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

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1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Deffense, Etienne. "From organic chemistry to fat and oil chemistry." Oléagineux, Corps gras, Lipides 16, no. 1 (2009): 14–24. http://dx.doi.org/10.1051/ocl.2009.0238.

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12

Wood, EJ. "Chemistry. An Introduction to General, Organic and Biological Chemistry." Biochemical Education 13, no. 1 (1985): 44. http://dx.doi.org/10.1016/0307-4412(85)90156-6.

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13

Weete, John D., Edward J. Parish, and W. David Nes. "Chemistry, biochemistry, and function of sterols." Lipids 35, no. 3 (2000): 241. http://dx.doi.org/10.1007/s11745-000-0517-y.

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14

Parish, Edward J., and W. David Nes. "Biochemistry, chemistry, and function of steroids." Lipids 32, no. 12 (1997): 1301. http://dx.doi.org/10.1007/s11745-006-0167-0.

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15

Debardieux, Laurent. "Organic and Biological Chemistry." Biochimie 85, no. 5 (2003): 563. http://dx.doi.org/10.1016/s0300-9084(03)00010-5.

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16

Zanda, Matteo. "Focus in Organic Chemistry." Letters in Organic Chemistry 2, no. 7 (2005): 573–75. http://dx.doi.org/10.2174/157017805774296858.

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17

Wiley, Richard H. "LASER ORGANIC CHEMISTRY." Annals of the New York Academy of Sciences 122, no. 2 (2006): 685–88. http://dx.doi.org/10.1111/j.1749-6632.1965.tb20250.x.

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18

Eaborn, Colin. "Advanced organic chemistry." Journal of Organometallic Chemistry 297, no. 2 (1985): c23. http://dx.doi.org/10.1016/0022-328x(85)80425-3.

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19

Chandru, Mamajanov, Cleaves, and Jia. "Polyesters as a Model System for Building Primitive Biologies from Non-Biological Prebiotic Chemistry." Life 10, no. 1 (2020): 6. http://dx.doi.org/10.3390/life10010006.

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A variety of organic chemicals were likely available on prebiotic Earth. These derived from diverse processes including atmospheric and geochemical synthesis and extraterrestrial input, and were delivered to environments including oceans, lakes, and subaerial hot springs. Prebiotic chemistry generates both molecules used by modern organisms, such as proteinaceous amino acids, as well as many molecule types not used in biochemistry. As prebiotic chemical diversity was likely high, and the core of biochemistry uses a rather small set of common building blocks, the majority of prebiotically avail
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20

García-Río, Luis. "Preface." Pure and Applied Chemistry 81, no. 4 (2009): iv. http://dx.doi.org/10.1351/pac20098104iv.

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The 19th IUPAC Conference on Physical Organic Chemistry (ICPOC-19) was held at the University of Santiago de Compostela, Santiago, Spain, 13-18 July 2008 under the local auspices of the Universities of Santiago, A Coruña, and Vigo. About 400 delegates attended ICPOC-19 from 39 countries, to participate in a scientific program comprising 11 plenary lectures, 22 invited lectures, 102 oral communications, and 224 posters.Physical organic chemistry, the study of the interrelationships between structure and reactivity in organic molecules, is a relatively young subfield of organic chemistry. At the
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21

Watkins, Ivor. "Essentials of Bio-organic Chemistry." Biochemical Education 13, no. 4 (1985): 185. http://dx.doi.org/10.1016/0307-4412(85)90085-8.

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22

Leadbeater, Nicholas E. "Microwaves in organic chemistry." Tetrahedron 62, no. 19 (2006): 4633. http://dx.doi.org/10.1016/j.tet.2006.02.077.

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23

Kennedy, John F., and Linda L. Lloyd. "Vitamin C: Its chemistry and biochemistry." Carbohydrate Polymers 22, no. 1 (1993): 77. http://dx.doi.org/10.1016/0144-8617(93)90168-4.

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24

Sturgcon, R. J. "Advances in Carbohydrate Chemistry and Biochemistry." Carbohydrate Research 279 (December 1995): C11—C12. http://dx.doi.org/10.1016/0008-6215(95)90201-5.

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25

Bishop, Claude T. "Advances in Carbohydrate Chemistry and Biochemistry." Carbohydrate Research 139 (June 1985): C5—C6. http://dx.doi.org/10.1016/0008-6215(85)90031-x.

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26

Prebble, John N. "Jeffrey Barry Harborne. 1 September 1928 — 21 July 2002." Biographical Memoirs of Fellows of the Royal Society 56 (January 2010): 131–47. http://dx.doi.org/10.1098/rsbm.2010.0012.

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Jeffrey Harborne made a major contribution to the discipline of phytochemistry. Originally an organic chemist, he became an academic leader in the biochemistry of secondary metabolites, particularly flavonoids and also other plant phenols. He contributed significantly to areas at the interface between chemistry and traditional areas of plant science, systematics and ecology. His early research was influential on the rise in importance of both plant chemotaxonomy and biochemical ecology.
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27

Feinman, Richard D. "Ethanol Metabolism and the Transition from Organic Chemistry to Biochemistry." Journal of Chemical Education 78, no. 9 (2001): 1215. http://dx.doi.org/10.1021/ed078p1215.

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28

LAUBE, T. "ChemInform Abstract: New Carbocations - From Physical Organic Chemistry to Biochemistry." ChemInform 28, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199713301.

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29

Loertscher, Jennifer, Jennifer E. Lewis, Allison M. Mercer, and Vicky Minderhout. "Development and use of a construct map framework to support teaching and assessment of noncovalent interactions in a biochemical context." Chemistry Education Research and Practice 19, no. 4 (2018): 1151–65. http://dx.doi.org/10.1039/c8rp00029h.

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Most chemistry educators agree that deep understanding of the nature of noncovalent interactions is essential for learning in chemistry. Yet decades of research have shown that students have persistent incorrect ideas about these interactions. We have worked in collaboration with a community of chemistry, biology, and biochemistry educators to develop a construct map to guide development of instructional and assessment resources related to the physical basis of noncovalent interactions in a biochemical context. This map was devised using data about student learning and expert perspectives on n
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30

Pryor, W. A. "Free radicals in organic chemistry." Free Radical Biology and Medicine 21, no. 2 (1996): 253–54. http://dx.doi.org/10.1016/0891-5849(96)90038-6.

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31

Carreira, Erick M., and Damiano M. Cereghetti. "Amphotericin B: 50 Years of Chemistry and Biochemistry." Synthesis, no. 6 (2006): 0914–42. http://dx.doi.org/10.1055/s-2006-926368.

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32

Marco-Contelles, José. "Cyclohexane Epoxides − Chemistry and Biochemistry of (+)-Cyclophellitol." European Journal of Organic Chemistry 2001, no. 9 (2001): 1607–18. http://dx.doi.org/10.1002/1099-0690(200105)2001:9<1607::aid-ejoc1607>3.0.co;2-6.

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33

Zheng, Zhan-Jiang, Ding Wang, Zheng Xu, and Li-Wen Xu. "Synthesis of bi- and bis-1,2,3-triazoles by copper-catalyzed Huisgen cycloaddition: A family of valuable products by click chemistry." Beilstein Journal of Organic Chemistry 11 (December 11, 2015): 2557–76. http://dx.doi.org/10.3762/bjoc.11.276.

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The Cu(I)-catalyzed azide-alkyne cycloaddition reaction, also known as click chemistry, has become a useful tool for the facile formation of 1,2,3-triazoles. Specifically, the utility of this reaction has been demonstrated by the synthesis of structurally diverse bi- and bis-1,2,3-triazoles. The present review focuses on the synthesis of such bi- and bistriazoles and the importance of using copper-promoted click chemistry (CuAAC) for such transformations. In addition, the application of bitriazoles and the related CuAAAC reaction in different fields, including medicinal chemistry, coordination
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34

Fisher, Grant. "Diagnostics in computational organic chemistry." Foundations of Chemistry 18, no. 3 (2016): 241–62. http://dx.doi.org/10.1007/s10698-016-9253-4.

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35

GOODWIN, WILLIAM. "Explanation in Organic Chemistry." Annals of the New York Academy of Sciences 988, no. 1 (2003): 141–53. http://dx.doi.org/10.1111/j.1749-6632.2003.tb06093.x.

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36

Vella, F. "Columbia review high-yield organic chemistry." Biochemical Education 25, no. 3 (1997): 177–78. http://dx.doi.org/10.1016/s0307-4412(97)84447-0.

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37

Cori, Osvaldo. "Worked examples in essential organic Chemistry." Biochemical Education 13, no. 1 (1985): 42. http://dx.doi.org/10.1016/0307-4412(85)90149-9.

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38

Leyva, Elisa, Denisse de Loera, Claudia G. Espinosa-González, and Saúl Noriega. "Physicochemical Properties and Photochemical Reactions in Organic Crystals." Current Organic Chemistry 23, no. 3 (2019): 215–55. http://dx.doi.org/10.2174/1385272822666190313152105.

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Background: Molecular organic photochemistry is concerned with the description of physical and chemical processes generated upon the absorption of photons by organic molecules. Recently, it has become an important part of many areas of science: chemistry, biology, biochemistry, medicine, biophysics, material science, analytical chemistry, among others. Many synthetic chemists are using photochemical reactions in crystals to generate different types of organic compounds since this methodology represents a green chemistry approach. Objective &amp; Method: Chemical reactions in crystals are quite
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39

Greer, Alexander. "Organic chemistry of singlet oxygen." Tetrahedron 62, no. 46 (2006): 10613. http://dx.doi.org/10.1016/j.tet.2006.08.096.

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40

Posner, G. H., and W. B. Motherwell. "Tetrahedron reports on organic chemistry." Tetrahedron 58, no. 52 (2002): I—XVI. http://dx.doi.org/10.1016/s0040-4020(02)01503-x.

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41

Posner, Professor G. H., and Professor W. B. Motherwell. "Tetrahedron reports on organic chemistry." Tetrahedron 59, no. 13 (2003): I—XVI. http://dx.doi.org/10.1016/s0040-4020(03)00323-5.

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42

Posner, Professor G. H., and Professor W. B. Motherwell. "Tetrahedron reports on organic chemistry." Tetrahedron 59, no. 26 (2003): I—XVII. http://dx.doi.org/10.1016/s0040-4020(03)00841-x.

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43

Posner, Professor G. H., and Professor W. B. Motherwell. "Tetrahedron reports on organic chemistry." Tetrahedron 59, no. 39 (2003): I—XVII. http://dx.doi.org/10.1016/s0040-4020(03)01130-x.

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44

Posner, Professor G. H., and Professor W. B. Motherwell. "Tetrahedron reports on organic chemistry." Tetrahedron 59, no. 52 (2003): I—XVII. http://dx.doi.org/10.1016/s0040-4020(03)01884-2.

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45

Posner, Professor G. H., and Professor W. B. Motherwell. "Tetrahedron reports on organic chemistry." Tetrahedron 60, no. 13 (2004): I—XVII. http://dx.doi.org/10.1016/s0040-4020(04)00315-1.

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46

Posner, Professor G. H., and Professor W. B. Motherwell. "Tetrahedron reports on organic chemistry." Tetrahedron 60, no. 40 (2004): I—XVIII. http://dx.doi.org/10.1016/s0040-4020(04)01396-1.

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47

Lectka, T., and W. B. Motherwell. "Tetrahedron reports on organic chemistry." Tetrahedron 62, no. 25 (2006): I—XIX. http://dx.doi.org/10.1016/s0040-4020(06)00771-x.

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48

Lectka, T., and W. B. Motherwell. "Tetrahedron reports on organic chemistry." Tetrahedron 62, no. 52 (2006): I—XX. http://dx.doi.org/10.1016/s0040-4020(06)01801-1.

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49

Lectka, T., and W. B. Motherwell. "Tetrahedron reports on organic chemistry." Tetrahedron 63, no. 12 (2007): I—XX. http://dx.doi.org/10.1016/s0040-4020(07)00205-0.

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Lectka, T., and W. B. Motherwell. "Tetrahedron reports on organic chemistry." Tetrahedron 63, no. 25 (2007): I—XX. http://dx.doi.org/10.1016/s0040-4020(07)00834-4.

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