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Title:	One-Pot Synthesis of Ferrocenyl Ketones Containing Biaryls and 6-Aryl-2-ferrocenylquinolines via Ir/Pd-Cocatalyzed α-Alkylation/Suzuki Reaction
Source:	Journal of Organic Chemistry [0022-3263] Xu, Chen yr:2013

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description	1.	Baumann, U. Fresenius' Zeitschrift für Analytische Chemie 174.4 (1960): 296-296.
description	2.	Khedkar, Mayur V. "Efficient, recyclable and phosphine-free carbonylative Suzuki coupling reaction using immobilized palladium ion-containing ionic liquid: synthesis of aryl ketones and heteroaryl ketones." RSC Advances 3.21 (2013): 7791-7797.
description	3.	Hamera, R. Synlett : accounts and rapid communications in synthetic organic chemistry 26.14 (2015): 2047-2048.
description	4.	Hudson, Zachary M. "Assembly and Disassembly of Ferrocene-Based Nanotubes." Science 344.6183 (2014): 482-483.
description	5.	Cao, Q. "Ferrocene-based novel electrochemical In3+ sensor." Tetrahedron letters 52.34 (2011): 4464-4467.
description	6.	KEALY, T. J. "A NEW TYPE OF ORGANO-IRON COMPOUND." Nature 168.4285 (1951): 1039-1040.
description	7.	Rausch, M. "Ferrocene: a novel organometallic compound." Journal of Chemical Education 34.6 (1957): 268-272.
description	8.	Wu, X. "Palladium-catalyzed carbonylative coupling of aryl iodides and benzyl acetylenes to 3-alkylidenefuran-2-ones under mild conditions and its density functional theory modeling." Chemistry - A European Journal 18.50 (2012): 16177-85.
description	9.	O'Keefe, B. "Facile access to sterically hindered aryl ketones via carbonylative cross-coupling: application to the total synthesis of luteolin." Tetrahedron 67.24 (2011): 4344-4351.
description	10.	Prediger, P. "Palladium-catalyzed Suzuki cross-coupling of 2-haloselenophenes: Synthesis of 2-arylselenophenes, 2,5-diarylselenophenes, and 2-arylselenophenyl ketones." Journal of organic chemistry 71.10 (2006): 3786-3792.
description	11.	Wilkinson, G. "The structure of iron biscyclopentadienyl." Journal of the American Chemical Society 74.8 (1952): 2125-2126.
description	12.	Astruc, D. "Why is Ferrocene so Exceptional?" European journal of inorganic chemistry 2017.1 (2016): 6-29.
description	13.	Togni, A. Ferrocenes: Homogeneous Catalysis, Organic Synthesis, Materials Science. VCH Publishers, 1995.
description	14.	Miller, Samuel A. "114. Dicyclopentadienyliron." Journal of the Chemical Society FEB (1952): 632-635.
description	15.	Miller, Samuel A. Journal of the Chemical Society 74.FEB (1952): 632-635.
description	16.	Jia, L. "A design strategy for the hierarchical fabrication of colloidal hybrid mesostructures." Nature communications 5 (2014): 3882-3882.
description	17.	Zherebetskyy, D. "Hydroxylation of the surface of PbS nanocrystals passivated with oleic acid." Science 344.6190 (2014): 1380-4.
description	18.	Hudson, Zachary M. "Metal-containing triarylboron compounds for optoelectronic applications." Dalton transactions 40.31 (2011): 7805-16.
description	19.	Werner, H. "At Least 60 Years of Ferrocene: The Discovery and Rediscovery of the Sandwich Complexes." Angewandte Chemie (International ed.) 51.25 (2012): 6052-6058.
description	20.	Li, H. "Ligand-Free Pd-Catalyzed Carbonylative Cross-Coupling Reactions under Atmospheric Pressure of Carbon Monoxide: Synthesis of Aryl Ketones and Heteroaromatic Ketones." European journal of organic chemistry 2011.14 (2011): 2662-2667.