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ChemComm
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DOI: 10.1039/C6CC07032A
COMMUNICATION
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1 For selected reviews on transition-metal-catalyzed C−H funcꢀonalizaꢀon,
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15 For selected examples of branched olefin synthesis starting from
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Aznar, Angew. Chem. Int. Ed., 2007, 46, 5587-5590; (b) A. T. Lindhardt, T.
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2
For selected examples of transition-metal-catalyzed C−H olefinaꢀon,
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3 For selected reviews on directing group assisted C−H olefinaꢀon, see: (a)
D. A. Colby, R. G. Bergman and J. A. Ellman, Chem. Rev., 2010, 110, 624-
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17 See the Supporting Information for a detailed description.
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4 (a) I. Moritanl and Y. Fujiwara, Tetrahedron Lett., 1967, 8, 1119-1122; (b)
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5 Olefin synthesis using unactivated olefin, see: (a) C. Jia, W. Lu, T.
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6 For selected examples of 1,2-disubstituted olefin synthesis via arene C–H
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19 J. Tang, D. Hackenberger and L. J. Goossen, Angew. Chem. Int. Ed. DOI:
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22 J. F. Hartwig, Organotransition Metal Chemistry: From Bonding to
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23 (a) M. Bera, A. Modak, T. Patra, A. Maji and D. Maiti, Org. Lett., 2014,
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24 For diaryl ketone synthesis, see: M. M. Hossain and S.-G. Shyu,
Tetrahedron, 2014, 70, 251-255.
25 For epoxide synthesis, see: M. W. C. Robinson, K. S. Pillinger, I.
Mabbett, D. A. Timms and A. E. Graham, Tetrahedron, 2010, 66, 8377-
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26 For vicinal iodo substituted alkane synthesis, see: M. Jereb, M. Zupan
and S. Stavber, Green Chem., 2005, 7, 100-104.
27 For oxidation of alkenes, see: M. S. Yusubov, R. Y. Yusubova, T. V. Funk,
K.-W. Chi and V. V. Zhdankin, Synthesis, 2009, 2009, 2505-2508.
28 For nitration of olefin, see: S. Maity, S. Manna, S. Rana, T. Naveen, A.
Mallick and D. Maiti, J. Am. Chem. Soc., 2013, 135, 3355-3358.
29 For reduction of olefin, see: G. R. A. Adair, K. K. Kapoor, A. L. B. Scolan
and J. M. J. Williams, Tetrahedron Letters, 2006, 47, 8943-8944.
4 | Chem. Commun., 2016, 00, 1-3
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