Protodeboronation (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Protodeboronation" in English language version.

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  • Roesner, S.; Blair, D. J.; Aggarwal, V. K. "Enantioselective installation of adjacent tertiary benzylic stereocentres using lithiation–borylation–protodeboronation methodology. Application to the synthesis of bifluranol and fluorohexestrol". Chem. Sci. 2015, 6, 3718. doi:10.1039/C4SC03901G
  • Klingensmith, L. M.; Bio, M. M.; Moniz, G. A., "Selective protodeboronation: synthesis of 4-methyl-2-thiopheneboronic anhydride and demonstration of its utility in Suzuki-Miyaura reactions". Tetrahedron Lett. 2007, 48, 8242. doi:10.1016/j.tetlet.2007.09.060
  • Cox, P. A.; Leach, A. G.; Campbell, A. D.; Lloyd-Jones, G. C. "Protodeboronation of Heteroaromatic, Vinyl, and Cyclopropyl Boronic Acids: pH–Rate Profiles, Autocatalysis, and Disproportionation" J. Am. Chem. Soc. 2016, 138, 9145. doi:10.1021/jacs.6b03283
  • Cox, P. A.; Reid, M.; Leach A. G.; Campbell, A. D.; King, E. J.; Lloyd-Jones, G. C. "Base-Catalyzed Aryl-B(OH)2 Protodeboronation Revisited: From Concerted Proton Transfer to Liberation of a Transient Aryl Anion". J. Am. Chem. Soc. 2017, 139, 13156. doi:10.1021/jacs.7b07444
  • Brown, H. C.; Zweifel, G. "Hydroboration. XI. The Hydroboration of Acetylenes—A Convenient Conversion of Internal Acetylenes into cis-Olefins and of Terminal Acetylenes into Aldehydes" J. Am. Chem. Soc. 1961, 83 (18), 3834. doi:10.1021/ja01479a024
  • Billingsley, K. L.; Anderson, K. W.; Buchwald, S. L. "A Highly Active Catalyst for Suzuki–Miyaura Cross-Coupling Reactions of Heteroaryl Compounds". Angew. Chemie Int. Ed. 2006, 45, 3484. doi:10.1002/anie.200600493
  • Chen, J.; Cammers-Goodwin, A. "2-(Fluorophenyl)pyridines by the Suzuki-Miyaura method: Ag2O accelerates coupling over undesired ipso substitution (SNAr) of fluorine" Tetrahedron Lett. 2003, 44, 1503.doi:10.1016/S0040-4039(02)02793-4
  • Nishihara, Y.; Onodera, H.; Osakada, K. "Synthesis and structural characterization of the first unsymmetrical from transmetallation between 2,4,6-trifluorophenylboronic acid and trans-Pd(C6F5)I(PEt3)2" Chem. Commun. 2004, 192. doi:10.1039/b308741g
  • Korenaga, T.; Kosaki, T.; Fukumura, R.; Ema, T.; Sakai, T. "Suzuki-Miyaura coupling reaction using pentafluorophenylboronic acid". Org. Lett. 2005, 7, 4915.doi:10.1021/ol051866i
  • Imao, D.; Glasspoole, B. W.; Laberge, V. S.; Crudden, C. M. "Cross Coupling Reactions of Chiral Secondary Organoboronic Esters With Retention of Configuration". J. Am. Chem. Soc. 2009, 131 (14), 5024.doi:10.1021/ja8094075
  • Leconte, N.; Keromnes-Wuillaume, A.; Suzenet, F.; Guillaumet, G. "Efficient Palladium-Catalyzed Synthesis of Unsymmetrical (Het)aryltetrazines". Synlett 2007, 204.doi:10.1055/s-2007-967991
  • Deng, J. Z.; Paone, D. V.; Ginnetti, A. T.; Kurihara, H.; Dreher, S. D.; Weissman, S. A.; Stauffer, S. R.; Burgey, C. S. "Copper-facilitated Suzuki reactions: application to 2-heterocyclic boronates". Org. Lett. 2009, 11, 345.doi:10.1021/ol802556f
  • Lennox, A. J. J.; Lloyd-Jones, G. C. "The Slow-Release Strategy in Suzuki–Miyaura Coupling". Isr. J. Chem. 2010, 50, 664.doi:10.1002/ijch.201000074
  • Knapp, D. M.; Gillis, E. P.; Burke, M. D. "A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates.". J. Am. Chem. Soc. 2009, 131, 6961.doi:10.1021/ja901416p
  • Molander, G. A.; Ellis, N. "Organotrifluoroborates:  Protected Boronic Acids That Expand the Versatility of the Suzuki Coupling Reaction". Acc. Chem. Res. 2007, 40, 275.doi:10.1021/ar050199q
  • Kuivila, H. G.; Reuwer, J. F.; Mangravite, J. A. "Electrophilic Displacement Reactions. X. General Acid Catalysis in the Protodeboronation of Areneboronic Acids". Can. J. Chem. 1963, 41, 3081. doi:10.1021/ja01470a028
  • Kuivila, H. G.; Nahabedian, K. V. "Electrophilic displacement reactions. XV. Kinetics and Mechanism of the Base-catalyzed Protodeboronation of Areneboronic Acids". J. Am. Chem. Soc. 1961, 83, 2159. doi:10.1139/v63-451