Готові списки джерел за темами / Organic Chemistry

Добірка наукової літератури з теми "Organic Chemistry"

Автор: Grafiati
Опубліковано: 4 червня 2021
Оновлено: 25 липня 2024

Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями

Оберіть тип джерела:

Зміст

Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Organic Chemistry".

Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.

Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.

Статті в журналах з теми "Organic Chemistry"

1

Mulyanti, Sri, Atik Rahmawati, and Ulfa Lutfianasari. "IMPLICATION OF MINI PROJECT ORGANIC CHEMISTRY EXPERIMENTS FOR IMPROVING ORGANIC CHEMISTRY CONCEPT." EDUSAINS 13, no. 2 (December 30, 2021): 129–37. http://dx.doi.org/10.15408/es.v13i2.16879.

Повний текст джерела
Анотація:
IMPLICATION OF MINI PROJECT ORGANIC CHEMISTRY EXPERIMENTS FOR IMPROVING ORGANIC CHEMISTRY CONCEPTAbstractOrganic Chemistry Practice is one of the courses in the chemical education department that must be taken by pre-service teacher of chemistry, still lack of mastery of students on organic chemistry concepts, requiring lecturers to be able to design the experiment in such a way so as to increase mastery of the concept of organic chemistry students in Organic Chemistry Practice. This study aims to apply the mini project model to the Organic Chemistry Practice so that it is expected to increase students' mastery of concepts in organic chemistry. The research was conducted using quantitative methods, its measuring conceptual change from the students from N-gain score. The results showed that there was an increase in students' mastery of concepts based on the% N-gain obtained. The majority of students are at a high criterion with% N-Gain> 70. The t test shows the significance of the implementation of the mini project model to increase students' mastery of concept concepts.AbstrakRendahnya penguasaan mahasiswa terhadap konsep-konsep kimia organik, menuntut pengajar untuk dapat mendesain praktikum sedemikian rupa, sehingga dapat meningkatkan penguasaan konsep kimia organik mahasiswa pada Praktikum Kimia Organik. Penelitian ini bertujuan untuk menerapkan model mini project pada Praktikum Kimia Organik sehingga diharapkan dapat meningkatkan penguasaan konsep mahasiswa pada materi kimia organik. Penelitian dilakukan dengan metode kuantitatif, yakni mengukur hasil tes penguasaan konsep mahasiswa. Hasil penelitian menunjukkan bahwa terjadi peningkatan penguasaan konsep mahasiswa berdasarkan hasil %N-Gain yang diperoleh. Mayoritas mahasiswa berada pada kriteria tinggi dengan %N-Gain > dari 70. Uji t menunjukkan signifikansi pelaksanaan model mini project terhadap peningkatan penguasaan konsep mahasiswa.
Стилі APA, Harvard, Vancouver, ISO та ін.
2

Dembinski, Roman, and Vadim Soloshonok. "Featured Reviews in Organic Chemistry." Molecules 28, no. 16 (August 9, 2023): 5975. http://dx.doi.org/10.3390/molecules28165975.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
3

Sagan, C., W. R. Thompson, and B. N. Khare. "Titan's Organic Chemistry." Symposium - International Astronomical Union 112 (1985): 107–21. http://dx.doi.org/10.1017/s007418090014642x.

Повний текст джерела
Анотація:
Voyager discovered nine simple organic molecules in the atmosphere of Titan. Complex organic solids, called tholins, produced by irradiation of simulated Titanian atmosphere are consistent with measured properties of Titan from ultraviolet to microwave frequencies, and are the likely main constituents of the observed red aerosols. The tholins contain many of the organic building blocks central to life on Earth. At least 100 m and possibly kms thickness of complex organics have been produced on Titan during the age of the solar system, and may exist today as submarine deposits beneath an extensive ocean of simple hydrocarbons.
Стилі APA, Harvard, Vancouver, ISO та ін.
4

Kaur, Navjeet. "Photochemical Reactions for the Synthesis of Six-Membered O-Heterocycles." Current Organic Synthesis 15, no. 3 (April 27, 2018): 298–320. http://dx.doi.org/10.2174/1570179414666171011160355.

Повний текст джерела
Анотація:
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 disposal. The formation of byproducts was diminished under photochemical substrate activation that usually occurred without additional reagents. Photochemical irradiation is becoming more interesting day by day because of easy purification of the products as well as green chemistry. Conclusion: This review article represents the high applicability of photochemical reactions for organic synthesis and research activities in organic photochemistry. The synthesis of heterocyclic molecules has been outlined in this review. Traditional approaches require expensive or highly specialized equipment or would be of limited use to the synthetic organic chemist due to their highly inconvenient approaches. Photochemistry can be used to prepare a number of heterocycles selectively, efficiently and in high yield.
Стилі APA, Harvard, Vancouver, ISO та ін.
5

Mijin, Dusan, and Slobodan Petrovic. "Microwaves in organic chemistry and organic chemical." Chemical Industry 59, no. 9-10 (2005): 224–29. http://dx.doi.org/10.2298/hemind0510224m.

Повний текст джерела
Анотація:
The usual way of applying heat to a chemical reaction is the use of a Bunsen burner, an oil or some other type of bath, or an electric heater. In inorganic chemistry, microwave technology has been used since the late 1970s while it has been implemented in organic chemistry since the mid-1980s. Microwave heating has been used in the food industry for almost fifty years. The shorter reaction times and expanded reaction range that is offered by microwave technology are suited to the increased demands in industry. For example, there is a requirement in the pharmaceutical industry for a higher number of a novel chemical entities to be produced, which requires chemists to employ a number of resources to reduce time for the production of compounds. Also, microwaves are used in the food industry, as well as in the pyrolysis of waste materials, sample preparation, the solvent extraction of natural products and the hydrolysis of proteins and peptides.
Стилі APA, Harvard, Vancouver, ISO та ін.
6

Williams, Ian H. "Physical Organic Chemistry in the 21st Century: A Q1 Progress Report." Chemistry International 44, no. 2 (April 1, 2022): 10–13. http://dx.doi.org/10.1515/ci-2022-0203.

Повний текст джерела
Анотація:
Abstract In 1997, a collection of twenty personal perspectives from eminent chemists was published in Pure and Applied Chemistry to mark the centenary of physical organic chemistry [1]. This Symposium in Print, entitled Physical Organic Chemistry in the 21st Century (POC21C), was organized by the IUPAC Commission on Physical Organic Chemistry, which was chaired at that time by Tom Tidwell, who contributed a historical prologue in which he suggested Stieglitz’s 1899 proposal of carbocations as reaction intermediates as (unwittingly) having given birth to the discipline. The principal authors were Edward Arnett, Daniel Bellus, Ron Breslow, Fulvio Cacace, Jan Engberts, Marye Anne Fox, Ken Houk, Keith Ingold, Alan Katritzky, Ed Kosower, Meir Lahav, Teruaki Mukaiyama, Oleg Nefedov, George Olah, John Roberts, Jean-Michel Savéant, Helmut Schwarz, Andrew Streitwieser, Frank Westheimer, and Akio Yamamoto. Tidwell noted that, whereas they were not all known as physical organic chemists, yet they had all used the tools of this discipline in their work and were able to comment upon the utility of physical organic chemistry for the practice of other areas of chemistry as well. The theme that ran through all the essays was that the future of the field lay in an interdisciplinary approach, that physical organic chemists would use all the tools available to them, and that they would not be fettered to narrow views.
Стилі APA, Harvard, Vancouver, ISO та ін.
7

Franzini, Raphael M., and Titas Deb. "The Unique Bioorthogonal Chemistry of Isonitriles." Synlett 31, no. 10 (March 20, 2020): 938–44. http://dx.doi.org/10.1055/s-0039-1690849.

Повний текст джерела
Анотація:
The isocyano group is the structurally most compact bioorthogonal group known. It reacts with tetrazines under physiological conditions and has great potential for widespread use in the biosciences. In this account, we highlight the unique properties of the isocyano group as a bioorthogonal functionality. Protecting group chemistry based on the reaction of isonitriles and tetrazines that allows releasing payloads is a particular focus of the article. We further discuss the atypical steric attractions that take place in the transition state of the reaction between isonitriles and tetrazines, which result in an increase in the rate of the reaction with steric bulk of the tetrazine substituents. These findings will open up new possibilities in bioorthogonal chemistry where reactivity and stability are simultaneously desired.1 Introduction2 The Isocyano Group: A Structurally Compact Group for Bioorthogonal Chemistry3 Bioorthogonal Protecting Group Chemistry4 Steric Attractions in the Transition State Accelerate the Cycloaddition of Isonitriles and Tetrazines5 Reactions of Tetrazines and Isonitriles are Compatible with Biomolecules and Living Organisms6 Conclusions
Стилі APA, Harvard, Vancouver, ISO та ін.
8

Stankus, Tony. "Organic Chemistry." Serials Librarian 27, no. 2-3 (April 8, 1996): 171–80. http://dx.doi.org/10.1300/j123v27n02_15.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
9

Wood, E. J. "Organic chemistry." Biochemical Education 23, no. 1 (January 1995): 44. http://dx.doi.org/10.1016/0307-4412(95)90196-5.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
10

Fox, Marye Anne. "A Perspective on Organic Chemistry: Physical Organic Chemistry." Journal of Organic Chemistry 74, no. 22 (November 20, 2009): 8497–509. http://dx.doi.org/10.1021/jo901731t.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
Більше джерел

Дисертації з теми "Organic Chemistry"

1

Stenta, Marco <1979&gt. "Computational models in organic and bio-organic chemistry." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2008. http://amsdottorato.unibo.it/1069/1/Tesi_Stenta_Marco.pdf.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
2

Stenta, Marco <1979&gt. "Computational models in organic and bio-organic chemistry." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2008. http://amsdottorato.unibo.it/1069/.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
3

Fisher, Grant Andrew. "Model construction in organic chemistry." Thesis, University of Leeds, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.401068.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
4

Yang, Hongfang. "Benzotriazole intermediates in organic chemistry." [Gainesville, Fla.] : University of Florida, 2004. http://purl.fcla.edu/fcla/etd/UFE0005743.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
5

Kulkarni, S. Y. "Analytical methods in organic chemistry." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 1985. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/3241.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
6

Goei, Elisabeth Rukmini. "Using Green Chemistry Experiments to Engage Sophomore Organic Chemistry." Miami University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=miami1280437800.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
7

Alcock, S. "Tobacco chemistry." Thesis, University of Nottingham, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.356015.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
8

Leste-Lasserre, Pierre. "Sulfur allotrope chemistry." Thesis, McGill University, 2001. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=38218.

Повний текст джерела
Анотація:
The synthesis of the sulfur homocycles S6, S9, S10, S12 and S20, which belong to the group of sulfur allotropes, has been achieved based on existing procedures. Polymeric sulfur Smu was also prepared.
The parameters of a small scale model reaction between 2,3-diphenyl-1,3-butadiene and S10 were optimized. Products were identified and 1H-NMR yields were calculated by comparison with an internal standard. The experimental parameters of this model served as a base for further reactions of S 10 with a variety of simple or conjugated olefins. The products of these reactions were fully isolated and characterized using standard spectroscopic techniques. The structures of a new bis-sulfurated compound having a norbornane framework and of the product obtained from the dimerization of norborn-5-ene-2,3-dithiol were also confirmed by single crystal X-ray crystallography.
The sulfur homocycles S9, S12 and S20 were also found to react with norbornene and two different 1,3-dienes. Products were identified and 1H-NMR yields for these small scale reactions were calculated by internal standard comparison. Differences and similarities with the products obtained with S10 are discussed. Sulfuration efficiencies of the different allotropes towards selected substrates are also compared.
A mechanistic study was carried out. The implication of sulfur radicals in the thermal decomposition of S10 has been suggested. Reaction mechanisms accounting for the formation of the different products observed are proposed.
Стилі APA, Harvard, Vancouver, ISO та ін.
9

Santangelo, Ellen M. "Stereoselective syntheses of semichemicals : Applications in ecological chemistry." Doctoral thesis, KTH, Chemistry, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-74.

Повний текст джерела
Анотація:

This thesis describes the syntheses of semiochemicals and their applications in the development of control methods for pest insects. The compounds synthesized are divided into three groups: 1) Lepidoptera pheromones; 2) methyl substituted chiral pheromones and 3) aphid pheromones.

Different purification techniques have been explored in order to provide > 99% pure semiochemicals for field tests. Examples of the techniques are uses of urea inclusion complexes, argentum chromatography, low temperature crystallization and what we call the Baeckström isolation technique.

Iridoids have been produced in a synthetic strategy including an intramolecular enal-enamine [4+2] cycloaddition, a dynamic acetylation and an enantioselective transesterification mediated by a lipase from Pseudomonas cepacia. The use of chiral auxiliaries to perform the intramolecular [4+2] cycloaddition has also been investigated. A useful asymmetric route to iridoids has been developed.

Стилі APA, Harvard, Vancouver, ISO та ін.
10

Liu, Zhijian. "Novel aryne chemistry in organic synthesis." [Ames, Iowa : Iowa State University], 2006.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
Більше джерел

Книги з теми "Organic Chemistry"

1

1944-, Rawn J. David, ed. Organic chemistry. Upper Saddle River, N.J: Prentice Hall, 1996.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
2

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

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
3

Organic chemistry. 3rd ed. Dubuque, IA: McGraw-Hill, 2010.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
4

Smith, Janice Gorzynski. Organic chemistry. 2nd ed. Boston: McGraw-Hill, 2008.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
5

Organic chemistry. 7th ed. Upper Saddle River, N.J: Pearson Prentice Hall, 2010.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
6

Jonathan, Clayden, ed. Organic chemistry. Oxford: Oxford University Press, 2001.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
7

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

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
8

B, Fryhle Craig, ed. Organic chemistry. 7th ed. New York: J. Wiley, 2002.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
9

Carey, Francis A. Organic chemistry. 6th ed. Dubuque, IA: McGraw-Hill, 2006.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
10

Hornback, Joseph M. Organic chemistry. Pacific Grove, CA: Brooks/Cole Pub. Co., 1998.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
Більше джерел

Частини книг з теми "Organic Chemistry"

1

Khan, JaVed I., Thomas J. Kennedy, and Donnell R. Christian. "Organic Chemistry." In Basic Principles of Forensic Chemistry, 31–57. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-59745-437-7_4.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
2

Gooch, Jan W. "Organic Chemistry." In Encyclopedic Dictionary of Polymers, 505. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_8238.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
3

Hoenig, Steven L. "Organic Chemistry." In Basic Chemical Concepts and Tables, 61–124. Boca Raton, FL : CRC Press, Taylor & Francis Group, [2019]: CRC Press, 2019. http://dx.doi.org/10.1201/9780429277948-3.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
4

Gooch, Jan W. "Organic Chemistry." In Encyclopedic Dictionary of Polymers, 912. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_14401.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
5

Barker, Alan, and Kathryn Knapp. "Organic Chemistry." In Work Out Chemistry GCSE, 133–43. London: Macmillan Education UK, 1990. http://dx.doi.org/10.1007/978-1-349-11950-9_18.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
6

Casparian, Armen S., Gergely Sirokman, and Ann O. Omollo. "Organic Chemistry." In Rapid Review of Chemistry for the Life Sciences and Engineering, 115–25. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.1201/9781003092759-8.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
7

Hoenig, Steven L. "Organic Chemistry." In Basic Chemical Concepts and Tables, 89–158. 2nd ed. Boca Raton: CRC Press, 2024. http://dx.doi.org/10.1201/9781003396512-3.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
8

Lewis, Rhobert, and Wynne Evans. "Organic Chemistry:Hydrocarbons." In Chemistry, 318–40. London: Macmillan Education UK, 2018. http://dx.doi.org/10.1057/978-1-137-61037-9_18.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
9

Lewis, Rhobert, and Wynne Evans. "Organic Mechanisms." In Chemistry, 362–71. London: Macmillan Education UK, 2018. http://dx.doi.org/10.1057/978-1-137-61037-9_20.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
10

Tucker, William B. "Organometallic Chemistry." In Organic Chemistry, 190–99. Boca Raton: CRC Press, 2024. http://dx.doi.org/10.1201/9781003479352-17.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.

Тези доповідей конференцій з теми "Organic Chemistry"

1

Van Aken, Koen. "Organic Chemistry Resources Worldwide: An Intuitive WWW Resource Guide for Synthetic Organic Chemists." In The 1st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02070.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
2

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.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
3

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

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
4

Handayani, Dewi. "ORGANIC CHEMISTRY 1 DIGITAL BOOK." In International Symposium on Open, Distance, and E-Learning. Pustekkom, 2018. http://dx.doi.org/10.32550/pi.v1i1.24.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
5

Khan, Ali Yousuf, Miguel Angel Luque-Nieto, Hifsa Ansari, Ubaid-ur-Rahman, Syed Inshal Waris, and Shariq uz Zaman Durrani. "Augmented Reality EleReactor Organic Chemistry." In 2022 Global Conference on Wireless and Optical Technologies (GCWOT). IEEE, 2022. http://dx.doi.org/10.1109/gcwot53057.2022.9772917.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
6

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

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
7

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.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
8

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.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
9

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.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
10

Magalhaes, Elizabeth, and Ray Jones. "About the Royal Society of Chemistry." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-2013-about.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.

Звіти організацій з теми "Organic Chemistry"

1

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

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
2

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

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
3

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

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
4

Hess, Nancy J., David L. Blanchard, Jr, James A. Campbell, Herman M. Cho, Rai, Dhanpat, Rai, Yuanxian Xia, and Steven D. Conradson. Technetium Chemistry in HLW: Role of Organic Complexants. Office of Scientific and Technical Information (OSTI), June 2002. http://dx.doi.org/10.2172/834840.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
5

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

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
6

Hess, Nancy J., David L. Blanchard, Jr, Herman M. Cho, Yuanxian Xia, James A. Campbell, Dhanpat Rai, and Steven D. Conradson. Technetium Chemistry in HLW: Role of Organic Complexants. Office of Scientific and Technical Information (OSTI), June 2004. http://dx.doi.org/10.2172/839063.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
7

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

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
8

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

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
9

Allendorf, Mark D., Jeffery A. Greathouse, and Blake Simmons. Creating a Discovery Platform for Confined-Space Chemistry and Materials: Metal-Organic Frameworks. Office of Scientific and Technical Information (OSTI), September 2008. http://dx.doi.org/10.2172/1130392.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
10

Lipsky, S. The contribution of electronically excited states to the radiation chemistry of organic systems. Office of Scientific and Technical Information (OSTI), January 1990. http://dx.doi.org/10.2172/6764782.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
Також вас можуть зацікавити розширені добірки на тему "Organic Chemistry" для конкретних типів джерел:
Статті в журналах Дисертації Книги
Ми пропонуємо знижки на всі преміум-плани для авторів, чиї праці увійшли до тематичних добірок літератури. Зв'яжіться з нами, щоб отримати унікальний промокод!

До бібліографії