Academic literature on the topic 'Synthetic'

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Journal articles on the topic "Synthetic"

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Singavarapu, Adilakshmi, Gowri Sankar Reddipalli, Venkat Reddy Ghojala, Narsimulu Akkapally, and Chandrashekar Reddy Guddeti. "Effective Synthetic Route for Large Scale Synthesis of Fluphenazine Hydrochloride and process related unknown impurity." Research Journal of Chemistry and Environment 27, no. 4 (March 15, 2023): 58–64. http://dx.doi.org/10.25303/2704rjce058064.

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A new synthetic route has been developed on a large scale for the synthesis of fluphenazine hydrochloride. We started the synthesis with the cheap and readily available tert-butyl piperazine-1-carboxylate and 1- bromo-3-chloropropane.This approach is scalable nucleophilic substitution reaction between tert-butyl piperazine-1-carboxylate and 1-bromo-3- chloropropane to afford tert-butyl 4-(3-chloropropyl) piperazine-1-carboxylate, the resulting amino chloro compound was used for N-alkylation with 2- (trifluoromethyl)-10H-phenothiazine and the obtained N- alkylated product was deprotected and then Nalkylated with chloro ethanol to afford fluphenazine hydrochloride. During the synthectic approach, we identified unknown impurity which was properly isolated and analysed by spectral data. Our synthetic strategy is very effective for large scale synthesis of fluphenazine hydrochloride.
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Hughes, Randall A., and Andrew D. Ellington. "Synthetic DNA Synthesis and Assembly: Putting the Synthetic in Synthetic Biology." Cold Spring Harbor Perspectives in Biology 9, no. 1 (January 2017): a023812. http://dx.doi.org/10.1101/cshperspect.a023812.

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Sokolov, N. A., E. P. Vasiliev, and A. A. Getmanskaya. "Generation and study of the synthetic brain electron microscopy dataset for segmentation purpose." Computer Optics 47, no. 5 (October 2023): 778–87. http://dx.doi.org/10.18287/-6179-co-1273.

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Advanced microscopy technologies such as electron microscopy have opened up a new field of vision for biomedical researchers. The use of artificial intelligence methods for processing EM data is largely difficult due to the small amount of annotated data at the training stage. Therefore, we add synthetic images to an annotated real EM dataset or use a fully synthetic training dataset. In this work, we present an algorithm for the synthesis of 6 types of organelles. Based on the EPFL dataset, a training set of 1161 real fragments 256×256 (ORG) and 2000 synthetic ones (SYN), as well as their combination (MIX), were generated. The experiment of training models for 6, 5-classes and binary segmentation showed that, despite the imperfections of synthetics, training on a mixed (MIX) dataset gave a significant increase (about 0.1) in the Dice metric for 6 and 5 and same results at binary. The synthetic data strategy gives annotations for free, but shifts the effort to producing sufficiently realistic images.
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Brücher, W., M. J. Kerschgens, and F. Steffany. "Synthetic wind climatologies." Meteorologische Zeitschrift 3, no. 3 (July 11, 1994): 183–86. http://dx.doi.org/10.1127/metz/3/1994/183.

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Falk, K. C., G. F. W. Rakow, and R. K. Downey. "The utilization of heterosis for seed yield in hybrid and synthetic cultivars of summer turnip rape." Canadian Journal of Plant Science 78, no. 3 (July 1, 1998): 383–87. http://dx.doi.org/10.4141/p97-076.

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Hybrids of summer turnip rape (Brassica rapa L. syn. B. campestris L.) have been shown to exhibit high levels of heterosis. This study was undertaken to determine whether the heterosis for seed yield observed in hybrids could be captured by synthetic cultivars of turnip rape. The agronomic performance of reciprocal inter-cultivar hybrids and their corresponding two-component synthetics was studied using four turnip rape cultivars. Hybrid seed was produced by hand pollination in the greenhouse and Syn1 seed was produced by mixing equal proportions of each parent to form the base seed (Syn0) of each synthetic, and planting these in isolation in the field. The seed yield of hybrids, synthetics and parents were similar in 1985 while in 1986, hybrids yielded 25% and synthetics 23% more than parents. Actual versus predicted synthetic yields were similar except for one synthetic, Echo-Torch in 1986, where the actual yield exceeded the predicted value. Hybrid yields may have been underestimated by the chosen prediction method and therefore the yield potential of hybrids would be greater than for synthetics in turnip rape. However, until a suitable pollination control system is developed in this species, synthetic cultivars are a viable alternative to hybrids. Key words: Turnip rape (summer), synthetic, hybrids, Brassica rapa, B. campestris
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Bachheimer, Jean-Pierre. "Comparative NIR and IR examination of natural, synthetic, and irradiated synthetic quartz." European Journal of Mineralogy 12, no. 5 (October 4, 2000): 975–86. http://dx.doi.org/10.1127/0935-1221/2000/0012-0975.

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Green, Alexander A. "Synthetic bionanotechnology: synthetic biology finds a toehold in nanotechnology." Emerging Topics in Life Sciences 3, no. 5 (October 23, 2019): 507–16. http://dx.doi.org/10.1042/etls20190100.

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Enabled by its central role in the molecular networks that govern cell function, RNA has been widely used for constructing components used in biological circuits for synthetic biology. Nucleic acid nanotechnology, which exploits predictable nucleic acid interactions to implement programmable molecular systems, has seen remarkable advances in in vitro nanoscale self-assembly and molecular computation, enabling the production of complex nanostructures and DNA-based neural networks. Living cells genetically engineered to execute nucleic acid nanotechnology programs thus have outstanding potential to significantly extend the current limits of synthetic biology. This perspective discusses the recent developments and future challenges in the field of synthetic bionanotechnology. Thus far, researchers in this emerging area have implemented dozens of programmable RNA nanodevices that provide precise control over gene expression at the transcriptional and translational levels and through CRISPR/Cas effectors. Moreover, they have employed synthetic self-assembling RNA networks in engineered bacteria to carry out computations featuring up to a dozen inputs and to substantially enhance the rate of chemical synthesis. Continued advancement of the field will benefit from improved in vivo strategies for streamlining nucleic acid network synthesis and new approaches for enhancing network function. As the field matures and the complexity gap between in vitro and in vivo systems narrows, synthetic bionanotechnology promises to have diverse potential applications ranging from intracellular circuits that detect and treat disease to synthetic enzymatic pathways that efficiently produce novel drug molecules.
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Huang, Yucan. "Exploring Strychnine from Synthesis and Reaction Mechanisms." Highlights in Science, Engineering and Technology 83 (February 27, 2024): 318–28. http://dx.doi.org/10.54097/3mbz8g41.

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Strychnine is a prominent organic compound with significant impacts in both organic synthesis and pharmaceuticals. This article provides a detailed account of various synthetic methods employed to produce strychnine over different decades, categorizing them into the 1950s-1960s, 1990s-2000s, and the modern era. It critically assesses the advantages and disadvantages of each synthetic approach within these time frames, with a particular focus on four advanced methods of recent times: transition-metal catalyzed synthesis, asymmetric synthesis, and biocatalysis synthesis. Furthermore, this review delves into the synthetic principles underlying these methods and examines their potential for achieving controlled synthesis reactions. The positive ramifications of controlled synthesis methods are explored in depth, encompassing areas such as education, synthetic reactions, criminal investigations, and pharmaceutical development. However, the research finds that each modern synthetic method still faces its own set of challenges, including issues related to reaction instability, scale limitations, and stringent reaction conditions. Consequently, researchers must dedicate extensive efforts to address these problems in order to realize the potential of controlled synthesis methods.
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Chatterjee, Bhaskar, Dhananjoy Mondal, and Smritilekha Bera. "Synthetic applications of the Cannizzaro reaction." Beilstein Journal of Organic Chemistry 20 (June 19, 2024): 1376–95. http://dx.doi.org/10.3762/bjoc.20.120.

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The Cannizzaro reaction has emerged as a versatile synthetic tool for the construction of functionalized molecules. Dating back to the 19th century, this reaction, though initially used for the synthesis of an alcohol and acid functionality from aldehydes, has henceforth proven useful to generate diverse molecular entities using both intermolecular and intramolecular synthetic strategies. Immense applications in the synthesis of hydroxy acids and esters, heterocycles, fused carbocycles, natural products, and others with broad substrate scope have raised profound interest from methodological and synthetic standpoints. The ongoing development of reagents, solvents, and technologies for the Cannizzaro reaction reflects the broader trend in organic synthesis towards more sustainable and efficient practices. The focus of this review is to highlight some recent advances in synthetic strategies and applications of the Cannizzaro reaction towards the synthesis of potentially useful molecules.
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Fairbanks, Antony J. "Synthetic and semi-synthetic approaches to unprotected N-glycan oxazolines." Beilstein Journal of Organic Chemistry 14 (February 15, 2018): 416–29. http://dx.doi.org/10.3762/bjoc.14.30.

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N-Glycan oxazolines have found widespread use as activated donor substrates for endo-β-N-acetylglucosaminidase (ENGase) enzymes, an important application that has correspondingly stimulated interest in their production, both by total synthesis and by semi-synthesis using oligosaccharides isolated from natural sources. Amongst the many synthetic approaches reported, the majority rely on the fabrication (either by total synthesis, or semi-synthesis from locust bean gum) of a key Manβ(1–4)GlcNAc disaccharide, which can then be elaborated at the 3- and 6-positions of the mannose unit using standard glycosylation chemistry. Early approaches subsequently relied on the Lewis acid catalysed conversion of peracetylated N-glycan oligosaccharides produced in this manner into their corresponding oxazolines, followed by global deprotection. However, a key breakthrough in the field has been the development by Shoda of 2-chloro-1,3-dimethylimidazolinium chloride (DMC), and related reagents, which can direct convert an oligosaccharide with a 2-acetamido sugar at the reducing terminus directly into the corresponding oxazoline in water. Therefore, oxazoline formation can now be achieved in water as the final step of any synthetic sequence, obviating the need for any further protecting group manipulations, and simplifying synthetic strategies. As an alternative to total synthesis, significant quantities of several structurally complicated N-glycans can be isolated from natural sources, such as egg yolks and soy bean flour. Enzymatic transformations of these materials, in concert with DMC-mediated oxazoline formation as a final step, allow access to a selection of N-glycan oxazoline structures both in larger quantities and in a more expedient fashion than is achievable by total synthesis.
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Dissertations / Theses on the topic "Synthetic"

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Coates, Helen Margaret. "Synthetic studies towards stemofoline synthesis." Thesis, University of Southampton, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.238730.

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Foley, Michael Andrew. "1-Acyldihydropyridones as Synthetic Intermediates." DigitalCommons@USU, 1988. https://digitalcommons.usu.edu/etd/7180.

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The most efficient and stereoselective total synthesis of (+/-) lausbine II to date has been achieved. The key steps in this are the copper-mediated conjugate addition reaction of the Grignard reagent of 1-bromo-4-chlorobutane to a dihydropyridone and a stereoselective reduction of a quinolizidinone. Methodology has been developed for the convenient synthesis of 1-acyl-2-substituted-1,2,5,6-tetrahydropyridines. This was accomplished by adding novel alkylzinc iodides to the 1-acyliminium ion derived from Nphenoxycarbonyl-4-methoxy-1, 2, 3, 4-tetrahydropyridine.
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Hale, Joshua G. "Biomimetic motion synthesis for synthetic humanoids." Thesis, University of Glasgow, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.270966.

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Liu, Yunqi. "Synthetic approaches toward natural product synthesis." Diss., The University of Arizona, 1995. http://hdl.handle.net/10150/187050.

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1,2-Dithiolan-3-one-1-oxide exists in antihumor antibiotic leinamycin and can cause DNA cleavage in the presence of thiols. Diastereoselective synthesis of this unique ring system has been achieved by low temperature oxidation of the corresponding 1,2-dithiolan-3-ones with 3,3-dimethyldioxirane. 5-Methyl-1,2-dithiolan-3-one-1-oxides were synthesized by oxidation of 5-methyl-1,2-dithiolan-3-one with 3,3-dimethyldioxirane. Eu(fod)₃ and C₆D₆ induced proton chemical shift studies showed that the major isomer in the product has a trans sulfoxide relative to the 5-methyl group. Low temperature oxidation of 4-substituted-amino-5,5-dimethyl-1,2-dithiolan-3-ones by 3,3-dimethyldioxirane preferentially led to the corresponding trans-1,2-dithiolan-3-one-1-oxides. This assignment was made on the basis of a X-ray crystallographic structure study. Formation of azlactones as well as 1,2-dithiolan-3-one-1,1-dioxide were also observed when some substituted 1,2-dithiolan-3-ones were oxidized by 3,3-ditnethyldioxirane. Three 2,2-dimethyl-1,3-dithian-4-ones were synthesized by SnCl₄ mediated condensation of β-mercaptothioacids and acetone. Oxidation of 2,2,6-trimethyl-1,3-dithian-4-one with Ce(IV) did not give 1,2-dithiolan-3-one or 1,2-dithiolan-3-one-1-oxides as anticipated; 1,3-dithian-5-en-4-one was detected as the product instead. Synthetic approaches toward loline were explored. Intramolecular photoaddition of bicyclic olefinic N-nitrosamine did not give the desired product. An epoxide approach did not furnish loline due to unsuccessful epoxide ring opening by azide ion. In the urea approach, the tertiary nitrogen of the bicyclic urea preferentially undergoes a transannular iodocyclization. The same results were obtained by halocyclizing bis-silylimidate or mono-silylimidate of the bicyclic urea.
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Stewart, Mark Richard. "The design and synthesis of synthetic receptors." Thesis, University of Leeds, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.400852.

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Swenson, Helen Rachel. "Studies in synthetic peptides and heterocyclic synthesis." Thesis, University of Edinburgh, 1999. http://hdl.handle.net/1842/13061.

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The following work documents three studies undertaken using solid phase synthesis techniques. Interaction of the zinc metalloprotease, endothelin converting enzyme-1(ECE-1), with its peptidic natural substrate big endothelum-1 has been investigated via an SAR study, using solid phase peptide synthesis (SPPS). Truncated forms of the substrate had been previously reported to inhibit ECE-1, this was confirmed however the big ET-1 analogues were shown to be substrates for the enzyme. A short study of the substrate specificity of ECE-1 was carried out. The synthesis of vast libraries of peptides using combinational synthesis has been used to accelerate the drug discovery process. Purification of these mixtures has not been previously attempted. 17-Tetrabenzo [a,c,g,i]fluoroeneyhethoxycarbonyl (Tbfmcc) developed for use with single peptides of proteins, has been used to achieve facile purification of five peptide libraries synthesised using SP. The methodology was fully optimised for the efficient separation of the desired library members from all impurities by exploiting the affinity of TBfmoc for carbon. A potential small molecule inhibitor of the zinc metalloenzyme, farnesyl transferase (FTase), was designed. The efficient solution phase synthesis of this novel structure is reported its adaptation to solid phase synthesis is described, with the view to using multiple parallel synthesis techniques to synthesise a range of analogous.
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Scott, Felicia Yi Xia. "Controlled Hybrid Material Synthesis using Synthetic Biology." Diss., Virginia Tech, 2017. http://hdl.handle.net/10919/86147.

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The concept of creating a hybrid material is motivated by the development of an improved product with acquired properties by amalgamation of components with specific desirable traits. These new attributes can range from improvements upon existing properties, such as strength and durability, to the acquisition of new abilities, such as magnetism and conductivity. Currently, the concept of an organic-inorganic hybrid material typically describes the integration of an inorganic polymer with organically derived proteins. By building on this idea and applying the advanced technologies available today, it is possible to combine living and nonliving components to synthesize functional materials possessing unique abilities of living cells such as self-healing, evolvability, and adaptability. Furthermore, artificial gene regulation, achievable through synthetic biology, allows for an additional dimension of the control of hybrid material function. Here, I genetically engineer E. coli with a tightly controlled artificial protein construct, allowing for inducible expression of different amounts of the surface anchored protein by addition of varying concentrations of L-arabinose. The presence of the surface protein allows the cells to bind nonliving nanoparticle substrates, effectively turning the cells into living crosslinkers. By using the living crosslinker, I was able to successfully synthesize a robust, macroscale living-nonliving hybrid material with magnetic characteristics. Furthermore, by varying the particle size and inducer concentration, the resulting material exhibited alterations in structure and function. Finally, I was able to manipulate material kinetics within a PDMS channel by applying fluctuating magnetic fields and demonstrate material durability. These results demonstrate the ability to manipulate synthesis of living-nonliving hybrid materials, which demonstrate the potential for use in promising applications in areas such as environmental monitoring and micromachining. Additionally, this work serves as a foundational step toward the integration of synthetic biology with tissue engineering by exploiting the possibility of controlling material properties with genetic engineering.
Ph. D.
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Kim, Charles. "Synthetic studies toward the synthesis of norrisolide /." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 2002. http://wwwlib.umi.com/cr/ucsd/fullcit?p3055785.

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Siddiq, Musab. "Synthetic Instruments an overview : Synthetic Instruments." Thesis, University of Gävle, Department of Technology and Built Environment, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-340.

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The rapid development within the field of measurement methods and techniques and software design that has taken place over the last years offers new possibilities for designers of measurement systems through the use of virtual instruments as building blocks. The concept of virtual instrumentation is developed within the interchangeable virtual instrument foundation. A closely related term is “synthetic instruments”, which is often used for essentially the same concept, but it is even more software oriented. Synthetic instruments as a research field are in an initial stage and a quick search on “Synthetic instruments” in Institute of Electrical and Electronics Engineers (IEEE) explorer match close to 30 documents. IEEE explorer is a database that provides full-text access to IEEE transactions, journals, magazines and conference proceedings, and all current IEEE Standards.

This Master Thesis is a theoretical work extracted from study material, IEEE documents and web-resources referenced. The work gives the reader an overview of the Synthetic Instruments and their functionality with respect to hardware and software. The papers were analyzed based upon the various trends in the research, development and productizing phases.

For this approach; kernel architecture of an ideal synthetic instrument has been introduced as a prototype around which current technologies and applications can be addressed. The major areas of focus in the architecture are the data conversion and signal conditioning; the knowledge of its working under current implemented technologies has been highlighted and discussed in regards to the software and hardware trends. The defense industry holds the major influence.

The work was aimed towards giving a state-of-the art introduction to synthetic instrument technology; also in order to provide the work an introductory nature, only one hardware & software example has been discussed.

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Gilmore, Laurie Ann. "Chlorination of synthetic dyes and synthetic brighteners." Thesis, Georgia Institute of Technology, 1991. http://hdl.handle.net/1853/20794.

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Books on the topic "Synthetic"

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Architecture, Office for Metropolitan. Educatorium: Synthetisch landschap = synthetic landscape. Utrecht: Universiteit Utrecht, 2000.

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Campbell, Marissa J. DNA microarrays, synthesis, and synthetic DNA. Hauppauge, N.Y: Nova Science, 2011.

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Balmer, Andrew S., Katie Bulpin, and Susan Molyneux-Hodgson. Synthetic Biology. London: Palgrave Macmillan UK, 2016. http://dx.doi.org/10.1057/9781137495426.

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Ryadnov, Maxim, Luc Brunsveld, and Hiroaki Suga, eds. Synthetic Biology. Cambridge: Royal Society of Chemistry, 2017. http://dx.doi.org/10.1039/9781782622789.

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Ryadnov, Maxim, Luc Brunsveld, and Hiroaki Suga, eds. Synthetic Biology. Cambridge: Royal Society of Chemistry, 2014. http://dx.doi.org/10.1039/9781849737845.

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Fourné, Franz. Synthetic Fibers. München: Carl Hanser Verlag GmbH & Co. KG, 1999. http://dx.doi.org/10.3139/9783446401334.

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Chatwal, Gurdeep R. Synthetic dyes. Mumbai [India]: Himalaya Pub. House, 2009.

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Kempt, Hendrik. Synthetic Friends. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-13631-3.

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Tiller, Thomas, ed. Synthetic Antibodies. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6857-2.

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Dixon, Wheeler Winston. Synthetic Cinema. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-12571-4.

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Book chapters on the topic "Synthetic"

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Kleschik, William A. "Synthesis of Synthetic Pyrethroids." In ACS Symposium Series, 189–98. Washington, DC: American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0355.ch017.

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Gooch, Jan W. "Resin, Synthetic (Synthetic Polymer)." In Encyclopedic Dictionary of Polymers, 624. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9952.

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Bährle-Rapp, Marina. "synthetic." In Springer Lexikon Kosmetik und Körperpflege, 540. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_10264.

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Gooch, Jan W. "Synthetic." In Encyclopedic Dictionary of Polymers, 725. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_11490.

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Guillot, Agnès, and Jean-Arcady Meyer. "Synthetic Animals in Synthetic Worlds." In Cyberworlds, 111–23. Tokyo: Springer Japan, 1998. http://dx.doi.org/10.1007/978-4-431-67941-7_7.

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Kubicek, Christian P. "Synthetic Biopolymers." In Synthetic Biology, 307–35. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-22708-5_9.

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Müller, Oliver. "Synthetic Biology." In Synthetic Biology, 31–45. Wiesbaden: Springer Fachmedien Wiesbaden, 2015. http://dx.doi.org/10.1007/978-3-658-10988-2_3.

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Kempt, Hendrik. "Synthetic Friends." In Synthetic Friends, 111–61. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-13631-3_7.

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Sánchez-Pascuala, Alberto, Pablo I. Nikel, and Víctor de Lorenzo. "Re-Factoring Glycolytic Genes for Targeted Engineering of Catabolism in Gram-Negative Bacteria." In Synthetic Biology, 3–24. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7795-6_1.

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Lebar, Tina, and Roman Jerala. "Designed Transcriptional Regulation in Mammalian Cells Based on TALE- and CRISPR/dCas9." In Synthetic Biology, 191–203. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7795-6_10.

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Conference papers on the topic "Synthetic"

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Cornwall, Patrick, Manuel Ballester, Heming Wang, and Florian Willomitzer. "Towards Synthetic Light-in-Flight." In Computational Optical Sensing and Imaging. Washington, D.C.: Optica Publishing Group, 2023. http://dx.doi.org/10.1364/cosi.2023.cth2b.3.

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We present a method for the computational synthesis of a shaped, synthetic light pulse from interferometric measurements under CW illumination. The pulse can be manipulated to travel through a captured scene, demonstrating synthetic light-in-flight videos.
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LE GALL, Y., N. BURLET, M. SIMON, F. NOVELLA, S. DUGELAY, and JP MALKASSE. "USING SHADOWS IN CIRCULAR SAS IMAGING FOR TARGET ANALYSIS." In Synthetic Aperture Sonar and Synthetic Aperture Radar 2023. Institute of Acoustics, 2023. http://dx.doi.org/10.25144/15947.

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SHOULDICE, E., S. SMITH, TO SAEBO, A. CRAWFORD, Ø. MIDTGAARD, J. KING, S. JOHNSON, et al. "THE IMPACTS OF SCENE STABILITY AND ACOUSTIC BACKSCATTER COHERENCE ON AUTOMATED SEABED CHANGE DETECTION." In Synthetic Aperture Sonar and Synthetic Aperture Radar 2023. Institute of Acoustics, 2023. http://dx.doi.org/10.25144/15925.

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HUNTER, AJ, Z. RYMANSAIB, CJ SANFORD, BW THOMAS, A. BURT, and R. BROTHERS. "ISOLATION OF RESONANT WAVE FEATURES IN LOW-FREQUENCY WIDEBAND SAS DATA PRODUCTS FROM CYLINDRICAL SHELLS." In Synthetic Aperture Sonar and Synthetic Aperture Radar 2023. Institute of Acoustics, 2023. http://dx.doi.org/10.25144/15917.

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LANE, RO, WJ HOLMES, and T. LAMONT-SMITH. "TARGET RECOGNITION IN SAR IMAGES WITH LOW-SWAP PROCESSING HARDWARE." In Synthetic Aperture Sonar and Synthetic Aperture Radar 2023. Institute of Acoustics, 2023. http://dx.doi.org/10.25144/15942.

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ANDRE, D., and FM WATSON. "REVERSE-PATH MULTISTATIC SAR FOR MOVING TARGET DETECTION IN CLUTTER." In Synthetic Aperture Sonar and Synthetic Aperture Radar 2023. Institute of Acoustics, 2023. http://dx.doi.org/10.25144/15920.

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OLSON, DR, and M. GEILHUFE. "COMPARISON OF MODEL SELECTION TECHNIQUES FOR SEAFLOOR SCATTERING STATISTICS." In Synthetic Aperture Sonar and Synthetic Aperture Radar 2023. Institute of Acoustics, 2023. http://dx.doi.org/10.25144/15924.

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EMIGH, MS, H. BAKER, CH MENDOZA-CARDENAS, and AJ BROCKMEIER. "WEAKLY SUPERVISED AUTOMATIC OBJECT MASKING FOR SAS." In Synthetic Aperture Sonar and Synthetic Aperture Radar 2023. Institute of Acoustics, 2023. http://dx.doi.org/10.25144/15934.

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CRAWFORD, A., J. SECKER, S. GONG, and E. SHOULDICE. "ADDING SAS IMAGE PROCESSING CAPABILITY TO SAR IMAGE PROCESSING SOFTWARE." In Synthetic Aperture Sonar and Synthetic Aperture Radar 2023. Institute of Acoustics, 2023. http://dx.doi.org/10.25144/15911.

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TODD, BD, II RODRIGUEZ-PINTO, DD STERNLICHT, J. WEAVER, and M. HARTZOG. "ADVANCED AUTONOMY FOR UUV-BASED SAS." In Synthetic Aperture Sonar and Synthetic Aperture Radar 2023. Institute of Acoustics, 2023. http://dx.doi.org/10.25144/15918.

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Reports on the topic "Synthetic"

1

Elowitz, Michael. Synthetic Origins. Asimov Press, April 2024. http://dx.doi.org/10.62211/21yr-22te.

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Stewart, John M., Karl Hahn, and Wieslaw A. Klis. Synthetic Helizyme Enzymes. Fort Belvoir, VA: Defense Technical Information Center, August 1989. http://dx.doi.org/10.21236/ada211789.

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Henninger, Amy E., Eric Chown, and Randy Jones. Emotional Synthetic Forces. Fort Belvoir, VA: Defense Technical Information Center, July 2004. http://dx.doi.org/10.21236/ada426234.

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Calvert, Paul D., H. K. Hall, and Jr. Intelligent Synthetic Polymers. Fort Belvoir, VA: Defense Technical Information Center, January 1995. http://dx.doi.org/10.21236/ada292905.

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Doudchenko, Nikolay, and Guido Imbens. Balancing, Regression, Difference-In-Differences and Synthetic Control Methods: A Synthesis. Cambridge, MA: National Bureau of Economic Research, October 2016. http://dx.doi.org/10.3386/w22791.

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Bello, Mollie. Synthetic Self-Healing Methods. Office of Scientific and Technical Information (OSTI), June 2014. http://dx.doi.org/10.2172/1133311.

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Sigman, David S. Synthetic sequence Specific Nucleases. Fort Belvoir, VA: Defense Technical Information Center, July 1989. http://dx.doi.org/10.21236/ada210751.

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Sigman, David S. Synthetic Sequence Specific Nucleases. Fort Belvoir, VA: Defense Technical Information Center, July 1988. http://dx.doi.org/10.21236/ada198570.

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Henyey, Frank, and Kevin Williams. Synthetic Aperture Sonar Primer. Fort Belvoir, VA: Defense Technical Information Center, September 1997. http://dx.doi.org/10.21236/ada627533.

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Frame, Edwin A., and Ruben A. Alvarez. Synthetic Fuel Lubricity Evaluations. Fort Belvoir, VA: Defense Technical Information Center, September 2003. http://dx.doi.org/10.21236/ada421822.

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