, Chem. Soc. Rev, vol.36, pp.67-76, 2007.
, Coord. Chem. Rev, vol.386, pp.96-118, 2019.
, Chem.-Asian J, vol.13, pp.2164-2173, 2018.
, Chem. Soc. Rev, vol.49, pp.1487-1516, 2020.
, J. Org. Chem, vol.73, pp.590-593, 2008.
, Adv. Synth. Catal, vol.350, pp.2967-2974, 2008.
, Nat. Chem, vol.10, pp.1016-1022, 2018.
, Chem. Sci, vol.6, pp.6190-6196, 2015.
, For an early study in the gas phase, vol.51, pp.3812-3817, 2012.
Ar)X] + complexes by halide abstraction using silver salts or supramolecular cages, see: (a), J. Am. Chem. Soc, vol.138, issue.3, pp.1701-1706, 2016. ,
, For the detection of aryl-phosphoniums as side-products in gold-catalyzed transformations, see: (a), vol.136, pp.11093-11099, 2014.
, Chem.-Eur. J, vol.26, pp.4226-4231, 2020.
, Chin. J. Chem, vol.36, pp.1213-1221, 2018.
, For reviews dealing with Cu-catalyzed C-P coupling reactions, vol.248, pp.52824-52831, 2004.
, Polyhedron, vol.8, pp.1039-1043, 1989.
, Organometallics, vol.34, pp.3497-3507, 2015.
, Chem. Commun, vol.52, pp.5057-5060, 2016.
For the C-H arylation of (benz)imidazolium salts with aryl iodides using 20 mol% of Cu 2 O, see: S, Chem. Commun, vol.53, pp.3489-3492, 2017. ,
, J. Am. Chem. Soc, vol.136, pp.1778-1781, 2014.
, Angew. Chem. Int. Ed, vol.54, pp.11920-11929, 2015.
, Organometallics, vol.35, pp.995-1001, 2016.
, Chem.-Eur. J, vol.24, pp.11922-11925, 2018.
, Angew. Chem. Int. Ed, vol.41, pp.2808-2817, 2002.
, Dalton Trans, pp.7883-7884, 2009.
, A peri-bridged naphthyl phosphonium has been proposed as a transient intermediate in the reaction of 1,8-bis(diphenylphosphino)naphthalene with 1,8-bis(bromomethyl)naphthalene, see, Tetrahedron, vol.69, pp.1628-1633, 2013.
, Angew. Chem. Int. Ed, vol.136, pp.1306-1310, 2014.
, See the ESI for details
, Dalton Trans, pp.1099-1106, 1987.
, For structurally characterized bis(phosphine)CuX complexes, see for example, vol.48, pp.12809-12820, 2009.
, J. Am. Chem. Soc, vol.135, pp.13827-13834, 2013.
, Angew. Chem. Int. Ed, vol.54, pp.15022-15045, 2015.
, Angew. Chem. Int. Ed, vol.55, pp.3414-3418, 2016.
, Angew. Chem. Int. Ed, vol.8, pp.12264-12267, 2017.
, Angew. Chem. Int. Ed, vol.57, pp.11732-11736, 2018.
, Angew. Chem. Int. Ed, vol.517, pp.7884-7887, 2015.
, Angew. Chem. Int. Ed, vol.54, pp.5556-5558, 2015.
, Stable organocopper(III) species have been prepared using macrocyclic N-containing ligands, vol.122, pp.6883-6892, 2000.
, Angew. Chem. Int. Ed, vol.41, pp.5696-5705, 2002.
, The differences in C-X bond strengths are roughly compensated by those in Cu-X bond strengths
, Toste et al assessed the possibility for (P,C)-cyclometallated Au(III) complexes to undergo P-C reductive elimination, but no peri-bridged naphthyl phosphonium was detected, p.10
, J. Am. Chem. Soc, vol.127, pp.1446-1453, 2005.
, J. Am. Chem. Soc, vol.126, pp.1755-1763, 2004.
, Chem.-Eur. J, vol.23, pp.5357-5360, 2017.
, Bull. Chem. Soc. Jpn, vol.92, pp.1131-1141, 2019.
, Acc. Chem. Res, vol.106, pp.8291-8331, 2006.