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CCDC 779156 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The via For more detailed crystallographic data, see the CIF
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CCDC 779156 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif. For more detailed crystallographic data, see the CIF.
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We have confirmed that the concept is also applicable to other types of carbon-carbon and carbon-heteroatom bond-forming events. Details will be summarized in due course.
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63849267472
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79953714956
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27544441150
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For the synthesis of spirocyclic compounds with the introduction of a nucleophile, see: a
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Most established methods for the synthesis of functionalized spirocyclic compounds could accommodate the introduction of electrophiles into the structures; for recent studies, see: a
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Most established methods for the synthesis of functionalized spirocyclic compounds could accommodate the introduction of electrophiles into the structures; for recent studies, see: a) X. Zhang, R. C. Larock, J. Am. Chem. Soc. 2005, 127, 12230;
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79953725817
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note
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2) could also be obtained from a series of aryl alkynes 3 in good yields.
-
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35
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0000491742
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For the general utility of alkenyl iodonium salts, see: a
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40
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77954836136
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For new reactivities of iodonium salts uncovered by us, see: a
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For new reactivities of iodonium salts uncovered by us, see: a) T. Dohi, M. Ito, N. Yamaoka, K. Morimoto, H. Fujioka, Y. Kita, Angew. Chem. 2010, 122, 3406;
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55049136075
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For chiral hypervalent iodine compounds developed by us with μ-oxo-bridged structures, see: a
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For chiral hypervalent iodine compounds developed by us with μ-oxo-bridged structures, see: a) T. Dohi, A. Maruyama, N. Takenaga, K. Senami, Y. Minamitsuji, H. Fujioka, S. Caemmerer, Y. Kita, Angew. Chem. 2008, 120, 3847;
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