Статті в журналах з теми "Heterocyclic Carbene"
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Longevial, Jean-François, Mamadou Lo, Aurélien Lebrun, Danielle Laurencin, Sébastien Clément, and Sébastien Richeter. "Molecular complexes and main-chain organometallic polymers based on Janus bis(carbenes) fused to metalloporphyrins." Dalton Transactions 49, no. 21 (2020): 7005–14. http://dx.doi.org/10.1039/d0dt00594k.
Повний текст джерелаZhu, Yannan, and You Huang. "Organocatalyzed [3+3] Annulations for the Construction of Heterocycles." Synthesis 52, no. 08 (February 5, 2020): 1181–202. http://dx.doi.org/10.1055/s-0039-1690810.
Повний текст джерелаFernando, Jared, Alison Levens, Daniel Moock, and David Lupton. "N-Heterocyclic Carbene Catalyzed Transformylation." Synthesis 49, no. 15 (June 12, 2017): 3505–10. http://dx.doi.org/10.1055/s-0036-1588449.
Повний текст джерелаLeitão, Maria Inês P. S., Giulia Francescato, Clara S. B. Gomes, and Ana Petronilho. "Synthesis of Platinum(II) N-Heterocyclic Carbenes Based on Adenosine." Molecules 26, no. 17 (September 4, 2021): 5384. http://dx.doi.org/10.3390/molecules26175384.
Повний текст джерелаDong, Zhaowen, Cristian Pezzato, Andrzej Sienkiewicz, Rosario Scopelliti, Farzaneh Fadaei-Tirani, and Kay Severin. "SET processes in Lewis acid–base reactions: the tritylation of N-heterocyclic carbenes." Chemical Science 11, no. 29 (2020): 7615–18. http://dx.doi.org/10.1039/d0sc01278e.
Повний текст джерелаFujita, Ken-ichi, Junichi Sato, and Hiroyuki Yasuda. "Tautomerization of 5-Alkylidene-2-Oxazolidinone to 2-Oxazolone by Use of an N-Heterocyclic Carbene Catalyst." Synlett 26, no. 08 (March 3, 2015): 1106–10. http://dx.doi.org/10.1055/s-0034-1380274.
Повний текст джерелаZhao, Shixian, Feifei Wu, Yuyu Ma, Wanzhi Chen, Miaochang Liu, and Huayue Wu. "Enhancement of N-heterocyclic carbenes on rhodium catalyzed olefination of triazoles." Organic & Biomolecular Chemistry 14, no. 8 (2016): 2550–55. http://dx.doi.org/10.1039/c5ob02397a.
Повний текст джерелаHollóczki, Oldamur. "Unveiling the peculiar hydrogen bonding behavior of solvated N-heterocyclic carbenes." Physical Chemistry Chemical Physics 18, no. 1 (2016): 126–40. http://dx.doi.org/10.1039/c5cp05369b.
Повний текст джерелаWu, Wenchao, Shuangli Xu, Yan Zhang, Xiu Wang, Ruotong Li, Fang Sun, Chenxia Yu, Tuanjie Li, Donghui Wei та Changsheng Yao. "NHC-catalyzed β-specific addition of N-based nucleophiles to allenoates". Organic Chemistry Frontiers 7, № 13 (2020): 1593–99. http://dx.doi.org/10.1039/d0qo00189a.
Повний текст джерелаHata, Kazuhiro, Hideto Ito, Yasutomo Segawa, and Kenichiro Itami. "Pyridylidene ligand facilitates gold-catalyzed oxidative C–H arylation of heterocycles." Beilstein Journal of Organic Chemistry 11 (December 28, 2015): 2737–46. http://dx.doi.org/10.3762/bjoc.11.295.
Повний текст джерелаGraham, David C., and Brian F. Yates. "Increased Stability of NO and NS Heterocyclic Carbenes?" Australian Journal of Chemistry 57, no. 4 (2004): 359. http://dx.doi.org/10.1071/ch03248.
Повний текст джерелаDas, Tamal Kanti, and Akkattu T. Biju. "Imines as acceptors and donors in N-heterocyclic carbene (NHC) organocatalysis." Chemical Communications 56, no. 61 (2020): 8537–52. http://dx.doi.org/10.1039/d0cc03290e.
Повний текст джерелаIversen, Kalon J., David J. D. Wilson, and Jason L. Dutton. "Activation of the C–N bond of N-heterocyclic carbenes by inorganic elements." Dalton Trans. 43, no. 34 (2014): 12820–23. http://dx.doi.org/10.1039/c4dt00946k.
Повний текст джерелаGehrke, Sascha, and Oldamur Hollóczki. "A molecular mechanical model for N-heterocyclic carbenes." Physical Chemistry Chemical Physics 18, no. 32 (2016): 22070–80. http://dx.doi.org/10.1039/c6cp02624a.
Повний текст джерелаAndrada, Diego M., Nicole Holzmann, Thomas Hamadi та Gernot Frenking. "Direct estimate of the internal π-donation to the carbene centre within N-heterocyclic carbenes and related molecules". Beilstein Journal of Organic Chemistry 11 (24 грудня 2015): 2727–36. http://dx.doi.org/10.3762/bjoc.11.294.
Повний текст джерелаZhang, Zhen-Zhen, Yongna Zhang, Hui-Xin Duan, Zhuo-Fei Deng та You-Qing Wang. "Enantioselective (3+2) cycloaddition via N-heterocyclic carbene-catalyzed addition of homoenolates to cyclic N-sulfonyl trifluoromethylated ketimines: synthesis of fused N-heterocycle γ-lactams". Chemical Communications 56, № 10 (2020): 1553–56. http://dx.doi.org/10.1039/c9cc09269b.
Повний текст джерелаGao, Yafei, Qi Chen, Xuebing Leng, and Liang Deng. "Cyclometallation reactions of a three-coordinate cobalt(i) complex bearing a nonsymmetric N-heterocyclic carbene ligand." Dalton Transactions 48, no. 26 (2019): 9676–83. http://dx.doi.org/10.1039/c9dt00731h.
Повний текст джерелаDe Vreese, Rob, and Matthias D’hooghe. "N-Heterocyclic carbene/Brønsted acid cooperative catalysis as a powerful tool in organic synthesis." Beilstein Journal of Organic Chemistry 8 (March 14, 2012): 398–402. http://dx.doi.org/10.3762/bjoc.8.43.
Повний текст джерелаWalker, James A., and Levi M. Stanley. "N-Heterocyclic carbene-catalysed intramolecular hydroacylation to form basic nitrogen-containing heterocycles." Organic & Biomolecular Chemistry 14, no. 42 (2016): 9981–84. http://dx.doi.org/10.1039/c6ob01956k.
Повний текст джерелаGehrke, Sascha, and Oldamur Hollóczki. "N‐Heterocyclic Carbene Organocatalysis: With or Without Carbenes?" Chemistry – A European Journal 26, no. 44 (July 23, 2020): 10140–51. http://dx.doi.org/10.1002/chem.202002656.
Повний текст джерелаGehrke, Sascha, and Oldamur Hollóczki. "Are There Carbenes in N-Heterocyclic Carbene Organocatalysis?" Angewandte Chemie International Edition 56, no. 51 (November 22, 2017): 16395–98. http://dx.doi.org/10.1002/anie.201708305.
Повний текст джерелаFrański, Rafał, Błażej Gierczyk, Grzegorz Schroeder, Stefan Pieper, Andreas Springer, and Michael Linscheid. "Electrospray ionization mass spectrometric study of mercury complexes of N-heterocyclic carbenes derived from 1,2,4-triazolium salt precursors." Open Chemistry 5, no. 1 (March 1, 2007): 316–29. http://dx.doi.org/10.2478/s11532-006-0050-0.
Повний текст джерелаAl Furaiji, Khalidah H. M., Andrew Molino, Jason L. Dutton, and David J. D. Wilson. "Theoretical Investigation of Main-Group Element Hydride Insertion into Phosphorus-Heterocyclic Carbenes (PHCs)." Australian Journal of Chemistry 73, no. 8 (2020): 787. http://dx.doi.org/10.1071/ch19487.
Повний текст джерелаNonnenmacher, Michael, Dominik M. Buck, and Doris Kunz. "Experimental and theoretical investigations on the high-electron donor character of pyrido-annelated N-heterocyclic carbenes." Beilstein Journal of Organic Chemistry 12 (August 23, 2016): 1884–96. http://dx.doi.org/10.3762/bjoc.12.178.
Повний текст джерелаHasson, Mohammed Mujbel, Basim H. Al-Zaidi, and Ahmad H. Ismail. "Synthesis and Characterization of Ag(I) Complexes Derived from New N-Heterocyclic Carbenes." Asian Journal of Chemistry 31, no. 5 (March 28, 2019): 1149–52. http://dx.doi.org/10.14233/ajchem.2019.21877.
Повний текст джерелаKelemen, Z., R. Streubel, and L. Nyulászi. "Zwitterionic carbene adducts and their carbene isomers." RSC Advances 5, no. 52 (2015): 41795–802. http://dx.doi.org/10.1039/c5ra07039b.
Повний текст джерелаKassam, Karim, and John Warkentin. "Reactions of dialkoxycarbenes with tethered triple bonds to form heterocyclic compounds." Canadian Journal of Chemistry 75, no. 2 (February 1, 1997): 120–28. http://dx.doi.org/10.1139/v97-016.
Повний текст джерелаDash, Chandrakanta, Animesh Das, and H. V. Rasika Dias. "Mercury(II) Complexes of Anionic N-Heterocyclic Carbene Ligands: Steric Effects of the Backbone Substituent." Molecules 25, no. 16 (August 16, 2020): 3741. http://dx.doi.org/10.3390/molecules25163741.
Повний текст джерелаBarnett, Harrison J., and Anthony F. Hill. "A Dirhoda‐Heterocyclic Carbene." Angewandte Chemie International Edition 59, no. 11 (January 29, 2020): 4274–77. http://dx.doi.org/10.1002/anie.201912650.
Повний текст джерелаBarnett, Harrison J., and Anthony F. Hill. "A Dirhoda‐Heterocyclic Carbene." Angewandte Chemie 132, no. 11 (March 9, 2020): 4304–7. http://dx.doi.org/10.1002/ange.201912650.
Повний текст джерелаOno, Shintaro, Takashi Watanabe, Yosuke Nakamura, Hiroyasu Sato, Toru Hashimoto, and Yoshitaka Yamaguchi. "Synthesis of N -heterocyclic carbene boranes via silver N -heterocyclic carbene complexes." Polyhedron 137 (November 2017): 296–305. http://dx.doi.org/10.1016/j.poly.2017.08.045.
Повний текст джерелаMichalak and Kośnik. "Chiral N-heterocyclic Carbene Gold Complexes: Synthesis and Applications in Catalysis." Catalysts 9, no. 11 (October 25, 2019): 890. http://dx.doi.org/10.3390/catal9110890.
Повний текст джерелаDzieszkowski, Krzysztof, and Zbigniew Rafiński. "N-Heterocyclic Carbene Catalysis under Oxidizing Conditions." Catalysts 8, no. 11 (November 16, 2018): 549. http://dx.doi.org/10.3390/catal8110549.
Повний текст джерелаZhou, Bi-Hui, Wei-Ping He, Lin-Lin Li, Li-Mei Fan, Xiang-Rong Li, and Jie Li. "Synthesis of Novel Chiral Pyrimidone Salts and their Application in Asymmetric Diethylzinc Addition of Arylaldehydes." Current Organic Synthesis 15, no. 1 (March 20, 2018): 137–42. http://dx.doi.org/10.2174/1570179414666170830130658.
Повний текст джерелаBoubakri, Lamia, A. Chakchouk-Mtibaa, Abdullah S. Al-Ayed, L. Mansour, Nael Abutaha, Abdel Halim Harrath, L. Mellouli, I. Özdemir, S. Yasar, and Naceur Hamdi. "Ru(ii)–N-heterocyclic carbene complexes: synthesis, characterization, transfer hydrogenation reactions and biological determination." RSC Advances 9, no. 59 (2019): 34406–20. http://dx.doi.org/10.1039/c9ra05605j.
Повний текст джерелаBrückner, Tobias, Merle Arrowsmith, Merlin Heß, Kai Hammond, Marcel Müller, and Holger Braunschweig. "Synthesis of fused B,N-heterocycles by alkyne cleavage, NHC ring-expansion and C–H activation at a diboryne." Chemical Communications 55, no. 47 (2019): 6700–6703. http://dx.doi.org/10.1039/c9cc02657f.
Повний текст джерелаLe, Nguyen Nhat Thu, Josefine Just, Jonathan M. Pankauski, Paul R. Rablen, and Dasan M. Thamattoor. "Ring Expansion of Alkylidenecarbenes Derived from Lactams, Lactones, and Thiolactones into Strained Heterocyclic Alkynes: A Theoretical Study." Molecules 24, no. 3 (February 7, 2019): 593. http://dx.doi.org/10.3390/molecules24030593.
Повний текст джерелаLin, Ivan JB, and Chandra Sekhar Vasam. "Review of gold(I) N-heterocyclic carbenes." Canadian Journal of Chemistry 83, no. 6-7 (June 1, 2005): 812–25. http://dx.doi.org/10.1139/v05-087.
Повний текст джерелаMariconda, Annaluisa, Marco Sirignano, Rubina Troiano, Simona Russo, and Pasquale Longo. "N-heterocyclic Carbene Gold Complexes Active in Hydroamination and Hydration of Alkynes." Catalysts 12, no. 8 (July 29, 2022): 836. http://dx.doi.org/10.3390/catal12080836.
Повний текст джерелаAzizi, Zahra, Mehdi Ghambarian, Mohammad A. Rezaei, and Mohammad Ghashghaee. "Saturated N,X-Heterocyclic Carbenes (X=N, O, S, P, Si, C, and B): Stability, Nucleophilicity, and Basicity." Australian Journal of Chemistry 68, no. 9 (2015): 1438. http://dx.doi.org/10.1071/ch14715.
Повний текст джерелаHo, Peter C., Hilary A. Jenkins, James F. Britten, and Ignacio Vargas-Baca. "Building new discrete supramolecular assemblies through the interaction of iso-tellurazole N-oxides with Lewis acids and bases." Faraday Discussions 203 (2017): 187–99. http://dx.doi.org/10.1039/c7fd00075h.
Повний текст джерелаGroso, Emilia, and Corinna Schindler. "Recent Advances in the Application of Ring-Closing Metathesis for the Synthesis of Unsaturated Nitrogen Heterocycles." Synthesis 51, no. 05 (February 8, 2019): 1100–1114. http://dx.doi.org/10.1055/s-0037-1611651.
Повний текст джерелаXu, Xinfang, and Michael P. Doyle. "Recent Developments in the Synthetic Uses of Silyl-protected Enoldiazoacetates for Heterocyclic Syntheses." Australian Journal of Chemistry 67, no. 3 (2014): 365. http://dx.doi.org/10.1071/ch13576.
Повний текст джерелаJandl, Christian, and Alexander Pöthig. "A hybrid carbocyclic/N-heterocyclic carbene ligand." Chemical Communications 53, no. 13 (2017): 2098–101. http://dx.doi.org/10.1039/c6cc08468k.
Повний текст джерелаRitleng, Vincent, and Christophe Michon. "Bidentate Donor-Functionalized N-Heterocyclic Carbenes: Valuable Ligands for Ruthenium-Catalyzed Transfer Hydrogenation." Molecules 27, no. 15 (July 23, 2022): 4703. http://dx.doi.org/10.3390/molecules27154703.
Повний текст джерелаŠegina, Jan, Luka Ciber, Helena Brodnik, Franc Požgan, Jurij Svete, Bogdan Štefane, and Uroš Grošelj. "Synthesis of Six-Membered N-Heterocyclic Carbene Precursors Based on Camphor." Molecules 28, no. 24 (December 6, 2023): 7973. http://dx.doi.org/10.3390/molecules28247973.
Повний текст джерелаTang, Xiang-Ting, Fan Yang, Ting-Ting Zhang, Yi-Fan Liu, Si-Yu Liu, Tong-Fu Su, Dong-Can Lv, and Wen-Bo Shen. "Recent Progress in N-Heterocyclic Carbene Gold-Catalyzed Reactions of Alkynes Involving Oxidation/Amination/Cycloaddition." Catalysts 10, no. 3 (March 20, 2020): 350. http://dx.doi.org/10.3390/catal10030350.
Повний текст джерелаOjha, Minita, Shweta Choudhary, and Raj K. Bansal. "3-Benzylbenzothiazolylidene Carbene Catalyzed Isomerization of Dimethyl Maleate to Dimethyl Fumarate: Experimental and Theoretical Results." Current Organocatalysis 7, no. 2 (July 2, 2020): 108–17. http://dx.doi.org/10.2174/2213337206666191018111354.
Повний текст джерелаHongfa, Chayanant, Haw-Lih Su, Hassan S. Bazzi, and David E. Bergbreiter. "Polyisobutylene-AnchoredN-Heterocyclic Carbene Ligands." Organic Letters 11, no. 3 (February 5, 2009): 665–67. http://dx.doi.org/10.1021/ol802728t.
Повний текст джерелаMaki, Brooks E., Audrey Chan, Eric M. Phillips, and Karl A. Scheidt. "N-Heterocyclic carbene-catalyzed oxidations." Tetrahedron 65, no. 16 (April 2009): 3102–9. http://dx.doi.org/10.1016/j.tet.2008.10.033.
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