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Готові списки джерел за темами / Novel c–c

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Добірка наукової літератури з теми "Novel c–c"

Автор: Grafiati

Опубліковано: 6 вересня 2023

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Статті в журналах з теми "Novel c–c"

1

Wentrup, C., B. E. Fulloon, D. W. J. Moloney, Hervé Bibas, and M. W. Wong. "Novel heterocumulene (RN=C=C=C=X) and ketene rearrangements." Pure and Applied Chemistry 68, no. 4 (January 1, 1996): 891–94. http://dx.doi.org/10.1351/pac199668040891.

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2

WENTRUP, C., B. E. FULLOON, D. W. J. MOLONEY, H. BIBAS, and M. W. WONG. "ChemInform Abstract: Novel Heterocumulene (RN=C=C=C=X) and Ketene Rearrangements." ChemInform 27, no. 50 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199650275.

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3

Wiedemann, Ralf, Paul Steinert, Olaf Gevert, and Helmut Werner. "Novel C−C and C−C−P Coupling Reactions Using an Allenylidenerhodium Complex as a Precursor." Journal of the American Chemical Society 118, no. 10 (January 1996): 2495–96. http://dx.doi.org/10.1021/ja953911v.

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4

Adams, Chris J., Michael I. Bruce, Brian W. Skelton, and Allan H. White. "A novel route to butatrienylidene complexes: stabilisation of :CCCCH2on Ru5clusters." Chem. Commun., no. 23 (1996): 2663–64. http://dx.doi.org/10.1039/cc9960002663.

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5

Niharika, Pedireddi, and Gedu Satyanarayana. "One-pot C–C/C–O bond formation: synthesis of spirocyclic lactones." RSC Advances 6, no. 2 (2016): 837–43. http://dx.doi.org/10.1039/c5ra22684h.

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6

Rozen, Shlomo, and Iris Ben-David. "BrF3, an Underutilized Reagent in Organic Chemistry: A Novel C−C−N to C−N−C Rearrangement." Journal of Organic Chemistry 66, no. 2 (January 2001): 496–500. http://dx.doi.org/10.1021/jo0013094.

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7

Mirzarakhmetova, Dilbar T., and Yulduz Yusupbaevna Baltaeva. "Molecular Genetic Analysis Of C-X-C Motif Chemokine Ligand 9 (CXCL9) As A Novel Biomarker In Atherosclerosis." American Journal of Applied sciences 3, no. 05 (May 7, 2021): 24–30. http://dx.doi.org/10.37547/tajas/volume03issue05-05.

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Анотація:

For almost a century, many have considered lipids as the sine qua non of atherosclerosis. However, in 1856 Rudolf Virchow introduced a theory that inflammation is the driving force of atherogenesis. Recruitment of blood leukocytes to the injured vascular endothelium characterizes the initiation and progression of atherosclerosis and involves many inflammatory mediators, modulated by cells of both innate and adaptive immunity. The pro-inflammatory cytokine, interferon (IFN)-γ derived from T cells, is vital for both innate and adaptive immunity and is also expressed at high levels in atherosclerotic lesions. As such, IFN-γ plays a crucial role in the pathology of atherosclerosis through activation of signal transducer and activator of transcription STAT1.Our study indeed provides evidence that in HMECs STAT1 coordinates a platform for cross-talk between IFNγ and TLR4, and identifies a STAT1-dependent gene signature that reflects a pro-atherogenic state in coronary artery disease (CAD) and carotid atherosclerosis. Taken together, our data indicate that in the presence of appropriate stimuli, HMECs are highly responsive and consistently express Cxcl9. HMECs may therefore provide a better model for in vitro studies of atherosclerosis.

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8

Leclère, Mathieu, Bonnie K. Kwok, Luke K. Wu, David S. Allan, and Robert N. Ben. "C-Linked Antifreeze Glycoprotein (C-AFGP) Analogues as Novel Cryoprotectants." Bioconjugate Chemistry 22, no. 9 (September 21, 2011): 1804–10. http://dx.doi.org/10.1021/bc2001837.

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9

Trost, Barry M., and Chao-Jun Li. "Novel "Umpolung" in C-C Bond Formation Catalyzed by Triphenylphosphine." Journal of the American Chemical Society 116, no. 7 (April 1994): 3167–68. http://dx.doi.org/10.1021/ja00086a074.

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10

Cauwelier, B., F. Nollet, A. Gadisseur, W. Schroyens, and Z. Berneman. "A novel HLA-C null allele,HLA-C*05:99N." Tissue Antigens 84, no. 4 (June 25, 2014): 420–21. http://dx.doi.org/10.1111/tan.12404.

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Дисертації з теми "Novel c–c"

1

Waterfield, P. C. "Novel C-organostannyl heterocycles." Thesis, University of Bath, 1988. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.384138.

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2

Balanta, Castillo Angelica. "Novel molecular and colloidal catalysts for c-c bond formation processes." Doctoral thesis, Universitat Rovira i Virgili, 2011. http://hdl.handle.net/10803/66243.

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Esta tesis doctoral se centró en la síntesis y la caracterización de nanopartículas metálicas (Pd, Ni, Pt) estabilizadas por varios tipos de ligandos y el uso de estas nanopartículas en reacciones de formación de nuevos C-C o C-heteroatomo: a) Reacción de substitución alílica catalizadas por Pd; b) Reacción de acoplamiento asimétrico de Suzuki-Miyaura; c) Reacción de acoplamiento de Suzuki-Miyaura; d) reacción de adición 1,4 de ácidos borónicos a cetonas. En cada una de estas reacciones se llevó a cabo la síntesis y caracterización de nanoparticulas metálica y complejos moleculares usando muchos tipos de ligandos en los sistemas moleculares y los sistemas análogos cataliazados por nanopartículas. Excelentes actividades y enatioselectividades fueron obtenidas en la reacción de alquilación y aminación alílica. Además, estos sistemas fueron reciclados usando líquidos iónicos. También, nuevos y selectivas nanoparticulas fueron sintetizadas y caracterizadas. Estas nanopartículas fueron usadas exitosamente en varias reacciones de formación de nuevos enlaces C-C.
This doctoral thesis focuses on the synthesis and characterization of metal nanoparticles (Pd, Ni, Pt) stabilized by several types of ligands and the used of these nanoparticles in new C-C or C-heteroatom bond formation reactions: a) Pd-catalysed asymmetric allylic substitution reactions; b) Pd-catalysed asymmetric Suzuki-Miyaura coupling reactions; c) Ni-catalysed Suzuki-Miyaura coupling reactions; d) Pt-catalysed 1,4-addition of phenylboronic acid to 2-cyclohexen-1-one reaction. For each reaction, the synthesis and characterization of metal nanoparticles and molecular complexes using several types of ligands were performed and both types of catalytic systems were tested in the appropriate reactions. Remarkably, excellent enantioselectivities using Pd/phosphite ligand were obtained in allylic substitution reaction. An efficient recovery of the catalytic system was carried out using ionic liquids as reaction medium. New active and selective nanoparticles were synthesized and characterized. These nanoparticles were applied successfully in various C-C bond formation reactions.

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3

Redpath, P. "A novel and versatile approach to C- and C-AZA-nucleosides." Thesis, Queen's University Belfast, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.517040.

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4

Edwards, Michael Gareth. "Borrowing hydrogen : a novel concept for C-C bond formation with alcohols." Thesis, University of Bath, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.397556.

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5

Ferguson, William James. "The nitrile oxide/isoxazoline route to novel C-glycosides and C-disaccharides." Thesis, University of Edinburgh, 1996. http://hdl.handle.net/1842/13815.

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Анотація:

A convergent route, based on nitrile oxide/isoxazoline chemistry to carbon-linked disaccharides (C-disaccharides) and C-glycosides with functionalised linkages has been investigated. The sequence involves three steps. Firstly, the cycloaddition of a sugar-derived nitrile oxide to a terminal alkene provides a 3,5-disubstituted 2-isoxazoline. Next, the substituents attached to the isoxazoline may be modified, and finally the heterocycle subjected to either hydrogenolysis or reductive cleavage to afford a C-glycoside with a carbonyl or an amino functionalised linkage. Four terminal alkenes were selected; two ω-unsaturated monosaccharide derivatives, methyl 5, 6-dideoxy-2,3-0-isopropylidene-α-D-lyxo-hex-5-enofuranoside (93) and 3-O-benzyl-5, 6-dideoxy-2, 3-O-isopropylidene-α-D-xylo-hex-5-enofuranose (84), and two non-carbohydrate model alkenes, methylenecyclohexane and styrene. The in situ Mukaiyama dehydration of the peracetylated 2,6-anhydro-1-deoxy-1-nitroalditol derivatives from nitromethane and D-xylose, D-galactose and D-mannose provided the source of nitrile oxides (79), (89) and (90) respectively. Cycloadditions of the xylopyranosyl and galactopyranosyl nitrile oxides (79) and (89) to alkenes (93) and (84) proceeded regiospecifically and with a high degree of π-facial selectivity (40-64% d.e.). In each case the major adduct was found to possess R-configuration at the newly formed chiral centre C-5, corresponding to an erythro relationship between it and the adjacent C-4 position of the attached furanose unit. The structure of the isoxazoline formed from xylopyranosyl nitrile oxide (79) and D-mannose derived alkene (93) was established by X-ray crystallography. The observed selectivies may be rationalised in terms of the "inside alkoxy effect" proposed by Houk and the "homoallylic" modification of De Micheli et al.

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6

Gonzalez, De Castro Angela. "Novel iron-pybisulidine catalysts for the selective aerobic oxidation and C-O/C-C cleavage of organic substrates." Thesis, University of Liverpool, 2014. http://livrepository.liverpool.ac.uk/19373/.

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The selective oxidation of organic compounds is one of the most attractive transformations for both, industry and academia. Industrial interest stems from the potential application of such oxidation methodologies in the economic, greener synthesis of valuable products, whereas academic research is challenged by the difficulties in achieving specific, direct functionalisation of the “inert” CH bonds in complex molecules. In this Ph. D. thesis, our contribution to the selective oxidation of organic substrates using a novel class of iron catalysts is presented. A general introduction covering the major challenges in the area of iron-catalysed selective oxidation of organic compounds is described in Chapter 1. Chapter 2 covers the design, synthesis and coordination properties of the novel PyBisulidine type ligands, which we have conceived for their potential use in selective oxidation, attempting to overcome some of the limitations of current methods. The efficiency of such PyBisulidine ligands is demonstrated in Chapter 3, where iron-PyBisulidine complexes are used for catalysing the aerobic α-oxidation of functionalised ethers. High catalytic efficiency, very good mass balance and excellent functional group tolerance were achieved with these catalysts under mild conditions. Such advantages stem from an unconventional reaction mechanism, involving the dehydrogenative oxygenation of the ether substrate to give a peroxobisether, followed by the cleavage of the peroxy bond to form two ester molecules. Unlike metalloenzymes and biomimetic iron complexes, H2 is released as the sole byproduct during the catalytic cycle. The oxidation mechanism is discussed in Chapter 4. Like natural dioxygenases, iron-PyBisulidine catalysts were found capable of promoting the aerobic cleavage of aliphatic C-C and C-O bonds. Even though biomimetic complexes are often seen as simplified models to study enzymatic processes, a more synthetic perspective of the selective aerobic cleavage of ethereal C-C and C-O bonds is described in Chapter 5.The great potential of such cleavages in organic synthesis is well exemplified in the iron-PyBisulidine catalysed direct conversion of natural isochromans into biologically active isochromanones with excellent selectivity. The ability of the iron-PyBisulidine complexes in catalysing aerobic C-C cleavages is further expanded in Chapter 6, where the oxidative cleavage of olefinic C=C bonds to carbonyl compounds is demonstrated. The catalytic reactions proceeded efficiently, showing a broad scope and a mechanism that involves the formation of dioxetane intermediates is postulated. Chapter 7 is an extension of Chapter 6, in which iron-PyBisulidine complexes were found to catalyse α-methylstyrene linear dimerisation under an inert atmosphere. Moreover, control in the regioselectivity of the double bond in the dimers can be achieved by modifications in the PyBisulidine ligands. Final conclusions and a perspective of the research covered in this Ph.D. thesis are provided in Chapter 8.

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7

Zhou, Yixing Harden T. Kendall. "Cloning and characterization of a novel phospholipase C enzyme, human phospholipase C eta2." Chapel Hill, N.C. : University of North Carolina at Chapel Hill, 2007. http://dc.lib.unc.edu/u?/etd,1271.

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Анотація:

Thesis (Ph. D.)--University of North Carolina at Chapel Hill, 2007.
Title from electronic title page (viewed Mar. 26, 2008). "... in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Pharmacology." Discipline: Pharmacology; Department/School: Medicine.

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8

Niblock, Helen Sarah. "Synthesis of the C(1)-C(9) fragment of disorazole C1 and novel heterocyclic analogues." Thesis, University of Edinburgh, 2012. http://hdl.handle.net/1842/6251.

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A highly convergent strategy for the synthesis of the antitubulin polyketide disorazole C1 is proposed based around the alkyne precursor I, featuring a novel Evans-Tishchenko/ring closing alkyne metathesis approach. Due to the inherent symmetry of the molecule this retrosynthesis leads to two fragments: a β- hydroxyketone II and the oxazole C(1)-(9) fragment III. A review of previous syntheses of disorazole C1 and established structure activity relationships (SARs) highlights a gap in current knowledge relating to the role of the oxazole in tubulin binding. Therefore, the focus of this research has been towards developing new routes for the synthesis of the C(1)-C(9) fragment that can be adapted to the synthesis of heterocyclic analogues to further establish the SAR of disorazole C1. Chapter 2 focuses on a disconnection at the C(5)-C(6) bond and a novel synthesis of the racemic C(1)-C(9) fragment has been achieved via a lithiation of methyl 2- methyl-1,3-oxazole-4-carboxylate and coupling to aldehyde V. First generation asymmetric routes to the C(1)-C(9) fragment centred on i. a biomimetic amino acid condensation route via an oxazoline intermediate based on the precedent of Meyers et al. and ii. a C(4)-C(5) disconnection approach based around the epoxide VII; are discussed in chapter 3. A second generation C(4)-C(5) disconnection centred on the novel tosylate VIII is discussed in chapter 4. Attempts to synthesise the parent C(1)- C(9) oxazole fragment using the tosylate VIII via i. a palladium catalysed C-H activation of ethyl 4-oxazole carboxylate and ii. lithiation of oxazole are reported. Coupling of fragment VIII (X = OTs) with ethyl 1H-pyrazole-4-carboxylate and a CuAAC coupling of the azide derived from tosylate VIII with methyl propiolate has allowed the successful completion of the synthesis of pyrazole and triazole analogues of this fragment.

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9

Rogers, Joshua Peter. "Photoelectron spectroscopy of (C₆F₆)-ₙ and C₆F₆ · I-clusters in a novel instrument". Thesis, Durham University, 2017. http://etheses.dur.ac.uk/12364/.

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The capabilities of a new photoelectron spectrometer are characterised in the study of (C6F6)n– and (C6F6)I– clusters. The photoelectron spectrometer consists of a series of vacuum chambers that facilitate a molecular beam of gas-phase anions. These anions and clusters are generated at the point of intersection between an electron beam and the supersonic expansion produced by a high temperature Even-Lavie pulsed valve. The anions are extracted orthogonally and mass-separated in a Wiley-McLaren time-of-flight mass spectrometer. The analyte is addressed by a laser pulse produced by either a tuneable nanosecond OPO for one-photon frequency-resolved measurements or a femtosecond pump-probe regime for two-photon time-resolved measurements. The kinetic energy of the resulting photoelectrons are measured in a velocity-map imaging spectrometer. C6F6- is of interest due to the prediction that it ought to host a meta-stable binding mode of the excess electron known as a correlation-bound state (CBS). Similar to other non-valence binding modes, such as the dipole-bound state, this CBS is thought to act as a doorway state in the mechanism of low energy electron capture. The CBS is characterised by a large and diffuse orbital in which the excess electron is bound primarily through charge:induced-dipole interactions with the molecule’s valence orbital system. In the CBS, C6F6- is predicted to adopt a planar geometry like that of the neutral species, in contrast to the buckled geometry adopted when the excess electron occupies a valence orbital. Frequency- and time-resolved measurements of the anion were made in an effort to generate and observe the CBS. Initially, frequency resolved measurements of (C6F6)n– revealed a vertical detachment energy of 1.60 ± 0.07 eV for n = 1, increasing by 200 meV per additional cluster unit up to n = 5. The broad shape of the direct detachment peak confirms the disparity in geometry between the anion and neutral species. However, no evidence of the CBS was evident in these data. In subsequent explorations, an in-situ electron donor was employed to mimic the electron impact process. An I– ion was introduced to the neutral C6F6 molecule to produce clusters of (C6F6)I–. Frequency-resolved measurements of this cluster revealed a mechanism for electron loss below the threshold for the single-photon direct detachment process. This suggested the presence of a charge-transfer channel centred around hv = 3.3 eV. Time-resolved measurements of (C6F6)I– confirmed the presence of the charge-transfer state and revealed an instantaneous and coherent transfer of the electron onwards into the valence orbital system of the C6F6 molecule. This transfer of charge causes the molecule to vibrate as its geometry changes from planar to buckled. The oscillations observed in the photoelectron spectra are coherent and sinusoidal and have a frequency of 121 ± 2 cm−1. This compares very favourably to the frequency of 122 cm−1 calculated by time-dependent density functional theory for the bending mode of C6F6 along the coordinate between the planar and buckled geometries. I argue that this charge-transfer state exhibits the predicted characteristics of a CBS.

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10

Godage, Himali Yasmin. "Novel approaches to the synthesis of C-glycosides." Thesis, University of Oxford, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.401067.

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Книги з теми "Novel c–c"

1

Gass, William H. Middle C: A novel. New York: Alfred A. Knopf, 2013.

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2

Jacob with a 'c': A novel. Cape Town: Carrefour Press, 1993.

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3

Bitely, Scott. Simmer down, Mr. C: A novel. Greenville, S.C: Ambassador International, 2012.

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4

The top prisoner of C-Max: A novel. Cape Town, South Africa: Umuzi, 2012.

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5

Osborne, Elizabeth. The natural history of Uncas Metcalfe: A novel /c Betsey Osborne. New York: St. Martin's Press, 2006.

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6

K, Dick Philip. C ovek u visokom dvorcu. Beograd: Editor, 2002.

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7

Crumley, James. Bordersnakes: A novel. New York, USA: Mysterious Press, 1996.

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8

Crumley, James. Bordersnakes: A novel. New York, USA: Mysterious Press, 1996.

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9

Hardpress. Aims and Ends, a Novel, by C. C. G. HardPress, 2020.

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10

Zuckerman, Al. Writing a Blockbuster Novel ?'C?'. Little, Brown Book Group Limited, 1994.

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Частини книг з теми "Novel c–c"

1

Cuatrecasas, Pedro. "Some Novel Phospholipase C Activities." In Cellular and Molecular Aspects of Inflammation, 405–12. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5487-1_20.

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2

Scalapino, D. J., R. T. Scalettar, and N. E. Bickers. "Polaron Effects in High-T c Oxide Superconductors." In Novel Superconductivity, 475–80. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1937-5_55.

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3

Kalogirou, O., C. Sarafidis, T. Bakas, and M. Gjoka. "57Fe Mössbauer study of novel series of intermetallic compounds R3(Fe1−xCox)29−yTy (R=Nd, Tb, Dy; T=Ti, V)." In Hyperfine Interactions (C), 153–56. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0281-3_38.

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4

Michalewicz, Marek T., and Mukunda P. Das. "Collective Electronic Oscillations on C 60." In Computational Approaches to Novel Condensed Matter Systems, 163–73. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4757-9791-6_8.

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5

Belokon, Yuri N., Michael North, and Henri B. Kagan. "Novel Types of Chiral Catalysts for Asymmetric C-C Bond Formation Reactions." In Current Trends in Organic Synthesis, 221–28. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-4801-0_28.

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6

Shuai, Wang, Cui Xiang, Liao Peng, and Li Dan. "S-URL Flux: A Novel C&C Protocol for Mobile Botnets." In Trustworthy Computing and Services, 412–19. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35795-4_52.

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7

Novák, Mihály, and Csaba Visy. "Some Observations on Intermediates of c-Hexene Bifunctionalization." In Novel Trends in Electroorganic Synthesis, 33–36. Tokyo: Springer Japan, 1998. http://dx.doi.org/10.1007/978-4-431-65924-2_9.

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8

Ramakrishnan, C., A. M. Thangakani, D. Velmurugan, and M. Michael Gromiha. "Identification of Novel c-Yes Kinase Inhibitors." In Intelligent Computing in Bioinformatics, 494–500. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-09330-7_57.

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9

Li, Cuixia, and Jian Yu. "A Novel Fuzzy C-Means Clustering Algorithm." In Rough Sets and Knowledge Technology, 510–15. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/11795131_74.

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10

Tsugita, Akira, Keiji Takamoto, Hiromoto Iwadate, Masaharu Kamo, Hiroyuki Yano, Norifumi Miyatake, and Kazuo Satake. "Development of Novel C-Terminal Sequencing Methods." In Methods in Protein Sequence Analysis, 55–62. Boston, MA: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4899-1603-7_7.

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Тези доповідей конференцій з теми "Novel c–c"

1

Zaman, A. N. K., Charlie Obimbo, and Rozita A. Dara. "A Novel Differential Privacy Approach that Enhances Classification Accuracy." In the Ninth International C* Conference. New York, New York, USA: ACM Press, 2016. http://dx.doi.org/10.1145/2948992.2949027.

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2

Vayadande, Kuldeep, Prajwal Atram, Hitashri Patil, Nupur Shinde, Vishal Singh, and Sameer Meshram. "A Novel Automatic Garbage Collector Tool for C/C++ Programs." In 2023 International Conference on Computational Intelligence and Sustainable Engineering Solutions (CISES). IEEE, 2023. http://dx.doi.org/10.1109/cises58720.2023.10183570.

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3

Konarev, Dmitry V., Natalia V. Drichko, Viktor N. Semkin, Yury M. Shul’ga, Andrzej Graja, and Rimma N. Lyubovskaya. "Spectroscopy of C[sub 60] and C[sub 70] complexes." In The 12th international winterschool on electronic properties of novel materials: progress in molecular nanostructures. AIP, 1998. http://dx.doi.org/10.1063/1.56477.

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4

Havlik, D., M. Steinmetz, P. Huber, W. Schranz, M. Enderle, and K. Knorr. "Phase diagram of the C[sub 60]/C[sub 70] system." In The 12th international winterschool on electronic properties of novel materials: progress in molecular nanostructures. AIP, 1998. http://dx.doi.org/10.1063/1.56465.

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5

Weidinger, A., B. Pietzak, M. Waiblinger, K. Lips, B. Nuber, and A. Hirsch. "Study of N@C[sub 60] and P@C[sub 60]." In The 12th international winterschool on electronic properties of novel materials: progress in molecular nanostructures. AIP, 1998. http://dx.doi.org/10.1063/1.56478.

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6

"The Stereotypical Women and Empowered Women Narration in the Novel Bidadari Bermata Bening." In Multi-Conference Proceeding Series C. Galaxy Science, 2022. http://dx.doi.org/10.11594/nstp.2022.2612.

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7

Karthikeyan, B., M. Murugavelu, S. Senthilvelan, and V. L. Chandraboss. "Novel Ag-Pt doped silicate catalyst for C-C coupling reaction." In FUNCTIONAL MATERIALS: Proceedings of the International Workshop on Functional Materials (IWFM-2011). AIP, 2012. http://dx.doi.org/10.1063/1.4736929.

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8

Sienkiewicz, A. "Singlet oxygen generation by C[sub 60] and C[sub 70]—an ESR study." In The 14th international winterschool on electronic properties of novel materials - molecular nanostructures. AIP, 2000. http://dx.doi.org/10.1063/1.1342469.

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9

Eisler, H. J., F. H. Hennrich, and M. M. Kappes. "C[sub 120] and C[sub 120]O: Vibrational spectroscopy and PM3 calculations." In The 12th international winterschool on electronic properties of novel materials: progress in molecular nanostructures. AIP, 1998. http://dx.doi.org/10.1063/1.56461.

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10

Zhang, Hai, and Yi Zhen. "A Novel Supervised C-V Segmentation." In 2011 International Conference on Intelligent Computation and Bio-Medical Instrumentation (ICBMI). IEEE, 2011. http://dx.doi.org/10.1109/icbmi.2011.37.

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Звіти організацій з теми "Novel c–c"

1

Wiser, W. H., and A. G. Oblad. Novel process for depolymerization of coal to C[sub 2]-C[sub 4] hydrocarbons. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/6454498.

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2

Wiser, W. H., and A. G. Oblad. Novel process for depolymerization of coal to C sub 2 -C sub 4 hydrocarbons. Office of Scientific and Technical Information (OSTI), June 1990. http://dx.doi.org/10.2172/6166612.

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3

Wiser, W. H., and A. G. Oblad. Novel process for depolymerization of coal to C[sub 2]--C[sub 4] hydrocarbons. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/7368636.

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4

Liu, Shih-Yuan, Zachary X. Giustra, Tom Autrey, David A. Dixon, and Paul Osenar. Novel Carbon (C)-Boron (B)-Nitrogen (N)-Containing H2 Storage Materials. Office of Scientific and Technical Information (OSTI), September 2017. http://dx.doi.org/10.2172/1393260.

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5

Zahnow, Cynthia A. A Novel Role for C/EBP in Mammary Development and Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, September 1997. http://dx.doi.org/10.21236/ada340339.

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6

Zahnow, Cynthia A. A Novel Role for C/EBP in Mammary Development and Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, July 1998. http://dx.doi.org/10.21236/ada359168.

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7

Zahnow, Cynthia A. A Novel Role for C/EBP In Mammary Development and Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, July 1999. http://dx.doi.org/10.21236/ada381707.

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8

Wiser, W. H., and A. G. Oblad. Novel process for depolymerization of coal to C{sub 2}-C{sub 4} hydrocarbons. Final report, 1 September 1989--31 August 1993. Office of Scientific and Technical Information (OSTI), July 1994. http://dx.doi.org/10.2172/10184719.

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9

Sternberg, Paul W. Identification of Novel Candidate Tumor Suppressor Genes Using C. elegans as a Model. Fort Belvoir, VA: Defense Technical Information Center, November 1996. http://dx.doi.org/10.21236/ada323557.

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10

Sternberg, Paul W. Identification of Novel Candidate Tumor Suppressor Genes Using C. elegans as a Model. Fort Belvoir, VA: Defense Technical Information Center, December 1997. http://dx.doi.org/10.21236/ada344938.

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