaction of various 1,1-disubstituted alkenes with ethyl trifluoropyruvate and to the cyclization of citronellal.
APA, Harvard, Vancouver, ISO, and other styles
9

Terada, M., K. Machioka, and K. Sorimachi. "Enantioselective Aza-Ene-Type Reaction." Synfacts 2006, no. 5 (May 2006): 0500. http://dx.doi.org/10.1055/s-2006-934450.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Corkey, Britton K., and F. Dean Toste. "Catalytic Enantioselective Conia-Ene Reaction." Journal of the American Chemical Society 127, no. 49 (December 2005): 17168–69. http://dx.doi.org/10.1021/ja055059q.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Ene reaction"

1

Braddock, D. C. "Towards an asymmetric ene reaction." Thesis, University of Oxford, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307037.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Ahmed, Ghafoor. "Novel transition metal catalysts for intramolecular ene-reaction." Thesis, University of Leicester, 1997. http://hdl.handle.net/2381/29970.

Full text
Abstract:
We have designed a new class of MII-catalysts, namely molybdenum and tungsten (II) complexes of the type PhCH2(Et)3N+[M(CO)4C1Br2]- and M(CO)5(OTf)2 (M = Mo or W), which induce intramolecular cyclization of olefinic aldehydes to afford products with a cis-configuration at the newly formed chiral centres in some cases. These catalysts can be tuned to drive the reaction either toward the end or Prins-type product (32 or 89). The latter reaction occurs via an anti addition of the carbonyl carbon and OH across the C=C bond, as evidenced by isotopic labeling. A chair-like transition state with an axial carbonyl oxygen is proposed to rationalise the stereoselectivities observed.
APA, Harvard, Vancouver, ISO, and other styles
3

Thompson, Michael Richard. "Maleation of polypropylene and EPDM through reactive extrusion using the Alder Ene reaction." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape17/PQDD_0024/NQ30654.pdf.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Dogan, Sengul Dilem. "Regioselectivity In The Ene Reaction Of Singlet Oxygen With Cyclic Alkenes And Application Of Ene Reaction To Stereoselective Synthesis Of Carbaheptopyranose Derivatives." Phd thesis, METU, 2010. http://etd.lib.metu.edu.tr/upload/12612648/index.pdf.

Full text
Abstract:
In the first part of this thesis is related to the regioselectivity in ene reaction of singlet oxygen with cyclic alkenes. The photooxygenation of 1-methyl-, 2,3-dimethyl-, 1,4-dimethylcyclohexa-1,4-dienes, 1,2,3,4,5,8-hexahydronaphthalene (16) and 2,3,4,7-tetrahydro-1H-indene (17) which are readily available through Birch reduction, yielded the ene products. The formed endocyclic dienes were trapped by the addition of singlet oxygen to give corresponding bicyclic endoperoxy-hydroperoxides. In the case of 1-methylcyclohexa-1,4-diene (13) and 1,4-dimethyl-cyclohexa-1,4-diene (15), cis-effect determined the product distribution. Photooxygenation of 2,3-dimethylcyclohexa-1,4-dienes (14) gave mainly exocyclic olefin, which was attributed to the lowered rotational barrier of the methyl group and increased reactivity of the methyl groups. Photooxygeneation of 1,2,3,4,5,8-hexahydronaphthalene (16) and 2,3,4,7-tetrahydro-1H-indene (17) shows importance of the geometry of the allylic hydrogen in the ground state. In the second part of this thesis is related to the stereoselective synthesis of carbaheptopyranose derivatives. Two new carbaheptopyranoses, 5a-carba-6-deoxy-&alpha
-DL-galacto-heptopyranose (184) and 5a-carba-6-deoxy-&alpha
-DL-gulo-heptopyranose (185) have been prepared starting from cyclohexa-1,4-diene. The addition of dichloroketene to cyclohexa-1,4-diene followed by subsequent reductive elimination and Baeyer-Villiger oxidation formed the bicyclic lactone 188. Reduction of the lactone moiety followed by acetylation gave the diacetate 182b with cis-configuration. Introduction of additional acetate functionality into the molecule was achieved by singlet oxygen ene-reaction. The formed hydroperoxide 189 was reduced and then acetylated. The double bond in triacetate was further functionalized either by direct cis-hydroxylation using OsO4 or epoxidation followed by ring-opening reaction to give the hepto-pyranose derivatives 184 and 185.
APA, Harvard, Vancouver, ISO, and other styles
5

Idris, M. S. H. "A study of the ene reactions of 1,2,3-tricarbonyl systems." Thesis, University of Nottingham, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.353550.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Sobanska, Anna W. "Application of the glyoxlate ene reaction to natural product synthesis." Thesis, University of Oxford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.670260.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Atkinson, Duncan. "Novel methods for allylic amination by an intramolecular nitroso ene reaction." Thesis, Loughborough University, 2013. https://dspace.lboro.ac.uk/2134/14069.

Full text
Abstract:
C-H functionalisation reactions aim for the selective cleavage of C-H bonds, and formation of a new carbon or heteroatom bond, often with the use of a transition metal catalyst. These reactions offer potential for functionalisation of hydrocarbons in fewer steps than conventional methods, and with high atom efficiency. They are therefore a subject of intense research in organic synthesis. Carbon-heteroatom bond forming reactions are particularly sought after, and useful in the efficient synthesis of many biologically significant groups such as oxazolidinone rings, 1,2 or 1,3 amino alcohols and amino acid analogues. An efficient, cheap and robust method for C-H amination would also be adaptable to varied syntheses of important large molecules. The necessity for complex and efficient transformations with a minimal number of steps means that heteroatom ring closures are also attractive and widely used reactions in such large molecule syntheses. The nitroso group is a highly reactive species which is normally generated in situ by oxidation of a hydroxylamine, for carbon-nitrogen bond forming reactions including the nitroso Heteroatomic Diels Alder reaction, nitroso ene reaction, and nitroso aldol reaction. Nitroso group reactions often show high stereo- and regioselectivity, and have formed key components of the syntheses of important biological molecules. Enantioselectivive protocols for the nitroso-ene reaction and, to a lesser extent, the nitroso HDA reaction, are poorly developed, however, and the range of available intramolecular nitroso reactions is limited. We aimed to establish efficient single-step intermolecular C-H amination reactions, to give 1,2 and 1,3 heteroatom functionalised molecules, and to develop the capacity for enantioselective induction in this reaction, if possible. Having synthesised a model set of unsaturated hydroxycarbamates, we identified a suitable system for nitroso generation, using a catalytic metal and stoichiometric oxidant. This resulted in in situ generation of cyclised product, with the olefin functionality intact. This cyclisation was then optimised and used to obtain a range of new heterocycles. The possibility of enantioselective induction via chiral catalysts was explored, as well as catalytic systems to increase the stereoselectivity of the reaction. In summary, a cheap, novel and reliable method was developed for formation of oxazolidinone rings from unsaturated hydroxycarbamates using an original intramolecular nitroso ene reaction, and a range of unsaturated heterocycles were synthesised in fairly good yields. Distereoselectivity of the nitroso ene cyclisations was optimised. However, to-date, we were unable to develop an enantioselective varient of the reaction. Several related aminations, as well as transformations of N-hydroxyoxazolidinone products, were also attempted during the project.
APA, Harvard, Vancouver, ISO, and other styles
8

Marcotte, Joel. "Formal Synthesis of (+/-) Morphine via an Oxy-cope/Claisen/Ene Reaction Cascade." Thèse, Université d'Ottawa / University of Ottawa, 2012. http://hdl.handle.net/10393/23560.

Full text
Abstract:
For years now, opium alkaloids and morphinans have been attractive synthetic targets for numerous organic chemists due to their important biological activity and interesting molecular architecture. Morphine is one of the most potent analgesic drugs used to alleviate severe pain. Our research group maintains a longstanding interest in tandem pericyclic reactions such as the oxy-Cope/Claisen/ene reaction cascade and their application to the total synthesis of complex natural products. Herein we report the ventures towards the formal synthesis of (+/-)-morphine based on the novel tandem oxy- Cope/Claisen/ene reaction developed in our laboratory. These three highly stereoselective pericyclic reactions occurring in a domino fashion generate the morphinan core structure after only 7 steps from commercially available material. The formal synthesis culminated in the production of a formal intermediate after a total of 18 linear steps, with an overall yield of 1.0%, successfully intersecting two previous syntheses of the alkaloids, namely the ones of Taber (2002) and Magnus (2009).
APA, Harvard, Vancouver, ISO, and other styles
9

Liu, Xingguo, and 刘兴国. "Concise synthesis of racemic and chiral fumagillol via intramolecular carbonyl ene reaction." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B46588292.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Abu, Ajaj Khalid. "Synthesis of Phosphonate Analogues of the Antibiotic Moenomycin A12." Doctoral thesis, Universitätsbibliothek Leipzig, 2004. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-37333.

Full text
Abstract:
SUMMARY The moenomycin-type compounds are known to inhibit selectively the enzyme penicillin binding protein 1b (PBP 1b) that catalyses the transglycosylation reaction in the biosynthesis of bacterial cell wall peptidoglycan. The moenomycins (see moenomycin A12) have been shown to interfere with this biosynthetic step interacting with the enzyme(s). The moenomycins do not induce resistance readily. A weak point in this respect may, however, be the phosphate bond to unit F. Its cleavage by a yet poorly characterized enzyme is the only enzymatic degradation reaction of the moenomycins that is known to-date. With this in mind we started a programme aimed at synthesizing trisaccharide analogues of moenomycin A12 in which the phosphate oxygen at C-1 of unit F is replaced by a CH2 group. It seemed important to retain all other functional groups in ring F as present in moenomycin since they are known to be of major importance as far as antibiotic activity is concerned. It appeared that the commercially available and cheap b-D-galactose-pentaacetate 30 would be an interesting starting material for this synthesis. In this work, the synthesis began with the introduction of the C-glycoside appendage at position 1 according to Giannis et al., thus forming the allyl C-galactopyranoside 34, a substance that represents the first C-glycosyl backbone for the synthesis of the glycosyl acceptors. The total synthesis of the glycosyl acceptors is shown in Scheme 6.1. We wanted to convert the C-allyl glycoside 34 into its propenyl analogue. Attempts to achieve this with singlet oxygen and palladium-mediated reaction proved fruitless. On the other hand, ene reaction of 34 with 4-phenyltriazolin-3,5-dione in CH2Cl2 provided 56 in 83 % yield. Ozonolysis of this alkene (-70 °C, MeOH-CH2Cl2) and subsequent quenching with dimethyl sulfide, followed by reduction of the crude aldehyde with sodium acetoxyborohydride (prepared from NaBH4 and AcOH in THF) furnished the primary alcohol 35 (85 %). This alcohol was converted into the mesylate 60 (60 %), and this in turn into the bromide 61 (80 %) by heating it at 80 °C with tetrabutylammonium bromide in toluene. The acetate groups were hydrolysed using Zemplén conditions to furnish 62 quantitatively. The primary hydroxyl group in 62 was protected as a tBuPh2Si ether 63 (85 %) on reaction with TBDPSCl in DMF at 0 °C, and as a tBuMe2Si ether 94 (87 %) on reaction with TBDMSCl in DMF at 0 °C in the presence of imidazole. PTScatalysed isopropylidenation of the 3,4-diols 63 and 94 with 2,2-dimethoxypropane in dry acetone gave the 3,4-O-acetonide derivatives 53 (88 %) and 95 (90 %), respectively. On the other hand, the glycosyl acceptor 53 was converted into the glycosyl acceptor 92. The free hydroxyl group in compound 53 was protected as an acetate group on reaction with acetic anhydride in pyridine in the presence of DMAP giving 89 (88 %). The silyl ether in 89 was cleaved with a molar solution of TBAF in THF affording compound 90 in 87 % yield. The free hydroxyl group in 90 was then subjected to an oxidation using the TEMPO method affording the aldehyde which was in turn oxidised with sodium chlorite to the corresponding acid. The acid was converted to the amide 91, making use of Staab's method, in which the acid was activated with CDI in dichloromethane to give the imidazolide, which upon reaction with ammonia furnished the amide 91 in an overall yield of 95 %. The required glycosyl acceptor 92 was obtained in quantitative yield by cleavage of the ester bond at position 5 under Zemplén conditions. Disaccharide formation was achieved employing the Jacquinet and Blatter method, which involves the use of glycosyl donor 67 and TMSOTf. No reaction was observed between this donor and acceptor 92, which may reflect the low nucleophilicity of the acceptor. On the contrary, glycosylation with acceptor 53 gave 68 (79 %). Deprotection of the silyl group in the disaccharide 68 was easily accomplished on treatment with a molar solution of TBAF in THF at RT affording 71 (89 %). Synthesis of the uronamide 72 was achieved after three major steps, in an overall yield of 98 %. Oxidation of the primary hydroxyl group in unit F to the corresponding aldehyde was accomplished with sodium hypochlorite and TEMPO. Oxidation of the crude aldehyde to the carboxylic acid with sodium chlorite followed by amide formation according to Staab gave 72. Removal of the isopropylidene group from 72 with trifluoroacetic acid (TFA) at RT furnished the diol 73 (89 %). Introduction of the carbamoyl group at C-4F position was achieved in two steps. Conversion of the diol 73 into the cyclic carbonate 76 with CDI in CH2Cl2 (84 %) and subsequent ring opening of this carbonate by bubbling a stream of gaseous ammonia into the CH2Cl2 solution at 0 °C gave 74 (62 %) as well as its isomer 77 (21 %). Dehalogenation of the N-trichloroacetyl group was intensively studied, but interactions of other functional groups in the studied substances could not be avoided. The base-labile carbonate in 76 and the carbamoyl group in urethane 74 were cleaved under the reaction conditions. Hydrolysis of 76 with 0.5 M LiOH in MeOH-THF (1:1) followed by acetylation gave 80 (73 %), while its reduction with NaBH4 in ethanol followed by acetylation gave 82 (60 °C, 85 %; RT, 83 %). On the other hand, reduction of 74 with NaBH4 in ethanol at 60 °C followed by acetylation gave 82 (78 %), while performing the reduction step at 5 °C (THF-MeOH 4:1) or at RT (ethanol or isopropanol) gave 80 in an average yield of 65 %. In a non reproducible reaction (NaBH4, EtOH, RT, then Ac2O, pyridine, RT), the desired compound 83 (42 %) was obtained accompanied by 82 (46 %) The reaction between the N-trichloroacetyl group and NaBH3CN was also fruitless. The phosphonate grouping was installed making use of Arbuzov reaction furnishing 85 (70 %). Trisaccharides could not be obtained from the oxazoline donor 42 (prepared from chitobiose octaacetate 86) through its reaction with acceptor 53. There was also no coupling product between the recently synthesized donor 88 and the acceptor 92. However, in this work, trisaccharide formation was achieved through the glycosylation reaction of donor 88 and acceptor 95 in 50 % yield (-30 °C, 1,2-dichloroethane, 3 Å, TMSOTf-TEA). Selective deprotection of the TBDMS group in compound 96 was accomplished at -10 °C with 1 eq of a molar solution of TBAF in THF. The free hydroxyl group of 97 was subjected to an oxidation using the TEMPO method affording the aldehyde. After oxidation of the aldehyde with sodium chlorite, the resulting carboxylic acid was converted according to Staab's method into the amide 93 in an overall yield of 95 % (based on 96). There were difficulties in converting the N-phthalimido group in 93 to the N-acetyl group which is necessary for biological activity of moenomycin-type compounds, since the reactions were accompanied by elimination of HBr. In conclusion, the synthetic methods employed in this work allow to prepare the di- and trisaccharides C-phosphonate analogues of moenomycin A12
Synthese von Phosphonat-Analoga des Antibiotikums Moenomycin A12 Universität Leipzig, Dissertation Diese Arbeit enthält 130 Seiten, 73 Abbildungen, 1 Tabelle, 156 Literaturangaben Referat: Im Rahmen der vorliegenden Arbeit wurden C-Glycosid-Di- und Trisaccharid-Bausteine des Antibiotikums Moenomycin A12 ausgehend von b-D-Galactose-pentaacetat hergestellt. Das Ausgangmaterial wurde in D-Galactoheptonamid übergeführt. Die Einheit F des Disaccharidbausteins hat alle Substituenten, die die Einheit F des Moenomycins A12 hat. Der ausgearbeitete Syntheseweg sollte zur Synthese anderer Analoga geeignet sein
APA, Harvard, Vancouver, ISO, and other styles
More sources

Books on the topic "Ene reaction"

1

Rakshit, D. End-modification reactions of Dextran. Birmingham: University of Birmingham, 1987.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
2

Mezzalira, Luca. Front-End Reactive Architectures. Berkeley, CA: Apress, 2018. http://dx.doi.org/10.1007/978-1-4842-3180-7.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Lutz, Bernd. Experimente und Behandlungsvorschläge zum Unterrichtsthema "Redox-Reaktionen": Eine Synopse. Kiel: Institut für die Pädagogik der Naturwissenschaften, 1986.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
4

Klibanoff, Peter. Investor reaction to salient news in closed-end country funds. Cambridge, MA: National Bureau of Economic Research, 1996.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
5

Kerekes, Amália. Mehr oder Weininger: Eine Textoffensive aus Österreich/Ungarn. Wien: Braumüller, 2005.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
6

Meyer, Matthias. Serielle versus parallele Verarbeitung visueller Information: Eine experimentelle Untersuchung am Beispiel eines Konzentrationstests. Bonn: Holos, 1994.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
7

Woodward, C. Vann. Reunion and reaction: The Compromise of 1877 and the end of Reconstruction. New York: Oxford University Press, 1991.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

Sterkenburg, P. G. J. van. Vloeken: Een cultuurbepaalde reactie op woede, irritatie en frustratie. [Den Haag]: Sdu Standaard, 1997.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
9

Bosch, Kees van den. De angst reactor: Kalkar, kroniek van een eeuwige belofte. Amsterdam: SUN, 2006.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
10

P. G. J. van Sterkenburg. Vloeken: Een cultuurbepaalde reactie op woede, irritatie en frustratie. 2nd ed. Den Haag: Sdu Standaard, 2001.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Book chapters on the topic "Ene reaction"

1

Li, Jie Jack. "Alder ene reaction." In Name Reactions, 2. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_2.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Li, Jie Jack. "Alder ene reaction." In Name Reactions, 1–2. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_1.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Li, Jie Jack. "Alder ene reaction." In Name Reactions, 2. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_2.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Li, Jie Jack. "Alder ene reaction." In Name Reactions, 1–2. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_1.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Li, Jie Jack. "Alder Ene Reaction." In Name Reactions, 1–3. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-50865-4_1.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Brummond, Kay M., and Jamie M. McCabe. "The Rhodium(I)-Catalyzed Alder-Ene Reaction." In Modern Rhodium-Catalyzed Organic Reactions, 151–72. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527604693.ch8.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Zhao, Da. "Ene Reaction of 1,3-Dehydro-o-Carborane." In Functionalization of Carborane via Carboryne Intermediates, 103–15. Singapore: Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-10-1569-4_6.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Carlsson, Ingemar, Adrian Harden, Stefan Lundmark, Ana Manea, Nicola Rehnberg, and Lennart Svensson. "Allyl Ethers in the Thiol-ene Reaction." In ACS Symposium Series, 65–75. Washington, DC: American Chemical Society, 2003. http://dx.doi.org/10.1021/bk-2003-0847.ch006.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Guan, Xiaoyuan, Guangxue Chen, Rui Guo, Zhaohui Yu, and Minghui He. "Thiol-ene Michael Addition Reaction Under Phototriggered Base Proliferation." In Lecture Notes in Electrical Engineering, 909–18. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-7629-9_113.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

"Ene Reaction." In Encyclopedia of Lubricants and Lubrication, 486. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-22647-2_200139.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Ene reaction"

1

Shirai, Masamitsu, Koichi Maki, Haruyuki Okamura, Koji Kaneyama, and Toshiro Itani. "Highly sensitive EUV-resist based on thiol-ene radical reaction." In SPIE Advanced Lithography, edited by Robert D. Allen. SPIE, 2010. http://dx.doi.org/10.1117/12.846339.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Rupp, Barbara, Thomas Bauer, and Christian Slugovc. "Thiol-ene reaction as tool for crosslinking of polynorbornene micelles in the nanoscale." In SPIE NanoScience + Engineering, edited by Stefano Cabrini and Taleb Mokari. SPIE, 2009. http://dx.doi.org/10.1117/12.829217.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Liu, Shuyan, Yabin Zhang, Congcong Zhai, Luqing Zhang, Chuanyong Zong, Jiachen Ma, Zhiyuan Huo, and Shuxiang Zhang. "Synthesis and Properties of a Novel Fluorinated Surfactant via “Thiol-ene” Click Reaction." In The Second International Conference on Materials Chemistry and Environmental Protection. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0008185400550058.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Grauželienė, Sigita, Deimantė Valaitytė, Jolita Ostrauskaitė, and Angels Serra. "Fully Bio-Based Polymers Derived from Acrylated Epoxidized Soybean Oil by Thiol-ene Reaction." In The First International Conference on “Green” Polymer Materials 2020. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/cgpm2020-07177.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Ahmed, Kumkum. "Facile fabrication of network polymers via thiol-ene click reaction for sensing applications (Conference Presentation)." In Behavior and Mechanics of Multifunctional Materials XVII, edited by Aimy Wissa, Mariantonieta Gutierrez Soto, and Russell W. Mailen. SPIE, 2023. http://dx.doi.org/10.1117/12.2661644.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Saito, T., T. Izumi, K. Tanaka, R. C. Advincula, and H. Usui. "Preparation of Surface-Tethered Polymer Thin Films by Vapor Deposition Assisted by Thiol-ene Reaction." In 2019 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2019. http://dx.doi.org/10.7567/ssdm.2019.a-2-05.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Shihui Wu, Lianhe Shu, and Kangnian Fan. "ENE reaction of fullerene C/sub 60/ and 4-allylanisole introduction of alkene to buckminsterfullerene." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835567.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Bermesheva, Evgeniya V., Pavel P. Chapala, and Maxim V. Bermeshev. "A new approach to the synthesis of polymers bearing 3,4-dihydroxyphenyl-moieties in side groups from eugenol and polybutadiene with help of thiol-ene reaction." In 9TH INTERNATIONAL CONFERENCE ON “TIMES OF POLYMERS AND COMPOSITES”: From Aerospace to Nanotechnology. Author(s), 2018. http://dx.doi.org/10.1063/1.5046040.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Hedayat Mofidi, Seyyed Ali, and Kent S. Udell. "Absorption Process in MgCl2-NH3 Thermochemical Batteries With Constant Mass Flow Rate." In ASME 2018 12th International Conference on Energy Sustainability collocated with the ASME 2018 Power Conference and the ASME 2018 Nuclear Forum. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/es2018-7512.

Full text
Abstract:
The working principle and performance of thermochemical batteries have been studied before [1–3]. In this paper, the performance of a thermochemical battery based on magnesium chloride and ammonia pair with a constant mass flow rate of ammonia gas is studied. It is shown that controlling the mass flow rate lowers the temperature of the reactive complex and increases the duration of the absorption process. However, it was observed that the reaction becomes mass transfer limited which slows the absorption rate and takes control of the reaction away from the mass flow controller. The progress of the reaction inside the reactor is studied in a single-cell reactor to understand the performance of these thermal batteries. It was shown that a reaction zone starts at the inlet and moves toward the end of the reactor. The mass transfer limited reaction zone movement reduces the absorption rate and temperature in the reaction zone.
APA, Harvard, Vancouver, ISO, and other styles
10

Mehta, Mayur, N. L. Singh, R. Makwana, S. Mukherjee, V. Vansola, Y. Santhi Sheela, S. Khirwadkar, et al. "Neutron induced reaction cross-section for the plasma facing fusion reactor material - Tungsten isotopes." In 2018 19th International Scientific Conference on Electric Power Engineering (EPE). IEEE, 2018. http://dx.doi.org/10.1109/epe.2018.8395989.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Reports on the topic "Ene reaction"

1

Klibanoff, Peter, Owen Lamont, and Thierry Wizman. Investor Reaction to Salient News in Closed-End Country Funds. Cambridge, MA: National Bureau of Economic Research, May 1996. http://dx.doi.org/10.3386/w5588.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Ramnath, Rishabh, Neale Kinnear, Sritika Chowdhury, and T. Hyatt. Interacting with Android Auto and Apple CarPlay when driving: The effect on driver performance. TRL, January 2020. http://dx.doi.org/10.58446/sjxj5756.

Full text
Abstract:
This study aimed to assess the impact of interacting with two infotainment systems, Android Auto and Apple CarPlay, on four driver performance measures: reaction time, driving behaviour, eyes-off road and self-reported performance. It also compared the results with other forms of driver impairment studied previously. Twenty regular Android users took part in the Android Auto trial and 20 regular Apple users took part in the Apple CarPlay trial. Each participant completed three 20 minute drives in TRL’s DigiCar simulator: control (no interaction with infotainment system), voice enabled and touch enabled. The route was divided into sections and participants performed music, navigation, texting and calling tasks at specific times during the drive. Compared with the control drive, participants in both trials showed a reduction in average speed, increase in deviation of headway and larger deviation of lane position for most tasks; this effect was greater when using touch features than voice features. Eye gaze measures indicated that participants did not meet the NHTSA criteria for most of the tasks when using touch controls for both systems, but they met the criteria when using voice control. Self-reported data suggested that participants found interacting through touch to be more difficult and distracting than voice. Most critically, reaction time to a stimulus on the road ahead was significantly higher when selecting music through Spotify when using Android Auto and Apple CarPlay. Participants also failed to react more to the stimulus on the road ahead when engaging with either Android Auto or Apple CarPlay compared with a control drive. Comparison with previous driver impairment studies showed that the increase in reaction time when interacting with either system using touch was higher than previously measured forms of impairment, including texting and hand-held calls.
APA, Harvard, Vancouver, ISO, and other styles
3

Lichtner, Peter C. End-Member Formulation of Solid Solutions and Reactive Transport. Office of Scientific and Technical Information (OSTI), September 2015. http://dx.doi.org/10.2172/1221523.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Benjamin Spencer, Yongfeng Zhang, Pritam Chakraborty, S. Bulent Biner, Marie Backman, Brian Wirth, Stephen Novascone, and Jason Hales. Light Water Reactor Sustainability Program Grizzly Year-End Progress Report. Office of Scientific and Technical Information (OSTI), September 2013. http://dx.doi.org/10.2172/1111509.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Galuszka, J., and T. Giddings. Methane to syngas in staged membrane reactor year-end report. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1996. http://dx.doi.org/10.4095/304637.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Hale, Richard Edward, David L. Fugate, Sacit M. Cetiner, and A. L. Qualls. Update on ORNL TRANSFORM Tool: Simulating Multi-Module Advanced Reactor with End-to-End I&C. Office of Scientific and Technical Information (OSTI), May 2015. http://dx.doi.org/10.2172/1239756.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Mueller, D., H. F. Dylla, M. G. Bell, W. R. Blanchard, C. E. Bush, G. Gettelfinger, R. J. Hawryluk, K. W. Hill, A. C. Janos, and F. C. Jobes. End points in discharge cleaning on TFTR (Tokamak Fusion Test Reactor). Office of Scientific and Technical Information (OSTI), July 1989. http://dx.doi.org/10.2172/6025693.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Read, Matthew. Estimating the Effects of Monetary Policy in Australia Using Sign-restricted Structural Vector Autoregressions. Reserve Bank of Australia, January 2023. http://dx.doi.org/10.47688/rdp2022-09.

Full text
Abstract:
Existing estimates of the macroeconomic effects of Australian monetary policy tend to be based on strong, potentially contentious, assumptions. I estimate these effects under weaker assumptions. Specifically, I estimate a structural vector autoregression identified using a variety of sign restrictions, including restrictions on impulse responses to a monetary policy shock, the monetary policy reaction function, and the relationship between the monetary policy shock and a proxy for this shock. I use an approach to Bayesian inference that accounts for the problem of posterior sensitivity to the choice of prior that arises in this setting, which turns out to be important. Some sets of identifying restrictions are not particularly informative about the effects of monetary policy. However, combining the restrictions allows us to draw some useful inferences. There is robust evidence that an increase in the cash rate lowers output and consumer prices at horizons beyond a year or so. The results are consistent with the macroeconomic effects of a 100 basis point increase in the cash rate lying towards the upper end of the range of existing estimates.
APA, Harvard, Vancouver, ISO, and other styles
9

Wang, Dou, Tao Li, Jie Rong, Nan Wang, Xianling Fan, and Yongmei Yan. Is fluoxetine necessary for preventive treatment of post-stroke depression in stroke patients? A meta-analysis of randomized controlled trials. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, March 2022. http://dx.doi.org/10.37766/inplasy2022.3.0137.

Full text
Abstract:
Review question / Objective: One third of patients may have post-stroke depression after a stroke. Poststroke depression seriously affects rehabilitation outcome, quality of life and mortality of stroke patients. Data on preventive treatment of fluoxetine for post-stroke depression in this setting are inconsistent. The purpose of this systematic review was to explore the efficacy and acceptability of fluoxetine for early antidepressant therapy in stroke patients, so as to better provide evidence-based medical evidence for clinical practice. To this end, the systematic review to be considered will address the following issues: P: stroke patients; I: Treatment interventions included: fluoxetine (Prozac), control group: conventional treatment, plus placebo or no other intervention; O: Primary outcome: incidence of PSD, secondary outcome: Hamilton Scale, neurological dysfunction, daily living ability, mortality, incidence of adverse reactions; S: This review includes only randomized controlled studies.
APA, Harvard, Vancouver, ISO, and other styles
10

Wang, Guanyi, Cezary Bojanowski, Dhongik Yoon, John Stillman, David Jaluvka, Leslie Foyto, and Erik Wilson. University of Missouri Research Reactor (MURR) Design Demonstration Element End Fitting Structural Rigidity Analysis. Office of Scientific and Technical Information (OSTI), January 2022. http://dx.doi.org/10.2172/1847307.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Ene reaction' for particular source types:
Journal articles Dissertations / Theses Books
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography