Literatura académica sobre el tema "Heteroaromatic rings"
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Artículos de revistas sobre el tema "Heteroaromatic rings"
Pitt, William R., David M. Parry, Benjamin G. Perry y Colin R. Groom. "Heteroaromatic Rings of the Future". Journal of Medicinal Chemistry 52, n.º 9 (14 de mayo de 2009): 2952–63. http://dx.doi.org/10.1021/jm801513z.
Texto completoDoerksen, Robert J. y Ajit J. Thakkar. "Bond orders in heteroaromatic rings". International Journal of Quantum Chemistry 90, n.º 2 (2002): 534–40. http://dx.doi.org/10.1002/qua.998.
Texto completoOrita, Akihiro, Fangguo Ye, Govindarajulu Babu, Tomohiro Ikemoto y Junzo Otera. "Double elimination protocol for the synthesis of arylene ethynylenes containing heteroaromatic rings". Canadian Journal of Chemistry 83, n.º 6-7 (1 de junio de 2005): 716–27. http://dx.doi.org/10.1139/v05-038.
Texto completoLandmana, Marilé, Helmar Görls, Chantelle Crause, Hubert Nienaber, Andrew Olivier y Simon Lotz. "Di-tungsten Bis-carbene Complexes Linked by Condensed Heteroaromatic Spacers". Zeitschrift für Naturforschung B 62, n.º 3 (1 de marzo de 2007): 419–26. http://dx.doi.org/10.1515/znb-2007-0316.
Texto completoDoerksen, Robert J. y Ajit J. Thakkar. "Quadrupole and Octopole Moments of Heteroaromatic Rings". Journal of Physical Chemistry A 103, n.º 48 (diciembre de 1999): 10009–14. http://dx.doi.org/10.1021/jp992524v.
Texto completoGamez, Patrick, Tiddo J. Mooibroek, Simon J. Teat y Jan Reedijk. "Anion Binding Involving π-Acidic Heteroaromatic Rings". Accounts of Chemical Research 40, n.º 6 (junio de 2007): 435–44. http://dx.doi.org/10.1021/ar7000099.
Texto completoKatritzky, Alan R. y Nicholas Dennis. "Cycloaddition reactions of heteroaromatic six-membered rings". Chemical Reviews 89, n.º 4 (junio de 1989): 827–61. http://dx.doi.org/10.1021/cr00094a006.
Texto completoMeena, Chhuttan L., Shubdha Ingole, Satyendra Rajpoot, Avinash Thakur, Prajwal P. Nandekar, Abhay T. Sangamwar, Shyam S. Sharma y Rahul Jain. "Discovery of a low affinity thyrotropin-releasing hormone (TRH)-like peptide that exhibits potent inhibition of scopolamine-induced memory impairment in mice". RSC Advances 5, n.º 70 (2015): 56872–84. http://dx.doi.org/10.1039/c5ra06935a.
Texto completoThorimbert, Serge, Candice Botuha y Kevin Passador. "‘Heteroaromatic Rings of the Future’: Exploration of Unconquered Chemical Space". Synthesis 51, n.º 02 (7 de noviembre de 2018): 384–98. http://dx.doi.org/10.1055/s-0037-1611279.
Texto completoSilva Júnior, P. E., L. C. D. Rezende, Julia Possamai Gimenes, Vinícius Gonçalves Maltarollo, James Dale, G. H. G. Trossini, F. S. Emery y A. Ganesan. "Synthesis of two ‘heteroaromatic rings of the future’ for applications in medicinal chemistry". RSC Advances 6, n.º 27 (2016): 22777–80. http://dx.doi.org/10.1039/c6ra01099g.
Texto completoTesis sobre el tema "Heteroaromatic rings"
Slater, Rachel. "Polyfunctional heteroaromatic fused ring systems". Thesis, Durham University, 2005. http://etheses.dur.ac.uk/2755/.
Texto completoVosswinkel, Michael. "Ring expansion and ring opening of heteroaromatic nitrenes". [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=968868576.
Texto completoMackay, C. "Spirocyclic intermediates in the electrophilic ring closures of heterocycles". Thesis, University of Manchester, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233067.
Texto completoCavitt, Marchello Alfonzo. "Stress relief: Exercising Lewis acid catalysis for donor-acceptor cyclopropane ring-opening annulations, a basis for new reaction methodologies". Diss., Georgia Institute of Technology, 2015. http://hdl.handle.net/1853/54448.
Texto completoYang, Hua. "Synthesis of novel polycyclic aromatics and heteroaromatics via cascade cyclizations of enyne-allenes and enyne-isocyanates". Morgantown, W. Va. : [West Virginia University Libraries], 2006. https://eidr.wvu.edu/etd/documentdata.eTD?documentid=4515.
Texto completoTitle from document title page. Document formatted into pages; contains xv, 110, [139] p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 102-110).
Aponte-Guzman, Joel. "Ring-Opening Benzannulations of Cyclopropenes, Alkylidene Cyclopropanes, and 2,3-Dihydrofuran Acetals: A complementary Approach to Benzo-fused (Hetero)aromatics". Diss., Georgia Institute of Technology, 2015. http://hdl.handle.net/1853/54916.
Texto completoVoßwinkel, Michael [Verfasser]. "Ring expansion and ring opening of heteroaromatic nitrenes / vorgelegt von Michael Voßwinkel". 2003. http://d-nb.info/968868576/34.
Texto completo楊保華. "Physical properties and photorearrangements of heteroaromatic ring-fused benzobarrelenes". Thesis, 1992. http://ndltd.ncl.edu.tw/handle/52744477482769872625.
Texto completoCapítulos de libros sobre el tema "Heteroaromatic rings"
Yamamoto, Takakazu, Isao Yamaguchi y Takuma Yasuda. "PAEs with Heteroaromatic Rings". En Poly(arylene etynylene)s, 181–208. Berlin, Heidelberg: Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/b101378.
Texto completoBuisson, J. P., J. Y. Mevellec, S. Zeraoui y S. Lefrant. "Vibrational Properties of Conducting Polymers with Aromatic or Heteroaromatic Rings". En Lower-Dimensional Systems and Molecular Electronics, 375–80. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-2088-1_41.
Texto completoDalvie, Deepak, Ping Kang, Cho-Ming Loi, Lance Goulet y Sajiv Nair. "Chapter 7. Influence of Heteroaromatic Rings on ADME Properties of Drugs". En Drug Discovery, 328–69. Cambridge: Royal Society of Chemistry, 2010. http://dx.doi.org/10.1039/9781849731102-00328.
Texto completoColthup, Norman B., Lawrence H. Daly y Stephen E. Wiberley. "AROMATIC AND HETEROAROMATIC RINGS". En Introduction to Infrared and Raman Spectroscopy, 261–88. Elsevier, 1990. http://dx.doi.org/10.1016/b978-0-08-091740-5.50011-9.
Texto completoRamsden, Christopher A. "Semi-Conjugated Heteroaromatic Rings". En Progress in Heterocyclic Chemistry, 1–25. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-08-100755-6.00001-6.
Texto completoLin-Vien, Daimay, Norman B. Colthup, William G. Fateley y Jeanette G. Grasselli. "Aromatic and Heteroaromatic Rings". En The Handbook of Infrared and Raman Characteristic Frequencies of Organic Molecules, 277–306. Elsevier, 1991. http://dx.doi.org/10.1016/b978-0-08-057116-4.50023-7.
Texto completo"Pd-Mediated Arylation of Aromatic and Heteroaromatic Rings". En Organic Synthesis: State of the 2005-2007, 25–26. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470385975.ch13.
Texto completo"Best Synthetic Methods: Construction of Aromatic and Heteroaromatic Rings". En Organic Synthesis, 170–71. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0470056312.ch86.
Texto completo"Best Synthetic Methods: Functionalization of Aromatic and Heteroaromatic Rings". En Organic Synthesis, 174–75. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0470056312.ch88.
Texto completoElnagdi, Mohamed Hilmy, Mohamed Rifaat, Hamza Elmoghayer y Kamal Usef Sadek. "Chemistry of Pyrazoles Condensed to Heteroaromatic Five- and Six-Membered Rings". En Advances in Heterocyclic Chemistry Volume 48, 223–99. Elsevier, 1990. http://dx.doi.org/10.1016/s0065-2725(08)60340-2.
Texto completoActas de conferencias sobre el tema "Heteroaromatic rings"
Padmaperuma, Asanga B. y Aaron W. Harper. "Photophysics of novel conjugated polymers with alternating heteroaromatic rings: synthesis and applications". En Optical Science and Technology, SPIE's 48th Annual Meeting, editado por Zakya H. Kafafi y Paul A. Lane. SPIE, 2004. http://dx.doi.org/10.1117/12.505952.
Texto completoJúnior, Paulo Eliandro da Silva, A. Ganesan, James Dale y Flavio Emery. "Synthesis and reactivity of pyrazolo-pyridone ring, an understudied heteroaromatic scaffold". En 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013915143915.
Texto completoDekamin, Mohammadghorban y Zahra Alirezvani. "A convenient synthesis of bis(indolyl)methane derivatives using heteroaromatic isocyanurate ring functionalized MCM-41 as a new and highly efficient reusable catalyst". En The 21st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04739.
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