Journal articles on the topic 'Cuprate addition'
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Snyder, James P. "Mechanism of Lithium Cuprate Conjugate Addition: Neutral Tetracoordinate CuI Cuprates as Essential Intermediates." Journal of the American Chemical Society 117, no. 44 (November 1995): 11025–26. http://dx.doi.org/10.1021/ja00149a033.
Full textLi, W. M., J. F. Zhao, L. P. Cao, Z. Hu, Q. Z. Huang, X. C. Wang, Y. Liu, et al. "Superconductivity in a unique type of copper oxide." Proceedings of the National Academy of Sciences 116, no. 25 (May 20, 2019): 12156–60. http://dx.doi.org/10.1073/pnas.1900908116.
Full textBreit, Bernhard. "ortho-Diphenylphosphanylbenzoyl-Directed Cuprate Addition to Acyclic Enoates." Angewandte Chemie International Edition 37, no. 4 (March 2, 1998): 525–27. http://dx.doi.org/10.1002/(sici)1521-3773(19980302)37:4<525::aid-anie525>3.0.co;2-m.
Full textWang, Qisi, Karin von Arx, Masafumi Horio, Deepak John Mukkattukavil, Julia Küspert, Yasmine Sassa, Thorsten Schmitt, et al. "Charge order lock-in by electron-phonon coupling in La1.675Eu0.2Sr0.125CuO4." Science Advances 7, no. 27 (June 2021): eabg7394. http://dx.doi.org/10.1126/sciadv.abg7394.
Full textClive, Derrick L. J., Chengzhi Zhang, Yuanxi Zhou, and Yong Tao. "Addition of dimethylphenylsilyl cuprates to vinyl epoxides: Effect of cuprate stoichiometry on stereochemistry and refiochemistry." Journal of Organometallic Chemistry 489, no. 1-2 (March 1995): C35—C37. http://dx.doi.org/10.1016/0022-328x(94)05224-y.
Full textAgterberg, Daniel F., J. C. Séamus Davis, Stephen D. Edkins, Eduardo Fradkin, Dale J. Van Harlingen, Steven A. Kivelson, Patrick A. Lee, Leo Radzihovsky, John M. Tranquada, and Yuxuan Wang. "The Physics of Pair-Density Waves: Cuprate Superconductors and Beyond." Annual Review of Condensed Matter Physics 11, no. 1 (March 10, 2020): 231–70. http://dx.doi.org/10.1146/annurev-conmatphys-031119-050711.
Full textHutchinson, D. K., S. A. Hardinger, and P. L. Fuchs. "Amine-directed addition of cuprate reagents to cyclopentenyl sulfones." Tetrahedron Letters 27, no. 13 (January 1986): 1425–28. http://dx.doi.org/10.1016/s0040-4039(00)84276-8.
Full textMulzer, Johann, Gerd Dürner, and Dirk Trauner. "Formal Total Synthesis of(—)-Morphine by Cuprate Conjugate Addition." Angewandte Chemie International Edition in English 35, no. 2324 (December 1996): 2830–32. http://dx.doi.org/10.1002/anie.199628301.
Full textLv, Bo, and Wei Guo. "The spin pairing symmetry of d-wave superconductor indicated by tunneling spectroscopy." International Journal of Modern Physics B 31, no. 25 (October 10, 2017): 1745017. http://dx.doi.org/10.1142/s0217979217450175.
Full textSalas, P., M. A. Solís, M. Fortes, and F. J. Sevilla. "Thermodynamic properties of underdoped YBa2Cu3O6+x cuprates for several doping values." International Journal of Modern Physics B 31, no. 13 (February 23, 2017): 1750100. http://dx.doi.org/10.1142/s0217979217501004.
Full textMayer, Theo, and Gerhard Maas. "Morpholinoallenes by Conjugate Cuprate Addition to (2-Propynylidene)morpholinium Triflates." Synlett 1990, no. 07 (1990): 399–400. http://dx.doi.org/10.1055/s-1990-21105.
Full textBREIT, B. "ChemInform Abstract: ortho-Diphenylphosphanylbenzoyl-Directed Cuprate Addition to Acyclic Enoates." ChemInform 29, no. 25 (June 22, 2010): no. http://dx.doi.org/10.1002/chin.199825081.
Full textVacher, Antoine, Anissa Amar, Franck Camerel, Yann Molard, Camille Latouche, Thierry Roisnel, Vincent Dorcet, Abdou Boucekkine, Huriye Akdas-Kiliç, and Mathieu Achard. "Modulation of emission properties of phosphine-sulfonate ligand containing copper complexes: playing with solvato-, thermo-, and mechanochromism." Dalton Transactions 48, no. 6 (2019): 2128–34. http://dx.doi.org/10.1039/c8dt04502j.
Full textLipshutz, Bruce H., Stuart H. Dimock, and Brian James. "The role of trimethylsilyl chloride in Gilman cuprate 1,4-addition reactions." Journal of the American Chemical Society 115, no. 20 (October 1993): 9283–84. http://dx.doi.org/10.1021/ja00073a052.
Full textYamanaka, Masahiro, and Eiichi Nakamura. "Theoretical Studies on Solvent and Substituent Effects of Cuprate Conjugate Addition." Organometallics 20, no. 26 (December 2001): 5675–81. http://dx.doi.org/10.1021/om0105270.
Full textÖzdemir, Z. Güven, Ö. Aslan Çataltepe, and Ü. Onbaşlı. "Impedance and dielectric properties of mercury cuprate at nonsuperconducting state." International Journal of Modern Physics B 29, no. 29 (November 13, 2015): 1550205. http://dx.doi.org/10.1142/s0217979215502057.
Full textKranke, Birgit, and Horst Kunz. "Stereoselective synthesis of chiral piperidine derivatives employing arabinopyranosylamine as the carbohydrate auxiliary." Canadian Journal of Chemistry 84, no. 4 (April 1, 2006): 625–41. http://dx.doi.org/10.1139/v06-060.
Full textNakamura, Yasunori, Takehiko Tsukamoto, Kuniyuki Koyama, and Seiichiro Noguchi. "Effect of Ag Addition on the Crystal Growth in Bi Cuprate Superconductors." Materials Transactions, JIM 33, no. 5 (1992): 525–28. http://dx.doi.org/10.2320/matertrans1989.33.525.
Full textSimonelli, Fabio, Giuliano C. Clososki, Alcindo A. dos Santos, Alfredo R. M. de Oliveira, Francisco de A. Marques, and Paulo H. G. Zarbin. "Oxazoline cuprate addition to nitroalkenes: a new route approaching γ-amino acids." Tetrahedron Letters 42, no. 42 (October 2001): 7375–78. http://dx.doi.org/10.1016/s0040-4039(01)01576-3.
Full textCorey, E. J., Reto Naef, and Francis J. Hannon. "Enantioselective conjugate addition of rationally designed chiral cuprate reagents to 2-cycloalkenones." Journal of the American Chemical Society 108, no. 22 (October 1986): 7114–16. http://dx.doi.org/10.1021/ja00282a052.
Full textVrancken, Emmanuel, Pierre Mangeney, and Hélène Gérard. "Li+-Controlled Diastereoselectivity of the Addition of Allenyl Cuprate Reagents to Aldehydes." Synthesis 49, no. 03 (October 18, 2016): 526–31. http://dx.doi.org/10.1055/s-0036-1588613.
Full textSunshine, S. A., T. Siegrist, and L. F. Schneemeyer. "Single crystal growth of cuprates from hydroxide fluxes." Journal of Materials Research 12, no. 5 (May 1997): 1210–13. http://dx.doi.org/10.1557/jmr.1997.0170.
Full textZiegler, Frederick E., and Burton H. Jaynes. "Formation of (±)-forskolin via a cuprate addition to a synthetic dihydropyran-4-one." Tetrahedron Letters 29, no. 17 (1988): 2031–32. http://dx.doi.org/10.1016/s0040-4039(00)87826-0.
Full textAhn, Kwang Hyun, R. Bryan Klassen, and Stephen J. Lippard. "Enantioselective conjugate addition of Grignard reagents to enones catalyzed by chiral cuprate complexes." Organometallics 9, no. 12 (December 1990): 3178–81. http://dx.doi.org/10.1021/om00162a032.
Full textGarside, Diana, David N. Kirk, and Norman M. Waldron. "Synthesis of hydroxylated steroid hormones via conjugate addition of a silyl-cuprate reagent." Steroids 59, no. 12 (December 1994): 702–11. http://dx.doi.org/10.1016/0039-128x(94)90102-3.
Full textEsteban, Gema, Rocío Rincón, Aurelio G. Csákÿ, and Joaquín Plumet. "A Convenient Synthesis of the Central Core of Helioporins, seco-Pseudopterosins and Pseudopterosins via BCA-Annulation Sequence." Natural Product Communications 3, no. 4 (April 2008): 1934578X0800300. http://dx.doi.org/10.1177/1934578x0800300405.
Full textChen, Yan L., Lijie Zhang, Helen M. Chan, and Martin P. Harmer. "Controlled heterogeneous nucleation of melt-textured YBa2Cu3O6+x by addition of Al2O3 particles." Journal of Materials Research 8, no. 9 (September 1993): 2128–33. http://dx.doi.org/10.1557/jmr.1993.2128.
Full textSimonelli, Fabio, Giuliano C. Clososki, Alcindo A. dos Santos, Alfredo R. M. de Oliveira, Francisco de A. Marques, and Paulo H. G. Zarbin. "ChemInform Abstract: Oxazoline Cuprate Addition to Nitroalkenes: A New Route Approaching γ-Amino Acids." ChemInform 33, no. 3 (May 23, 2010): no. http://dx.doi.org/10.1002/chin.200203135.
Full textCooksey, John, Philip Kocienski, and Ying-Fa Li. "A Synthesis of the C1-C9 Fragment of Ionomycin Using Cationic η3-Allylicmolybdenum and -Iron Complexes." Collection of Czechoslovak Chemical Communications 70, no. 10 (2005): 1653–68. http://dx.doi.org/10.1135/cccc20051653.
Full textBreit, Bernhard, and Stephan K. Zahn. "Stereoselective hydroformylation, cuprate addition and domino reactions with the aid of a catalyst directing group." Polyhedron 19, no. 5 (March 2000): 513–15. http://dx.doi.org/10.1016/s0277-5387(99)00397-6.
Full textHamblett, Christopher L., David L. Sloman, Laura T. Kliman, Bruce Adams, Richard G. Ball, and Matthew G. Stanton. "Synthesis of C2-symmetric trans-2,6-diarylpiperidinones via aryl cuprate addition: an unexpected stereochemical outcome." Tetrahedron Letters 48, no. 12 (March 2007): 2079–82. http://dx.doi.org/10.1016/j.tetlet.2007.01.135.
Full textSwingle, Nicole M., K. Vasavi Reddy, and Bryant E. Rossiter. "Enantioselective conjugate addition, part V. Synthesis and testing of scalemic tetraamines as chiral cuprate ligands." Tetrahedron 50, no. 15 (April 1994): 4455–66. http://dx.doi.org/10.1016/s0040-4020(01)89378-9.
Full textSaengchantara, Suthiweth T., and Timothy W. Wallace. "Conjugate addition of cuprate reagents to chromones: A route to 2-substituted chroman-4-ones." Tetrahedron 46, no. 8 (January 1990): 3029–36. http://dx.doi.org/10.1016/s0040-4020(01)88394-0.
Full textAHN, K. H., R. B. KLASSEN, and S. J. LIPPARD. "ChemInform Abstract: Enantioselective Conjugate Addition of Grignard Reagents to Enones Catalyzed by Chiral Cuprate Complexes." ChemInform 22, no. 13 (September 1, 2010): no. http://dx.doi.org/10.1002/chin.199113077.
Full textCHAN, L. P., K. G. LYNN, and D. R. HARSHMAN. "CAN POSITRON 2D–ACAR RESOLVE THE ELECTRONIC STRUCTURE OF HIGH-Tc SUPERCONDUCTORS?" Modern Physics Letters B 06, no. 11 (May 10, 1992): 617–35. http://dx.doi.org/10.1142/s0217984992000715.
Full textBack, Thomas G., Peter G. Blazecka, and M. Vijaya Krishna. "A new synthesis of castasterone and brassinolide from stigmasterol. A concise and stereoselective elaboration of the side chain from a C-22 aldehyde." Canadian Journal of Chemistry 71, no. 2 (February 1, 1993): 156–63. http://dx.doi.org/10.1139/v93-022.
Full textDevaux, Jean-François, Steven V. O'Neil, Nathalie Guillo, and Leo A. Paquette. "Studies Toward an Asymmetric Synthesis of CP-263,114 and CP-225,917." Collection of Czechoslovak Chemical Communications 65, no. 4 (2000): 490–510. http://dx.doi.org/10.1135/cccc20000490.
Full textCossy, Janine, Olivier Mirguet, Domingo Gomez Pardo, and Jean-Roger Desmurs. "A short formal synthesis of paroxetine. Diastereoselective cuprate addition to a chiral racemic olefinic amido ester." Tetrahedron Letters 42, no. 44 (October 2001): 7805–7. http://dx.doi.org/10.1016/s0040-4039(01)01666-5.
Full textKant, Joydeep, Jeanine A. Roth, Carl E. Fuller, Donald G. Walker, Daniel A. Benigni, and Vittorio Farina. "A Novel Approach to Cephalosporins From Allenylazetidinones: A New Cyclization Strategy via Tandem Cuprate Addition-Sulfenylation." Journal of Organic Chemistry 59, no. 17 (August 1994): 4956–66. http://dx.doi.org/10.1021/jo00096a045.
Full textYamanaka, Masahiro, Seiji Mori, and Eiichi Nakamura. "Density Functional Studies on Kinetic Reactivity of “Higher Order” Lipshutz Cuprate in Addition Reaction to Acetylene." Bulletin of the Chemical Society of Japan 75, no. 8 (August 2002): 1815–18. http://dx.doi.org/10.1246/bcsj.75.1815.
Full textJameleddine, Khiari, Kacem Yakdhan, Kraiem Jamil, Ben Hassine Bechir, and Gravel Denis. "STEREOCHEMISTRY OF CONJUGATE ADDITION REACTIONS OF CUPRATE REAGENTS ON CYCLIC ENONES POSSESSING A PROTECTED γ-OXYGEN." Synthetic Communications 32, no. 17 (January 2002): 2719–22. http://dx.doi.org/10.1081/scc-120006038.
Full textKoot, Wim-Jan, Henk Hiemstra, and W. Nico Speckamp. "Stereoselective synthesis of enantiopure 4,5-disubstituted pyrrolidin-2-ones by consecutive cuprate addition and N-acyliminium coupling." Tetrahedron Letters 33, no. 51 (December 1992): 7969–72. http://dx.doi.org/10.1016/s0040-4039(00)74791-5.
Full textBreit, Bernhard. "Controlling Stereoselectivity with the Aid of a Reagent-Directing Group: Hydroformylation, Cuprate Addition, and Domino Reaction Sequences." Chemistry – A European Journal 6, no. 9 (April 28, 2000): 1519–24. http://dx.doi.org/10.1002/(sici)1521-3765(20000502)6:9<1519::aid-chem1519>3.0.co;2-6.
Full textBreit, Bernhard. "Controlling Stereoselectivity with the Aid of a Reagent-Directing Group: Hydroformylation, Cuprate Addition, and Domino Reaction Sequences." Chemistry - A European Journal 6, no. 9 (May 2, 2000): 1519–24. http://dx.doi.org/10.1002/(sici)1521-3765(20000502)6:9<1519::aid-chem1519>3.3.co;2-y.
Full textCanisius, Johannes, T. Andrew Mobley, Stefan Berger, and Norbert Krause. "Mechanism of 1,6-Addition Reactions of Organocuprates: Detailed NMR Spectroscopic Study of a Cuprate–Enyne π Complex." Chemistry - A European Journal 7, no. 12 (June 18, 2001): 2671–75. http://dx.doi.org/10.1002/1521-3765(20010618)7:12<2671::aid-chem26710>3.0.co;2-s.
Full textCini, Melchior, Tracey D. Bradshaw, William Lewis, and Simon Woodward. "Cuprate Addition to a 6-Substituted Pentafulvene - Preparation ofsec-Alkyl-Substituted Titanocene Dichlorides and Their Biological Activity." European Journal of Organic Chemistry 2013, no. 19 (May 15, 2013): 3997–4007. http://dx.doi.org/10.1002/ejoc.201300474.
Full textWelker, Matthias, Simon Woodward, Luis F Veiros, and Maria José Calhorda. "Chemoselectivity as a Delineator of Cuprate Structure in Catalytic 1,4-Addition of Diorganozinc Reagents to Michael Acceptors." Chemistry - A European Journal 16, no. 19 (April 13, 2010): 5620–29. http://dx.doi.org/10.1002/chem.200903310.
Full textNakamura, Eiichi, Masahiro Yamanaka, and Seiji Mori. "Complexation of Lewis Acid with Trialkylcopper(III): On the Origin of BF3-Acceleration of Cuprate Conjugate Addition." Journal of the American Chemical Society 122, no. 8 (March 2000): 1826–27. http://dx.doi.org/10.1021/ja993124o.
Full textYañez-Aulestia, Ana, Qiang Wang, and Heriberto Pfeiffer. "Enhancing CO2 chemisorption on lithium cuprate (Li2CuO2) at moderate temperatures and different pressures by alkaline nitrate addition." Physical Chemistry Chemical Physics 22, no. 5 (2020): 2803–13. http://dx.doi.org/10.1039/c9cp05512f.
Full textBRANDOW, B. H. "PHENOMENOLOGY OF THE VALENCE-FLUCTUATION PAIRING MECHANISM: Tc SYSTEMATICS OF CUPRATES, AND EVIDENCE FOR THIS MECHANISM IN OTHER SUPERCONDUCTORS." International Journal of Modern Physics B 08, no. 27 (December 15, 1994): 3859–86. http://dx.doi.org/10.1142/s0217979294001664.
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