Academic literature on the topic 'MBFT’s'
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Journal articles on the topic "MBFT’s"
郑, 轶天. "A New MBFGS Algorithm." Advances in Applied Mathematics 11, no. 08 (2022): 5981–85. http://dx.doi.org/10.12677/aam.2022.118630.
Full textLi, Shilong, Liang Duan, Yang Zhao, Fu Gao, and Slawomir W. Hermanowicz. "Analysis of Microbial Communities in Membrane Biofilm Reactors Using a High-Density Microarray." Membranes 13, no. 3 (2023): 324. http://dx.doi.org/10.3390/membranes13030324.
Full textBonne, Damien, Thierry Constantieux, Yoann Coquerel, and Jean Rodriguez. "Stereoselective Multiple Bond-Forming Transformations (MBFTs): The Power of 1,2- and 1,3-Dicarbonyl Compounds." Chemistry - A European Journal 19, no. 7 (2013): 2218–31. http://dx.doi.org/10.1002/chem.201204018.
Full textBortolini, Jascieli Carla, Luzia Cleide Rodrigues, Susicley Jati, and Sueli Train. "Phytoplankton functional and morphological groups as indicators of environmental variability in a lateral channel of the Upper Paraná River floodplain." Acta Limnologica Brasiliensia 26, no. 1 (2014): 98–108. http://dx.doi.org/10.1590/s2179-975x2014000100011.
Full textBizon, Agnes Meire Branco Leria, Camila Giugliani, and Elsa Regina Justo Giugliani. "Women’s Satisfaction with Breastfeeding and Risk of Exclusive Breastfeeding Interruption." Nutrients 15, no. 24 (2023): 5062. http://dx.doi.org/10.3390/nu15245062.
Full textBonne, Damien, Thierry Constantieux, Yoann Coquerel, and Jean Rodriguez. "ChemInform Abstract: Stereoselective Multiple Bond-Forming Transformations (MBFTs): The Power of 1,2- and 1,3-Dicarbonyl Compounds." ChemInform 44, no. 29 (2013): no. http://dx.doi.org/10.1002/chin.201329231.
Full textDunleavy, Trisha. "Transnational co-production, multiplatform television and My Brilliant Friend." Critical Studies in Television: The International Journal of Television Studies 15, no. 4 (2020): 336–56. http://dx.doi.org/10.1177/1749602020953755.
Full textDi Mauro, María Florencia, María José Iglesias, Débora Pamela Arce, et al. "MBF1s regulate ABA-dependent germination of Arabidopsis seeds." Plant Signaling & Behavior 7, no. 2 (2012): 188–92. http://dx.doi.org/10.4161/psb.18843.
Full textTojo, Takuto, Kenichi Tsuda, Takeshi Yoshizumi, et al. "Arabidopsis MBF1s Control Leaf Cell Cycle and its Expansion." Plant and Cell Physiology 50, no. 2 (2008): 254–64. http://dx.doi.org/10.1093/pcp/pcn187.
Full textSugikawa, Yoichi, Satoe Ebihara, Kenichi Tsuda, Yasuo Niwa, and Ken-ichi Yamazaki. "Transcriptional coactivator MBF1s from Arabidopsis predominantly localize in nucleolus." Journal of Plant Research 118, no. 6 (2005): 431–37. http://dx.doi.org/10.1007/s10265-005-0238-y.
Full textDissertations / Theses on the topic "MBFT’s"
Raimondi, Wilfried. "Nouvelles transformations organocatalysées énantiosélectives à partir de composés dicarbonyles et de nitroalcènes." Thesis, Aix-Marseille, 2012. http://www.theses.fr/2012AIXM4350/document.
Full textThis work focused on the development of novel transformations combining MBFT's and organocatalysis, the latest powerful tools of organic synthesis, and involving the reactivity of nitroalkenes. We first developed a highly stereoselective consecutive Michael – [3+2] Heterocyclisation – Fragmentation reaction where two C–C bonds, one C–O bond and a cycle are formed to make optically active cyclopentanoximes bearing up to three stereocenters. These products can be converted into hydroxylamines or indoles. We then exploited the nucleophilic potential of 1,2-dicarbonyl compounds in the design of the first organocatalyzed diastereo- and enantioselective Michael additions of 1,2-ketoamides and 1,2-ketoesters onto nitroalkenes. The corresponding adducts are valuable synthetic platforms towards the synthesis of five- and six-membered carbo- and heterocycles with wide functional variety. This work led to the development of a domino transformation involving 1,2-dicarbonyl compounds and halogenated nitroolefines to efficiently access 2-carbonyl- and 2-phosphorylfuranes whose reported synthetic pathways remain rare. The first encouraging trials carried out to make atropisomers enable a potential asymmetric version of this methodology
Raimondi, Wilfried. "Nouvelles transformations organocatalysées énantiosélectives à partir de composés dicarbonyles et de nitroalcènes." Electronic Thesis or Diss., Aix-Marseille, 2012. http://www.theses.fr/2012AIXM4350.
Full textThis work focused on the development of novel transformations combining MBFT's and organocatalysis, the latest powerful tools of organic synthesis, and involving the reactivity of nitroalkenes. We first developed a highly stereoselective consecutive Michael – [3+2] Heterocyclisation – Fragmentation reaction where two C–C bonds, one C–O bond and a cycle are formed to make optically active cyclopentanoximes bearing up to three stereocenters. These products can be converted into hydroxylamines or indoles. We then exploited the nucleophilic potential of 1,2-dicarbonyl compounds in the design of the first organocatalyzed diastereo- and enantioselective Michael additions of 1,2-ketoamides and 1,2-ketoesters onto nitroalkenes. The corresponding adducts are valuable synthetic platforms towards the synthesis of five- and six-membered carbo- and heterocycles with wide functional variety. This work led to the development of a domino transformation involving 1,2-dicarbonyl compounds and halogenated nitroolefines to efficiently access 2-carbonyl- and 2-phosphorylfuranes whose reported synthetic pathways remain rare. The first encouraging trials carried out to make atropisomers enable a potential asymmetric version of this methodology
Sasso, d'Elia Cecilia. "Organocatalyse et multiple bond-forming transformations (MBFTs) comme outils pour le contrôle de la chiralité." Thesis, Aix-Marseille, 2017. http://www.theses.fr/2017AIXM0371.
Full textIn the last century, the ability of organic chemists to build complex molecules has grown exponentially. Despite these achievements, the challenge of synthesizing new molecules efficiently and selectively remains open. In the first chapter, we will discuss the definition of chirality as a transversal topic in science. Subsequently we will discuss the different strategies to control chirality in organic synthesis, with a special attention to organocatalysis. In the second and third chapter we will focus on the attempt to control central chirality for the synthesis of substituted tetrahydropyrans and the investigation of the reactivity of α,β-unsaturated 1,3-ketoamides in Michael addition. In the fourth chapter, other less conventional types of chirality will be examined. First, a study on the racemization of atropisomer furans will be conducted. Then, innovative strategies will be implemented for the synthesis [4] - and [5] helicenes via, in particular, chirality conversion approaches
Sasso, d'Elia Cecilia. "Organocatalyse et multiple bond-forming transformations (MBFTs) comme outils pour le contrôle de la chiralité." Electronic Thesis or Diss., Aix-Marseille, 2017. http://www.theses.fr/2017AIXM0371.
Full textIn the last century, the ability of organic chemists to build complex molecules has grown exponentially. Despite these achievements, the challenge of synthesizing new molecules efficiently and selectively remains open. In the first chapter, we will discuss the definition of chirality as a transversal topic in science. Subsequently we will discuss the different strategies to control chirality in organic synthesis, with a special attention to organocatalysis. In the second and third chapter we will focus on the attempt to control central chirality for the synthesis of substituted tetrahydropyrans and the investigation of the reactivity of α,β-unsaturated 1,3-ketoamides in Michael addition. In the fourth chapter, other less conventional types of chirality will be examined. First, a study on the racemization of atropisomer furans will be conducted. Then, innovative strategies will be implemented for the synthesis [4] - and [5] helicenes via, in particular, chirality conversion approaches
Lee, Mike Y. J., and 李耀中. "Evolution and emerging trends in HFT research." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/mbfxts.
Full text國立政治大學
資訊管理學系
107
In this research, the evolution and emerging trends of High Frequency Trading (HFT) research is conducted by examining papers published in the Web of Science (WOS) from 1993 to 2017. A total of 241 papers are included, and 1876 keywords from these articles were extracted and analyzed. For tracing the dynamic changes of the HFT Research, the whole 24 years are further separated into three consecutive periods: 1993-2002, 2003-2012, and 2013-2017. The Ucinet is adopted to get keywords network, or knowledge network, to study the relationship of each research theme. NetDraw is applied to visualize network. The social network analysis (SNA) technique is used to reveal patterns and trends in the research by measuring the association strength of terms representative of relevant publications produced in HFT field. Results indicate that HFT research has been strongly influenced by these keywords: “market”, “prices”, “finance”, “liquidity”, “statistics”, “financial markets”, “stock”, “stochastic”, “model” and “trades” as shown in Table 3, which represent some established research themes. These are major focuses and the bridges connecting to other research themes in HFT. The detailed analysis in “Discussions and implications” provides an overview of evolution and emerging trends in HFT Research. It concludes that “market performance” related keywords, which represent some established research themes, have become the major focus in HFT research. It also changes rapidly to embrace new themes. Especially, this research may make contribution to enlarge research method in that there is no SNA research in HFT research before.
CHANG, JUNE-PEI, and 張戎佩. "Cell-Aware Utilization of MBFFs under Setup-Time and Hold-Time Constraints." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/16669475137858783266.
Full text中華大學
資訊工程學系
104
Utilization of multi-bit flip-flops(MBFFs) in a synchronous design has become a significant methodology for clock power reduction. It is known that power reduction in utilization of MBFFs mainly depends on timing constraints on 1-bit flip-flops in a synchronous design. Given a synchronous design with a set of 1-bit flip-flops inside a placement plane and a set of available MBFFs in a cell library, firstly, the possibility of merging 1-bit flip-flops into available MBFFs in utilization of MBFFs can be increased by considering some sets of timing constraints on the 1-bit flip-flops under setup-time and hold-time constraints. Furthermore, based on the establishment of the timing-constrained merging graphs(TCMGs) using some sets of timing constraints on the 1-bit flip-flops and the power information of the MBFFs in a given cell library, the corresponding cell-aware reduced extraction tree can be constructed from the established TCMGs by using the concept of clique extraction and dominated and isomorphic reduction on tree size. Finally, an edge-weighted extraction diagraph can be constructed from the corresponding reduced extraction trees and the utilization of MBFFs in a synchronous design can be obtained from the edge-weighted extraction diagraph to maximize the reduction of the total consumed power in a given synchronous design. Compared with four published approaches[20] [24][25][26] with a given set of timing constraints on the given 1-bit flip-flops, the experimental results show that our proposed approach can reduce 0.23%, 2.19%, 1.84% and 0.01% of the clock power for six tested examples on the average, respectively.
Book chapters on the topic "MBFT’s"
Bonne, Damien, and Jean Rodriguez. "Definitions and Classifications of MBFTs." In Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis. John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781119006220.ch1.
Full textJIA, YANXING, and SHIQIANG ZHOU. "MBFTs for the Total Synthesis of Natural Products." In Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis. John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781119006220.ch13.
Full textZarganes-Tzitzikas, Tryfon, Ahmad Yazbak, and Alexander Dömling. "Industrial Applications of Multiple Bond-Forming Transformations (MBFTs)." In Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis. John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781119006220.ch15.
Full textKuan, Ta-Wen, Xiaodong Yu, Qi Wang, and Yihan Wang. "Yolo V3 for Market MBFVS Food Materials Detection." In Lecture Notes in Electrical Engineering. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-0068-4_15.
Full textMuth, Lydia. "Ergebnisse." In Ermittlung der Teilhabeförderung und des Finanzierungsbedarfs bei Chronisch Mehrfachgeschädigt/Mehrfachbeeinträchtigt Abhängigkeitskranken. Springer Fachmedien Wiesbaden, 2022. http://dx.doi.org/10.1007/978-3-658-39487-5_7.
Full textAuricchio, Gennaro, and Jie Zhang. "On the Manipulability of Maximum Vertex-Weighted Bipartite b-Matching Mechanisms." In Frontiers in Artificial Intelligence and Applications. IOS Press, 2023. http://dx.doi.org/10.3233/faia230262.
Full textConference papers on the topic "MBFT’s"
Yue, Zheng, and Liu June. "A Nonmonotone MBFGS Method for Solving Nonconvex Minimization Problems." In 2008 3rd International Conference on Innovative Computing Information and Control. IEEE, 2008. http://dx.doi.org/10.1109/icicic.2008.66.
Full textZhao, Lin, Dali Wang, and Yueting Yang. "The quadratic property of the L-MBFGS methods for training neural networks." In 2011 International Conference on Mechatronic Science, Electric Engineering and Computer (MEC). IEEE, 2011. http://dx.doi.org/10.1109/mec.2011.6025596.
Full textPennell, Douglas, Luis Tay-Wo-Chong, Richard Smith, Patricia Sierra Sanchez, and Andrea Ciani. "GT36 First Stage Development Enabling Load and Fuel (H2) Flexibility With Low Emissions." In ASME Turbo Expo 2023: Turbomachinery Technical Conference and Exposition. American Society of Mechanical Engineers, 2023. http://dx.doi.org/10.1115/gt2023-103568.
Full textYang, Gang, Gang Yang, Jun Wu, Fei Shen, and Li-ping Xie. "Notice of Retraction: Research on Phosphorus Removals from Wastewater by Modified Blast-Furnace Slag (MBFS)." In 2011 5th International Conference on Bioinformatics and Biomedical Engineering. IEEE, 2011. http://dx.doi.org/10.1109/icbbe.2011.5781116.
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