Статті в журналах з теми "Atropisomerismo"
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Clayden, Jonathan. "Atropisomerism." Tetrahedron 60, no. 20 (May 2004): 4335. http://dx.doi.org/10.1016/j.tet.2004.03.002.
Повний текст джерелаCzarnocki, Zbigniew, and Piotr Pomarański. "Arylpyridines: A Review from Selective Synthesis to Atropisomerism." Synthesis 51, no. 03 (December 14, 2018): 587–611. http://dx.doi.org/10.1055/s-0037-1611365.
Повний текст джерелаSiegel, Jay. "Prologue: Atropisomerism." Synlett 29, no. 16 (September 21, 2018): 2122–25. http://dx.doi.org/10.1055/s-0037-1610908.
Повний текст джерелаFordyce, Euan A. F., S. Fraser Hunt, Damien Crepin, Stuart T. Onions, Guillaume F. Parra, Chris J. Sleigh, John King-Underwood, Harry Finch, and John Murray. "Conformationally restricted benzothienoazepine respiratory syncytial virus inhibitors: their synthesis, structural analysis and biological activities." MedChemComm 9, no. 3 (2018): 583–89. http://dx.doi.org/10.1039/c8md00033f.
Повний текст джерелаBirepinte, Mélodie, Frédéric Robert, Sandra Pinet, Laurent Chabaud, and Mathieu Pucheault. "Non-biaryl atropisomerism at the C–B bond in sterically hindered aminoarylboranes." Organic & Biomolecular Chemistry 18, no. 16 (2020): 3007–11. http://dx.doi.org/10.1039/d0ob00421a.
Повний текст джерелаBischetti, Martina, Giuseppe Pomarico, Sara Nardis, Federica Mandoj, Daniel O. Cicero, and Roberto Paolesse. "5,10,15-Triarylcorrole atropisomerism." Journal of Porphyrins and Phthalocyanines 24, no. 01n03 (January 2020): 153–60. http://dx.doi.org/10.1142/s1088424619500706.
Повний текст джерелаSiegel, Jay. "Cluster Preface: Atropisomerism." Synlett 29, no. 16 (September 21, 2018): 2120–21. http://dx.doi.org/10.1055/s-0037-1610998.
Повний текст джерелаBoiadjiev, Stefan E., and David A. Lightner. "Atropisomerism in monopyrroles." Tetrahedron: Asymmetry 13, no. 16 (August 2002): 1721–32. http://dx.doi.org/10.1016/s0957-4166(02)00481-0.
Повний текст джерелаCiogli, A., S. Vivek Kumar, M. Mancinelli, A. Mazzanti, S. Perumal, C. Severi, and C. Villani. "Atropisomerism in 3-arylthiazolidine-2-thiones. A combined dynamic NMR and dynamic HPLC study." Organic & Biomolecular Chemistry 14, no. 47 (2016): 11137–47. http://dx.doi.org/10.1039/c6ob02145j.
Повний текст джерелаKöster, Roland, Günther Seidel, Susanna Kerschl, and Bernd Wrackmeyer. "Atropisomerism in Boron-Nitrogen Heterocycles/Atropisomerism in Boron-Nitrogen Heterocycles." Zeitschrift für Naturforschung B 42, no. 2 (February 1, 1987): 191–94. http://dx.doi.org/10.1515/znb-1987-0212.
Повний текст джерелаMeininger, Daniel J., Nicanor Muzquiz, Hadi D. Arman, and Zachary J. Tonzetich. "Synthesis, characterization, and atropisomerism of iron complexes containing the tetrakis(2-chloro-6-fluorophenyl)porphyrinate ligand." Dalton Transactions 44, no. 20 (2015): 9486–95. http://dx.doi.org/10.1039/c5dt01122a.
Повний текст джерелаBoiadjiev, Stefan E., and David A. Lightner. "Atropisomerism in linear tetrapyrroles." Tetrahedron 58, no. 37 (September 2002): 7411–21. http://dx.doi.org/10.1016/s0040-4020(02)00827-x.
Повний текст джерелаBaker, Robert W., Zinka Brkic, Melvyn V. Sargent, Brian W. Skelton, and Allan H. White. "Atropisomerism of 2,2'-Binaphthalenes." Australian Journal of Chemistry 53, no. 12 (2000): 925. http://dx.doi.org/10.1071/ch00122.
Повний текст джерелаTietze, Lutz F., Heiko J. Schuster, J. Marian von Hof, Sonja M. Hampel, Juan F. Colunga, and Michael John. "Atropisomerism of Aromatic Carbamates." Chemistry – A European Journal 16, no. 42 (September 30, 2010): 12678–82. http://dx.doi.org/10.1002/chem.201001047.
Повний текст джерелаDoulain, Pierre-Emmanuel, Christine Goze, Ewen Bodio, Philippe Richard, and Richard A. Decréau. "BODIPY atropisomer interconversion, face discrimination, and superstructure appending." Chemical Communications 52, no. 24 (2016): 4474–77. http://dx.doi.org/10.1039/c5cc10526a.
Повний текст джерелаUrban, S., and RJ Capon. "Lamellarin-S: a New Aromatic Metabolite From an Australian Tunicate, Didemnum sp." Australian Journal of Chemistry 49, no. 6 (1996): 711. http://dx.doi.org/10.1071/ch9960711.
Повний текст джерелаRyan, Sarah J., Craig L. Francis, and G. Paul Savage. "N-Aryl Atropisomerism Induces Facial Selectivity in Benzonitrile Oxide Cycloadditions with Exocyclic Methylene Benzosultams." Australian Journal of Chemistry 66, no. 8 (2013): 874. http://dx.doi.org/10.1071/ch13270.
Повний текст джерелаAllaoud, S., and B. Frange. "Atropisomerism in aryl-substituted borazines." Inorganic Chemistry 24, no. 16 (July 1985): 2520–23. http://dx.doi.org/10.1021/ic00210a011.
Повний текст джерелаTakahashi, Hideyo, Shintaro Wakamatsu, Hidetsugu Tabata, Tetsuta Oshitari, Ayako Harada, Keizo Inoue, and Hideaki Natsugari. "Atropisomerism Observed in Indometacin Derivatives." Organic Letters 13, no. 4 (February 18, 2011): 760–63. http://dx.doi.org/10.1021/ol103008d.
Повний текст джерелаNa, Lu-Xin, Xu-Lin Sun, Meng Wang, Kun-Feng Li, Lei Xing, Zhuo Chen, Zhu Guan, and Zhen-Jun Yang. "Atropisomerism of diastereomer diribonucleoside phosphotriester." Chinese Chemical Letters 24, no. 1 (January 2013): 13–16. http://dx.doi.org/10.1016/j.cclet.2013.01.018.
Повний текст джерелаSummers, Thomas J., Hrishikesh Tupkar, Tyler M. Ozvat, Zoë Tregillus, Kenneth A. Miller, and Nathan J. DeYonker. "Computational Insight into the Rope-Skipping Isomerization of Diarylether Cyclophanes." Symmetry 13, no. 11 (November 9, 2021): 2127. http://dx.doi.org/10.3390/sym13112127.
Повний текст джерелаWang, Haimang, Jianfeng Li, and W. Robert Scheidt. "Picket fence porphyrin challenges. Unexpected atropisomerism." Journal of Porphyrins and Phthalocyanines 22, no. 11 (October 18, 2018): 981–88. http://dx.doi.org/10.1142/s1088424618500943.
Повний текст джерелаAllaoud, Smail, Touriya Zair, Abdallah Karim, and Bernard Frange. "Atropisomerism in o-aryl-substituted borazines." Inorganic Chemistry 29, no. 7 (April 1990): 1447–49. http://dx.doi.org/10.1021/ic00332a035.
Повний текст джерелаCrossley, Maxwell J., Leslie D. Field, Adrienne J. Forster, Margaret M. Harding, and Sever Sternhell. "Steric effects on atropisomerism in tetraarylporphyrins." Journal of the American Chemical Society 109, no. 2 (January 1987): 341–48. http://dx.doi.org/10.1021/ja00236a008.
Повний текст джерелаPaul, Bishwajit, Glenn L. Butterfoss, Mikki G. Boswell, Mia L. Huang, Richard Bonneau, Christian Wolf, and Kent Kirshenbaum. "N-Naphthyl Peptoid Foldamers Exhibiting Atropisomerism." Organic Letters 14, no. 3 (January 24, 2012): 926–29. http://dx.doi.org/10.1021/ol203452f.
Повний текст джерелаZhang, Kan, Yuqi Liu, Zhikun Shang, Corey Evans, and Shengfu Yang. "Effects of End-Caps on the Atropisomerization, Polymerization, and the Thermal Properties of ortho-Imide Functional Benzoxazines." Polymers 11, no. 3 (March 1, 2019): 399. http://dx.doi.org/10.3390/polym11030399.
Повний текст джерелаMöhrle, H., and M. Jeandrée. "Darstellung und Atropisomerie von 1-[2-(2,2-Dimethylpiperidino)phenyl]ethanol." Scientia Pharmaceutica 69, no. 1 (March 30, 2001): 1–10. http://dx.doi.org/10.3797/scipharm.aut-01-01.
Повний текст джерелаBeattie, Nicola J., Craig L. Francis, Andris J. Liepa, and G. Paul Savage. "Spiroheterocycles via Regioselective Cycloaddition Reactions of Nitrile Oxides with 5-Methylene-1H-pyrrol-2(5H)-ones." Australian Journal of Chemistry 63, no. 3 (2010): 445. http://dx.doi.org/10.1071/ch09479.
Повний текст джерелаGu, Zhenhua, and Jia Feng. "Atropisomerism in Styrene: Synthesis, Stability, and Applications." SynOpen 05, no. 01 (January 2021): 68–85. http://dx.doi.org/10.1055/s-0040-1706028.
Повний текст джерелаToenjes, Sean T., and Jeffrey L. Gustafson. "Atropisomerism in medicinal chemistry: challenges and opportunities." Future Medicinal Chemistry 10, no. 4 (February 2018): 409–22. http://dx.doi.org/10.4155/fmc-2017-0152.
Повний текст джерелаConsoli, Grazia M. L., Francesca Cunsolo, Corrada Geraci, Enrico Gavuzzo, and Placido Neri. "Atropisomerism in 1,5-Bridged Calix[8]arenes†." Organic Letters 4, no. 16 (August 2002): 2649–52. http://dx.doi.org/10.1021/ol026185r.
Повний текст джерелаAlcock, Nathaniel W., John M. Brown, and Jesús J. Pérez-Torrente. "Atropisomerism in asymmetric cis-diphosphine arylplatinum complexes." Tetrahedron Letters 33, no. 3 (January 1992): 389–92. http://dx.doi.org/10.1016/s0040-4039(00)74139-6.
Повний текст джерелаVeljković, Jelena, Ivana Antol, Nikola Basarić, Vilko Smrečki, Krešimir Molčanov, Norbert Müller, and Kata Mlinarić-Majerski. "Atropisomerism in 1-(2-adamantyl)naphthalene Derivatives." Journal of Molecular Structure 1046 (August 2013): 101–9. http://dx.doi.org/10.1016/j.molstruc.2013.04.027.
Повний текст джерелаGlunz, Peter W. "Recent encounters with atropisomerism in drug discovery." Bioorganic & Medicinal Chemistry Letters 28, no. 2 (January 2018): 53–60. http://dx.doi.org/10.1016/j.bmcl.2017.11.050.
Повний текст джерелаClayden, Jonathan, Wesley J Moran, Paul J Edwards, and Steven R LaPlante. "The Challenge of Atropisomerism in Drug Discovery." Angewandte Chemie International Edition 48, no. 35 (August 17, 2009): 6398–401. http://dx.doi.org/10.1002/anie.200901719.
Повний текст джерелаConstable, Edwin C., Richard M. Hartshorn, and Catherine E. Housecroft. "1,1′-Biisoquinolines—Neglected Ligands in the Heterocyclic Diimine Family That Provoke Stereochemical Reflections." Molecules 26, no. 6 (March 13, 2021): 1584. http://dx.doi.org/10.3390/molecules26061584.
Повний текст джерелаCarroll, AR, and WC Taylor. "Constituents of Eupomatia Species. xiv. The Structures of Eupomatilone-1, -2, -3, -4, -5, -6 and -7 Isolated From Eupomatia Bennettii." Australian Journal of Chemistry 44, no. 12 (1991): 1705. http://dx.doi.org/10.1071/ch9911705.
Повний текст джерелаRyan, Sarah J., Craig L. Francis, and G. Paul Savage. "Benzonitrile Oxide Cycloadditions with Exocyclic Methylene Benzothiazepine Dioxides." Australian Journal of Chemistry 67, no. 3 (2014): 381. http://dx.doi.org/10.1071/ch13444.
Повний текст джерелаAlkorta, Ibon, José Elguero, Artur M. S. Silva, and Augusto C. Tomé. "A theoretical study of the conformation of meso-tetraphenylporphyrin (TPPH2), its anions, cations and metal complexes (Mg2+, Ca2+ and Zn2+)." Journal of Porphyrins and Phthalocyanines 14, no. 07 (July 2010): 630–38. http://dx.doi.org/10.1142/s1088424610002409.
Повний текст джерелаTomé, Augusto C., Artur M. S. Silva, Ibon Alkorta, and José Elguero. "Atropisomerism and conformational aspects of meso-tetraarylporphyrins and related compounds." Journal of Porphyrins and Phthalocyanines 15, no. 01 (January 2011): 1–28. http://dx.doi.org/10.1142/s1088424611002994.
Повний текст джерелаLloyd-Williams, Paul, and Ernest Giralt. "Atropisomerism, biphenyls and the Suzuki coupling: peptide antibiotics." Chemical Society Reviews 30, no. 3 (2001): 145–57. http://dx.doi.org/10.1039/b001971m.
Повний текст джерелаBoger, Dale L., Steven L. Castle, Susumu Miyazaki, Jason H. Wu, Richard T. Beresis, and Olivier Loiseleur. "Vancomycin CD and DE Macrocyclization and Atropisomerism Studies." Journal of Organic Chemistry 64, no. 1 (January 1999): 70–80. http://dx.doi.org/10.1021/jo980880o.
Повний текст джерелаNakamura, Takashi, Nobuaki Waizumi, Koichi Tsuruta, Yoshiaki Horiguchi, and Isao Kuwajima. "Synthesis of the Taxol Derivatives: Control of Atropisomerism." Synlett 1994, no. 08 (1994): 584–86. http://dx.doi.org/10.1055/s-1994-22934.
Повний текст джерелаWang, C. H., J. Reilly, N. Brand, S. Schwartz, S. Alluri, T. M. Chan, A. V. Buevich, and A. K. Ganguly. "Synthesis and atropisomerism of 2,2′-ortho disubstituted biphenyls." Tetrahedron Letters 51, no. 48 (December 2010): 6213–15. http://dx.doi.org/10.1016/j.tetlet.2010.09.010.
Повний текст джерелаHowarth, Ashlee J., David L. Davies, Francesco Lelj, Michael O. Wolf, and Brian O. Patrick. "Atropisomerism in a thermally switchable, cyclometallated iridium complex." Dalton Transactions 41, no. 34 (2012): 10150. http://dx.doi.org/10.1039/c2dt31120h.
Повний текст джерелаSeifert, Nathan A., Cristóbal Pérez, Justin L. Neill, Brooks H. Pate, Montserrat Vallejo-López, Alberto Lesarri, Emilio J. Cocinero, and Fernando Castaño. "Chiral recognition and atropisomerism in the sevoflurane dimer." Physical Chemistry Chemical Physics 17, no. 28 (2015): 18282–87. http://dx.doi.org/10.1039/c5cp01025j.
Повний текст джерелаNguyen, Thanh V, David J Sinclair, Anthony C Willis, and Michael S Sherburn. "Guest Binding Drives Reversible Atropisomerism in Cavitand Hosts." Chemistry - A European Journal 15, no. 24 (June 8, 2009): 5892–95. http://dx.doi.org/10.1002/chem.200900695.
Повний текст джерелаO’Connor, Stephen P., Ying Wang, Ligaya M. Simpkins, Robert P. Brigance, Wei Meng, Aiying Wang, Mark S. Kirby, Carolyn A. Weigelt, and Lawrence G. Hamann. "Synthesis, SAR, and atropisomerism of imidazolopyrimidine DPP4 inhibitors." Bioorganic & Medicinal Chemistry Letters 20, no. 21 (November 2010): 6273–76. http://dx.doi.org/10.1016/j.bmcl.2010.08.090.
Повний текст джерелаRoszkowski, Piotr, Dariusz Błachut, Jan K. Maurin, Magdalena Woźnica, Jadwiga Frelek, Franciszek Pluciński, and Zbigniew Czarnocki. "Atropisomerism in 3,4,5-Tri-(2-methoxyphenyl)-2,6-lutidine." European Journal of Organic Chemistry 2013, no. 35 (November 12, 2013): 7867–71. http://dx.doi.org/10.1002/ejoc.201301378.
Повний текст джерелаOntiveros-Rodríguez, Julio C., Eleuterio Burgueño-Tapia, Javier Porras-Ramírez, Pedro Joseph-Nathan, and L. Gerardo Zepeda. "Configurational Study of an Aporphine Alkaloid from Annona purpurea." Natural Product Communications 13, no. 7 (July 2018): 1934578X1801300. http://dx.doi.org/10.1177/1934578x1801300711.
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