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Статті в журналах з теми "Novel c–c"

Щоб переглянути інші типи публікацій з цієї теми, перейдіть за посиланням: Novel c–c.

Автор: Grafiati

Опубліковано: 6 вересня 2023

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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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11

Zhang, X., and E. F. Reed. "A novel HLA-C null allele,HLA-C*08:121N." HLA 87, no. 1 (December 9, 2015): 55–56. http://dx.doi.org/10.1111/tan.12719.

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12

Srinivas, Malladi, and K. B. De. "A novel baker's yeast mediated C-C bond cleavage reaction." Biotechnology Letters 14, no. 8 (August 1992): 679–82. http://dx.doi.org/10.1007/bf01021642.

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13

Ohta, Shunsaku, Kentaro Sato, Ikuo Kawasaki, Yuko Yamaguchi, Satoko Nishio, and Masayuki Yamashita. "Novel nucleophilic CC bond-formingtele-reaction of imidazole ring." Journal of Heterocyclic Chemistry 41, no. 3 (May 2004): 335–41. http://dx.doi.org/10.1002/jhet.5570410305.

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14

Alper, O., and E. Bowden. "Novel Insights Into c-Src." Current Pharmaceutical Design 11, no. 9 (April 1, 2005): 1119–30. http://dx.doi.org/10.2174/1381612053507576.

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15

Ahmed, M. T., N. Minhaj, and I. A. Khan. "Novel electronically tunable C-multipliers." Electronics Letters 31, no. 1 (January 5, 1995): 9–11. http://dx.doi.org/10.1049/el:19950018.

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16

Hauteville, Marcelle, Pascale Gaillard, Marie-Christine Duclos, and Mourad Kaouadji. "Synthesis of Novel C-Methylflavones." Liebigs Annalen 1996, no. 7 (January 25, 2006): 1217–22. http://dx.doi.org/10.1002/jlac.199619960724.

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17

Sagare, Sandipkumar Chandrakant, and Dattatraya Vishnu Kodavade. "C-HUIM." International Journal of Software Innovation 10, no. 1 (January 1, 2022): 1–11. http://dx.doi.org/10.4018/ijsi.307015.

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Анотація:

High-utility itemset mining is one of the highly researched area. Many research enthusiasts have discovered various techniques and algorithms to mine high-utility itemsets from transaction databases. One of the limitations of the existing high-utility itemset mining techniques is that there is no any generalized framework for applying the custom combinations of input parameters and any other constraints for mining high utility itemsets. This paper proposes a novel customizable framework to discover customized high utility itemsets (C-HUI). Users can customize the constraints and/or input parameters as per their requirements. A novel C-HUIM algorithm is used to discover customized high utility itemsets (C-HUI) from real-life datasets. The experimental results of the proposed framework and C-HUIM algorithm highlight the effectiveness of the approach.

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18

Gao, Sisi, Ashish Radadiya, Wenbo Li, Huanting Liu, Wen Zhu, Valérie de Crécy-Lagard, Nigel G. J. Richards, and James H. Naismith. "Uncovering the chemistry of C–C bond formation in C-nucleoside biosynthesis: crystal structure of a C-glycoside synthase/PRPP complex." Chemical Communications 56, no. 55 (2020): 7617–20. http://dx.doi.org/10.1039/d0cc02834g.

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19

Romero, Antonio, Daniel Peron, and Pierre H. Dixneuf. "Metallacumulenes: preparation of novel alkenyl–allenylidene– and diynyl–ruthenium complexes. Crystal structure of a Ru–CC–CC–C(OSiMe3)Ph2derivative." J. Chem. Soc., Chem. Commun., no. 20 (1990): 1410–12. http://dx.doi.org/10.1039/c39900001410.

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20

Akita, Munetaka, Min-Chul Chung, Aizoh Sakurai, and Yoshihiko Moro-oka. "Formation of novel conjugated polycarbon–metal systems via metal migration on a M–CC–CC–M linkage." Chemical Communications, no. 14 (2000): 1285–86. http://dx.doi.org/10.1039/b003722m.

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21

Qiu, Jun, and Ronghua Zhang. "Transition-metal-free oxidative carboazidation of acrylamides via cascade C–N and C–C bond-forming reactions." Org. Biomol. Chem. 12, no. 25 (2014): 4329–34. http://dx.doi.org/10.1039/c4ob00720d.

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Анотація:

A novel transition-metal-free oxidative carboazidation of acrylamides using inexpensive NaN₃ and K₂S₂O₈ was achieved, which not only provided an efficient method to prepare various N₃-substituted oxindoles, but also represented a novel strategy for C–N and C–C bond formation via a free-radical cascade process.

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22

Deng, Z. H., H. Y. Zhou, D. M. Wang, and Y. P. Xu. "A novel HLA-C*01 variant allele, HLA-C*01:38." Tissue Antigens 77, no. 1 (September 6, 2010): 81–83. http://dx.doi.org/10.1111/j.1399-0039.2010.01556.x.

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23

Merritt, J. Robert, Jinqi Liu, Elizabeth Quadros, Michelle L. Morris, Ruiyan Liu, Rui Zhang, Biji Jacob, et al. "Novel Pyrrolidine Ureas as C−C Chemokine Receptor 1 (CCR1) Antagonists." Journal of Medicinal Chemistry 52, no. 5 (March 12, 2009): 1295–301. http://dx.doi.org/10.1021/jm801416q.

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24

Joshi, Uday, Solen Josse, Muriel Pipelier, Floris Chevallier, Jean-Paul Pradère, Roland Hazard, Stéphanie Legoupy, François Huet, and Didier Dubreuil. "Novel pyrrole C-nucleosides by nitrogen extrusion from pyridazine C-nucleosides." Tetrahedron Letters 45, no. 5 (January 2004): 1031–33. http://dx.doi.org/10.1016/j.tetlet.2003.11.088.

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25

Datta, Apurba, David G. Vander Velde, Gunda I. Georg, and Richard H. Himes. "Syntheses of novel C-9 and C-10 modified bioactive taxanes." Tetrahedron Letters 36, no. 12 (March 1995): 1985–88. http://dx.doi.org/10.1016/0040-4039(95)00208-t.

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26

Khouzam, Amirah, Julia Platt, Rachel Cox, and Gregory M. Enns. "Novel c.316G>C mutation in PDHA1 causes PDH deficiency." Mitochondrion 13, no. 6 (November 2013): 925. http://dx.doi.org/10.1016/j.mito.2013.07.072.

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27

Nhari, Laila M., Elham N. Bifari, Aisha R. Al-Marhabi, Huda A. Al-Ghamdi, Sameera N. Al-Ghamdi, Fatimah A. M. Al-Zahrani, Khalid O. Al-Footy, and Reda M. El-Shishtawy. "Synthesis of Novel Key Chromophoric Intermediates via C-C Coupling Reactions." Catalysts 12, no. 10 (October 21, 2022): 1292. http://dx.doi.org/10.3390/catal12101292.

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Анотація:

The fundamentals of Pd-catalyzed Csp2−Csp2 Miyaura borylation, Suzuki cross-coupling, and Stille cross-coupling reactions for a variety of borylated precursors based on phenothiazine (PTZ), phenoxazine (POZ), carbazole (Cz), and quinoxaline (QX) units have been explored. Three palladium-based catalysts were chosen for this study: Pd(PPh3)4, Pd(PPh3)2Cl2, and Pd(dppf)Cl2, applying different reaction conditions. Around 16 desired chromophores were successfully designed and synthesized using C-C cross-coupling reactions in moderate to excellent yields, including PTZ, POZ, and Cz units coupled with QX, indolinium iodide, thienyl, phenyl, or triphenylamine moieties. Additionally, PTZ, POZ, and Cz have been employed in synthesizing various pinacol boronate ester derivatives in good to moderate yields. Interestingly, Pd(dppf)Cl2 was found to be the best catalyst for borylation, and C-C cross-coupling reactions occurred in as little as 30 min, with an excellent yield exceeding 98%. Pd(PPh3)4 and Pd(PPh3)2Cl2 catalyzed the reaction to obtain the desired products in moderate to good yields after a long time (20–24 h). On the other hand, the Suzuki-Miyaura cross-coupling between N-(2-methyl)hexyl carbazole pinacol boronate ester derivative 10c and three halogenated quinoxaline derivatives—4-(3-(5-bromothiophen-2-yl)quinoxalin-2-yl)benzaldehyde (27), 4-(5-(3-(5-bromothiophen-2-yl)quinoxalin-2-yl)thiophen-2-yl)benzaldehyde (30), and 4-(3-chloroquinoxalin-2-yl)benzaldehyde (25) catalyzed by Pd(PPh3)4—afforded three carbazole-quinoxaline chromophores (28, 30, and 31, respectively) in 2–3 h, with good to excellent yields reaching 86%. The electron-deficient QX couplers proved to be coupled efficiently using the Stille coupling reaction, which involves the coupling between electron-rich orgaostannane and electron-deficient halide. The synthesized precursors and desired chromophores were characterized by FTIR, 1H-NMR, 13C-NMR, and HRMS.

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28

Pfundheller, Henrik M, Torsten Bryld, Carl E Olsen, and Jesper Wengel. "Oligonucleotides Containing Novel 4′-C- or 3′-C-(Aminoalkyl)-Branched Thymidines." Helvetica Chimica Acta 83, no. 1 (January 19, 2000): 128–51. http://dx.doi.org/10.1002/(sici)1522-2675(20000119)83:1<128::aid-hlca128>3.0.co;2-q.

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29

Hackeloer, Kristina, Gregor Schnakenburg, and Siegfried R. Waldvogel. "Novel Domino Oxidative Coupling: C−C Bond Formation Sequence to Highly Functionalized Dibenzo[a,c]cycloheptenes." Organic Letters 13, no. 5 (March 4, 2011): 916–19. http://dx.doi.org/10.1021/ol102969k.

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30

Severengiz, Tevfik, Wolf-Walther du Mont, Dieter Lenoir, and Heike Voss. "Novel Reactions of Acyl Halides with Bis(trimethylsilyl) Telluride: C,Te and C,C Bond Formation." Angewandte Chemie International Edition in English 24, no. 12 (December 1985): 1041–42. http://dx.doi.org/10.1002/anie.198510411.

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31

Schaub, Thomas, and Udo Radius. "Efficient CF and CC Activation by a Novel N-Heterocyclic Carbene-Nickel(0) Complex." Chemistry - A European Journal 11, no. 17 (August 19, 2005): 5024–30. http://dx.doi.org/10.1002/chem.200500231.

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32

Sun, Kai, Yunhe Lv, Zhonghong Zhu, Liping Zhang, Hankui Wu, Lin Liu, Yongqing Jiang, Beibei Xiao та Xin Wang. "Oxidative C–S bond cleavage reaction of DMSO for C–N and C–C bond formation: new Mannich-type reaction for β-amino ketones". RSC Advances 5, № 4 (2015): 3094–97. http://dx.doi.org/10.1039/c4ra14249g.

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33

Machiry, Aravind, John Kastner, Matt McCutchen, Aaron Eline, Kyle Headley, and Michael Hicks. "C to checked C by 3c." Proceedings of the ACM on Programming Languages 6, OOPSLA1 (December 8, 2022): 1–29. http://dx.doi.org/10.1145/3527322.

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Анотація:

Owing to the continued use of C (and C++), spatial safety violations (e.g., buffer overflows) still constitute one of today's most dangerous and prevalent security vulnerabilities. To combat these violations, Checked C extends C with bounds-enforced checked pointer types. Checked C is essentially a gradually typed spatially safe C - checked pointers are backwards-binary compatible with legacy pointers, and the language allows them to be added piecemeal, rather than necessarily all at once, so that safety retrofitting can be incremental. This paper presents a semi-automated process for porting a legacy C program to Checked C. The process centers on 3C, a static analysis-based annotation tool. 3C employs two novel static analysis algorithms - typ3c and boun3c - to annotate legacy pointers as checked pointers, and to infer array bounds annotations for pointers that need them. 3C performs a root cause analysis to direct a human developer to code that should be refactored; once done, 3C can be re-run to infer further annotations (and updated root causes). Experiments on 11 programs totaling 319KLoC show 3C to be effective at inferring checked pointer types, and experience with previously and newly ported code finds 3C works well when combined with human-driven refactoring.

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34

AlGhamdi, Khalid M. "C-punch excision: a novel technique." International Journal of Dermatology 55, no. 10 (June 23, 2016): 1154–56. http://dx.doi.org/10.1111/ijd.13202.

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35

Chen, Liliang, Tsutomu Mashimo, Chihiro Iwamoto, Hiroki Okudera, Emil Omurzak, Hullathy Subban Ganapathy, Hirotaka Ihara, et al. "Synthesis of novel CoCx@C nanoparticles." Nanotechnology 24, no. 4 (January 7, 2013): 045602. http://dx.doi.org/10.1088/0957-4484/24/4/045602.

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36

Au, J. S., and P. J. Pockros. "Novel Therapeutic Approaches for Hepatitis C." Clinical Pharmacology & Therapeutics 95, no. 1 (January 2013): 78–88. http://dx.doi.org/10.1038/clpt.2013.206.

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37

Christiansen, J. S., and J. P. Monson. "Workshop C: Novel topics in endocrinology." Growth Hormone & IGF Research 13 (August 2003): S93. http://dx.doi.org/10.1016/s1096-6374(03)00062-5.

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38

Edser, Caroline. "Novel chemistries: c-linkages and rearrangements." Focus on Surfactants 2012, no. 11 (November 2012): 1–2. http://dx.doi.org/10.1016/s1351-4210(12)70293-7.

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39

Bhattacharyya, Debdatta, and Ayan Kar. "TCTAP C-045 Novel Bifurcation Technique." Journal of the American College of Cardiology 71, no. 16 (April 2018): S112—S113. http://dx.doi.org/10.1016/j.jacc.2018.03.241.

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40

Su, Kankan, Haiyue Zhang, Weiwei Fang, Feng Zhang, Lihong Yang, Yanhui Jin, and Mingshan Wang. "Protein C deficiency (a novel mutation." Blood Coagulation & Fibrinolysis 29, no. 8 (December 2018): 714–19. http://dx.doi.org/10.1097/mbc.0000000000000778.

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41

Gray, Alana L., David T. Coleman, Reneau F. Castore, Mohamed M. Mohyeldin, Khalid A. El Sayed, and James A. Cardelli. "Isothiocyanatostilbenes as novel c-Met inhibitors." Oncotarget 6, no. 38 (October 31, 2015): 41180–93. http://dx.doi.org/10.18632/oncotarget.5748.

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42

Shields, William W., and Paul J. Pockros. "Novel drugs for hepatitis C virus." Current Hepatitis Reports 8, no. 2 (May 2009): 52–58. http://dx.doi.org/10.1007/s11901-009-0008-8.

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43

Aguado-Ruiz, Jesus, Antonio J. Lopez-Martin, and Jaime Ramirez-Angulo. "Three novel improved CMOS C-multipliers." International Journal of Circuit Theory and Applications 40, no. 6 (January 14, 2011): 607–16. http://dx.doi.org/10.1002/cta.745.

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44

Agh-Atabay, Naz M., Jack L. Davidson, Graeme Douglas та Kenneth W. Muir. "Metal-promoted alkyne trimerisation leading to novel metallacycles. The molecular structures of [Mo{η3-C(CF3)C(CF3)C(Me)C(Ph)SPri}(CF3CCCF3)(η5-C5H5)], [WSPri{η5-C(CF3)C(CF3)C(CF3)C(CF3)C(Me)C(Ph)}(η5-C5H5)], and [W(SC6H4Me-4){η4-C(CF3)C(CF3)C(CO2Me)C(CO2Me)C(CF3)C(CF3)}(η5-C5H5)]". J. Chem. Soc., Chem. Commun., № 9 (1989): 549–51. http://dx.doi.org/10.1039/c39890000549.

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45

Bacsa, Ildikó, Csilla Konc, Anna Orosz, Gábor Kecskeméti, Réka Rigó, Csilla Özvegy-Laczka, and Erzsébet Mernyák. "Synthesis of Novel C-2- or C-15-Labeled BODIPY—Estrone Conjugates." Molecules 23, no. 4 (April 3, 2018): 821. http://dx.doi.org/10.3390/molecules23040821.

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46

Wang, D. M., Y. P. Xu, and Z. H. Deng. "Identification of a novel HLA-C*01 variant allele, C*01:46." Tissue Antigens 78, no. 1 (April 19, 2011): 70–71. http://dx.doi.org/10.1111/j.1399-0039.2011.01654.x.

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47

Tedebark, Ulf, Morten Meldal, Luigi Panza, and Klaus Bock. "C-Linked glycosyl azido acid in novel solid-phase C-glycopeptide synthesis." Tetrahedron Letters 39, no. 13 (March 1998): 1815–18. http://dx.doi.org/10.1016/s0040-4039(98)00095-1.

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48

Fleaca, Claudiu Teodor, Florian Dumitrache, Ion Morjan, Rodica Alexandrescu, Catalin Luculescu, Ana Niculescu, Eugeniu Vasile, and Victor Kuncser. "Novel Fe@C–TiO2 and Fe@C–SiO2 water-dispersible magnetic nanocomposites." Applied Surface Science 278 (August 2013): 284–88. http://dx.doi.org/10.1016/j.apsusc.2013.01.172.

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49

Zhou, X. Y., L. Q. Zhang, Y. Xiao, X. Q. Yang, and J. P. Cai. "Characterization of a novel HLA-C*04 allele, HLA-C*04:277." HLA 90, no. 5 (September 3, 2017): 315–16. http://dx.doi.org/10.1111/tan.13110.

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Huo, M. R., Y. Yu, B. Xi, and D. Li. "Identification of a novel HLA-C*12 allele, HLA-C*12:221." HLA 91, no. 3 (February 22, 2018): 215–16. http://dx.doi.org/10.1111/tan.13213.

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