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Artículos de revistas sobre el tema "C.002.782.815.440"

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Publicado: 25 de julio de 2024
Última modificación: 31 de julio de 2025

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1

Arijit, Kundu, Bhattacharyya Bhaswati, Dhara Kaliprasanna та Patra Amarendra. "Zinc mediated ring size tuned C=C reduction and C-C coupling of α,α'-(E,E)- bis(benzylidene)cycloalkanones". Journal of Indian Chemical Society Vol. 89, Dec 2012 (2012): 1711–22. https://doi.org/10.5281/zenodo.5773484.

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Department of Chemistry, University College of Science and Technology, University of Calcutta, Kolkata-700 009, India <em>E-mail</em> : kali.dhara@gmail.com Department of Chemistry, Hooghly Mohsin College, Hooghly-712 101, West Bengal, India <em>Manuscript received online 09 January 2012, revised 29 February 2012, accepted 21 March 2012</em> Reduction of substituted &alpha;,&alpha;&#39;-(<em>E,E</em>)-bis(benzylidene)cycloalkanones bearing five- and six-membered rings using zinc-amalgam in glacial acetic acid yielded C = C bond reduced products and C-C coupled compounds with the carbonyl funct
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2

Smith, Alice M., Jürgen Agreiter, and Vladimir E. Bondybey. "Laser-induced fluorescence of matrix-isolated HCCCCCN+ and HCCCCCCCN+." Chemical Physics Letters 244, no. 5-6 (1995): 379–87. http://dx.doi.org/10.1016/0009-2614(95)00915-q.

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3

Bartel, Christoph, Peter Botschwina, Hans Bürger, et al. "Cyanisocyanacetylen, N≡C−C≡C−N≡C." Angewandte Chemie 110, no. 20 (1998): 3036–40. http://dx.doi.org/10.1002/(sici)1521-3757(19981016)110:20<3036::aid-ange3036>3.0.co;2-n.

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4

Bartel, Christoph, Peter Botschwina, Hans Bürger, et al. "Cyanoisocyanoacetylene, N≡C−C≡C−N≡C." Angewandte Chemie International Edition 37, no. 20 (1998): 2879–82. http://dx.doi.org/10.1002/(sici)1521-3773(19981102)37:20<2879::aid-anie2879>3.0.co;2-0.

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5

Frances, Mary. "Glossary. The C-P-C cycle." Rivista Italiana Costruttivismo 6, no. 2 (2018): 61–63. http://dx.doi.org/10.69995/pqwp4764.

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6

Okabayashi, T., M. Tanimoto, K. Tanaka, and E. Hirota. "Microwave spectroscopy of fluorocyanobutadiyne (F-CC-CC-CN)." Chemical Physics Letters 230, no. 6 (1994): 530–35. http://dx.doi.org/10.1016/0009-2614(94)01205-9.

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7

Makovicky, Emil, and Sven Karup-Møller. "Exploratory studies of the Cu–Pd–Se system at 650°C, 550°C, 400°C, and 300°C." European Journal of Mineralogy 29, no. 4 (2017): 645–52. http://dx.doi.org/10.1127/ejm/2017/0029-2651.

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8

Sinha, Narayan, Dorus Heijnen, Ben L. Feringa, and Michael G. Organ. "Murahashi Cross‐Coupling at −78 °C: A One‐Pot Procedure for Sequential C−C/C−C, C−C/C−N, and C−C/C−S Cross‐Coupling of Bromo‐Chloro‐Arenes." Chemistry – A European Journal 25, no. 39 (2019): 9180–84. http://dx.doi.org/10.1002/chem.201901678.

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9

Bartel, Christoph, Peter Botschwina, Hans Buerger, et al. "ChemInform Abstract: Cyanoisocyanoacetylene, NC-CC-NC." ChemInform 30, no. 14 (2010): no. http://dx.doi.org/10.1002/chin.199914088.

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10

Smith, Alice M., Günter Schallmoser, Anton Thoma, and Vladimir E. Bondybey. "Infrared spectral evidence of N≡C–C≡C–N≡C: Photoisomerization of N≡C–C≡C–C≡N in an argon matrix." Journal of Chemical Physics 98, no. 3 (1993): 1776–85. http://dx.doi.org/10.1063/1.464266.

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11

A. Adrio, Luis, and King Kuok (Mimi) Hii. "Palladium-Catalyzed Heterofunctionalization of C-H, C=C and C≡ C Bonds." Current Organic Chemistry 15, no. 18 (2011): 3337–61. http://dx.doi.org/10.2174/138527211797248003.

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12

Allen, Gregory W., Robert S. Armstrong, Manuel J. Aroney, Raymond K. Pierens, and Alan J. Williams. "Polarisability anisotropies of C—H, C—C, C—Cl and C—Br bonds." J. Chem. Soc., Faraday Trans. 2 84, no. 11 (1988): 1775–78. http://dx.doi.org/10.1039/f29888401775.

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13

TANABE, YASUHIRO, and EIICHI YASUDA. "C/C Composite." Sen'i Gakkaishi 44, no. 11 (1988): P440—P443. http://dx.doi.org/10.2115/fiber.44.11_p440.

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14

Monnier, Florian, and Marc Taillefer. "Katalytische C-C-, C-N- und C-O-Ullmann-Kupplungen." Angewandte Chemie 121, no. 38 (2009): 7088–105. http://dx.doi.org/10.1002/ange.200804497.

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15

Chen, Tieqiao, and Li-Biao Han. "Nickelkatalysierte C-O/C-H-Kreuzkupplungen zur C-C-Bindungsbildung." Angewandte Chemie 127, no. 30 (2015): 8722–24. http://dx.doi.org/10.1002/ange.201503204.

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16

Monnier, Florian, and Marc Taillefer. "Katalytische C-C-, C-N- und C-O-Ullmann-Kupplungen." Angewandte Chemie 120, no. 17 (2008): 3140–43. http://dx.doi.org/10.1002/ange.200703209.

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17

Karamanis, Panaghiotis, and George Maroulis. "Single (C–C) and triple (CC) bond-length dependence of the static electric polarizability and hyperpolarizability of H–CC–CC–H." Chemical Physics Letters 376, no. 3-4 (2003): 403–10. http://dx.doi.org/10.1016/s0009-2614(03)00784-x.

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18

SMITH, A. M., G. SCHALLMOSER, A. THOMA, and V. E. BONDYBEY. "ChemInform Abstract: IR Spectral Evidence of NC-CC-NC: Photoisomerization of NC-CC-CN in an Argon Matrix." ChemInform 24, no. 28 (2010): no. http://dx.doi.org/10.1002/chin.199328112.

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19

Kulchat, Sirinan, Kamel Meguellati, and Jean-Marie Lehn. "Organocatalyzed and Uncatalyzed CC/CC and CC/CN Exchange Processes betweenKnoevenageland Imine Compounds in Dynamic Covalent Chemistry." Helvetica Chimica Acta 97, no. 9 (2014): 1219–36. http://dx.doi.org/10.1002/hlca.201400187.

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20

Nguyen, Trang T., Jeffery A. Bertke, Danielle L. Gray, and Kami L. Hull. "Facile C–H, C–F, C–Cl, and C–C Activation by Oxatitanacyclobutene Complexes." Organometallics 34, no. 17 (2015): 4190–93. http://dx.doi.org/10.1021/acs.organomet.5b00470.

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21

Savitskiy, V. O., and D. V. Sidorov. "Incremental source code analysis for C/C++ languages." Proceedings of the Institute for System Programming of RAS 22 (2012): 119–30. http://dx.doi.org/10.15514/ispras-2012-22-8.

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22

Kumar Roy, Gaurav. "New Pre-Processor EXCLUDE Directive of C/C++." International Journal of Scientific Engineering and Research 5, no. 8 (2017): 49–52. https://doi.org/10.70729/2081701.

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23

Reed, Ishmael. "The C above C above High C." Antioch Review 57, no. 3 (1999): 333. http://dx.doi.org/10.2307/4613883.

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24

Reed, Ishmael. "The C above C above High C." Antioch Review 59, no. 2 (2001): 460. http://dx.doi.org/10.2307/4614179.

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25

Yeang, Calvin, Joseph L. Witztum, and Sotirios Tsimikas. "‘LDL-C’ = LDL-C + Lp(a)-C." Current Opinion in Lipidology 26, no. 3 (2015): 169–78. http://dx.doi.org/10.1097/mol.0000000000000171.

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26

Cataldo, F. "Structural relationships between dicopper diacetylide (Cu-C≡C-C≡C-Cu) and dicopper acetylide (Cu-C≡C-Cu)." European Journal of Solid State and Inorganic Chemistry 35, no. 3 (1998): 281–91. http://dx.doi.org/10.1016/s0992-4361(98)80009-x.

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27

Dembitsky, Valery M., Hijazi Abu Ali, and Morris Srebnik. "Recent developments in bisdiborane chemistry: B?C?B, B?C?C?B, B?C?C?B and B?C?C?B compounds." Applied Organometallic Chemistry 17, no. 6-7 (2003): 327–45. http://dx.doi.org/10.1002/aoc.430.

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28

Kulchat, Sirinan, Kamel Meguellati, and Jean-Marie Lehn. "Erratum: Organocatalyzed and Uncatalyzed CC/CC and CC/CN Exchange Processes betweenKnoevenageland Imine Compounds in Dynamic Covalent Chemistry." Helvetica Chimica Acta 98, no. 1 (2015): 153. http://dx.doi.org/10.1002/hlca.201590000.

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29

Yokota, Akira, Emiko Hiyama, and Makoto Oka. "Possible Existence of $${(c\bar{c})}$$ ( c c ¯ ) –Nucleus Bound States." Few-Body Systems 55, no. 8-10 (2014): 761–65. http://dx.doi.org/10.1007/s00601-014-0895-2.

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30

Cataldo, F. "From dicopper diacetylide (Cu-C≡C-C≡C-Cu) to carbyne." European Journal of Solid State and Inorganic Chemistry 35, no. 3 (1998): 293–304. http://dx.doi.org/10.1016/s0992-4361(98)80018-0.

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31

Okabayashi, Toshiaki, Noriko Yamashita, Yoshiko Sakai, and Mitsutoshi Tanimoto. "Millimeter-Wave Spectrum of Fluorodiacetylene (HCCCCF)." Journal of Molecular Spectroscopy 193, no. 2 (1999): 273–76. http://dx.doi.org/10.1006/jmsp.1998.7738.

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32

Thomas, Phillip S., Nathan P. Bowling, Nicola J. Burrmann, and Robert J. McMahon. "Dialkynyl Carbene Derivatives: Generation and Characterization of Triplettert-Butylpentadiynylidene (t-Bu−C≡C−C̈−C≡C−H) and Dimethylpentadiynylidene (Me−C≡C−C̈−C≡C−Me)." Journal of Organic Chemistry 75, no. 19 (2010): 6372–81. http://dx.doi.org/10.1021/jo101096n.

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33

Shaimov, A. Yu. "ORGANIZATION AND MAINTENANCE OF PROGRAM TIMERS IN C/C++." Vektor of development 1, no. 12 (2023): 129–34. http://dx.doi.org/10.53852/2782-3962-2023-1-12-129-134.

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34

Wang, Wen-Xue, Yoshihiro Takao, and Terutake Matsubara. "Tensile strength and fracture toughness of C/C and metal infiltrated composites Si–C/C and Cu–C/C." Composites Part A: Applied Science and Manufacturing 39, no. 2 (2008): 231–42. http://dx.doi.org/10.1016/j.compositesa.2007.11.004.

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35

Bürger, Hans, Dieter Lentz, Britta Meisner, Natascha Nickelt, Dagmar Preugschat, and Michael Senzlober. "Syntheses and1H-,13C- and15N-NMR Spectra of Ethynyl Isocyanide, H−C≡C−N≡C, D−C≡C−N≡C and Prop-1-ynyl Isocyanide, H3C−C≡C−N≡C, D3C−C≡C−N≡C: High Resolution Infrared Spectrum of Prop-1-ynyl Isocyanide." Chemistry - A European Journal 6, no. 18 (2000): 3377–85. http://dx.doi.org/10.1002/1521-3765(20000915)6:18<3377::aid-chem3377>3.0.co;2-1.

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36

KOGO, Yasuo, Akihiro KIKKAWA, Wataru SAITO, and Hiroshi HATTA. "Tensile properties of monofilament C/C composites." Proceedings of Conference of Kanto Branch 2004.10 (2004): 347–48. http://dx.doi.org/10.1299/jsmekanto.2004.10.347.

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37

Andreas, Enge. "[Re] Volume computation for polytopes: Vingt ans après." ReScience C 6, no. 1 (2020): #17. https://doi.org/10.5281/zenodo.4242972.

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38

Dr., Priyanka Surendran. "Understanding the Botnet Phenomenon." International Journal of Engineering and Management Research 8, no. 4 (2018): 193–95. https://doi.org/10.31033/ijemr.v8i4.13240.

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Internet threats have increased manifold with the arrival of botnets. Many organizations worldwide and the social networks have been affected by botnets. Numerous researches have been carried to understand the concept of bots, C&amp;C channels, botnet and botmasters. These botnets have been able to update itself regularly which makes them very difficult to be detected. The purpose of this paper is to understand the of behavior of botnets and its affect on the virtual world. The paper has also analyzed the types of botnets, lifecycle and elements of botnets.
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39

Lussier, L. S., C. Sandorfy, H. OA L E-Thanh, and D. Vocelle. "THE EFFECT OF ACIDS ON THE INFRARED SPECTRA OF SCHIFF BASES—II. IMINES CONTAINING THE C=C-C=N AND C=C-C=C-C=N UNITS." Photochemistry and Photobiology 45, s1 (1987): 801–8. http://dx.doi.org/10.1111/j.1751-1097.1987.tb07886.x.

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40

Dr., Amruta B. Hooli, Kishore G. Bhat Dr., and Preeti. Ingalgi Mrs. "COMPARISON OF DIFFERENT PHENOYPIC TESTS FOR IDENTIFICATION OF CANDIDA ISOLATED FROM ORAL CAVITY." International Journal of Research - Granthaalayah 8, no. 1 (2020): 32–39. https://doi.org/10.5281/zenodo.3630698.

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Background and Objectives: Oral candidiasis is one of the most common fungal infections affecting the oral mucosa. Candida genus is comprised of numerous species amongst which C.albicans is the commonest followed by C. dubliniensis. Interest has been increased towards identifying the non-albicans resistant to antifungal drugs. Various techniques are developed for species identification such as traditional, rapid, molecular and automated methods. These methods have their own advantages and limitations. Though the traditional methods are complex, time consuming, they are simple and economical as
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41

Yam, Vivian Wing-Wah, Samuel Hung-Fai Chong, Chi-Chiu Ko, and Kung-Kai Cheung. "Synthesis and Luminescence Behavior of Rhenium(I) Triynyl Complexes. X-ray Crystal Structures of [Re(CO)3(tBu2bpy)(C⋮C−C⋮C−C⋮CPh)] and [Re(CO)3(Me2bpy)(C⋮C−C⋮C−C⋮CSiMe3)]." Organometallics 19, no. 24 (2000): 5092–97. http://dx.doi.org/10.1021/om000725b.

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42

Nodelman, Vladimir. "OOP via C++, C#...?" ACM SIGCSE Bulletin 36, no. 3 (2004): 255. http://dx.doi.org/10.1145/1026487.1008087.

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43

RITTER, STEPHEN K. "EXTREME C–C BONDS." Chemical & Engineering News 87, no. 19 (2009): 32–33. http://dx.doi.org/10.1021/cen-v087n019.p032.

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44

Accardi, Luigi, Ameur Dhahri, and Habib Rebei. "$$C^*$$ C ∗ -Quadratic Quantization." Journal of Statistical Physics 172, no. 5 (2018): 1187–209. http://dx.doi.org/10.1007/s10955-018-2085-y.

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45

Kaupp, Gerd, and Jürgen Boy. "Überlange C-C-Einfachbindungen." Angewandte Chemie 109, no. 1-2 (1997): 48–50. http://dx.doi.org/10.1002/ange.19971090108.

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46

Huntley, Deborah R., Georgios Markopoulos, Patrick M. Donovan, Lawrence T. Scott, and Roald Hoffmann. "Squeezing CC Bonds." Angewandte Chemie 117, no. 46 (2005): 7721–25. http://dx.doi.org/10.1002/ange.200502721.

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47

Huntley, Deborah R., Georgios Markopoulos, Patrick M. Donovan, Lawrence T. Scott, and Roald Hoffmann. "Squeezing CC Bonds." Angewandte Chemie International Edition 44, no. 46 (2005): 7549–53. http://dx.doi.org/10.1002/anie.200502721.

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48

Liu, Liang, Hui Chen, Zhenqiang Yang, Junnian Wei, and Zhenfeng Xi. "C,C- and C,N-Chelated Organocopper Compounds." Molecules 26, no. 19 (2021): 5806. http://dx.doi.org/10.3390/molecules26195806.

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Copper-catalyzed and organocopper-involved reactions are of great significance in organic synthesis. To have a deep understanding of the reaction mechanisms, the structural characterizations of organocopper intermediates become indispensable. Meanwhile, the structure-function relationship of organocopper compounds could advance the rational design and development of new Cu-based reactions and organocopper reagents. Compared to the mono-carbonic ligand, the C,N- and C,C-bidentate ligands better stabilize unstable organocopper compounds. Bidentate ligands can chelate to the same copper atom via
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49

DePinto, Jeffrey T., Wendy A. deProphetis, Jessica L. Menke, and Robert J. McMahon. "Triplet 1,3-Diphenylpropynylidene (Ph−C−C−C−Ph)." Journal of the American Chemical Society 129, no. 8 (2007): 2308–15. http://dx.doi.org/10.1021/ja066300j.

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50

Zheng, Qing-Zhong, and Ning Jiao. "Ag-catalyzed C–H/C–C bond functionalization." Chemical Society Reviews 45, no. 16 (2016): 4590–627. http://dx.doi.org/10.1039/c6cs00107f.

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