Academic literature on the topic 'Chemistry, Biochemistry. Chemistry, Organic'

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Journal articles on the topic "Chemistry, Biochemistry. Chemistry, Organic"

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Kaur, Navjeet. "Photochemical Reactions for the Synthesis of Six-Membered O-Heterocycles." Current Organic Synthesis 15, no. 3 (2018): 298–320. http://dx.doi.org/10.2174/1570179414666171011160355.

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Background: The chemists have been interested in light as an energy source to induce chemical reactions since the beginning of the scientific chemistry. This review summarizes the chemistry of photochemical reactions with emphasis of their synthetic applications. The organic photochemical reactions avoid the polluting or toxic reagents and therefore offer perspectives for sustainable processes and green chemistry. In summary, this review article describes the synthesis of a number of six-membered O-heterocycles. Objective: Photochemistry is indeed a great tool synthetic chemists have at their
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Wright, Robin, Sehoya Cotner, and Amy Winkel. "Minimal Impact of Organic Chemistry Prerequisite on Student Performance in Introductory Biochemistry." CBE—Life Sciences Education 8, no. 1 (2009): 44–54. http://dx.doi.org/10.1187/cbe.07-10-0093.

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Curriculum design assumes that successful completion of prerequisite courses will have a positive impact on student performance in courses that require the prerequisite. We recently had the opportunity to test this assumption concerning the relationship between completion of the organic chemistry prerequisite and performance in introductory biochemistry. We found no statistically significant differences between average biochemistry grades or grade distribution among students with or without the organic chemistry prerequisite. However, students who had not completed the organic chemistry prereq
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McRae, Marc P. "Correlation of Preadmission Organic Chemistry Courses and Academic Performance in Biochemistry at a Midwest Chiropractic Doctoral Program*." Journal of Chiropractic Education 24, no. 1 (2010): 30–34. http://dx.doi.org/10.7899/1042-5055-24.1.30.

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Purpose: Organic chemistry has been shown to correlate with academic success in the preclinical years of medicine, dentistry, and graduate physiology. The purpose of this study is to examine the relationship between undergraduate organic chemistry grades and first-semester biochemistry grades at a Midwest chiropractic doctoral program. Methods: Students enrolled in a first-semester biochemistry course who had completed the prerequisite courses in organic chemistry offered at this same institution were entered into the study. The total grade for each of the three courses was calculated using th
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Mlinac-Jerković, Kristina, Vladimir Damjanović, Svjetlana Kalanj-Bognar, and Jasna Lovrić. "Marking a Century of the Department of Chemistry and Biochemistry at School of Medicine in Zagreb." Croatica chemica acta 92, no. 3 (2019): 435–42. http://dx.doi.org/10.5562/cca3554.

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In 2018 the Department of Chemistry and Biochemistry at Zagreb School of Medicine celebrated 100 years since it was established by professor Fran Bubanović. This essay is focused on his successors, outstanding teachers and scientists, professors Tomislav Pinter and Mihovil Proštenik, members of Yugoslavian (today Croatian) Academy of Sciences and Arts. Tomislav Pinter was a prominent physical chemist who had an original approach and gave novel interpretation of van der Waals and Wohl’s equations. He also served as the president of Croatian Chemical Society. Neurobiochemist Mihovil Proštenik st
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Wood, E. J. "Organic chemistry." Biochemical Education 23, no. 1 (1995): 44. http://dx.doi.org/10.1016/0307-4412(95)90196-5.

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Rosenfeld, Louis. "Justus Liebig and Animal Chemistry." Clinical Chemistry 49, no. 10 (2003): 1696–707. http://dx.doi.org/10.1373/49.10.1696.

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Abstract Justus Liebig was one of the individuals making chemistry almost a German monopoly in the 19th century. At Giessen he established the first organic chemistry laboratory and offered a systematic course for training new chemists. His comprehensive survey of plant nutrition changed the nature of scientific agriculture. In a study of animal chemistry, Liebig treated physiologic processes as chemical reactions and inferred the transformations from the chemical properties of the elements and compounds in laboratory reactions. He constructed hypothetical chemical equations derived from the f
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RICHTER-ADDO, GEORGE B. "Interactions of nitric oxide and organic nitroso compounds with metalloporphyrins and heme." Journal of Porphyrins and Phthalocyanines 04, no. 04 (2000): 354–57. http://dx.doi.org/10.1002/(sici)1099-1409(200006/07)4:4<354::aid-jpp240>3.0.co;2-v.

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The chemistry of nitric oxide (NO) has taken on new dimensions since the discovery, about a decade ago, of a myriad of biological events that NO participates in. Many of the foundations of metal-NO chemistry were laid out earlier by inorganic chemists and biochemists investigating the structures and electronic properties of the heme-NO moiety or its model compounds. Certainly, the persistent work over the last three decades by chemists working with metal nitrosyls has paid off. Current areas of research in heme-NO chemistry include (i) how the NO group approaches and binds to the metal center
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Houk, K. N., and Fang Liu. "Holy Grails for Computational Organic Chemistry and Biochemistry." Accounts of Chemical Research 50, no. 3 (2017): 539–43. http://dx.doi.org/10.1021/acs.accounts.6b00532.

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Laube, Thomas. "New Carbocations—From Physical Organic Chemistry to Biochemistry." Angewandte Chemie International Edition in English 35, no. 2324 (1996): 2765–66. http://dx.doi.org/10.1002/anie.199627651.

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Reddy, Neelesh C., Mohan Kumar, Rajib Molla, and Vishal Rai. "Chemical methods for modification of proteins." Organic & Biomolecular Chemistry 18, no. 25 (2020): 4669–91. http://dx.doi.org/10.1039/d0ob00857e.

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The field of protein bioconjugation draws attention from stakeholders in chemistry, biology, and medicine. This review provides an overview of the present status, challenges, and opportunities for organic chemists.
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Dissertations / Theses on the topic "Chemistry, Biochemistry. Chemistry, Organic"

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Easton, Christopher J. "Aspects of biological and organic chemistry, particularly amino acid, cyclodextrin, and free radical chemistry /." Title page, contents and abstract only, 1997. http://web4.library.adelaide.edu.au/theses/09S.D/09s.de13.pdf.

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Orrling, Kristina M. "On the Versatility of Microwave-Assisted Chemistry : Exemplified by Applications in Medicinal Chemistry, Heterocyclic Chemistry and Biochemistry." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-101356.

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Ding, Xiao Dong. "Synthesis and characterization of heme models and spectroelectrochemical studies of heme proteins." Diss., The University of Arizona, 1997. http://hdl.handle.net/10150/282523.

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To better understand the relationship between the structure and electronic properties of the iron center and the functions of heme proteins, both naturally occurring heme proteins and synthetically prepared heme models have been studied. The reduction potential (E°') and the pH dependence of E°' of nitrophorin 1 (NP1) and myoglobin (Mb) were determined by spectroelectrochemical techniques. The difference in the electrostatic interaction of the Fe(III) center with buried charged groups in the heme pocket of Mb and NP1 is the major factor that causes the 300 mV difference in E°. The pH dependenc
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Agha, Kazim Ally. "Synthesis, physicochemical and biochemical properties of C3'-modified 2',5'-linked oligonucleotides." Thesis, McGill University, 2003. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=84457.

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Oligoribonucleotides comprising of 2',5' -linked internucleotide linkages are known to bind selectively to RNA over DNA. The ability to bind to RNA renders them suitable as probes for many biological applications, such as 'antisense technology'. Little is known about the effect of sugar structure (and conformation) on the binding properties of 2',5'-linked oligonucleotides. To get insight into the role of sugar conformation, 2 ',5'-linked oligonucleotides modified at the C3'-position of the furanose ring were synthesized via solid phase synthesis and their binding to complementary singl
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Morley, Krista Louise. "Focusing mutagenesis into the active site to improve hydrolase selectivity." Thesis, McGill University, 2005. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=111830.

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Occasionally, researchers need to modify enzymes through amino acid substitutions to make them more efficient catalysts for organic synthesis. There is still debate over the best protein engineering strategy for improving enzyme enantioselectivity: rational design or directed evolution. Rational design experiments focus mutations close to the active site, while directed evolution experiments often find mutations far from the active site.<br>In this thesis, a combination of the two strategies improved Pseudomonas fluorescens esterase (PFE) for production of a useful synthetic building block for
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Roman, Miguel Angel. "Synthesis of branched nucleosides and oligonucleotides containing flexible alkylamine linkers on the heterocyclic bases." Thesis, McGill University, 1995. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=22797.

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The N3 position of thymidine was alkylated with different sized bromoalkyl phthalimide linkers in generally good yields, with no alkylation observed on the sugar ring. The free amino group, available after methylamine deprotection of the phthalimide linker, was protected with the levulinyl protecting group (e.g., 20). Branched 'Y'-shaped nucleic acids containing branching monomer 20 were synthesized using standard solid phase synthetic methodology and complexes of these branched nucleic acids with one and two mole-equivalents of linear complement dA$ sb{10}$ are investigated by thermal melting
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Park, Seongsoon. "Enhancing hydrolase activity and selectivity by medium, substrate, and protein engineering." Thesis, McGill University, 2003. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=83088.

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Researchers use enzymes for enantio- and regioselective reactions because of their high selectivity and activity toward natural substrates. However, researchers sometimes need to modify the reaction system or the enzyme itself to get reliable selectivity and activity when they deal with unnatural substrates. To obtain researcher's need, one can change the solvent, modify the substrates, or alter the enzyme itself. These processes are called medium, substrate, and protein engineering, respectively.<br>This thesis deals with hydrolases, which are classified by EC 3. We applied the proper
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Zhou, Wen-Qiang. "The synthesis of amide-linked 2',3'-cyclopropanated dinucleosides and the effect of their incorporation into DNA-strands on duplexation." Thesis, McGill University, 1995. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=40024.

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In order to establish if binding affinity could be improved by conformationally restricting the amide backbone, exo-amide-linked and endo-amide-linked 2$ sp prime$,3$ sp prime$-cyclopropanated dinucleoside analogs (e.g. dimers 35, 54, and 55) have been studied. The dimers were synthesized by coupling the corresponding cyclopropyl acids (5$ sp prime$-end building unit) with aminothymidines (3$ sp prime$-end building unit) by standard peptide synthesis methodology. After proper functionalizations, the dimers were incorporated into DNA sequences, and the effects of their incorporation into DNA-st
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Mangos, Maria M. "Factors governing the design, selection and cleavage of sugar-modified duplexes by ribonuclease H." Thesis, McGill University, 2005. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=85579.

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The antisense principle bases its premise in the exquisite complementarity of a synthetic, chemically-modified oligonucleotide to tightly bind with a unique target RNA sequence. Rapid and selective genetic discrimination, as driven by the formation of multiple points of target contact, constitutes a central goal of oligonucleotide therapies. Most synthetic designs have, however, provided little structural insight on the role of the antisense oligonucleotide (AON) in triggering RNA cleavage of preformed hybrids, as catalyzed by a ubiquitous, intracellular enzyme known as ribonuclease H.
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Kutterer, Kristina M. K. "Urea and carbamate backbone modified DNA & work towards a synthesis of polyoxin L and analogues." Thesis, McGill University, 1995. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=28808.

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Urea, N-methylurea and carbamate linked thymidine dimers, 38, 37 and 39 respectively, were synthesized efficiently and incorporated into 12- and 19-mer DNA oligonucleotide strands, via solid-phase synthesis. Thermal denaturation studies utilizing complementary single stranded DNA, RNA and duplex DNA, indicated selectivity of binding of all three backbone modified oligomers to single stranded DNA. The oligomer containing dimer 37 exhibited the strongest binding to single stranded DNA. Carbamate and 5$ sp prime$-N-methylurea modified dimers suitable for the preparation of longer nucleoside homop
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Books on the topic "Chemistry, Biochemistry. Chemistry, Organic"

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Organic chemistry. 5th ed. Brooks/Cole, Cengage Learning, 2011.

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P, Rogers Elizabeth, ed. General, organic, and biochemistry. 3rd ed. Brooks/Cole Pub. Co., 1987.

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General organic & biochemistry. Thomson Brooks/Cole, 2007.

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K, Whitesell James, ed. Organic chemistry. 2nd ed. Jones and Bartlett, 1997.

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K, Whitesell James, ed. Organic chemistry. 3rd ed. Jones and Bartlett Publishers, 2003.

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Fox, Marye Anne. Organic chemistry. Jones and Bartlett, 1994.

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Brown, William H. Introduction to organicand biochemistry. 4th ed. Brooks/Cole Pub. Co., 1987.

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Mundy, Bradford P. Organic and biological chemistry. Saunders College Pub, 1993.

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Organic and biological chemistry. Rinton Press, 2001.

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Solomons, T. W. Graham. Organic chemistry. Wiley, 2011.

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Book chapters on the topic "Chemistry, Biochemistry. Chemistry, Organic"

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Noble, W. J. "Organic Synthesis at High Pressure." In High Pressure Chemistry and Biochemistry. Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3827-4_12.

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Gupta, M. N. "Enzyme function in organic solvents." In Interface between Chemistry and Biochemistry. Birkhäuser Basel, 1995. http://dx.doi.org/10.1007/978-3-0348-9061-8_3.

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Noble, W. J. "Kinetics of Organic Reactions at High Pressure." In High Pressure Chemistry and Biochemistry. Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3827-4_11.

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Kirby, Anthony J. "The Organic Chemistry of Phosphate Transfer." In Ciba Foundation Symposium 57 - Phosphorus in the Enviroment: Its Chemistry and Biochemistry. John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470720387.ch7.

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Heimbach, Paul, and Tamás Bartik. "Information from Alternatives in Biochemistry." In Reactivity and Structure Concepts in Organic Chemistry. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-83806-4_9.

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Jenner, G. "The Future of High Pressure Organic Synthesis." In High Pressure Chemistry, Biochemistry and Materials Science. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1699-2_19.

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Jenner, G. "High Pressure Kinetic Effects as Mechanistic Probes in Organic Chemistry." In High Pressure Chemistry, Biochemistry and Materials Science. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1699-2_18.

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Paz, Y., and R. Naaman. "Mode Specifity in Collisions of Aniline with Surfaces covered with Organized Organic Monolayers." In The Jerusalem Symposia on Quantum Chemistry and Biochemistry. Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-2642-7_30.

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Burrington, J. D. "Selective Oxidation Catalysis: An Organic Chemist’s View of Mechanism." In Computational Materials, Chemistry, and Biochemistry: From Bold Initiatives to the Last Mile. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-18778-1_32.

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Goddard, William A. "Superconductors: Cuprate High Tc and BEDT-TTF Organic Superconductors." In Computational Materials, Chemistry, and Biochemistry: From Bold Initiatives to the Last Mile. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-18778-1_61.

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Conference papers on the topic "Chemistry, Biochemistry. Chemistry, Organic"

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Москалев, Владимир Борисович. "PREDICTION OF THE CONDITIONS OF CHEMICAL ORGANIC REACTIONS USING THE EDGE ATTENTION GRAPH CONVOLUTION NETWORK." In Наука. Исследования. Практика: сборник избранных статей по материалам Международной научной конференции (Санкт-Петербург, Апрель 2020). Crossref, 2020. http://dx.doi.org/10.37539/srp290.2020.84.35.019.

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Моделирование структуры химической реактивности с точки зрения структуры участвующих веществ имеет важные последствия во всех областях химии и биохимии, от синтеза до понимания метаболических процессов. Для предсказания условий реакций органической химии на основе графов была взята модель графовой сверточной нейронной сети с механизмом внимания на ребрах Edge Attention Graph Convolution Network. Modeling the structure of chemical reactivity from the point of view of the structure of the substances involved has important consequences in all areas of chemistry and biochemistry, from synthesis to
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Porto, Caio M., and Nelson H. Morgon. "Quantum Tunneling and Reaction Rates in Selenoxides and Sulfoxides Elimination." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol202062.

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Selenoxides and sulfoxides elimination reactions are important, not only to Organic Chemistry synthesis, but also to other areas, as Biochemistry. These reactions were studied, using direct dynamics calculations, at the canonical variational theory (CVT) and small curvature tunneling (SCT) level. The calculated rate constants for the selenoxide reaction were in good agreement with experimental data, 8.83 × 10-5 s -1 and 3.20 × 10-5 s -1 , respectively. The rate constants for the sulfoxide reaction are very small at 37°C, namely 2.43 × 10-9 , and there is also a significant tunneling correction
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Pereira, Jose A. "A biochemistry-inspired artificial chemistry: LAC." In 2005 Purtuguese Conference on Artificial Intelligence. IEEE, 2005. http://dx.doi.org/10.1109/epia.2005.341269.

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GenTan, Xie, Lin Na, Bi ZhiLi, Shan Jie, and LI HongMei. "Application of Molecular Chemistry in Biochemistry and Chemistry and Biology Application of Traditional in Medicine." In 2021 10th International Conference on Applied Science, Engineering and Technology (ICASET 2021). Atlantis Press, 2021. http://dx.doi.org/10.2991/aer.k.210817.013.

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Fauzi’ah, Lina, Artina Diniaty, Widinda Normalia Arlianty, and Beta Wulan Febriana. "Modified spiral organic curriculum on organic chemistry courses for chemistry education undergraduate students." In INTERNATIONAL CONFERENCE AND WORKSHOP ON MATHEMATICAL ANALYSIS AND ITS APPLICATIONS (ICWOMAA 2017). Author(s), 2017. http://dx.doi.org/10.1063/1.5015999.

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Cannan, Brian. "Comprehensive Synthetic Organic Chemistry Information." In The 1st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02066.

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Aires de Sousa, João. "JavaScript and Chemistry." In The 1st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02072.

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Yang, Yu-ying. "Curriculum reform in organic chemistry teaching." In 2012 IEEE Conference on Technology and Society in Asia (T&SA). IEEE, 2012. http://dx.doi.org/10.1109/tsasia.2012.6397990.

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Ramirez, Jorge Alvarez, and Ana Maria Villarreal Bueno. "Learning organic chemistry with virtual reality." In 2020 IEEE International Conference on Engineering Veracruz (ICEV). IEEE, 2020. http://dx.doi.org/10.1109/icev50249.2020.9289672.

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HUNTER, DUNCAN H., MUSTAFA JANABI, BRIAR MANNING, XIZHEN ZHU, and GIAN GOBBI. "RADIOIODINATION VIA SOLID PHASE ORGANIC CHEMISTRY." In Proceedings of the 3rd International Conference on Isotopes. WORLD SCIENTIFIC, 2000. http://dx.doi.org/10.1142/9789812793867_0007.

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Reports on the topic "Chemistry, Biochemistry. Chemistry, Organic"

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Liu, Zhijian. Novel Aryne Chemistry in Organic Synthesis. Office of Scientific and Technical Information (OSTI), 2006. http://dx.doi.org/10.2172/897369.

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Tolbert, Laren Malcolm. The Organic Chemistry of Conducting Polymers. Office of Scientific and Technical Information (OSTI), 2014. http://dx.doi.org/10.2172/1165261.

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Munavalli, Shekar, Dennis K. Rohrbaugh, and H. D. Durst. Chemistry, Biochemistry, Pharmacology, and Toxicology of CS and Synthesis of Its Novel Analogs. Defense Technical Information Center, 2007. http://dx.doi.org/10.21236/ada474594.

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Hess, Nancy J., David L. Blanchard, Jr, James A. Campbell, et al. Technetium Chemistry in HLW: Role of Organic Complexants. Office of Scientific and Technical Information (OSTI), 2002. http://dx.doi.org/10.2172/834840.

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Hess, Nancy S., and Steven D. Conradsen. Tc Chemistry in HLW: Role of Organic Complexants. Office of Scientific and Technical Information (OSTI), 2003. http://dx.doi.org/10.2172/834842.

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Hess, Nancy J., David L. Blanchard, Jr, Herman M. Cho, et al. Technetium Chemistry in HLW: Role of Organic Complexants. Office of Scientific and Technical Information (OSTI), 2004. http://dx.doi.org/10.2172/839063.

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Madronich, Sasha. Modeling the Explicit Chemistry of Anthropogenic and Biogenic Organic Aerosols. Office of Scientific and Technical Information (OSTI), 2015. http://dx.doi.org/10.2172/1227953.

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Hartman, F. (CO/sub 2/ chemistry and biochemistry, Ginosa Marina, Italy, June 17-28, 1989): Foreign trip report. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/5855377.

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STOCK, L. M., and J. E. MEACHAM. OCCURRENCE & CHEMISTRY OF ORGANIC COMPOUNDS IN HANFORD SITE WASTE TANKS. Office of Scientific and Technical Information (OSTI), 2004. http://dx.doi.org/10.2172/827712.

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Baluyut, John. Cellulose and cellobiose. Adventures of a wandering organic chemist in theoretical chemistry. Office of Scientific and Technical Information (OSTI), 2012. http://dx.doi.org/10.2172/1048525.

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